T. Lerman-Sagie

发表

Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutation

E. Leshinsky‐Silver, D. Lev, S. Gras, 2012, Acta Neuropathologica.

Clinical Correlates of Occipital Intermittent Rhythmic Delta Activity (OIRDA) in Children

T. Lerman-Sagie, N. Watemberg, Ilan Linder, 2007, Epilepsia.

Muscle Glycogen Depletion and Increased Oxidative Phosphorylation Following Status Epilepticus

T. Lerman-Sagie, M. Sadeh, N. Watemberg, 2003, Journal of child neurology.

Clinical phenotypes of infantile onset CACNA1A-related disorder.

E. Bertini, D. Lev, B. Pode-Shakked, 2020, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features

P. May, R. Krause, S. Haas, 2017, Brain : a journal of neurology.

De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies.

Michael R. Johnson, G. Carvill, I. Scheffer, 2016, American journal of human genetics.

GRIN1 mutations cause encephalopathy with infantile‐onset epilepsy, and hyperkinetic and stereotyped movement disorders

D. Lev, N. Matsumoto, M. Shiina, 2015, Epilepsia.

Early onset epileptic encephalopathy caused by de novo SCN8A mutations

E. Leshinsky‐Silver, D. Lev, M. Kubota, 2014, Epilepsia.

Adding Video Recording Increases the Diagnostic Yield of Routine Electroencephalograms in Children with Frequent Paroxysmal Events

T. Lerman-Sagie, N. Watemberg, R. Dabby, 2005, Epilepsia.

Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene

E. Leshinsky‐Silver, D. Lev, M. Knaap, 2014, neurogenetics.

Recurrent Absence Status Epilepticus (Spike-and-Wave Stupor) Associated With Lamotrigine Therapy

D. Lev, T. Lerman-Sagie, N. Watemberg, 2006, Journal of child neurology.

Multiplex families with epilepsy

G. Carvill, I. Scheffer, H. Mefford, 2016, Neurology.

Founder Effect with Variable Age at Onset in Arab Families with Lafora Disease and EPM2A Mutation

S. Berkovic, D. Lev, J. Serratosa, 2007, Epilepsia.

NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvement.

A. Munnich, E. Leshinsky‐Silver, D. Lev, 2009, Molecular genetics and metabolism.

Clinical Presentations of Mitochondrial Cardiomyopathies

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2004, Pediatric Cardiology.

Neurologic Presentations of Mitochondrial Disorders

D. Lev, A. Fattal-Valevski, S. Harel, 2000, Journal of child neurology.

Multiple presentation of mitochondrial disorders

Alisa R Gutman, D. Lev, S. Harel, 1999, Archives of disease in childhood.

The cerebellar "tilted telephone receiver sign" enables prenatal diagnosis of PHACES syndrome.

D. Lev, C. Garel, L. Ben‐Sira, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Paternal germline mosaicism of a SCN2A mutation results in Ohtahara syndrome in half siblings.

E. Leshinsky‐Silver, D. Lev, N. Matsumoto, 2014, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Effect of Early Corticosteroid Therapy for Landau‐Kleffner Syndrome

T. Lerman-Sagie, P. Lerman, S. Kivity, 1991, Developmental medicine and child neurology.

Sulthiame in childhood epilepsy

B. Ben-Zeev, T. Lerman-Sagie, N. Watemberg, 2004, Pediatrics international : official journal of the Japan Pediatric Society.

Major brain malformations: corpus callosum dysgenesis, agenesis of septum pellucidum and polymicrogyria in patients with BCORL1-related disorders

D. Lev, E. Sherr, T. Lerman-Sagie, 2021, Journal of human genetics.

Multiple Causes of Pediatric Early Onset Chorea—Clinical and Genetic Approach

D. Lev, H. Ben-Pazi, T. Lerman-Sagie, 2018, Neuropediatrics.

Developmental coordination disorder in children with attention‐deficit–hyperactivity disorder and physical therapy intervention

T. Lerman-Sagie, N. Watemberg, Nathan Watemberg, 2007, Developmental medicine and child neurology.

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1

J. Shendure, G. Carvill, I. Scheffer, 2013, Nature Genetics.

Systematic review and meta‐analysis of isolated posterior fossa malformations on prenatal ultrasound imaging (part 1): nomenclature, diagnostic accuracy and associated anomalies

A. Papageorghiou, C. Garel, A. Khalil, 2016, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Cerebrospinal fluid findings in infants with nonpolio enteroviral meningitis.

T. Lerman-Sagie, M. Shohat, Y. Levy, 1988, Israel journal of medical sciences.

Severe Refractory Status Epilepticus Owing to Presumed Encephalitis

B. Ben-Zeev, T. Lerman-Sagie, U. Kramer, 2005, Journal of child neurology.

REMOVED: Short-chain acyl-CoA dehydrogenase gene mutation (319 C>T) presents with clinical heterogeneity and is candidate founder mutation in Ashkenazi Jewish population.

D. Lev, S. Korman, N. Gregersen, 2007, Molecular genetics and metabolism.

Prenatal diagnosis of rhombencephalosynapsis: neuroimaging features and severity of vermian anomaly

D. Lev, A. Fink, M. Severino, 2021, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Diagnostic approach to fetal microcephaly.

T. Lerman-Sagie, Z. Leibovitz, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Prediction of microcephaly at birth using three reference ranges for fetal head circumference: can we improve prenatal diagnosis?

D. Lev, L. Ben‐Sira, T. Lerman-Sagie, 2016, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Application of a novel prenatal vertical cranial biometric measurement can improve accuracy of microcephaly diagnosis in utero

D. Lev, L. Ben‐Sira, T. Lerman-Sagie, 2016, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Microcephaly at birth ‐ the accuracy of three references for fetal head circumference. How can we improve prediction?

D. Lev, L. Ben‐Sira, T. Lerman-Sagie, 2015 .

Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological features.

D. Lev, W. Dobyns, L. Ben‐Sira, 2020, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Israeli Children With Autism Spectrum Disorder Are not Macrocephalic

D. Lev, T. Lerman-Sagie, M. Davidovitch, 2011, Journal of child neurology.

Prenatal and postnatal presentation of PRMT7 related syndrome: Expanding the phenotypic manifestations

D. Lev, T. Lerman-Sagie, G. Malinger, 2018, American journal of medical genetics. Part A.

Delineation of the interstitial 6q25 microdeletion syndrome: Refinement of the critical causative region

E. Leshinsky‐Silver, D. Lev, A. Frumkin, 2012, American journal of medical genetics. Part A.

Prenatal exclusion of Leigh syndrome due to T8993C mutation in the mitochondrial DNA

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2003, Prenatal diagnosis.

Benign Childhood Epilepsy With Centrotemporal Spikes: Clinical Characteristics and Identification of Patients at Risk for Multiple Seizures

E. Shahar, T. Lerman-Sagie, U. Kramer, 2002, Journal of child neurology.

The molecular and phenotypic spectrum of IQSEC2‐related epilepsy

R. Pfundt, E. Kossoff, E. Leshinsky‐Silver, 2016, Epilepsia.

Refractory epilepsy associated with ventriculoperitoneal shunt over-drainage: case report

S. Constantini, J. Roth, T. Lerman-Sagie, 2019, Child's Nervous System.

Abnormal sulcation as an early sign for migration disorders

D. Lev, T. Lerman-Sagie, G. Malinger, 2004, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Fetal Brain Development: Regulating Processes and Related Malformations

L. Haddad, T. Lerman-Sagie, Z. Leibovitz, 2022, Life.

Congenital Ataxia, Mental Retardation, and Dyskinesia Associated With a Novel CACNA1A Mutation

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2010, Journal of child neurology.

Delineating FOXG1 syndrome

E. Haan, D. Lev, F. Rivier, 2018, Neurology: Genetics.

White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation.

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2002, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Heterozygous Mutations in the ADCK3 Gene in Siblings with Cerebellar Atrophy and Extreme Phenotypic Variability.

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2013, JIMD reports.

Does a SCN1A gene mutation confer earlier age of onset of febrile seizures in GEFS+?

I. Scheffer, S. Berkovic, D. Lev, 2009, Epilepsia.

Prenatal brain imaging in congenital toxoplasmosis

T. Lerman-Sagie, G. Malinger, H. Werner, 2011, Prenatal diagnosis.

A newly recognized syndrome of severe growth deficiency, microcephaly, intellectual disability, and characteristic facial features.

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2014, European journal of medical genetics.

Malformations of Cortical Development: From Postnatal to Fetal Imaging

T. Lerman-Sagie, Z. Leibovitz, 2016, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Fourth ventricle index: sonographic marker for severe fetal vermian dysgenesis/agenesis

D. Lev, T. Lerman-Sagie, G. Malinger, 2019, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

A new locus (SPG47) maps to 1p13.2–1p12 in an Arabic family with complicated autosomal recessive hereditary spastic paraplegia and thin corpus callosum

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2011, Journal of the Neurological Sciences.

Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation.

E. Leshinsky‐Silver, D. Lev, A. Suls, 2012, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Clinical Experience With Open-Label Topiramate Use in Infants Younger Than 2 Years of Age

B. Ben-Zeev, T. Lerman-Sagie, Itai Berger, 2003, Journal of child neurology.

Rare copy number variants are an important cause of epileptic encephalopathies

I. Scheffer, H. Mefford, E. Eichler, 2011, Annals of neurology.

Frequency of CNKSR2 mutation in the X‐linked epilepsy‐aphasia spectrum

I. Scheffer, S. Berkovic, R. Burgess, 2017, Epilepsia.

Can syndromic macrocephaly be diagnosed in utero?

D. Lev, L. Ben‐Sira, T. Lerman-Sagie, 2011, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The first nonsense mutation in alsin results in a homogeneous phenotype of infantile‐onset ascending spastic paralysis with bulbar involvement in two siblings

D. Lev, G. Rouleau, T. Lerman-Sagie, 2003, Clinical genetics.

Infantile Onset of Hereditary Ascending Spastic Paralysis With Bulbar Involvement

T. Lerman-Sagie, J. Filiano, M. Korson, 1996, Journal of child neurology.

Central Apnea in a Child With Congenital Autonomic Dysfunction and Universal Pain Loss

T. Lerman-Sagie, A. Hansen, N. Guerina, 1996, Journal of child neurology.

Epilepsy and mental retardation limited to females: an under-recognized disorder.

K. Friend, I. Scheffer, M. Shaw, 2008, Brain : a journal of neurology.

Febrile Convulsions, Ataxia, Developmental Delay, and Obesity: A New Syndrome?

D. Lev, T. Lerman-Sagie, N. Watemberg, 2001, Journal of child neurology.

Mutations disrupting selenocysteine formation cause progressive cerebello-cerebral atrophy.

D. Söll, E. Leshinsky‐Silver, D. Lev, 2010, American journal of human genetics.

Primary disorders of metabolism and disturbed fetal brain development.

T. Lerman-Sagie, G. Malinger, A. Prasad, 2009, Clinics in perinatology.

Megalencephaly‐capillary malformation (MCAP) and megalencephaly‐polydactyly‐polymicrogyria‐hydrocephalus (MPPH) syndromes: Two closely related disorders of brain overgrowth and abnormal brain and body morphogenesis

J. Graham, D. Lev, K. Gripp, 2012, American journal of medical genetics. Part A.

Cone and rod dysfunction in the NARP syndrome

I. Chowers, A. Shaag, O. Elpeleg, 1999, British Journal of Ophthalmology.

Acute Intermittent Porphyria, Rasmussen Encephalitis, or Both?

D. Lev, N. Schoenfeld, T. Lerman-Sagie, 2007, Journal of child neurology.

Infant botulism in Israel: knowledge enables prompt diagnosis.

T. Lerman-Sagie, O. Yanay, N. Watemberg, 2004, The Israel Medical Association journal : IMAJ.

Prenatal diagnosis of malformations of cortical development by dedicated neurosonography

D. Lev, L. Ben‐Sira, T. Lerman-Sagie, 2007, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Is fetal magnetic resonance imaging superior to neurosonography for detection of brain anomalies?

D. Lev, T. Lerman-Sagie, G. Malinger, 2002, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Authors' reply re: Neuropsychological follow‐up at school age of children with asymmetric ventricles or unilateral ventriculomegaly identified in utero

T. Lerman-Sagie, G. Malinger, 2015, BJOG : an international journal of obstetrics and gynaecology.

Fetal pericallosal lipomas - Clues to diagnosis in the second trimester.

L. Ben‐Sira, T. Lerman-Sagie, G. Malinger, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Focus on the fetal Sylvian fissure

T. Lerman-Sagie, G. Malinger, 2008, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Fetal cerebellar disorders.

T. Lerman-Sagie, G. Malinger, S. Stöcklein, 2018, Handbook of clinical neurology.

Fetal central nervous system: MR imaging versus dedicated US--need for prospective, blind, comparative studies.

D. Lev, T. Lerman-Sagie, G. Malinger, 2004, Radiology.

The fetal cerebellum. Pitfalls in diagnosis and management

D. Lev, T. Lerman-Sagie, G. Malinger, 2009, Prenatal diagnosis.

Thick corpus callosum in the second trimester can be transient and is of uncertain significance

T. Lerman-Sagie, G. Malinger, S. Shinar, 2015, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The Fetal vermis, pons and brainstem: normal longitudinal development as shown by dedicated neurosonography

D. Lev, T. Lerman-Sagie, G. Malinger, 2013, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Dominantly Inherited Nonprogressive Cerebellar Hypoplasia Identified in Utero

D. Lev, L. Ben‐Sira, T. Lerman-Sagie, 2012, Journal of child neurology.

37 – Cerebellar Anomalies

T. Lerman-Sagie, G. Malinger, 2018 .

Significant overlap and possible identity of macrocephaly capillary malformation and megalencephaly polymicrogyria‐polydactyly hydrocephalus syndromes

D. Lev, K. Gripp, W. Dobyns, 2009, American journal of medical genetics. Part A.

Delineation of the phenotype of MED17-related disease in Caucasus-Jewish families.

A. Fattal-Valevski, S. Edvardson, T. Lerman-Sagie, 2021, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

The use of fetal neurosonography and brain MRI in cases of cytomegalovirus infection during pregnancy: A retrospective analysis with outcome correlation

L. Ben‐Sira, T. Lerman-Sagie, G. Malinger, 2017, Prenatal diagnosis.

Imaging of Fetal Cytomegalovirus Infection

D. Lev, T. Lerman-Sagie, G. Malinger, 2010, Fetal Diagnosis and Therapy.

Decreased bone density in carriers and patients of an Israeli family with the osteoporosis-pseudoglioma syndrome.

D. Lev, A. Foldes, T. Lerman-Sagie, 2003, The Israel Medical Association journal : IMAJ.

“Virtual patch clamp analysis” for predicting the functional significance of pathogenic variants in sodium channels

R. Sokol, D. Lev, H. Bassan, 2022, Epilepsy Research.

Dramatic improvement in mitochondrial cardiomyopathy following treatment with idebenone

A. Munnich, E. Leshinsky‐Silver, D. Lev, 2001, Journal of Inherited Metabolic Disease.

White matter abnormalities and dystonic motor disorder associated with mutations in the SLC16A2 gene

P. Fallon, C. Bönnemann, A. Siddiqui, 2009, Developmental medicine and child neurology.

Familial Brain Periventricular Pseudocysts

E. Leshinsky‐Silver, D. Lev, L. Ben‐Sira, 2016, Fetal Diagnosis and Therapy.

Low Erythrocyte Zinc Content in Acquired Aphasia With Convulsive Disorder (Landau-Kleffner Syndrome)

T. Lerman-Sagie, M. Statter, P. Lerman, 1987, Journal of child neurology.

Costeff syndrome: clinical features and natural history

D. Lev, A. Schweiger, B. Pode-Shakked, 2014, Journal of Neurology.

A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletion.

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2008, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Reversible fulminant lactic acidosis and liver failure in an infant with hepatic cytochrome-c oxidase deficiency

E. Leshinsky‐Silver, D. Lev, Ann Saada, 2002, Journal of Inherited Metabolic Disease.

Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome

I. Scheffer, S. Berkovic, D. Lev, 2015, Epilepsia.

A prospective, multicenter, open-label assessment of atomoxetine in non-North American children and adolescents with ADHD

J. Buitelaar, J. Gádoros, V. Harpin, 2004, European Child & Adolescent Psychiatry.

Technetium-99m-ethyl cysteinate dimer brain perfusion loss in pediatric postictal psychosis.

T. Lerman-Sagie, E. Avrahami, M. Lorberboym, 2000, Seminars in nuclear medicine.

Benign Intracranial Hypertension Associated With Budesonide Treatment in Children With Crohn's Disease

T. Lerman-Sagie, A. Levine, N. Watemberg, 2001, Journal of child neurology.

De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes

J. Shendure, B. O’Roak, C. Cytrynbaum, 2012, Nature Genetics.

Efficacy of corticosteroid therapy in treating epileptic encephalopathies and refractory epilepsies other than West syndrome

E. Shahar, B. Ben-Zeev, T. Lerman-Sagie, 2006, Journal of Pediatric Neurology.

CSF glucose levels in febrile infants

T. Lerman-Sagie, M. Shohat, M. Nitzan, 1988, European Journal of Pediatrics.

Molecular and functional studies of retinal degeneration as a clinical presentation of SACS-related disorder.

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2015, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Methylenetetrahydrofolate Reductase Deficiency: Importance of Early Diagnosis

A. Fattal-Valevski, H. Bassan, S. Korman, 2000, Journal of child neurology.

Prenatal Brain Disruption in Molybdenum Cofactor Deficiency

H. Mandel, D. Lev, T. Lerman-Sagie, 2011, Journal of child neurology.

Reply to: The many faces of TUBB4A mutations

E. Leshinsky‐Silver, D. Lev, M. S. van der Knaap, 2014, neurogenetics.

Fetal Neurology.

T. Lerman-Sagie, G. Malinger, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Safety and recommendations for vaccinations of children with inborn errors of metabolism.

B. Plecko, T. Lerman-Sagie, P. Dragoumi, 2021, European journal of paediatric neurology.

Expanding the phenotype of IBA57 mutations: related leukodystrophy can remain asymptomatic

K. Yokochi, D. Lev, A. Takata, 2018, Journal of Human Genetics.

Expanding the natural history of CASK‐related disorders to the prenatal period

E. Boltshauser, R. Battini, G. Zanni, 2022, Developmental medicine and child neurology.

X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

Andrew Menzies, Sarah Edkins, Sara Widaa, 2008, Nature Genetics.

Familial leukoencephalopathy with slowly progressive dystonia and ataxia.

H. Mandel, D. Lev, T. Lerman-Sagie, 2009, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Walker-Warburg syndrome and tectocerebellar dysraphia: A novel association caused by a homozygous DAG1 mutation.

H. Mandel, D. Lev, W. Dobyns, 2017, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Neuroimaging of Fetal Infection

M. L. Rossi, L. Tychsen, M. Recio, 2017, Journal of Pediatric Neurology.

A Possible Genotype-Phenotype Correlation in Ashkenazi-Jewish Individuals With Aicardi-Goutières Syndrome Associated With SAMHD1 Mutation

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2015, Journal of child neurology.

A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi–Goutiéres syndrome associated with mtDNA deletions

E. Leshinsky‐Silver, D. Lev, L. Ben‐Sira, 2011, European Journal of Human Genetics.

Deficiency of Asparagine Synthetase Causes Congenital Microcephaly and a Progressive Form of Encephalopathy

Dipendra K. Aryal, D. Goldstein, J. McNamara, 2013, Neuron.

Postictal Psychosis in a Child

T. Lerman-Sagie, Y. Bujanover, M. Lorberboym, 1999, Journal of child neurology.

Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy

T. Walsh, M. King, Ming K. Lee, 2013, Epilepsia.

Fetal cytomegalovirus infection of the brain: the spectrum of sonographic findings.

D. Lev, T. Lerman-Sagie, G. Malinger, 2003, AJNR. American journal of neuroradiology.

Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus.

I. Scheffer, S. Berkovic, D. Lev, 2001, American journal of human genetics.

Mortality in Dravet syndrome

I. Scheffer, E. Wirrell, V. Ramesh, 2016, Epilepsy Research.

Paroxysmal tonic upward gaze as a presentation of de-novo mutations in CACNA1A.

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2015, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

The Differential Diagnosis of Fetal Intracranial Cystic Lesions

T. Lerman-Sagie, G. Malinger, Edgardo Corral Sereño, 2008 .

RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections

E. Zackai, E. Bermejo, B. Weschke, 2003, Journal of medical genetics.

Mitochondrial Myopathy, Sideroblastic Anemia, and Lactic Acidosis: An Autosomal Recessive Syndrome in Persian Jews Caused by a Mutation in the PUS1 Gene

D. Lev, Y. Bykhovskaya, T. Lerman-Sagie, 2005, Journal of child neurology.

Fulminant neurological deterioration in a neonate with Leigh syndrome due to a maternally transmitted missense mutation in the mitochondrial ND3 gene.

E. Leshinsky‐Silver, D. Lev, Ann Saada, 2005, Biochemical and biophysical research communications.

Progressive cerebellocerebral atrophy: a new syndrome with microcephaly, mental retardation, and spastic quadriplegia

D. Lev, B. Ben-Zeev, T. Lerman-Sagie, 2003, Journal of medical genetics.

Progressive cerebello-cerebral atrophy and progressive encephalopathy with edema, hypsarrhythmia and optic atrophy may be allelic syndromes.

D. Lev, T. Lerman-Sagie, Keren Yosovich, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

White matter involvement in mitochondrial diseases.

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2005, Molecular genetics and metabolism.

Primary and maternal 3-methylcrotonyl-CoA carboxylase deficiency: insights from the Israel newborn screening program

S. Almashanu, H. Mandel, A. Luder, 2016, Journal of Inherited Metabolic Disease.

Utility of Whole Exome Sequencing for Genetic Diagnosis of Previously Undiagnosed Pediatric Neurology Patients

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2016, Journal of child neurology.

Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome

D. Lev, D. Chitayat, N. Matsumoto, 2013, Neurology.

De novo mutations in GRIN1 cause extensive bilateral polymicrogyria

H. Mefford, A. Fry, D. Pilz, 2018, Brain : a journal of neurology.

Pediatric Refractory Partial Status Epilepticus Responsive to Topiramate

T. Lerman-Sagie, N. Watemberg, L. Blumkin, 2005, Journal of child neurology.

Metabolic stroke in a patient with bi-allelic OPA1 mutations

D. Lev, L. Ben‐Sira, T. Lerman-Sagie, 2019, Metabolic Brain Disease.

Familial partial trisomy 15q11-13 presenting as intractable epilepsy in the child and schizophrenia in the mother.

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2011, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Building Bridges Between the Clinic and the Laboratory: A Meeting Review – Brain Malformations: A Roadmap for Future Research

W. Klonowski, L. Nguyen, Mercedes F. Paredes, 2019, Front. Cell. Neurosci..

The Spinal Muscular Atrophy with Pontocerebellar Hypoplasia Gene VRK1 Regulates Neuronal Migration through an Amyloid-β Precursor Protein-Dependent Mechanism

D. Lev, O. Reiner, P. Lazo, 2015, The Journal of Neuroscience.

De novo hotspot variants in CYFIP2 cause early‐onset epileptic encephalopathy

D. Lev, N. Matsumoto, M. Shiina, 2018, Annals of neurology.

Behavioral phenotypes of genetic syndromes: a reference guide for psychiatrists.

D. Lev, T. Lerman-Sagie, M. Moldavsky, 2001, Journal of the American Academy of Child and Adolescent Psychiatry.

TO JMG Characterisation of deletions of the ZFHX 1 B region and genotype-phenotype analysis in Mowat-Wilson syndrome

E. Zackai, B. Weschke, I. Temple, 2003 .

Autistic regression in a child with Silver-Russell syndrome and maternal UPD 7.

D. Lev, T. Lerman-Sagie, M. Davidovitch, 2012, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

The myth of vaccination and autism spectrum

T. Lerman-Sagie, Shahar Shefer, L. Gabis, 2021, European Journal of Paediatric Neurology.

Carnitine-Deficient Myopathy as a Presentation of Tyrosinemia Type I

S. Korman, T. Lerman-Sagie, A. Levine, 2001, Journal of child neurology.

Absence Seizures Aggravated by Valproic Acid

E. Shahar, T. Lerman-Sagie, U. Kramer, 2001, Epilepsia.

Autoimmune epilepsy: Distinct subpopulations of epilepsy patients harbor serum autoantibodies to either glutamate/AMPA receptor GluR3, glutamate/NMDA receptor subunit NR2A or double-stranded DNA

T. Lerman-Sagie, Y. Ganor, M. Levite, 2005, Epilepsy Research.

Fetal optic nerve sheath measurement as a non‐invasive tool for assessment of increased intracranial pressure

D. Lev, L. Ben‐Sira, T. Lerman-Sagie, 2011, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Ultrasound Nomograms of the Fetal Optic Nerve Sheath Diameter

D. Lev, T. Lerman-Sagie, G. Malinger, 2018, Ultraschall in der Medizin - European Journal of Ultrasound.

Ultrasound Nomograms of the Fetal Optic Nerve Sheath Diameter

D. Lev, T. Lerman-Sagie, G. Malinger, 2018, Ultraschall in der Medizin - European Journal of Ultrasound.

Glycogen storage disease type 1a in Israel: biochemical, clinical, and mutational studies.

H. Mandel, S. Korman, N. Bashan, 1997, American journal of medical genetics.

The role of orotic acid measurement in routine newborn screening for urea cycle disorders

S. Almashanu, H. Mandel, A. Fattal-Valevski, 2020, Journal of inherited metabolic disease.

Central Nervous System Involvement in X-Linked Myotubular Myopathy

S. Harel, T. Lerman-Sagie, A. Tomer, 1997, Journal of child neurology.

A benign congenital myopathy in an inbred Samaritan family.

D. Lev, T. Lerman-Sagie, M. Ginzberg, 2006, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Skewed X-inactivation in a manifesting carrier of X-linked myotubular myopathy and in her non-manifesting carrier mother

D. Lev, T. Lerman-Sagie, S. M. Tanner, 1999, Human Genetics.

CHAMP1 Mutations cause Refractory Infantile Myoclonic Epilepsy

D. Lev, H. Bassan, N. Matsumoto, 2019, Journal of Pediatric Neurology.

A clinical diagnostic algorithm for early onset cerebellar ataxia.

E. Bertini, G. Vasco, C. Catsman-Berrevoets, 2019, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Congenital Mirror Movements Associated With Brain Malformations

D. Lev, T. Lerman-Sagie, L. Blumkin, 2021, Journal of child neurology.

Thick fetal corpus callosum: an ominous sign?

D. Lev, L. Ben‐Sira, R. Achiron, 2009, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Mosaic marker chromosome 16 resulting in 16q11.2–q12.1 gain in a child with intellectual disability, microcephaly, and cerebellar cortical dysplasia

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2011, American journal of medical genetics. Part A.

Brain white matter abnormalities associated with copy number variants

A. Vanderver, D. Lev, L. Ben‐Sira, 2020, American journal of medical genetics. Part A.

CHARGE association in a child with de novo chromosomal aberration 46,X,der(X)t(X;2)(p22.1;q33) detected by spectral karyotyping

I. Bar-Am, D. Lev, T. Lerman-Sagie, 2000, Journal of medical genetics.

Differential diagnosis in fetuses with absent septum pellucidum

D. Lev, T. Lerman-Sagie, G. Malinger, 2005, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Hypomyelinating leukoencephalopathy with paroxysmal tonic upgaze and absence of psychomotor development

D. Lev, T. Lerman-Sagie, N. Watemberg, 2007, Movement disorders : official journal of the Movement Disorder Society.

Acute Pediatric Rhabdomyolysis

T. Lerman-Sagie, N. Watemberg, Nathan Watemberg, 2000, Journal of child neurology.

Developmental outcome of isolated fetal microcephaly

D. Lev, A. Schweiger, T. Lerman-Sagie, 2010, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Congenital periventricular pseudocysts: prenatal sonographic appearance and clinical implications

D. Lev, T. Lerman-Sagie, G. Malinger, 2002, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Progressive neurological deterioration in a child with distal arthrogryposis and whistling face

D. Lev, M. Yanoov, T. Lerman-Sagie, 2000, Journal of medical genetics.

Periventricular pseudocysts of noninfectious origin: Prenatal associated findings and prognostic factors

D. Lev, T. Lerman-Sagie, G. Malinger, 2020, Prenatal diagnosis.

Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin.

E. Leshinsky‐Silver, D. Lev, J. Vockley, 2008, Molecular genetics and metabolism.

Developmental Outcome of Children With Enlargement of the Cisterna Magna Identified in Utero

D. Lev, L. Ben‐Sira, T. Lerman-Sagie, 2009, Journal of child neurology.

Fetal brain imaging: a comparison between magnetic resonance imaging and dedicated neurosonography

D. Lev, Z. Ben-Aroya, L. Ben‐Sira, 2004, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Nonprogressive Familial Leukoencephalopathy With Porencephalic Cyst and Focal Seizures

D. Lev, B. Ben-Zeev, T. Lerman-Sagie, 2006, Journal of child neurology.

Autoimmune Epilepsy: Some Epilepsy Patients Harbor Autoantibodies to Glutamate Receptors and dsDNA on both Sides of the Blood-brain Barrier, which may Kill Neurons and Decrease in Brain Fluids after Hemispherotomy

P. van Bogaert, A. Futerman, D. Pelled, 2004, Clinical & developmental immunology.

Demyelinative Brainstem Encephalitis Responsive to Intravenous Immunoglobulin Therapy

T. Lerman-Sagie, A. Assa, N. Watemberg, 1999, Pediatrics.

Inborn errors of metabolism

B. Ben-Zeev, T. Lerman-Sagie, A. Nissenkorn, 2001, Neurology.

A cause of abnormal brain development

B. Ben-Zeev, T. Lerman-Sagie, A. Nissenkorn, 2001 .

Neurologic Involvement in a Child With Systemic Capillary Leak Syndrome

T. Lerman-Sagie, I. Cohen, L. Blumkin, 2010, Pediatrics.

Familial Intracranial Hypertension in 2 Brothers With PTEN Mutation: Expansion of the Phenotypic Spectrum

D. Lev, S. Constantini, T. Lerman-Sagie, 2019, Journal of child neurology.

Addition of galactose‐1‐phosphate measurement enhances newborn screening for classical galactosemia

S. Almashanu, H. Mandel, A. Fattal-Valevski, 2022, Journal of inherited metabolic disease.

Congenital Myopathies in Israeli Families

Y. Shapira, E. Shahar, H. Goez, 2007, Journal of child neurology.

Agenesis of the septum pellucidum: Prenatal diagnosis and outcome

L. Ben‐Sira, T. Lerman-Sagie, G. Malinger, 2020, Prenatal diagnosis.

Non‐visualization of the cavum septi pellucidi is not synonymous with agenesis of the corpus callosum

D. Lev, T. Lerman-Sagie, G. Malinger, 2012, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

VPS53 mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2)

E. Leshinsky‐Silver, D. Lev, O. Birk, 2014, Journal of Medical Genetics.

Common Peroneal Neuropathy due to Surfing

T. Lerman-Sagie, M. Sadeh, N. Watemberg, 2000 .

Clinical and Radiologic Correlates of Frontal Intermittent Rhythmic Delta Activity

T. Lerman-Sagie, A. Towne, N. Watemberg, 2002, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.

Clinical Correlates of Frontal Intermittent Rhythmic Delta Activity in Children

T. Lerman-Sagie, M. Neufeld, U. Kramer, 2003, Journal of child neurology.

Genetic Counseling and Testing for FSHD (Facioscapulohumeral Muscular Dystrophy) in the Israeli Population

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2012, Journal of Genetic Counseling.

Unique Imaging Features Enabling the Prenatal Diagnosis of Developmental Venous Anomalies: A Persistent Echogenic Brain Lesion Drained by a Collecting Vein in Contrast with Normal Brain Parenchyma on MRI

D. Lev, L. Ben‐Sira, T. Lerman-Sagie, 2017, Fetal Diagnosis and Therapy.

Expanding the phenotype of TRAK1 mutations: hyperekplexia and refractory status epilepticus.

D. Lev, H. Lerche, T. Lerman-Sagie, 2018, Brain : a journal of neurology.

Inborn errors of metabolism: A cause of abnormal brain development

B. Ben-Zeev, T. Lerman-Sagie, A. Nissenkorn, 2001 .

A practical approach to prenatal diagnosis of malformations of cortical development.

T. Lerman-Sagie, G. Malinger, Z. Leibovitz, 2021, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Expanding the genotype-phenotype spectrum of ISCA2-related multiple mitochondrial dysfunction syndrome-cavitating leukoencephalopathy and prolonged survival

D. Lev, L. Ben‐Sira, T. Lerman-Sagie, 2020, neurogenetics.

Medical Cannabis for Pediatric Moderate to Severe Complex Motor Disorders

T. Lerman-Sagie, Ilan Linder, L. Blumkin, 2018, Journal of child neurology.

Familial Hyperekplexia and Refractory Status Epilepticus: A New Autosomal Recessive Syndrome

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2004, Journal of child neurology.

Prenatal diagnosis of brainstem anomalies.

T. Lerman-Sagie, K. Haratz, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Assessment of fetal midbrain and hindbrain in mid‐sagittal cranial plane by three‐dimensional multiplanar sonography. Part 2: application of nomograms to fetuses with posterior fossa malformations

T. Lerman-Sagie, G. Malinger, Z. Leibovitz, 2014, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Re: Additional value of fetal magnetic resonance imaging in the prenatal diagnosis of central nervous system anomalies: a systematic review of the literature

T. Lerman-Sagie, G. Malinger, 2015, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Neuropsychological follow‐up at school age of children with asymmetric ventricles or unilateral ventriculomegaly identified in utero

D. Lev, A. Schweiger, T. Lerman-Sagie, 2015, BJOG : an international journal of obstetrics and gynaecology.

Neuropsychological outcome of children with asymmetric ventricles or unilateral mild ventriculomegaly identified in utero

D. Lev, A. Schweiger, T. Lerman-Sagie, 2007, BJOG : an international journal of obstetrics and gynaecology.

Leigh disease presenting in utero due to a novel missense mutation in the mitochondrial DNA-ND3.

E. Leshinsky‐Silver, D. Lev, Ann Saada, 2010, Molecular genetics and metabolism.

Familial Mitochondrial Intestinal Pseudo-Obstruction and Neurogenic Bladder

D. Lev, T. Lerman-Sagie, Y. Bujanover, 2000, Journal of child neurology.

The Neuropsychological profile of patients with 3‐Methylglutaconic aciduria type III, Costeff syndrome

D. Lev, A. Schweiger, Y. Anikster, 2015, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Urinary organic acid screening in children with developmental language delay

T. Lerman-Sagie, A. Gutman, S. Harel, 1999, Journal of Inherited Metabolic Disease.

Neonatal liver failure and Leigh syndrome possibly due to CoQ-responsive OXPHOS deficiency.

S. Polak‐Charcon, E. Leshinsky‐Silver, D. Lev, 2003, Molecular genetics and metabolism.

Hepatic coma culminating in severe brain damage in a child with a SCN1A mutation.

E. Leshinsky‐Silver, D. Lev, S. Zuberi, 2007, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Successful pregnancy in a patient with mitochondrial cardiomyopathy due to ACAD9 deficiency

D. Lev, T. Lerman-Sagie, Talia Jacobi-Polishook, 2020, JIMD reports.

Diagnostic Yield of Electroencephalograms in Infants and Young Children With Frequent Paroxysmal Eye Movements

T. Lerman-Sagie, U. Kramer, N. Watemberg, 2008, Journal of child neurology.

Cerebrospinal fluid zinc concentrations in febrile convulsions.

T. Lerman-Sagie, B. Garty, M. Nitzan, 1995, Archives of disease in childhood.

Cerebrospinal fluid zincconcentrations infebrile convulsions

T. Lerman-Sagie, R. Olomucki, 2011 .

Effect of Valproic Acid Therapy on Zinc Metabolism in Children with Primary Epilepsy

T. Lerman-Sagie, M. Statter, P. Lerman, 1987, Clinical neuropharmacology.

Fatal outcome following foetal cerebellar haemorrhage associated with placental thrombosis.

D. Lev, L. Ben‐Sira, T. Lerman-Sagie, 2006, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Sulthiame Revisited

T. Lerman-Sagie, P. Lerman, 1995, Journal of child neurology.

Juvenile Leigh Syndrome, Optic Atrophy, Ataxia, Dystonia, and Epilepsy due to T14487C Mutation in the mtDNA-ND6 Gene: A Mitochondrial Syndrome Presenting From Birth to Adolescence

E. Leshinsky‐Silver, D. Lev, Shani Inbar, 2011, Journal of child neurology.

RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasia.

E. Leshinsky‐Silver, D. Lev, N. Matsumoto, 2015, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Refining the phenotype of the THG1L (p.Val55Ala mutation)‐related mitochondrial autosomal recessive congenital cerebellar ataxia

D. Lev, K. Swoboda, T. Lerman-Sagie, 2019, American journal of medical genetics. Part A.

Significance of Microcephaly Among Children With Developmental Disabilities

S. Harel, T. Lerman-Sagie, N. Watemberg, 2002, Journal of child neurology.

Normal and abnormal fetal brain development during the third trimester as demonstrated by neurosonography.

D. Lev, T. Lerman-Sagie, G. Malinger, 2006, European journal of radiology.

Medullary Tegmental Cap Dysplasia: Fetal and Postnatal Presentations of a Unique Brainstem Malformation

D. Lev, M. Lequin, E. Boltshauser, 2023, American Journal of Neuroradiology.

Assessment of fetal midbrain and hindbrain in mid‐sagittal cranial plane by three‐dimensional multiplanar sonography. Part 1: comparison of new and established nomograms

T. Lerman-Sagie, G. Malinger, Z. Leibovitz, 2014, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

A normal second‐trimester ultrasound does not exclude intracranial structural pathology

D. Lev, T. Lerman-Sagie, G. Malinger, 2002, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Infantile onset progressive cerebellar atrophy and anterior horn cell Degeneration-A novel phenotype associated with mutations in the PLA2G6 gene.

D. Lev, T. Lerman-Sagie, L. Blumkin, 2020, European journal of medical genetics.

33 – Prenatal Diagnosis of Structural Brain Anomalies

C. Garel, L. Ben‐Sira, T. Lerman-Sagie, 2017 .

Diagnosis by whole exome sequencing of atypical infantile onset Alexander disease masquerading as a mitochondrial disorder.

E. Leshinsky‐Silver, D. Lev, M. Henneke, 2014, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Transient ‘primary’ carnitine deficiency

T. Lerman-Sagie, A. Gutman, I. Meshulach, 1998, Journal of Inherited Metabolic Disease.

Lissencephaly associated with congenital hypomyelinating and axonal neuropathy.

T. Lerman-Sagie, A. Nissenkorn, M. Sadeh, 1998, Pediatric Neurology.

Technetium 99m Ethylcysteinate Dimer Single-Photon Emission Computed Tomography (SPECT) During Intellectual Stress Test in Children and Adolescents With Pure Versus Comorbid Attention-Deficit Hyperactivity Disorder (ADHD)

T. Lerman-Sagie, N. Watemberg, A. Nissenkorn, 2004, Journal of child neurology.

Alexander Disease in Israel: Megalencephaly and Leukoencephalopathy and Its Differential Diagnosis

T. Lerman-Sagie, N. Zelnik, M. Mahajnah, 2015, Journal of Pediatric Neurology.

Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47)

P. Bauer, L. Schöls, E. Leshinsky‐Silver, 2012, neurogenetics.

The fetal cerebellar vermis: normal development as shown by transvaginal ultrasound

D. Lev, T. Lerman-Sagie, G. Malinger, 2001, Prenatal diagnosis.

A Prospective Evaluation of Pediatric Patients With Syncope

T. Lerman-Sagie, L. Blieden, M. Mukamel, 1994, Clinical pediatrics.

Effect of cyclic, low dose pyrimethamine treatment in patients with Late Onset Tay Sachs: an open label, extended pilot study

A. Fattal-Valevski, A. Valevski, T. Lerman-Sagie, 2015, Orphanet Journal of Rare Diseases.

Pyrimethamine increases β-hexosaminidase A activity in patients with Late Onset Tay Sachs.

A. Fattal-Valevski, A. Valevski, T. Lerman-Sagie, 2011, Molecular genetics and metabolism.

Bilateral polymicrogyria associated with dystonia: A new neurogenetic syndrome?

K. Bhatia, D. Lev, W. Dobyns, 2020, American journal of medical genetics. Part A.

A new autosomal recessive syndrome with Zellweger‐like manifestations

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2003, American journal of medical genetics. Part A.

Neonatal vocal cord paralysis-an early presentation of hereditary neuralgic amyotrophy due to a mutation in the SEPT9 gene.

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2013, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Congenital Cytomegalovirus Infection Presenting as an Apparent Neurodegenerative Disorder

D. Lev, T. Lerman-Sagie, N. Watemberg, 2002, Clinical pediatrics.

Developmental outcome of isolated fetal macrocephaly

D. Lev, A. Schweiger, T. Lerman-Sagie, 2010, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Mitochondrial DNA Mutations Are Where to Look

O. Elpeleg, T. Lerman-Sagie, S. Houri, 1999, Journal of child neurology.

Does normal fetal brain ultrasound predict normal neurodevelopmental outcome in congenital cytomegalovirus infection?

D. Lev, A. Schweiger, L. Ben‐Sira, 2011, Prenatal diagnosis.

Adverse reactions of Topiramate and Lamotrigine in children

T. Lerman-Sagie, U. Kramer, Z. Shorer, 2005, Pharmacoepidemiology and drug safety.

Hereditary orotic aciduria identified by newborn screening

S. Almashanu, H. Mandel, A. Fattal-Valevski, 2023, Frontiers in Genetics.

Genotype & Phenotype of Ohtahara Syndrome-What's SCN2A Got to Do With It? A Clinician's Read

D. Lev, D. Chitayat, N. Matsumoto, 2014 .

Major brain malformations: corpus callosum dysgenesis, agenesis of septum pellucidum and polymicrogyria in patients with BCORL1-related disorders

D. Lev, E. Sherr, T. Lerman-Sagie, 2021, Journal of Human Genetics.

Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene

E. Leshinsky‐Silver, D. Lev, M. Knaap, 2014, neurogenetics.

A novel missense mutation in the NDP gene in a child with Norrie disease and severe neurological involvement including infantile spasms

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2007, American journal of medical genetics. Part A.

Carbamazepine versus Sulthiame in Treating Benign Childhood Epilepsy With Centrotemporal Spikes

E. Shahar, Y. Nevo, B. Ben-Zeev, 2002, Journal of child neurology.

Phenobarbital Still Has a Role in Epilepsy Treatment

T. Lerman-Sagie, P. Lerman, 1999, Journal of child neurology.

Sonographic developmental milestones of the fetal cerebral cortex: a longitudinal study

D. Lev, T. Lerman-Sagie, G. Malinger, 2006, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The subarachnoid space: normal fetal development as demonstrated by transvaginal ultrasound

R. Achiron, T. Lerman-Sagie, G. Malinger, 2000, Prenatal diagnosis.

Dramatic Effect of Lamotrigine in Young Adults Suffering from Intractable Absences and Generalized Tonic–Clonic Seizures Since Childhood

T. Lerman-Sagie, P. Lerman, 1998 .

Expanding the phenotype of IBA57 mutations: related leukodystrophy can remain asymptomatic

K. Yokochi, D. Lev, A. Takata, 2018, Journal of Human Genetics.

Fat Intolerance in Developmentally Impaired Children With Severe Feeding Intolerance

R. Shamir, T. Lerman-Sagie, A. Levine, 2006, Journal of child neurology.

Should Autistic Children Be Evaluated for Mitochondrial Disorders?

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2004, Journal of child neurology.

The ‘Brain Shadowing Sign': A Novel Marker of Fetal Craniosynostosis

D. Lev, T. Lerman-Sagie, G. Malinger, 2016, Fetal Diagnosis and Therapy.

Diagnosis of fetal cortical abnormalities by new reference charts for assessment of sylvian fissure biometry

D. Lev, T. Lerman-Sagie, Z. Leibovitz, 2023, Prenatal diagnosis.

Case report 416

T. Lerman-Sagie, M. Mimouni, M. Grunebaum, 2004, Skeletal Radiology.

Utility of genetic testing in children with leukodystrophy.

D. Lev, A. Fattal-Valevski, A. Mory, 2023, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Myoclonic tremor status as a presenting symptom of adenylosuccinate lyase deficiency.

D. Lev, N. Matsumoto, H. Saitsu, 2020, European journal of medical genetics.

Assessment of fetal intracranial pathologies first demonstrated late in pregnancy: cell proliferation disorders

D. Lev, T. Lerman-Sagie, G. Malinger, 2003 .

The fetal corpus callosum. ‘The truth is out there’

D. Lev, T. Lerman-Sagie, G. Malinger, 2007, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Three‐dimensional sagittal reconstruction of the corpus callosum: fact or artifact?

T. Lerman-Sagie, G. Malinger, F. Viñals, 2006, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Systematic review and meta‐analysis of isolated posterior fossa malformations on prenatal imaging (part 2): neurodevelopmental outcome

A. Papageorghiou, C. Garel, A. Khalil, 2016, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Atypical presentation of Costeff syndrome-severe psychomotor involvement and electrical status epilepticus during slow wave sleep.

E. Leshinsky‐Silver, D. Lev, Y. Anikster, 2015, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

A novel mutation in the TPR6 domain of the RAPSN gene associated with congenital myasthenic syndrome

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2012, Journal of the Neurological Sciences.

A compound heterozygous missense mutation and a large deletion in the KCTD7 gene presenting as an opsoclonus-myoclonus ataxia-like syndrome

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2012, Journal of Neurology.

Does normal fetal brain ultrasound predict normal neurodevelopmental outcome in congenital cytomegalovirus infection?

D. Lev, A. Schweiger, L. Ben‐Sira, 2011, Prenatal diagnosis.

Familial optic atrophy with white matter changes

E. Leshinsky‐Silver, D. Lev, T. Lerman-Sagie, 2003, American journal of medical genetics. Part A.

Diagnostic Utility of Genome-wide DNA Methylation Analysis in Genetically Unsolved Developmental and Epileptic Encephalopathies and Refinement of a CHD2 Episignature

G. Carvill, H. Mefford, S. Berkovic, 2023, medRxiv.

Severe growth deficiency, microcephaly, intellectual disability, and characteristic facial features are due to a homozygous QARS mutation

E. Leshinsky‐Silver, D. Lev, Jiqiang Ling, 2017, neurogenetics.

Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome

D. Lev, D. Chitayat, N. Matsumoto, 2013, Neurology.

Progressive cerebellocerebral atrophy: a new syndrome with microcephaly, mental retardation, and spastic quadriplegia

D. Lev, B. Ben-Zeev, T. Lerman-Sagie, 2003, Journal of medical genetics.

Familial leukoencephalopathy with slowly progressive dystonia and ataxia.

H. Mandel, D. Lev, T. Lerman-Sagie, 2009, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Rhabdomyolysis

T. Lerman-Sagie, N. Watemberg, Brent A. Armstrong, 2007, Internal and emergency medicine.

Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47)

P. Bauer, L. Schöls, E. Leshinsky‐Silver, 2012, neurogenetics.

De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies.

Michael R. Johnson, G. Carvill, I. Scheffer, 2016, American journal of human genetics.

Periventricular Brain Heterotopias in a Child With Adrenocortical Insufficiency, Achalasia, Alacrima, and Neurologic Abnormalities (Allgrove Syndrome)

T. Lerman-Sagie, A. Shuper, L. Kornreich, 1999, Journal of child neurology.