H. Sarnat

H. Sarnat, 2004, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Population meta-analysis of low plasma glucose thresholds in full-term normal newborns.

J. Elashoff, H. Sarnat, S. Farber, 2006, American journal of perinatology.

MicroRNA Expression Patterns in Human Astrocytes in Relation to Anatomical Location and Age

S. Ludwin, A. Bar-Or, J. Antel, 2016, Journal of neuropathology and experimental neurology.

Genetics of neural crest and neurocutaneous syndromes.

H. Sarnat, L. Flores‐Sarnat, 2013, Handbook of clinical neurology.

Embryology of Neurocutaneous Syndromes

H. Sarnat, L. Flores‐Sarnat, 2008 .

Embryology of the Neural Crest: Its Inductive Role in the Neurocutaneous Syndromes

H. Sarnat, L. Flores‐Sarnat, 2005, Journal of child neurology.

Juvenile Dermatomyositis Induced by Toxoplasmosis

H. Sarnat, T. Seland, D. Matheson, 1987, Journal of child neurology.

Hereditary Motor Sensory Neuropathy Type I Presenting as Scapuloperoneal Atrophy (Davidenkow Syndrome) Electrophysiological and Pathological Studies

G. Ronen, H. Sarnat, N. Lowry, 1986, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Mitochondrial “Hypermetabolic” Neurons in Paediatric Epileptic Foci

W. Hader, L. Bello-Espinosa, H. Sarnat, 2011, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Repeatedly discharging neurons in epileptic foci have a high energy requirement derived from their mitochondria, and become “hypermetabolic”. Increased mitochondrial activity might be demonstrated histochemically in individual neurons within foci identified as epileptogenic by preoperative electroen

W. Hader, L. Bello-Espinosa, H. Sarnat, 2011 .

Guillain-Barré Syndrome

H. Sarnat, 2011 .

Mitochondrial Myopathy of Cerebro-Hepato-Renal (Zellweger) Syndrome

H. Darwish, H. Sarnat, S. Rubin, 1983, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Ependymal Reactions to Injury. A Review

H. Sarnat, 1995, Journal of neuropathology and experimental neurology.

Role of human fetal ependyma.

H. Sarnat, 1992, Pediatric neurology.

Ectopic or heterotopic? An appeal for semantic precision in describing developmental disorders of the nervous system.

H. Sarnat, 1995, Pediatric neurology.

Heterotopic Growth of Dysplastic Cerebellum in Frontal Encephalocele in an Infant of a Diabetic Mother

D. Demello, H. Sarnat, J. Blair, 1982, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Hemimegalencephaly: part 2. Neuropathology suggests a disorder of cellular lineage.

H. Sarnat, A. Alvarez, L. Flores‐Sarnat, 2003, Journal of child neurology.

Intermediate filament proteinopathies: from cytoskeletons to genes to functional nosology.

H. Sarnat, W. Graf, 2002, Neurology.

Intravascular lymphomatosis

G. Kraft, H. Sarnat, Melina E. Oei, 2002, Muscle & nerve.

The Case Report: Clutter or Contribution to Medical Literature?

R. Lee, H. Sarnat, 1988, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Muscle Biopsy for Diagnosis of Neuromuscular and Metabolic Diseases

S. Carpenter, H. Sarnat, 2015 .

Phenotype/genotype correlations in epidermal nevus syndrome as a neurocristopathy.

H. Sarnat, L. Flores‐Sarnat, 2015, Handbook of clinical neurology.

Vimentin Immunohistochemistry in Human Fetal Brain: Methods of Standard Incubation versus Thermal Intensification Achieve Different Objectives

H. Sarnat, 1998, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Bilateral dissecting aneurysms of the internal carotid arteries

L. Adelman, H. Sarnat, F. Doe, 2004, Acta Neuropathologica.

Evolution of the nervous system

M. Netsky, H. Sarnat, 1974 .

Synaptophysin immunocytochemistry with thermal intensification: a marker of terminal axonal maturation in the human fetal nervous system

D. Born, H. Sarnat, 1999, Brain and Development.

Axonal pathfinding during the development of the nervous system

H. Sarnat, 2022, Annals of the Child Neurology Society.

Developmental Disorders of Muscle

H. Sarnat, 2011 .

D-2-Hydroxyglutaric Aciduria: Hypotonia, Cortical Blindness, Seizures, Cardiomyopathy, and Cylindrical Spirals in Skeletal Muscle

D. Shaw, R. Jack, H. Sarnat, 1997, Journal of child neurology.

MRI Findings in an Immunocompromised Boy with CNS Fungal Infection

E. Wirrell, H. Glass, W. Morrish, 2007, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

The Pachygyria-Polymicrogyria Spectrum of Cortical Dysplasia in X-Linked Hydrocephalus

D. Born, H. Sarnat, W. Graf, 1998, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Immunocytochemical markers of neuronal maturation in human diagnostic neuropathology

H. Sarnat, 2014, Cell and Tissue Research.

New insights into a spectrum of developmental malformations related to mTOR dysregulations: challenges and perspectives

E. Aronica, A. Bongaarts, A. Mühlebner, 2019, Journal of anatomy.

Area Postrema: Fetal Maturation, Tumors, Vomiting Center, Growth, Role in Neuromyelitis Optica.

E. Boltshauser, H. Sarnat, L. Flores‐Sarnat, 2019, Pediatric neurology.

Synaptophysin Immunoreactivity in the Human Hippocampus and Neocortex From 6 to 41 Weeks of Gestation

H. Sarnat, C. Trevenen, L. Flores‐Sarnat, 2010, Journal of neuropathology and experimental neurology.

Clinical neuropathology practice guide 5-2013: markers of neuronal maturation

H. Sarnat, 2013, Clinical neuropathology.

Review: The international consensus classification of Focal Cortical Dysplasia – a critical update 2018

I. Blümcke, I. Najm, H. Sarnat, 2018, Neuropathology and applied neurobiology.

Alteration of developing and adult rat muscle membranes by zuclomiphene and other hypocholesterolemic agents

R. B. Ramsey, J. McGarry, V. Fischer, 1978, Acta Neuropathologica.

Development of the human olfactory system.

H. Sarnat, L. Flores‐Sarnat, 2019, Handbook of clinical neurology.

Cerebellar networks and neuropathology of cerebellar developmental disorders.

H. Sarnat, 2018, Handbook of clinical neurology.

Olfactory Development, Part 2: Neuroanatomic Maturation and Dysgeneses

H. Sarnat, L. Flores‐Sarnat, 2017, Journal of child neurology.

139 – Development of Olfaction and Taste in the Human Fetus and Neonate

H. Sarnat, 2017 .

Maturation and Dysgenesis of the Human Olfactory Bulb

H. Sarnat, Weiming Yu, 2016, Brain pathology.

Myopathy of the Proteus syndrome: Hypothesis of muscular dysgenesis

H. Sarnat, P. Diadori, C. Trevenen, 1993, Neuromuscular Disorders.

The 2016 Bernard Sachs Lecture: Timing in Morphogenesis and Genetic Gradients During Normal Development and in Malformations of the Nervous System.

H. Sarnat, 2018, Pediatric neurology.

Timing in neural maturation: arrest, delay, precociousness, and temporal determination of malformations.

X. Wei, H. Sarnat, M. Philippart, 2015, Pediatric neurology.

New Insights Into the Pathogenesis of Congenital Myopathies

H. Sarnat, 1994, Journal of child neurology.

Clinical effects of myotonic dystrophy on pregnancy and the neonate.

H. Sarnat, P. Byrne, T. O'Connor, 1976, Archives of neurology.

Changes in RNA and oxidative enzymes in Nephelopsis obscura (Erpobdellidae) as indices of environmental stress

H. Sarnat, R. Davies, R. Singhal, 1989 .

Effects of anoxia and hyperoxia on the neurons in the leech Nephelopsis obscura (Erpobdellidae): ultrastructural studies

H. Sarnat, R. Davies, R. Singhal, 1988 .

Unimpaired RNA synthesis in neurons and epithelial cells in a freshwater leech exposed to the organophosphate insecticide chlorpyrifos.

H. Sarnat, R. Davies, R. Singhal, 1989, The Science of the total environment.

Type II arnold-chiari malformation with normal spine in trisomy 18

H. Sarnat, M. Case, P. Monteleone, 1977, Acta Neuropathologica.

The Brain of the Planarian as the Ancestor of the Human Brain

M. Netsky, H. Sarnat, 1985, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

The Authors’ Reply: Practical Advantages to Acridine Orange

H. Sarnat, C. Trevenen, 1986 .

Sacral agenesis

H. Sarnat, M. Case, R. Graviss, 1976, Neurology.

Infantile muscular dystrophy in Canadian aboriginals is an αB‐crystallinopathy

M. D. Del Bigio, C. Campbell, A. Chudley, 2011, Annals of neurology.

Novel Inflammatory Neuropathology in Immature Brain: (1) Fetal Tuberous Sclerosis, (2) Febrile Seizures, (3) α-B-crystallin, and (4) Role of Astrocytes.

Morris H. Scantlebury, H. Sarnat, 2017, Seminars in pediatric neurology.

Ependymal abnormalities in cerebro-hepato-renal disease of Zellweger

H. Darwish, H. Sarnat, C. Trevenen, 1993, Brain and Development.

Dysmaturation neuromyopathy.

H. Sarnat, M. Verity, 1989, Journal of child neurology.

Ganglion cell maturation in peripheral neuroblastic tumours of children.

H. Sarnat, Weiming Yu, 2022, Clinical neuropathology.

A 10-Year-Old Girl with Progressive Generalized Weakness

J. Mah, H. Sarnat, 2006, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Neurocutaneous Syndromes as Embryonic Neurocristopathies

H. Sarnat, L. Flores‐Sarnat, 2016, Journal of Pediatric Epilepsy.

DSCAM: an endogenous promoter drives expression in the developing CNS and neural crest.

G. Lyons, J. Korenberg, J. Richardson, 2002, Biochemical and biophysical research communications.

Fetal Brain Lesions in Tuberous Sclerosis Complex: TORC1 Activation and Inflammation

E. Aronica, P. Crino, A. Prabowo, 2013, Brain pathology.

Toward a better definition of focal cortical dysplasia: An iterative histopathological and genetic agreement trial

M. Honavar, F. Cendes, Í. Lopes-Cendes, 2021, Epilepsia.

Morphogenesis timing of genetically programmed brain malformations in relation to epilepsy.

H. Sarnat, L. Flores‐Sarnat, 2014, Progress in brain research.

Fetal brain mTOR signaling activation in tuberous sclerosis complex.

E. Aronica, M. Baybis, P. Crino, 2014, Cerebral cortex.

Disturbances of late neuronal migrations in the perinatal period.

H. Sarnat, 1987, American journal of diseases of children.

Regional Differentiation of the Human Fetal Ependyma: Immunocytochemical Markers

H. Sarnat, H B Sarnat, Harvey B. Sarnat, 1992, Journal of neuropathology and experimental neurology.

The Discovery, Proof and Reproof of Neurosecretion: (Speidel, 1917; Scharrer and Scharrer, 1934)

H. Sarnat, 1983, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Inverse prominence of ependyma and capillaries in the spinal cord of vertebrates: a comparative histochemical study.

H. Sarnat, J. Lloyd, J. F. Campa, 1975, The American journal of anatomy.

Histochemical Mapping of Vertebrate Brains for Study of Evolution

H. Sarnat, 1985 .

Myotubular Myopathy: Arrest of Morphogenesis of Myofibres Associated with Persistence of Fetal Vimentin and Desmin Four cases compared with fetal and neonatal muscle

H. Sarnat, 1990, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Developmental Disorders of the Nervous System

H. Sarnat, L. Flores‐Sarnat, 2008 .

Maturational arrest of fetal muscle in neonatal myotonic dystrophy. A pathologic study of four cases.

H. Sarnat, S. Silbert, 1976, Archives of neurology.

Chapter 65 – Neonatal Neuromuscular Disorders

H. Sarnat, L. Flores‐Sarnat, 2005 .

Does increased desmin in myofibres constitute a storage disease?

H. Sarnat, 1993, Neuromuscular Disorders.

Vimentin and desmin in maturing skeletal muscle and developmental myopathies

H. Sarnat, 1992, Neurology.

Vimentin/desmin Immunoreactivity of Myofibres in Developmental Myopathies

H. Sarnat, 1991, Acta paediatrica Japonica : Overseas edition.

[Spinal muscular atrophy: disappearance of RNA fluorescence of degenerating motor neurons. An acridine orange study].

H. Sarnat, C. Jiménez, P. Jacob, 1989, Revue neurologique.

Hypoxic alterations in neonatal neurons: An acridine orange fluorochromic study of nucleic acids

H. Sarnat, 1987, Brain and Development.

[Does the brain influence the muscular development of the human fetus? Evidence in 21 cases].

H. Sarnat, 1985, The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques.

Neonatal Myotubular Myopathy: Neuropathy and Failure of Postnatal Maturation of Fetal Muscle

H. Sarnat, Sanford I. Roth, J. Jimenez, 1981, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Diagnostic value of the muscle biopsy in the neonatal period.

H. Sarnat, 1978, American journal of diseases of children.

How to construct a neural tube.

Harvey B. Sarnat, Menkes Jh, H. Sarnat, 2000 .

NEONATAL ENCEPHALOPATHY FOLLOWING FETAL DISTRESS

Harvey B. Sarnat, H. Sarnat, M. S. Sarnat, 1977 .

Respiratory chain deficiencies.

A. Rötig, P. Delonlay, H. Sarnat, 2013, Handbook of clinical neurology.

Embryology and neuropathological examination of central nervous system malformations.

H. Sarnat, 2008, Handbook of clinical neurology.

Histochemistry and immunocytochemistry of the developing ependyma and choroid plexus

H. Sarnat, Harvey B. Sarnat, 1998, Microscopy research and technique.

Acquired, induced and secondary malformations of the developing central nervous system.

H. Sarnat, 2008, Handbook of clinical neurology.

Nervous System, Neuroembryology of

H. Sarnat, L. Flores‐Sarnat, 2003 .

Plasma Glucose Concentrations in Profound Neonatal Hypoglycemia

H. Sarnat, S. Farber, A. Alkalay, 2006, Clinical pediatrics.

Synaptogenesis in the Foetal and Neonatal Cerebellar System. 2. Pontine Nuclei and Cerebellar Cortex

R. Auer, H. Sarnat, L. Flores‐Sarnat, 2013, Developmental Neuroscience.

Molecular genetic and morphologic integration in malformations of the nervous system for etiologic classification.

H. Sarnat, L. Flores‐Sarnat, 2002, Seminars in pediatric neurology.

Acute unilateral oculomotor palsy associated with echo 9 viral infection.

D. O'connor, H. Sarnat, J. Hertenstein, 1976, The Journal of pediatrics.

mTOR Inhibitors as a New Therapeutic Strategy in Treatment Resistant Epilepsy in Hemimegalencephaly: A Case Report

A. Shlien, M. Connolly, C. Dunham, 2018, Journal of child neurology.

Watershed infarcts in the fetal and neonatal brainstem. An aetiology of central hypoventilation, dysphagia, Möibius syndrome and micrognathia.

H. Sarnat, 2004, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Embryology and malformations of the forebrain commissures.

Harvey B Sarnat, H. Sarnat, 2008, Handbook of clinical neurology.

Perinatal sudanophilic leukodystrophy.

L. Adelman, H. Sarnat, 1973, American journal of diseases of children.

Cytoplasmic RNA in Nervous System Tumours in Children: A Fluorochromic Histochemical Study using Acridine Orange

H. Sarnat, N. Rewcastle, C. Trevenen, 1986, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Neuropathology of pediatric epilepsy.

H. Sarnat, L. Flores‐Sarnat, 2013, Handbook of clinical neurology.

International recommendation for a comprehensive neuropathologic workup of epilepsy surgery brain tissue: A consensus Task Force report from the ILAE Commission on Diagnostic Methods

E. Aronica, M. Thom, R. Spreafico, 2016, Epilepsia.

Focal cortical dysplasia type 1

R. Coras, H. Holthausen, H. Sarnat, 2021, Brain pathology.

Brain Imaging Findings in Neonatal Hypoglycemia: Case Report and Review of 23 Cases

H. Sarnat, F. Moser, A. Alkalay, 2005, Clinical pediatrics.

Academic productivity after retirement in pediatric neurology and neuropathology

H. Sarnat, 2018, Neurology.

Neurologic aspects of neonatal hypoglycemia.

H. Sarnat, A. Alkalay, L. Flores‐Sarnat, 2005, The Israel Medical Association journal : IMAJ.

Epilepsies associated with focal cortical dysplasias (FCDs)

Giorgio Lo Russo, Laura Tassi, L. Tassi, 2014, Acta Neuropathologica.

Cerebral embryopathy in late first trimester: possible association with swine influenza vaccine.

S. Kotagal, H. Sarnat, J. Blair, 1979, Teratology.

Synaptogenesis and Myelination in the Nucleus/Tractus Solitarius

H. Sarnat, L. Flores‐Sarnat, 2016, Journal of child neurology.

Sudden infant death syndrome: an update and new perspectives of etiology.

H. Sarnat, D. Rubens, 2013, Handbook of clinical neurology.

Do the Corticospinal and Corticobulbar Tracts Mediate Functions in the Human Newborn?

H. Sarnat, 1989, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Sequences of synaptogenesis in the human fetal and neonatal brain by synaptophysin immunocytochemistry

H. Sarnat, 2023, Frontiers in Cellular Neuroscience.

Niemann Pick C: First Case in a Canadian Nakoda Nation Child

Aneal Khan, X. Wei, Colleen Curtis, 2014, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Synaptic plexi of U-fibre layer beneath focal cortical dysplasias: Role in epileptic networks.

W. Hader, L. Bello-Espinosa, H. Sarnat, 2018, Clinical neuropathology.

Precocious and delayed neocortical synaptogenesis in fetal holoprosencephaly.

H. Sarnat, L. Flores‐Sarnat, 2013, Clinical neuropathology.

Sequence of Synaptogenesis in the Fetal and Neonatal Cerebellar System - Part 1: Guillain-Mollaret Triangle (Dentato-Rubro-Olivo-Cerebellar Circuit)

R. Auer, H. Sarnat, L. Flores‐Sarnat, 2013, Developmental Neuroscience.

Synaptogenesis in the Fetal Corpus Striatum, Globus Pallidus, and Substantia Nigra

R. Auer, H. Sarnat, L. Flores‐Sarnat, 2013, Journal of child neurology.

Pathogenesis of decrebrate “seizures” in the premature infant with intraventricular hemorrhage

H. Sarnat, 1975 .

Sarnat Grading Scale for Neonatal Encephalopathy after 45 Years: An Update Proposal.

C. Wusthoff, L. Leijser, K. Mohammad, 2020, Pediatric neurology.

Editorial Commentary: Inter-observer concordance in applying the Sarnat Grading Scale of neonatal encephalopathy to mildly preterm infants

H. Sarnat, 2019, Pediatric Research.

Functions of the corticospinal and corticobulbar tracts in the human newborn

H. Sarnat, 2003, Journal of Pediatric Neurology.

Cerebral dysgeneses and their influence on fetal muscle development

H. Sarnat, 1986, Brain and Development.

A new classification of malformations of the nervous system: an integration of morphological and molecular genetic criteria as patterns of genetic expression.

H. Sarnat, L. Flores‐Sarnat, 2001, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

CNS malformations: gene locations of known human mutations.

H. Sarnat, 2005, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

CNS malformations: gene locations of known human mutations.

H. Sarnat, 2004, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Central nervous system malformations: locations of known human mutations.

H. Sarnat, H B Sarnat, 2000, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

In Memoriam: Ellsworth C. Alvord, Jr (1923-2010)

H. Sarnat, E. S. Johnson, 2010, Journal of child neurology.

Hypothesis: Phylogenetic Diseases of the Nervous System

M. Netsky, H. Sarnat, 1984, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Congenital cervical spinal atrophy

S. Kotagal, C. Archer, H. Sarnat, 1981, Muscle & nerve.

Alpers Syndrome

A. Kirton, Aneal Khan, X. Wei, 2012, Journal of child neurology.

Idiopathic torticollis: Sternocleidomastoid myopathy and accessory neuropathy

R. Morrissy, H. Sarnat, 1981, Muscle & nerve.

Might the olfactory bulb be an origin of olfactory auras in focal epilepsy?

H. Sarnat, L. Flores‐Sarnat, 2016, Epileptic disorders : international epilepsy journal with videotape.

Sarnat With Striosomes of Graybiel and Dyskinesias in Premature Infants Synaptogenesis in the Fetal Corpus Striatum , Globus Pallidus , and Substantia Nigra : Correlations

R. Auer, H. Sarnat, -. LauraFlores, 2012 .

Agenesis of the Mesencephalon and Metencephalon with Cerebellar Hypoplasia: Putative Mutation in the EN2 Gene—Report of 2 Cases in Early Infancy

Harvey B Sarnat, G. Kletter, J. Siebert, 2002, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Acridine orange‐RNA fluorescence of maturing neurons in the perinatal rat brain

H. Topaloglu, H. Sarnat, H. Topaloğlu, 1989, The Anatomical record.

Cerebral Dysplasias as Expressions of Altered Maturational Processes

H. Sarnat, 1991, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Pathology of Mitochondrial Encephalomyopathies

J. Marín-García, H. Sarnat, 2005, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Neuropathologic research strategies in holoprosencephaly.

H. Sarnat, L. Flores‐Sarnat, 2001, Journal of child neurology.

Malformations of Central Nervous System

H. Sarnat, 2014 .

Clinicopathological findings in mitochondrial disorders

H. Sarnat, 2005, Journal of Pediatric Neurology.

Central nervous system malformations: locations of known human mutations.

H. Sarnat, H B Sarnat, 2000, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Lipid storage myopathy in infantile Pompe's disease.

B. Brown, H. Sarnat, J. Carroll, 1982, Archives of neurology.

Axes and gradients of the neural tube for a morphological/molecular genetic classification of nervous system malformations.

H. Sarnat, L. Flores‐Sarnat, 2008, Handbook of clinical neurology.

Human cerebellar hypoplasia: a syndrome of diverse causes.

H. Alcalá, H. Sarnat, 1980, Archives of neurology.

Prevention of Neuroblast Migratory Disorders

H. Sarnat, Louanne Hudgins, 1999 .

Commentary by Series Editor on Article by Rosa Russo

H. Sarnat, 2007 .

Central nervous system malformations: gene locations of known human mutations.

H. Sarnat, 2003, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Commentary by Series Editor

H. Sarnat, 2001 .

Molecular Genetic Classification of Central Nervous System Malformations

H. Sarnat, 2000, Journal of child neurology.

When does a ganglion become a brain? Evolutionary origin of the central nervous system.

M. Netsky, H. Sarnat, 2002, Seminars in pediatric neurology.

Why should neurologists be interested in Williams syndrome?

M. Rossen, H. Sarnat, 1998, Neurology.

Embryology and Clinical Development of the Human Olfactory System

H. Sarnat, L. Flores‐Sarnat, 2022, Journal of Pediatric Neurology.

Transitory and Vestigial Structures of the Developing Human Nervous System.

H. Sarnat, 2021, Pediatric neurology.

Survey on Olfactory Testing by Pediatric Neurologists: Is the Olfactory a “True” Cranial Nerve?

H. Sarnat, L. Flores‐Sarnat, 2020, Journal of child neurology.

Olfactory Development, Part 1: Function, From Fetal Perception to Adult Wine-Tasting

X. Wei, H. Sarnat, L. Flores‐Sarnat, 2017, Journal of child neurology.

Hereditary Motor-Sensory Neuropathies

H. Sarnat, 2011 .

Fetal anomaly diagnosis and termination of pregnancy

P. Pearl, H. Sarnat, W. Graf, 2023, Developmental medicine and child neurology.

Myopathies associated with hypothyroidism: a review based upon 13 cases.

F. Mastaglia, B. Kakulas, H. Sarnat, 1988, Australian and New Zealand journal of medicine.

Endocrine and Toxic Myopathies

H. Sarnat, 2011 .

The Utility of Simulation-Based Training in Teaching Frontline Providers Modified Sarnat Encephalopathy Examination: A Randomized Controlled Pilot Trial.

K. Mohammad, H. Sarnat, R. Bashir, 2022, Pediatric neurology.

Effects of denervation and tenotomy on the gastrocnemius muscle in the frog: A histologic and histochemical study

H. Sarnat, Jay M. Portnoy, D. Chi, 1977, The Anatomical record.

Endothelial ultrastructural alterations of intramuscular capillaries in infantile mitochondrial cytopathies: “Mitochondrial angiopathy”

Aneal Khan, H. Sarnat, R. Casey, 2012, Neuropathology : official journal of the Japanese Society of Neuropathology.

Blake's pouch cyst in 13q deletion syndrome: Posterior fossa malformations may occur due to disruption of multiple genes

M. Newton, M. Wallis, G. Fitt, 2017, American journal of medical genetics. Part A.

Cerebral Dysgenesis: Embryology and Clinical Expression

H. Sarnat, 1992 .

Marin-Garcia et al: Striated Muscle Mitochondrial Phenotype

J. Marín-García, H. Sarnat, M. Goldenthal, 2003 .

Probing striated muscle mitochondrial phenotype in neuromuscular disorders.

J. Marín-García, H. Sarnat, M. Goldenthal, 2003, Pediatric neurology.

Kearns-Sayre Syndrome With a Novel Mitochondrial DNA Deletion

J. Marín-García, H. Sarnat, M. Goldenthal, 2000, Journal of child neurology.

Central Nervous System, Malformations

H. Sarnat, 2003 .

[Neuroblastic migration: embryological aspects and mechanisms].

H. Sarnat, 1998, Revista de neurologia.

Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome.

M. M. Morrow, M. Shinawi, D. Chitayat, 2021, Pediatric neurology.

Motor Neuron Degeneration in a 20-Week Male Fetus: Spinal Muscular Atrophy Type 0

H. Sarnat, C. Trevenen, 2007, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Fetal Opercular Cavernous Angioma Causing Cerebral Cleft

K. Barlow, X. Wei, H. Sarnat, 2012, Journal of child neurology.

Role of Cajal-Retzius and subplate neurons in cerebral cortical development.

H. Sarnat, L. Flores‐Sarnat, 2002, Seminars in pediatric neurology.

Bilateral Agenesis of the Hippocampal Dentate Gyrus in a Neurologically Normal Adult

A. Clark, H. Sarnat, 2006, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Is focal cortical dysplasia sporadic? Family evidence for genetic susceptibility

I. Scheffer, G. Jackson, P. Crino, 2014, Epilepsia.

Precocious synapses in 13.5-week fetal holoprosencephalic cortex and cyclopean retina

L. Resch, H. Sarnat, Weiming Yu, 2014, Brain and Development.

Diagnostic value of histochemistry in embryonal rhabdomyosarcoma.

D. Demello, H. Sarnat, S. Siddiqui, 1979, American Journal of Surgical Pathology.

Semantics do Matter! Precision in Scientific Communication in Pediatric Neurology

Harvey B Sarnat, H. Sarnat, 2007, Journal of child neurology.

α-B-Crystallin as a Tissue Marker of Epileptic Foci in Paediatric Resections

H. Sarnat, L. Flores‐Sarnat, 2009, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Disorders of segmentation of the neural tube: agenesis of selective neuromeres.

H. Sarnat, 2008, Handbook of clinical neurology.

Severe mitochondrial cytopathy with complete A-V block, PEO, and mtDNA deletions.

J. Marín-García, H. Sarnat, M. Goldenthal, 2002, Pediatric neurology.

Malformations of the nervous system

Paolo Curatolo, P. Curatolo, Harvey B. Sarnat, 2008 .

The Alberta Congenital Anomalies Surveillance System: a 40-year review with prevalence and trends for selected congenital anomalies, 1997-2019.

M. Brindle, S. Greenway, R. Lowry, 2023, Health Promotion and Chronic Disease Prevention in Canada.

Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria

I. Scheffer, Siddharth Srivastava, B. Bourgeois, 2023, JAMA neurology.

Evolution of the nervous system

M. Netsky, H. Sarnat, 1974 .

Hemimegalencephaly: Part 2. Neuropathology Suggests a Disorder of Cellular Lineage

H. Sarnat, L. Flores‐Sarnat, G. Dávila-Gutiérrez, 2003 .

Updated clinical recommendations for the management of tuberous sclerosis complex associated epilepsy.

L. Lagae, E. Aronica, S. Auvin, 2023, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Progressive Spinal Muscular Atrophies

I. Gamstorp, H. Sarnat, 1984 .

Embryology and malformations of the forebrain commissures.

H. Sarnat, 2008, Handbook of clinical neurology.

Commentary by Series Editor

H. Sarnat, 2003 .

Immunocytochemical markers of neuronal maturation in human diagnostic neuropathology

H. Sarnat, 2014, Cell and Tissue Research.

Effects of anoxia, hyperoxia, and salinity on neurons in the leech Nephelopsis obscura (Erpobdellidae): RNA redistribution by fluorescence histochemistry.

H. Sarnat, R. Davies, Ram N. Singhal, 1989, Journal of invertebrate pathology.

Vagal nerve maturation in the fetal lamb: An ultrastructural and morphometric study

S. Hasan, R. Auer, H. Sarnat, 1993, The Anatomical record.