Tung-Ming Chang

发表

Delay Maturation in Occipital Lobe in Girls With Inattention Subtype of Attention-Deficit Hyperactivity Disorder

R. Wu, Lung-Chang Lin, Ching-Tai Chiang, 2020, Clinical EEG and neuroscience.

New-born screening in large teaching hospital-six years of experience

Kuender D Yang, Ming-Tsung Lee, Haomin Yang, 2017 .

Generalized epilepsy in a patient with mosaic Turner syndrome: a case report

Chin-San Liu, Tung-Ming Chang, Kai-Ming Jhang, 2014, Journal of Medical Case Reports.

Therapeutic effects of children with refractory epilepsy after vagus nerve stimulation in Taiwan.

N. Chiu, Lung-Chang Lin, Rei-Cheng Yang, 2020, Pediatrics and neonatology.

KCNQ2 mutations in childhood nonlesional epilepsy: Variable phenotypes and a novel mutation in a case series

Shuan-yow Li, Inn-Chi Lee, Jao-Shwann Liang, 2019, Molecular genetics & genomic medicine.

KCNQ2-Associated Neonatal Epilepsy: Phenotype Might Correlate With Genotype

Jiann-Jou Yang, Shuan-yow Li, Inn-Chi Lee, 2017, Journal of child neurology.

Cognitive Development in Children With Language Impairment, and Correlation Between Language and Intelligence Development in Kindergarten Children With Developmental Delay

S. Liao, C-L. Hsu, Helen Cheng, 2015, Journal of child neurology.

Revascularization of Concurrent Renal and Cerebral Artery Stenosis in a 14-Year-Old Girl with Takayasu Arteritis and Moyamoya Syndrome

Rei-Cheng Yang, A. Yang, Meng-Luen Lee, 2018, Journal of Korean medical science.

Mucopolysaccharidosis III in Taiwan: Natural history, clinical and molecular characteristics of 28 patients diagnosed during a 21‐year period

W. Hwu, F. Tsai, Shio‐Jean Lin, 2018, American journal of medical genetics. Part A.

Clinical Spectrum and Comorbidities of Dravet Syndrome in Taiwan

Inn-Chi Lee, Shyi-Jou Chen, H. Fan, 2021 .

Ictal and interictal electroencephalographic findings can contribute to early diagnosis and prompt treatment in KCNQ2-associated epileptic encephalopathy.

Inn-Chi Lee, Jao-Shwann Liang, Tung-Ming Chang, 2020, Journal of the Formosan Medical Association = Taiwan yi zhi.

Preimplantation and prenatal genetic diagnosis of aromatic L-amino acid decarboxylase deficiency with an amplification refractory mutation system-quantitative polymerase chain reaction.

S. Kuo, Chih-ping Chen, W. Hwu, 2011, Taiwanese journal of obstetrics & gynecology.

Impact of mycoplasma pneumonia infection on urticaria: A nationwide, population-based retrospective cohort study in Taiwan

Jing-Yang Huang, Huang-Hsi Chen, Tung-Ming Chang, 2019, PloS one.

Natural progression of cardiac features and long-term effects of enzyme replacement therapy in Taiwanese patients with mucopolysaccharidosis II

Hsiang-Yu Lin, Shuan-Pei Lin, C. Chuang, 2021, Orphanet Journal of Rare Diseases.

Capillary electrophoresis for analysis of deletion and duplication in exon 44–55 of Duchenne muscular dystrophy gene

Y. Jong, Shou‐Mei Wu, Chung-An Chen, 2013, Electrophoresis.

Critical Trio Exome Benefits In-Time Decision-Making for Pediatric Patients With Severe Illnesses.

Y. Chien, W. Hwu, F. Lai, 2019, Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.

An At-Risk Population Screening Program for Mucopolysaccharidoses by Measuring Urinary Glycosaminoglycans in Taiwan

Hsiang-Yu Lin, Shuan-Pei Lin, Ya-Hui Chang, 2019, Diagnostics.

Cardiac characteristics and natural progression in Taiwanese patients with mucopolysaccharidosis III

Hsiang-Yu Lin, Shuan-Pei Lin, C. Chuang, 2019, Orphanet Journal of Rare Diseases.

Causes of death and clinical characteristics of 34 patients with Mucopolysaccharidosis II in Taiwan from 1995–2012

Y. Chien, W. Hwu, F. Tsai, 2016, Orphanet Journal of Rare Diseases.

Relationships among Height, Weight, Body Mass Index, and Age in Taiwanese Children with Different Types of Mucopolysaccharidoses

W. Hwu, F. Tsai, Shio‐Jean Lin, 2019, Diagnostics.

Functional independence of Taiwanese patients with mucopolysaccharidoses

W. Hwu, F. Tsai, Hsiang-Yu Lin, 2019, Molecular genetics & genomic medicine.

Aortic Root Dilatation in Taiwanese Patients with Mucopolysaccharidoses and the Long-Term Effects of Enzyme Replacement Therapy

Hsiang-Yu Lin, Shuan-Pei Lin, C. Chuang, 2020, Diagnostics.

Survival and diagnostic age of 175 Taiwanese patients with mucopolysaccharidoses (1985–2019)

Y. Chien, W. Hwu, F. Tsai, 2020, Orphanet Journal of Rare Diseases.

Cardiac Evaluation Using Two-Dimensional Speckle-Tracking Echocardiography and Conventional Echocardiography in Taiwanese Patients with Mucopolysaccharidoses

Hsiang-Yu Lin, Shuan-Pei Lin, C. Chuang, 2020, Diagnostics.

Genotype and phenotype studies of Lowe syndrome in three families in Taiwan.

M. Chao, Tung-Ming Chang, Ming Chen, 2021, Pediatrics and neonatology.

Aromatic L-amino acid decarboxylase deficiency in Taiwan.

Hsiu-Fen Lee, C. Chi, Tung-Ming Chang, 2009, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Clinical spectrum and the comorbidities of Dravet syndrome in Taiwan and the possible molecular mechanisms

Inn-Chi Lee, Shyi-Jou Chen, H. Fan, 2021, Scientific Reports.

Paralytic ileus in MELAS with phenotypic features of MNGIE.

Hsiu-Fen Lee, C. Chi, Mu-Chun Li, 2004, Pediatric neurology.

A Young Girl Presenting with Acute Respiratory Failure and Paralysis Due to a Suspected Taiwan Banded Krait Bite

Tung-Ming Chang, Han-Yao Chiu, Yu-Ching Tseng, 2013 .

Objective diagnosis of ADHD through movement analysis by using a smart chair with piezoelectric material.

R. Wu, Lung-Chang Lin, Ching-Tai Chiang, 2022, Pediatrics and neonatology.

Unilateral agenesis of the internal carotid artery in CHARGE syndrome.

A. Yang, Tung-Ming Chang, Ming Chen, 2010, Pediatrics and neonatology.

Infective endocarditis caused by community-associated methicillin-resistant Staphylococcus aureus in a previously healthy preschool child.

Yhu-Chering Huang, Tung-Ming Chang, Chao-jen Lin, 2014, Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi.

Novel Compound Heterozygous Variants in TBCD Gene Associated with Infantile Neurodegenerative Encephalopathy

Y. Chien, W. Hwu, Chien-Nan Lee, 2021, Children.