A. Prasad

发表

Do clinical variables predict an abnormal EEG in patients with complex febrile seizures?

Charuta N. Joshi, T. Wawrykow, J. Patrick, 2005, Seizure.

Review article Menkes disease and infantile epilepsy

C. A. Rupar, C. Prasad, A. Prasad, 2011 .

C. A. Rupar, C. Prasad, A. Prasad, 2011, Brain and Development.

Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease: Case and Review

D. Debicki, C. A. Rupar, C. Prasad, 2019, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

De novo STXBP1 Mutations in Two Patients With Developmental Delay With or Without Epileptic Seizures

J. Knoll, C. Prasad, A. Prasad, 2021, Frontiers in Neurology.

Pitfalls in Genetic Testing for Consanguineous Pediatric Populations

C. A. Rupar, C. Prasad, A. Prasad, 2022, Case reports in genetics.

MELAS: A Multigenerational Impact of the MTTL1 A3243G MELAS Mutation

D. Ramsay, M. Prasad, C. A. Rupar, 2014, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Treating Intellectual Disability; Look for Creatine Peaks in the Brain

A. Prasad, 2011, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Early Onset Epilepsy and Inherited Metabolic Disorders: Diagnosis and Management

G. Hoffmann, A. Prasad, 2010, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Argininemia: A Treatable Genetic Cause of Progressive Spastic Diplegia Simulating Cerebral Palsy: Case Reports and Literature Review

N. Rosman, J. Breen, A. Prasad, 1997, Journal of child neurology.

Altered activation and functional asymmetry of exner's area but not the visual word form area in a child with sudden-onset, persistent mirror writing

R. Cusack, A. Linke, E. Vriezen, 2018, Neuropsychologia.

The expanding phenotype of MELAS caused by the m.3291T > C mutation in the MT-TL1 gene

C. A. Rupar, C. Prasad, K. Tay, 2016, Molecular genetics and metabolism reports.

Genetic Testing in Children with Epilepsy: Report of a Single-Center Experience

B. Sadikovic, A. Prasad, T. Balci, 2020, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

The Burden of Seizures in Manitoba Children: A Population-Based Study

A. Kozyrskyj, A. Prasad, 2004, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Pyruvate dehydrogenase deficiency and epilepsy

C. Prasad, A. Prasad, T. Rupar, 2011, Brain and Development.

Risk factors for nonsyndromic holoprosencephaly: A Manitoba case–control study

J. Seabrook, A. Chudley, C. Prasad, 2012, American journal of medical genetics. Part A.

Predictive Value of the Lymphocyte Toxicity Assay in the Diagnosis of Drug Hypersensitivity Syndrome

G. Koren, S. Knowles, M. Rieder, 2010, Molecular Diagnosis & Therapy.

Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder

C. Greenberg, C. Prasad, A. Prasad, 2007, Pediatric Nephrology.

Vertebral Artery Dissection Causing Stroke After Trampoline Use

C. Casserly, R. Lim, A. Prasad, 2015, Pediatric emergency care.

Genetic Testing of Epileptic Encephalopathies of Infancy: An Approach

Suvasini Sharma, A. Prasad, 2013, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Development of Criteria for Epilepsy Genetic Testing in Ontario, Canada

O. Snead, K. Boycott, E. Donner, 2018, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Susceptibility to Febrile Seizures: More Than Just a Faulty Thermostat!

A. Prasad, S. Seshia, 2009, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Primary disorders of metabolism and disturbed fetal brain development.

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

De novo interstitial long arm deletion of chromosome 3 with facial dysmorphism, Dandy-Walker variant malformation and hydrocephalus.

C. Prasad, A. Prasad, A. Dawson, 2001, Clinical Dysmorphology.

Genetic evaluation of the floppy infant.

C. Prasad, A. Prasad, 2011, Seminars in fetal & neonatal medicine.

Recurrent Encephalopathy: NAGS (N-Acetylglutamate Synthase) Deficiency in Adults

M. Tuchman, C. A. Rupar, C. Prasad, 2013, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Electron Microscopic Examination of Skin Biopsy as a Cost-Effective Tool in the Diagnosis of Lysosomal Storage Diseases

J. Alroy, E. Kaye, A. Prasad, 1996, Journal of child neurology.

Smith-Lemli-Opitz syndrome: new mutation with a mild phenotype.

M. Nowaczyk, S. Longstaffe, B. Eng, 2002, American journal of medical genetics.

Implementation of Epilepsy Multigene Panel Testing in Ontario, Canada

O. Snead, K. Boycott, T. Hartley, 2019, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Dietary therapy of epilepsy in the nineties; renewed experience with the ketogenic diet

C. Stafstrom, A. Prasad, 1998 .

Recent Advances in the Genetics of Epilepsy: Insights from Human and Animal Studies

C. Stafstrom, C. Prasad, A. Prasad, 1999, Epilepsia.

Progress in Epilepsy Research Recent Advances in the Genetics of Epilepsy: Insights from Human and Animal Studies

C. Stafstrom, A. Prasad, T. Prasad, 1999 .

Chapter 6 Progress in Understanding the Genetics of Epilepsy

C. Stafstrom, C. Prasad, J. Slevin, 1999 .

Genetic Aspects of Human Epilepsy

C. Prasad, A. Prasad, 2013 .

Agenesis of the corpus callosum and cerebral anomalies in inborn errors of metabolism

C. Greenberg, C. Prasad, B. Chodirker, 2007, Congenital anomalies.

Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): evidence for a founder effect and results of a pilot study on a DNA-based newborn screening program.

J. Thompson, C. Greenberg, C. Prasad, 2001, Molecular genetics and metabolism.

Association Between Lysine Reduction Therapies and Cognitive Outcomes in Patients With Pyridoxine-Dependent Epilepsy

P. Striano, M. Lamb, N. Longo, 2022, Neurology.

Outcome of the first 3-years of a DNA-based neonatal screening program for glutaric acidemia type 1 in Manitoba and northwestern Ontario, Canada.

J. Thompson, C. Greenberg, C. Prasad, 2002, Molecular genetics and metabolism.

Pyridoxine Dependent Epilepsy: Enduring Mystery and Continuing Challenges

C. Prasad, A. Prasad, 2012, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Amish microcephaly: Long‐term survival and biochemical characterization

V. Siu, C. A. Rupar, C. Prasad, 2010, American journal of medical genetics. Part A.

Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype

L. Jocelyn, A. Chudley, C. Prasad, 2000, Clinical genetics.

Heterozygous De Novo UBTF Gain-of-Function Variant Is Associated with Neurodegeneration in Childhood.

T. Mullen, S. Edvardson, A. Shaag, 2017, American journal of human genetics.

High diagnostic yield of direct Sanger sequencing in the diagnosis of neuronal ceroid lipofuscinoses

S. Blaser, C. Prasad, J. Mathieu, 2019, JIMD reports.

Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole‐exome sequencing

B. Fernandez, K. Boycott, T. Hartley, 2017, Clinical genetics.

Epilepsy with Complex Genetics: Looking Beyond the Channelopathies

C. Prasad, A. Prasad, 2010 .

Old gene, new phenotype: mutations in heparan sulfate synthesis enzyme, EXT2 leads to seizure and developmental disorder, no exostoses

John F. Robinson, R. Hegele, V. Siu, 2015, Journal of Medical Genetics.

Cyproheptadine for central hypertension

G. Filler, A. Prasad, L. Hart, 2014 .

Methylenetetrahydrofolate reductase (MTHFR) deficiency and infantile epilepsy

C. A. Rupar, C. Prasad, A. Prasad, 2011, Brain and Development.

The floppy infant: contribution of genetic and metabolic disorders

C. Prasad, A. Prasad, 2003, Brain and Development.

The Floppy Infant: Retrospective Analysis of Clinical Experience (1990—2000) in a Tertiary Care Facility

A. Chudley, C. Prasad, B. Chodirker, 2005, Journal of child neurology.

Predictive value of the lymphocyte toxicity assay in the diagnosis of drug hypersensitivity syndrome.

G. Koren, S. Knowles, M. Rieder, 2010, Molecular diagnosis & therapy.

Alternative Epilepsy Therapies: The Ketogenic Diet, Immunoglobulins, and Steroids

G. Holmes, A. Prasad, Carl F. Stafstrom, 1996, Epilepsia.

Möbius sequence, Robin complex, and hypotonia: Severe expression of brainstem disruption spectrum versus Carey–Fineman–Ziter syndrome

M. Patton, A. Toutain, A. Verloes, 2004, American journal of medical genetics. Part A.

Inborn Errors of Metabolism and Epilepsy: Current Understanding, Diagnosis, and Treatment Approaches

Suvasini Sharma, A. Prasad, 2017, International journal of molecular sciences.

The Role of Vigabatrin in Childhood Seizure Disorders: Results from a Clinical Audit

S. Penney, D. Buckley, A. Prasad, 2001, Epilepsia.

Clinical and radiologic features of pediatric opioid use‐associated neurotoxicity with cerebellar edema (POUNCE) syndrome

A. Prasad, D. D. Kim, 2020, Neurology.

Menkes disease: what a multidisciplinary approach can do

A. Prasad, R. Ojha, 2016, Journal of multidisciplinary healthcare.

Exome sequencing reveals a homozygous mutation in TWINKLE as the cause of multisystemic failure including renal tubulopathy in three siblings.

J. Majewski, C. A. Rupar, C. Prasad, 2013, Molecular genetics and metabolism.

Epilepsy as a Network Disorder (2): What can we learn from other network disorders such as dementia and schizophrenia, and what are the implications for translational research?

H. Scharfman, A. Grace, A. Fenton, 2018, Epilepsy & Behavior.

Relationship between antiepileptic drugs and biological markers affecting long-term cardiovascular function in children and adolescents.

M. Rieder, A. Prasad, L. Cheng, 2010, The Canadian journal of clinical pharmacology = Journal canadien de pharmacologie clinique.

Fever, Seizures and Encephalopathy: From Bush Fires to Firestorms

Ramesh Konanki, Suvasini Sharma, A. Prasad, 2022, Annals of Indian Academy of Neurology.

Neurodevelopmental Disabilities in Canadian Children: Prevalence Data from the National Longitudinal Study of Children and Youth

B. Corbett, A. Prasad, 2019, Journal of Pediatric Neurology.

Parental psychosocial aspects and stressors involved in the management of inborn errors of metabolism

B. Potter, C. Prasad, A. Prasad, 2020, Molecular genetics and metabolism reports.

Does the duration of video-EEG recording influence diagnostic yield in pediatric epilepsy: Results from a single center study

A. Prasad, A. Andrade, Mohammed A. Al-Omari, 2023, Epilepsy & Behavior.

Natural History of Temporal Lobe Epilepsy: Antecedents and Progression

G. Shukla, A. Prasad, 2012, Epilepsy research and treatment.

Epilepsy, comorbid conditions in Canadian children: Analysis of cross-sectional data from Cycle 3 of the National Longitudinal Study of Children and Youth

J. Burneo, B. Corbett, A. Prasad, 2014, Seizure.

Status epilepticus in pediatric practice: neonate to adolescent.

A. Prasad, S. Seshia, 2006, Advances in neurology.

A study of the significance of photoparoxysmal responses and spontaneous epileptiform discharges in the EEG in childhood epilepsy

A. Prasad, F. Booth, J. G. Barnes, 2020, Epilepsy & Behavior.

Myoclonus‐Dystonia Presentation of ATM Gene Mutation in a Canadian Mennonite

M. Jog, A. Prasad, S. Goobie, 2021, Movement disorders clinical practice.

Magnetic resonance imaging in the diagnosis of white matter signal abnormalities

C. A. Rupar, C. Prasad, K. Tay, 2018, The neuroradiology journal.

Unusual presentation of Chiari I in toddlers: case reports and review of the literature

K. Tay, S. Ribaupierre, A. Prasad, 2012, Child's Nervous System.

Iron deficiency; non-hematological manifestations.

C. Prasad, A. Prasad, P. An, 1991, Progress in food & nutrition science.

Prevalence of Childhood Epilepsy in Canada

B. Corbett, A. Prasad, J. Burneo, 2011, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Linkage analysis and exome sequencing identify a novel mutation in KCTD7 in patients with progressive myoclonus epilepsy with ataxia

John F. Robinson, R. Hegele, V. Siu, 2014, Epilepsia.

A live-online mindfulness-based intervention for children living with epilepsy and their families: protocol for a randomized controlled trial of Making Mindfulness Matter©

K. Speechley, G. Zou, A. Prasad, 2020, Trials.

Electron Microscopic Examination of Skin Biopsy as a Cost-Effective Tool in the Diagnosis of Lysosomal Storage Diseases

J. Alroy, E. Kaye, A. Prasad, 1996, Journal of child neurology.

Homocystinuria: Challenges in diagnosis and management.

C. Prasad, C. Vardy, C. Prasad, 1999, Paediatrics & child health.

Update in Pediatric Neurology

A. Prasad, A. Andrade, 2018 .

Epilepsy as a network disorder: What can we learn from other network disorders such as dementia and schizophrenia, and what are the implications for translational research?

H. Scharfman, A. Grace, A. Fenton, 2018 .