Chang Yong Tsao

Summary

Affiliation: The Ohio State University
Country: USA

Publications

  1. ncbi request reprint Mitochondrial respiratory-chain defects presenting as nonspecific features in children
    C Y Tsao
    Department of Pediatrics, College of Medicine and Public Health, Ohio State University, Columbus, USA
    J Child Neurol 15:445-8. 2000
  2. ncbi request reprint Isolated neurosarcoidosis presenting as headache and multiple brain and spinal cord lesions mimicking central nervous system metastases
    Chang Yong Tsao
    Department of Pediatrics and Neurology, The Ohio State University, OH, USA
    Brain Dev 29:514-8. 2007
  3. ncbi request reprint Coexisting muscular dystrophies and epilepsy in children
    Chang Yong Tsao
    Department of Pediatrics, The Ohio State University, Columbus, OH, USA
    J Child Neurol 21:148-50. 2006
  4. ncbi request reprint Type 1 ataxia with oculomotor apraxia with aprataxin gene mutations in two American children
    Chang Y Tsao
    Department of Pediatrics and Neurology, The Ohio State University, Columbus, Ohio, USA
    J Child Neurol 20:619-20. 2005
  5. ncbi request reprint Cri du chat syndrome and complex karyotype in a patient with infantile spasms, hypsarrhythmia, nonketotic hyperglycinemia, and heterotopia
    Chang Y Tsao
    Department of Pediatrics and Neurology, The Ohio State University, Columbus, Ohio, USA
    Am J Med Genet A 134:198-201. 2005
  6. ncbi request reprint Effective treatment with oxcarbazepine in paroxysmal kinesigenic choreoathetosis
    Chang Yong Tsao
    Department of Pediatrics, The Ohio State University, Columbus, Ohio 43205, USA
    J Child Neurol 19:300-1. 2004
  7. ncbi request reprint Leigh disease with mitochondrial DNA A8344G mutation: case report and brief review
    Chang 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
  8. ncbi request reprint Mitochondrial DNA depletion in children
    C 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
  9. ncbi request reprint Dermatomyositis in two siblings and a brief review of familial dermatomyositis
    Chang Yong Tsao
    Department of Pediatrics, The Ohio State University, Columbus, USA
    J Child Neurol 17:540-2. 2002
  10. ncbi request reprint Combined partial deficiencies of carnitine palmitoyltransferase II and mitochondrial complex I presenting as increased serum creatine kinase level
    Chang 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

Collaborators

  • Jerry R Mendell
  • Thomas W Prior
  • Catherine E Cottrell
  • S Anne Joseph
  • Julie M Gastier-Foster
  • Devon Lamb Thrush
  • Robert Pyatt
  • Kandamurugu Manickam
  • Roula Al-Dahhak
  • Caroline Astbury
  • Matthew Pastore
  • Dennis Bartholomew
  • Shalini Reshmi
  • Amy Newmeyer
  • Joan Atkin

Detail Information

Publications19

  1. ncbi request reprint Mitochondrial respiratory-chain defects presenting as nonspecific features in children
    C 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...
  2. ncbi request reprint Isolated neurosarcoidosis presenting as headache and multiple brain and spinal cord lesions mimicking central nervous system metastases
    Chang 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...
  3. ncbi request reprint Coexisting muscular dystrophies and epilepsy in children
    Chang Yong Tsao
    Department of Pediatrics, The Ohio State University, Columbus, OH, USA
    J Child Neurol 21:148-50. 2006
    ....
  4. ncbi request reprint Type 1 ataxia with oculomotor apraxia with aprataxin gene mutations in two American children
    Chang 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...
  5. ncbi request reprint Cri du chat syndrome and complex karyotype in a patient with infantile spasms, hypsarrhythmia, nonketotic hyperglycinemia, and heterotopia
    Chang 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...
  6. ncbi request reprint Effective treatment with oxcarbazepine in paroxysmal kinesigenic choreoathetosis
    Chang 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...
  7. ncbi request reprint Leigh disease with mitochondrial DNA A8344G mutation: case report and brief review
    Chang 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...
  8. ncbi request reprint Mitochondrial DNA depletion in children
    C 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...
  9. ncbi request reprint Dermatomyositis in two siblings and a brief review of familial dermatomyositis
    Chang 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...
  10. ncbi request reprint Combined partial deficiencies of carnitine palmitoyltransferase II and mitochondrial complex I presenting as increased serum creatine kinase level
    Chang 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...
  11. ncbi request reprint Complete biotinidase deficiency presenting as reversible progressive ataxia and sensorineural deafness
    Chang Y Tsao
    Department of Pediatrics, The Ohio State University, Columbus, USA
    J Child Neurol 17:146. 2002
    ....
  12. ncbi request reprint Lambert-Eaton myasthenic syndrome in children
    Chang 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...
  13. ncbi request reprint High mitochondrial DNA T8993G mutation (<90%) without typical features of Leigh's and NARP syndromes
    C 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...
  14. doi request reprint Hypotonia, weakness, and pontocerebellar hypoplasia in siblings
    Chang 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...
  15. doi request reprint The efficacy of vagus nerve stimulation in intractable epilepsy associated with nonketotic hyperglycinemia in two children
    Chang 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...
  16. doi request reprint Unexpected detection of dystrophin gene deletions by array comparative genomic hybridization
    Catherine 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...
  17. ncbi request reprint Autistic disorder in 2 children with mitochondrial disorders
    Chang Yong Tsao
    Department of Pediatrics, The Ohio State University, Columbus, Ohio, USA
    J Child Neurol 22:1121-3. 2007
    ....
  18. ncbi request reprint Guillain-Barré syndrome
    S 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...
  19. doi request reprint Partial epilepsy in an adolescent male with limb-girdle muscular dystrophy 1B
    Chang 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...