List of works - Tai-Heng Chen

A Taiwanese boy with congenital generalized lipodystrophy caused by homozygous Ile262fs mutation in the BSCL2 gene

scientific article published on 01 November 2010

A child with severe stridor ⬇️

scientific article published on November 12, 2012

A lytic rib lesion in a neonate

scientific article published on 01 May 2010

An intra-abdominal oval-shaped mass

scientific article published in February 2014

An unusual orbital mass with dural tail signs

scientific article published on 01 August 2012

Benign reversible course in infants manifesting clinicopathological features of fatal mitochondrial myopathy due to m.14674 T>C mt-tRNAGlu mutation

scientific article published on 10 July 2013

Bluish discoloration of hemiscrotum ⬇️

scientific article published on 01 May 2011

Combined noninvasive ventilation and mechanical insufflator-exsufflator for acute respiratory failure in patients with neuromuscular disease: effectiveness and outcome predictors

scientific article published on 01 January 2019

Comment on: "Myostatin inhibition in combination with antisense oligonucleotide therapy improves outcomes in spinal muscular atrophy" by Zhou et al

scientific article published on 27 July 2020

Community-acquired pneumonia in pediatric patients with acute neuromuscular respiratory failure: a microbiologic perspective

scientific article published on 09 April 2014

Comparison of Clinical Characteristics Between Febrile and Afebrile Seizures Associated With Acute Gastroenteritis in Childhood

scientific article published on 16 April 2020

Correlation between muscle involvement, phenotype and D4Z4 fragment size in facioscapulohumeral muscular dystrophy ⬇️

scientific article published on December 7, 2011

Early-Onset Infantile Facioscapulohumeral Muscular Dystrophy: A Timely Review

scientific article published on 21 October 2020

Emergency room visits and admission rates of children with neuromuscular disorders: A 10-year experience in a medical center in Taiwan

scientific article published on 02 October 2018

Hair-on-end skull in an infant without anemia

scientific article

Hemifacial atrophy with intracranial calcification

scientific article published on 01 July 2013

Identification of KLHL40 mutations by targeted next-generation sequencing facilitated a prenatal diagnosis in a family with three consecutive affected fetuses with fetal akinesia deformation sequence.

scientific article published on 20 October 2016

Identification of bidirectional gene conversion between SMN1 and SMN2 by simultaneous analysis of SMN dosage and hybrid genes in a Chinese population ⬇️

scientific article published on June 25, 2011

Increasing recognition of cases with male Aicardi syndrome

scientific article published on 01 January 2010

Infantile facioscapulohumeral muscular dystrophy revisited: Expansion of clinical phenotypes in patients with a very short EcoRI fragment.

scientific article published on 21 February 2013

Massive cerebral air embolism in a preterm with fetal alcohol syndrome.

scientific article published in March 2009

Metabolic and Nutritional Issues Associated with Spinal Muscular Atrophy

scientific article published on 16 December 2020

Methodological considerations in combined noninvasive ventilation and mechanical in-exsufflator.

scientific article

Multifaceted roles of microRNAs: From motor neuron generation in embryos to degeneration in spinal muscular atrophy

scientific article published on 18 November 2019

Neonatal lupus

scientific article published on 20 April 2020

Neurological involvement associated with COVID-19 infection in children

scientific article published on 13 August 2020

New and Developing Therapies in Spinal Muscular Atrophy: From Genotype to Phenotype to Treatment and Where Do We Stand?

scientific article published on 07 May 2020

Noninvasive airway approaches for acute neuromuscular respiratory failure in emergency departments.

scientific article

Posterior Reversible Encephalopathy Syndrome With Spinal Cord Involvement in Children.

scientific article published on 10 October 2016

Posterior Reversible Encephalopathy Syndrome in Children: Case Series and Systematic Review.

scientific article published on 23 September 2013

Posterior reversible encephalopathy syndrome in critically ill children: a case series ⬇️

scientific article published on September 28, 2012

Prevalence and risk factors for feeding and swallowing difficulties in spinal muscular atrophy types II and III

scientific article

Prostaglandin I(2) analogues enhance growth-related oncogene-alpha expression in human monocyte-derived dendritic cells.

scientific article published in October 2010

Reliability and validity of outcome measures of in-hospital and at-home visits in a randomized, double-blind, placebo-controlled trial for spinal muscular atrophy.

scientific article published on 24 October 2013

Respiratory management for patients with neuromuscular disorders during the COVID-19 pandemic

scientific article published on 01 January 2020

Selective Neuromuscular Denervation in Taiwanese Severe SMA Mouse Can Be Reversed by Morpholino Antisense Oligonucleotides

scientific article

Spontaneous hemopneumothorax simulating acute abdominal affections

scientific article published on 20 November 2012

Symmetric atrophy of bilateral distal upper extremities and hyperIgEaemia in a male adolescent with Hirayama disease

scientific article published on 24 September 2009

The football sign in a neonate

scientific article published on 24 May 2013

The peeling dermatitis with a peculiar demarcation.

scientific article published in November 2013

List of works by Tai-Heng Chen

A Taiwanese boy with congenital generalized lipodystrophy caused by homozygous Ile262fs mutation in the BSCL2 gene

A child with severe stridor ⬇️

A lytic rib lesion in a neonate

An intra-abdominal oval-shaped mass

An unusual orbital mass with dural tail signs

Benign reversible course in infants manifesting clinicopathological features of fatal mitochondrial myopathy due to m.14674 T>C mt-tRNAGlu mutation

Bluish discoloration of hemiscrotum ⬇️

Combined noninvasive ventilation and mechanical insufflator-exsufflator for acute respiratory failure in patients with neuromuscular disease: effectiveness and outcome predictors

Comment on: "Myostatin inhibition in combination with antisense oligonucleotide therapy improves outcomes in spinal muscular atrophy" by Zhou et al

Community-acquired pneumonia in pediatric patients with acute neuromuscular respiratory failure: a microbiologic perspective

Comparison of Clinical Characteristics Between Febrile and Afebrile Seizures Associated With Acute Gastroenteritis in Childhood

Correlation between muscle involvement, phenotype and D4Z4 fragment size in facioscapulohumeral muscular dystrophy ⬇️

Early-Onset Infantile Facioscapulohumeral Muscular Dystrophy: A Timely Review

Emergency room visits and admission rates of children with neuromuscular disorders: A 10-year experience in a medical center in Taiwan

Hair-on-end skull in an infant without anemia

Hemifacial atrophy with intracranial calcification

Identification of KLHL40 mutations by targeted next-generation sequencing facilitated a prenatal diagnosis in a family with three consecutive affected fetuses with fetal akinesia deformation sequence.

Identification of bidirectional gene conversion between SMN1 and SMN2 by simultaneous analysis of SMN dosage and hybrid genes in a Chinese population ⬇️

Increasing recognition of cases with male Aicardi syndrome

Infantile facioscapulohumeral muscular dystrophy revisited: Expansion of clinical phenotypes in patients with a very short EcoRI fragment.

Massive cerebral air embolism in a preterm with fetal alcohol syndrome.

Metabolic and Nutritional Issues Associated with Spinal Muscular Atrophy

Methodological considerations in combined noninvasive ventilation and mechanical in-exsufflator.

Multifaceted roles of microRNAs: From motor neuron generation in embryos to degeneration in spinal muscular atrophy

Neonatal lupus

Neurological involvement associated with COVID-19 infection in children

New and Developing Therapies in Spinal Muscular Atrophy: From Genotype to Phenotype to Treatment and Where Do We Stand?

Noninvasive airway approaches for acute neuromuscular respiratory failure in emergency departments.

Posterior Reversible Encephalopathy Syndrome With Spinal Cord Involvement in Children.

Posterior Reversible Encephalopathy Syndrome in Children: Case Series and Systematic Review.

Posterior reversible encephalopathy syndrome in critically ill children: a case series ⬇️

Prevalence and risk factors for feeding and swallowing difficulties in spinal muscular atrophy types II and III

Prostaglandin I(2) analogues enhance growth-related oncogene-alpha expression in human monocyte-derived dendritic cells.

Reliability and validity of outcome measures of in-hospital and at-home visits in a randomized, double-blind, placebo-controlled trial for spinal muscular atrophy.

Respiratory management for patients with neuromuscular disorders during the COVID-19 pandemic

Selective Neuromuscular Denervation in Taiwanese Severe SMA Mouse Can Be Reversed by Morpholino Antisense Oligonucleotides

Spontaneous hemopneumothorax simulating acute abdominal affections

Symmetric atrophy of bilateral distal upper extremities and hyperIgEaemia in a male adolescent with Hirayama disease

The football sign in a neonate

The peeling dermatitis with a peculiar demarcation.