List of works - Chih-Chao Yang

A novel XK gene mutation in a Taiwanese family with McLeod syndrome.

scientific article published on 27 February 2014

Additional benefit of combined therapy with melatonin and apoptotic adipose-derived mesenchymal stem cell against sepsis-induced kidney injury

scientific article published on 15 May 2014

Cardioembolic stroke related to limb-girdle muscular dystrophy 1B.

scientific article

Carrier screening for spinal muscular atrophy (SMA) in 107,611 pregnant women during the period 2005-2009: a prospective population-based cohort study

scientific article published in 2011

Characterization of a familial case with primary erythromelalgia from Taiwan.

scientific article

Clinical characteristics and treatment delay of cerebral infarction in tuberculous meningitis.

scientific article published on 11 May 2010

Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese.

scientific article

Correlation of Survival Motor Neuron Expression in Leukocytes and Spinal Cord in Spinal Muscular Atrophy

scientific article published on 01 February 2009

Cutaneous polyarteritis nodosa in a patient with fabry disease.

scientific article published in January 2008

Cyclosporine-assisted adipose-derived mesenchymal stem cell therapy to mitigate acute kidney ischemia-reperfusion injury.

scientific article published on 31 May 2013

DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients

scientific article

Efficacy, safety, and tolerability of pramipexole in untreated and levodopa-treated patients with Parkinson's disease

scientific article

Exendin-4 and sitagliptin protect kidney from ischemia-reperfusion injury through suppressing oxidative stress and inflammatory reaction

scientific article

Fabry disease: a rare cause of Fever of unknown origin

scientific article published on 01 January 2012

HMBS mutations in Chinese patients with acute intermittent porphyria.

scientific article published in September 2008

Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: a comparison

scientific article published in February 2008

Identification of eight novel mutations of the acid α-glucosidase gene causing the infantile or juvenile form of glycogen storage disease type II

article

Identification of forty-five novel and twenty-three knownNF1 mutations in Chinese patients with neurofibromatosis type 1

scientific article published on 01 August 2006

Immunolocalization of transcription factor NF-kappaB in inclusion-body myositis muscle and at normal human neuromuscular junctions

scientific article published on 01 September 1998

Leukoencephalopathy induced by levamisole alone for the treatment of recurrent aphthous ulcers

scientific article published on 01 September 2006

Levamisole-induced multifocal inflammatory leukoencephalopathy: clinical characteristics, outcome, and impact of treatment in 31 patients

scientific article published on 01 July 2006

Long-term efficacy of miglustat in paediatric patients with Niemann-Pick disease type C.

scientific article

Melatonin treatment further improves adipose-derived mesenchymal stem cell therapy for acute interstitial cystitis in rat.

scientific article

Multiple sclerosis with childhood onset: report of 21 cases in Taiwan

scientific article published in November 2006

Mutation analysis and characterization of alternative splice variants of the Wilson disease gene ATP7B

scientific article published on 01 November 2010

Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum

scientific article published on 01 May 2008

Myopathy in Gaucher disease

scientific article

Nephrogenic systemic fibrosis associated with gadolinium use.

scientific article published in March 2008

Nerve function and dysfunction in acute intermittent porphyria

scientific article published on 17 July 2008

Neuroimaging findings in a brain with Niemann-Pick type C disease

scientific article published in August 2011

Neurosarcoidosis affecting the spinal cord.

scientific article published on September 2010

Nitric oxide-induced oxidative stress in autosomal recessive and dominant inclusion-body myopathies.

scientific article published in June 1998

Predictors for outcome and treatment delay in patients with tuberculous meningitis

scientific article published on August 2009

Probable variant Creutzfeldt–Jakob disease in Asia: a case report from Taiwan and review of two prior cases

scientific article

Scleromyxedema with myopathy was successfully treated by thalidomide.

scientific article published on 23 April 2008

Six novel NPC1 mutations in Chinese patients with Niemann-Pick disease type C.

scientific article

The effect of interferon beta-1a on optic neuritis relapse in patients with multiple sclerosis

scientific article published on 6 October 2009

The mutational spectrum in a cohort of Charcot-Marie-Tooth disease type 2 among the Han Chinese in Taiwan

scientific article

The spectrum of WRN mutations in Werner syndrome patients

scientific article

Transthyretin Ala97Ser in Chinese-Taiwanese patients with familial amyloid polyneuropathy: genetic studies and phenotype expression

scientific article published on 26 November 2007

Two novel mutations in the alpha-galactosidase A gene in Chinese patients with Fabry disease

scientific article published in March 2003

Valproic acid treatment in six patients with spinal muscular atrophy

scientific article published in December 2007

List of works by Chih-Chao Yang

A novel XK gene mutation in a Taiwanese family with McLeod syndrome.

Additional benefit of combined therapy with melatonin and apoptotic adipose-derived mesenchymal stem cell against sepsis-induced kidney injury

Cardioembolic stroke related to limb-girdle muscular dystrophy 1B.

Carrier screening for spinal muscular atrophy (SMA) in 107,611 pregnant women during the period 2005-2009: a prospective population-based cohort study

Characterization of a familial case with primary erythromelalgia from Taiwan.

Clinical characteristics and treatment delay of cerebral infarction in tuberculous meningitis.

Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese.

Correlation of Survival Motor Neuron Expression in Leukocytes and Spinal Cord in Spinal Muscular Atrophy

Cutaneous polyarteritis nodosa in a patient with fabry disease.

Cyclosporine-assisted adipose-derived mesenchymal stem cell therapy to mitigate acute kidney ischemia-reperfusion injury.

DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients

Efficacy, safety, and tolerability of pramipexole in untreated and levodopa-treated patients with Parkinson's disease

Exendin-4 and sitagliptin protect kidney from ischemia-reperfusion injury through suppressing oxidative stress and inflammatory reaction

Fabry disease: a rare cause of Fever of unknown origin

HMBS mutations in Chinese patients with acute intermittent porphyria.

Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: a comparison

Identification of eight novel mutations of the acid α-glucosidase gene causing the infantile or juvenile form of glycogen storage disease type II

Identification of forty-five novel and twenty-three knownNF1 mutations in Chinese patients with neurofibromatosis type 1

Immunolocalization of transcription factor NF-kappaB in inclusion-body myositis muscle and at normal human neuromuscular junctions

Leukoencephalopathy induced by levamisole alone for the treatment of recurrent aphthous ulcers

Levamisole-induced multifocal inflammatory leukoencephalopathy: clinical characteristics, outcome, and impact of treatment in 31 patients

Long-term efficacy of miglustat in paediatric patients with Niemann-Pick disease type C.

Melatonin treatment further improves adipose-derived mesenchymal stem cell therapy for acute interstitial cystitis in rat.

Multiple sclerosis with childhood onset: report of 21 cases in Taiwan

Mutation analysis and characterization of alternative splice variants of the Wilson disease gene ATP7B

Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum

Myopathy in Gaucher disease

Nephrogenic systemic fibrosis associated with gadolinium use.

Nerve function and dysfunction in acute intermittent porphyria

Neuroimaging findings in a brain with Niemann-Pick type C disease

Neurosarcoidosis affecting the spinal cord.

Nitric oxide-induced oxidative stress in autosomal recessive and dominant inclusion-body myopathies.

Predictors for outcome and treatment delay in patients with tuberculous meningitis

Probable variant Creutzfeldt–Jakob disease in Asia: a case report from Taiwan and review of two prior cases

Scleromyxedema with myopathy was successfully treated by thalidomide.

Six novel NPC1 mutations in Chinese patients with Niemann-Pick disease type C.

The effect of interferon beta-1a on optic neuritis relapse in patients with multiple sclerosis

The mutational spectrum in a cohort of Charcot-Marie-Tooth disease type 2 among the Han Chinese in Taiwan

The spectrum of WRN mutations in Werner syndrome patients

Transthyretin Ala97Ser in Chinese-Taiwanese patients with familial amyloid polyneuropathy: genetic studies and phenotype expression

Two novel mutations in the alpha-galactosidase A gene in Chinese patients with Fabry disease

Valproic acid treatment in six patients with spinal muscular atrophy