Research Topics
| Chang Yong TsaoSummaryAffiliation: The Ohio State University Country: USA Publications
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Detail Information
Publications
Mitochondrial respiratory-chain defects presenting as nonspecific features in childrenC Y Tsao
Department of Pediatrics, College of Medicine and Public Health, Ohio State University, Columbus, USA
J Child Neurol 15:445-8. 2000..Mitochondrial respiratory-chain defects should be considered in the differential diagnosis when persistent, progressive features and especially multiple organ involvement occur...- Isolated neurosarcoidosis presenting as headache and multiple brain and spinal cord lesions mimicking central nervous system metastasesChang Yong Tsao
Department of Pediatrics and Neurology, The Ohio State University, OH, USA
Brain Dev 29:514-8. 2007..We herein report a case of isolated brain biopsy-confirmed neurosarcoidosis in a 17-year-old boy presenting with severe unilateral headache and multiple brain and spinal cord MRI lesions mimicking central nervous system metastases... - Coexisting muscular dystrophies and epilepsy in childrenChang Yong Tsao
Department of Pediatrics, The Ohio State University, Columbus, OH, USA
J Child Neurol 21:148-50. 2006.... - Type 1 ataxia with oculomotor apraxia with aprataxin gene mutations in two American childrenChang Y Tsao
Department of Pediatrics and Neurology, The Ohio State University, Columbus, Ohio, USA
J Child Neurol 20:619-20. 2005..We report two American children, a sister and a brother, with type 1 ataxia with oculomotor apraxia and aprataxin gene mutations and briefly review type 1 ataxia with oculomotor apraxia... - Cri du chat syndrome and complex karyotype in a patient with infantile spasms, hypsarrhythmia, nonketotic hyperglycinemia, and heterotopiaChang Y Tsao
Department of Pediatrics and Neurology, The Ohio State University, Columbus, Ohio, USA
Am J Med Genet A 134:198-201. 2005..This is the first case with Cri du chat syndrome associated with nonketotic hyperglycinemia, infantile spasms, hypsarrhythmia, and heterotopia... - Effective treatment with oxcarbazepine in paroxysmal kinesigenic choreoathetosisChang Yong Tsao
Department of Pediatrics, The Ohio State University, Columbus, Ohio 43205, USA
J Child Neurol 19:300-1. 2004..We report a boy with paroxysmal kinesigenic choreoathetosis, which is dramatically relieved by oxcarbazepine even after unsatisfactory treatment with carbamazepine and other medications... - Leigh disease with mitochondrial DNA A8344G mutation: case report and brief reviewChang Yong Tsao
Department of Pediatrics, The Ohio State University, Children s Radiological Institute, Children s Hospital, Columbus, USA
J Child Neurol 18:62-4. 2003..The A8344G mitochondrial DNA mutation may present with Leigh disease or other different atypical clinical features without myoclonic epilepsy and ragged red fibers... - Mitochondrial DNA depletion in childrenC Y Tsao
Department of Pediatrics and Neurology, College of Medicine and Public Health, The Ohio State University, Columbus 43205, USA
J Child Neurol 15:822-4. 2000..Mitochondrial DNA depletion should be considered in the differential diagnosis in children with developmental delay or failure to thrive of unknown etiology... - Dermatomyositis in two siblings and a brief review of familial dermatomyositisChang Yong Tsao
Department of Pediatrics, The Ohio State University, Columbus, USA
J Child Neurol 17:540-2. 2002..Familial dermatomyositis can occur in different family members, and even dermatomyositis and polymyositis can coexist in the same family... - Combined partial deficiencies of carnitine palmitoyltransferase II and mitochondrial complex I presenting as increased serum creatine kinase levelChang Yong Tsao
Department of Pediatrics and Neurology, College of Medicine and Public Health, The Ohio State University, Columbus, USA
J Child Neurol 17:304-6. 2002..Metabolic myopathy may present with chronic fatigue and a persistently high serum creatine kinase level but without muscle weakness and may be attributable to combined enzyme defects... - Complete biotinidase deficiency presenting as reversible progressive ataxia and sensorineural deafnessChang Y Tsao
Department of Pediatrics, The Ohio State University, Columbus, USA
J Child Neurol 17:146. 2002.... - Lambert-Eaton myasthenic syndrome in childrenChang Yong Tsao
Department of Pediatrics and Neurology, College of Medicine and Public Health, The Ohio State University, USA
J Child Neurol 17:74-6. 2002..High-frequency repetitive nerve stimulation and P/Q-type calcium-channel antibodies may confirm the diagnosis... - High mitochondrial DNA T8993G mutation (<90%) without typical features of Leigh's and NARP syndromesC Y Tsao
Department of Pediatrics and Neurology, The Ohio State University, Columbus 43205, USA
J Child Neurol 16:533-5. 2001..High mitochondrial DNA T8993G mutation is not always associated with typical features of Leigh's and NARP syndromes... - Hypotonia, weakness, and pontocerebellar hypoplasia in siblingsChang Yong Tsao
Department of Pediatrics and Neurology, The Ohio State University, Nationwide Children s Hospital, Columbus, OH 43205, USA
Semin Pediatr Neurol 15:151-3. 2008..We herein briefly review familial spinal muscular atrophy with type 1 pontocerebellar hypoplasia in children... - The efficacy of vagus nerve stimulation in intractable epilepsy associated with nonketotic hyperglycinemia in two childrenChang Yong Tsao
Department of Pediatric, The Ohio State University, Columbus, Ohio 43205, USA
J Child Neurol 25:375-8. 2010..The efficacy in seizure reduction persists for at least 3 years in both children... - Autistic disorder in 2 children with mitochondrial disordersChang Yong Tsao
Department of Pediatrics, The Ohio State University, Columbus, Ohio, USA
J Child Neurol 22:1121-3. 2007.... - Unexpected detection of dystrophin gene deletions by array comparative genomic hybridizationCatherine E Cottrell
Department of Pathology and Laboratory Medicine, Nationwide Children s Hospital, Columbus, OH 43205, USA
Am J Med Genet A 152:2301-7. 2010..Ultimately, it is up to the clinician to promote informed decision-making within the family prior to testing, and ensure that adequate counseling is provided during follow-up... - Partial epilepsy in an adolescent male with limb-girdle muscular dystrophy 1BChang Yong Tsao
Departments of Pediatric and Neurology, The Ohio State University, Columbus, Ohio, USA
J Child Neurol 24:346-8. 2009..We now report another rare case of partial epilepsy and limb-girdle muscular dystrophy type 1B with lamin A/C gene mutation... - Guillain-Barré syndromeS Anne Joseph
The Ohio State University Columbus Children's Hospital, Columbus, Ohio 43205, USA
Adolesc Med 13:487-94. 2002..This chapter reviews the epidemiology, clinical presentation, diagnostic criteria, pathogenesis, treatment, and outcome of this condition...