C. Tsao

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Current trends in the treatment of infantile spasms

C. Tsao, 2009, Neuropsychiatric disease and treatment.

NDT-4488-current trends in the treatment of infantile

C. Tsao, 2009 .

ACTIVE (Ability Captured Through Interactive Video Evaluation) workspace volume video game to quantify meaningful change in spinal muscular atrophy

J. Kissel, L. Alfano, L. Lowes, 2020, Developmental medicine and child neurology.

Muscle Disease

C. Tsao, 2014, Pediatrics In Review.

Leigh Disease With Mitochondrial DNA A8344G Mutation: Case Report and Brief Review

J. Atkin, D. Boue, G. Herman, 2003, Journal of child neurology.

Diagnostic Utility of Whole Exome Sequencing in the Neuromuscular Clinic

K. Flanigan, D. Bartholomew, Emily Sites, 2019, Neuropediatrics.

Myasthenia Gravis and Associated Autoimmune Diseases in Children

J. Mendell, C. Tsao, W. Lo, 2000, Journal of child neurology.

Hypotonia, weakness, and pontocerebellar hypoplasia in siblings.

J. Mendell, D. Boue, Z. Sahenk, 2008, Seminars in pediatric neurology.

Practice patterns of mitochondrial disease physicians in North America. Part 1: diagnostic and clinical challenges.

Marni J. Falk, J. Ganesh, M. Tarnopolsky, 2014, Mitochondrion.

Critical Illness Polyneuropathy in a 2-Year-Old Girl With Hemorrhagic Shock Encephalopathy Syndrome

J. Mendell, C. Tsao, W. Lo, 1995, Journal of child neurology.

Combined Partial Deficiencies of Carnitine Palmitoyltransferase II and Mitochondrial Complex I Presenting as Increased Serum Creatine Kinase Level

J. Mendell, C. Tsao, 2002, Journal of child neurology.

Childhood onset of limb-girdle muscular dystrophy.

C. Tsao, X. Rosales, R. Al-dahhak, 2012, Pediatric neurology.

Congenital Muscular Dystrophy With Complete Laminin-α2-Deficiency, Cortical Dysplasia, and Cerebral White-Matter Changes in Children

J. Mendell, J. Rusin, C. Tsao, 1998, Journal of child neurology.

Isolated neurosarcoidosis presenting as headache and multiple brain and spinal cord lesions mimicking central nervous system metastases

D. Boue, J. Rusin, C. Tsao, 2007, Brain and Development.

Muscle disease.

C. Tsao, 2014, Pediatrics in review.

Dermatomyositis in Two Siblings and a Brief Review of Familial Dermatomyositis

J. Mendell, J. Kissel, C. Tsao, 2002, Journal of child neurology.

Type 1 Ataxia With Oculomotor Apraxia With Aprataxin Gene Mutations in Two American Children

G. Paulson, C. Tsao, 2005, Journal of child neurology.

Effective Treatment With Oxcarbazepine in Paroxysmal Kinesigenic Choreoathetosis

C. Tsao, 2004, Journal of child neurology.

Pathogenic missense variants altering codon 336 of GARS1 lead to divergent dominant phenotypes

W. Wiszniewski, A. Antonellis, Stefan Nicolau, 2022, Human mutation.

Infantile encephalopathy associated with the MELAS A3243G mutation.

S. Dimauro, J. Mendell, J. Paolicchi, 1999, The Journal of pediatrics.

Recovery of Cognition from Persistent Vegetative State in a Child with Normal Somatosensory Evoked Potentials

R. J. Ellingson, C. Tsao, F. Wright, 1991, Clinical EEG.

Unexpected detection of dystrophin gene deletions by array comparative genomic hybridization

J. Gastier-Foster, J. Mendell, R. Pyatt, 2010, American journal of medical genetics. Part A.

Dystrophin expression in a Duchenne muscular dystrophy Patient with a frame shift deletion

J. Mendell, A. Papp, T. Prior, 1997, Neurology.

Coexisting Muscular Dystrophies and Epilepsy in Children

C. Tsao, J. Mendel, 2006, Journal of child neurology.

Gene Therapy for Spinal Muscular Atrophy: Safety and Early Outcomes

J. Mendell, A. Connolly, L. Alfano, 2020, Pediatrics.

Mitochondrial Respiratory-Chain Defects Presenting as Nonspecific Features in Children

J. Mendell, J. Rusin, C. Tsao, 2000, Journal of child neurology.

Partial NADH dehydrogenase defect presenting as spastic cerebral palsy

C. Tsao, C. Boesel, F. Wright, 1994, Brain and Development.

Natural History of Steroid-Treated Young Boys With Duchenne Muscular Dystrophy Using the NSAA, 100m, and Timed Functional Tests.

J. Mendell, K. Flanigan, A. Connolly, 2020, Pediatric neurology.

Mitochondrial DNA Depletion in Children

J. Mendell, C. Tsao, M. Luquette, 2000, Journal of child neurology.

Cri du chat syndrome and complex karyotype in a patient with infantile spasms, hypsarrhythmia, nonketotic hyperglycinemia, and heterotopia

D. Bartholomew, C. Tsao, G. Wenger, 2005, American journal of medical genetics. Part A.

The Efficacy of Vagus Nerve Stimulation in Intractable Epilepsy Associated With Nonketotic Hyperglycinemia in Two Children

C. Tsao, 2010, Journal of child neurology.

Complete Biotinidase Deficiency Presenting as Reversible Progressive Ataxia and Sensorineural Deafness

C. L. Kien, C. Tsao, 2002, Journal of child neurology.

Generalized Tonic-Clonic Status Epilepticus in a Child with Cat-Scratch Disease and Encephalopathy

C. Tsao, 1992, Clinical EEG.

Acute Chemical Pancreatitis Associated with Carbamazepine Intoxication

C. Tsao, F. Wright, 1993, Epilepsia.

Aicardi syndrome, metastatic angiosarcoma of the leg, and scalp lipoma.

C. Tsao, A. Hamoudi, A. Sommer, 1993, American journal of medical genetics.

Infantile spasms in two children with Williams syndrome.

J. Westman, C. Tsao, 1997, American journal of medical genetics.

Lambert-Eaton Myasthenic Syndrome in Children

J. Mendell, J. Kissel, M. Friemer, 2002, Journal of child neurology.

Role of the Ketogenic Diet in Children with Intractable Seizures

M. Nahata, C. Tsao, K. Tallian, 1998, The Annals of pharmacotherapy.

Partial Epilepsy in an Adolescent Male With Limb-Girdle Muscular Dystrophy 1B

J. Mendell, C. Tsao, 2009, Journal of child neurology.

Autistic Disorder in 2 Children With Mitochondrial Disorders

J. Mendell, C. Tsao, 2007, Journal of child neurology.

Intractable Epilepsy, Audio-Visual Hallucinations and Charcot-Marie-Tooth Disease 1A in an African-American Boy

C. Tsao, 2011, Clinical EEG and neuroscience.

Gabapentin Associated with Aggressive Behavior in Pediatric Patients with Seizures

M. Nahata, C. Tsao, W. Lo, 1996, Epilepsia.

Leigh Syndrome, Cytochrome C Oxidase Deficiency and Hypsarrhythmia with Infantile Spasms

C. L. Kien, J. Rusin, C. Tsao, 1997, Clinical EEG.

Familial cerebellar ataxia with muscle coenzyme Q10 deficiency

S. Dimauro, B. Weissman, J. Mendell, 2001, Neurology.

Congestive heart failure and cardiac thrombus as first presentations of Friedreich ataxia.

C. Tsao, W. Lo, J. Craenen, 1992, Pediatric neurology.

2010 Publications - The Biopathology Center

P. Stankiewicz, J. Gastier-Foster, J. Mendell, 2010 .

Novel compound heterozygous laminina2‐chain gene (LAMA2) mutations in congenital muscular dystrophy

J. Mendell, J. Mendell, G. Marzluf, 1998, Human mutation.

High Mitochondrial DNA T8993G Mutation (>90%) Without Typical Features of Leigh's and NARP Syndromes

J. Mendell, D. Bartholomew, C. Tsao, 2001, Journal of child neurology.

Clinical variability in distal spinal muscular atrophy type 1 (DSMA1): determination of steady-state IGHMBP2 protein levels in five patients with infantile and juvenile disease

G. Dittmar, J. Mendell, U. Stephani, 2008, Journal of Molecular Medicine.

Practice patterns of mitochondrial disease physicians in North America. Part 1: diagnostic and clinical challenges.

Marni J. Falk, J. Ganesh, M. Tarnopolsky, 2014, Mitochondrion.

A Hypotonic Infant With Complete Deficiencies of Acid Maltase and Debrancher Enzyme

C. Tsao, C. Boesel, F. Wright, 1994, Journal of child neurology.