David T. Hsieh

Oncology

6202 Harry Hines Blvd
Dallas, TX 75390

Last Updated: 09/26/2026

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Found 19 publications

Multiple Sclerosis Exacerbation Associated With High-Altitude Climbing Exposure.

Multiple Sclerosis Exacerbation Associated With High-Altitude Climbing Exposure.

Journal: Military medicine

Published: December 12, 2019

Headache and Hypoglossal Nerve Palsy in a Child With Idiopathic Hypertrophic Pachymeningitis.

Headache and Hypoglossal Nerve Palsy in a Child With Idiopathic Hypertrophic Pachymeningitis.

Journal: Headache

Published: May 13, 2019

Hairless regulates p53 target genes to exert tumor suppressive functions in glioblastoma.

Hairless regulates p53 target genes to exert tumor suppressive functions in glioblastoma.

Journal: Journal of cellular biochemistry

Published: May 09, 2018

Human Hairless Protein Roles in Skin/Hair and Emerging Connections to Brain and Other Cancers.

Human Hairless Protein Roles in Skin/Hair and Emerging Connections to Brain and Other Cancers.

Journal: Journal of cellular biochemistry

Published: May 19, 2017

Somatic Mosaicism of PCDH19 in a male with early infantile epileptic encephalopathy and review of the literature.

Somatic Mosaicism of PCDH19 in a male with early infantile epileptic encephalopathy and review of the literature.

Journal: American journal of medical genetics. Part A

Published: October 17, 2016

Tuberous sclerosis complex: Five new things.

Tuberous sclerosis complex: Five new things.

Journal: Neurology. Clinical practice

Published: August 01, 2016

Three cases of Troyer syndrome in two families of Filipino descent.

Three cases of Troyer syndrome in two families of Filipino descent.

Journal: American journal of medical genetics. Part A

Published: December 08, 2015

Visual Diagnosis: Newborn With a Facial Vascular Birthmark.

Visual Diagnosis: Newborn With a Facial Vascular Birthmark.

Journal: Pediatrics in review

Published: September 03, 2015

Infantile onset Vanishing White Matter disease associated with a novel EIF2B5 variant, remarkably long life span, severe epilepsy, and hypopituitarism.

Infantile onset Vanishing White Matter disease associated with a novel EIF2B5 variant, remarkably long life span, severe epilepsy, and hypopituitarism.

Journal: American journal of medical genetics. Part A

Published: August 06, 2014

Index of suspicion. Case 1: Global developmental delay and seizures in a 34-month-old boy. Case 2: Ecchymoses on legs and refusal to walk in a 16-year-old autistic boy. Case 3: Progressive breathing difficulty in a 5-year-old girl.

Index of suspicion. Case 1: Global developmental delay and seizures in a 34-month-old boy. Case 2: Ecchymoses on legs and refusal to walk in a 16-year-old autistic boy. Case 3: Progressive breathing difficulty in a 5-year-old girl.

Journal: Pediatrics in review

Published: August 03, 2014

Epilepsy at a summer camp for children and young adults with developmental disabilities: a 3-year experience.

Epilepsy at a summer camp for children and young adults with developmental disabilities: a 3-year experience.

Journal: Military medicine

Published: January 10, 2014

Grip and percussion myotonia in myotonic dystrophy type 1.

Grip and percussion myotonia in myotonic dystrophy type 1.

Journal: The Journal of pediatrics

Published: December 19, 2013

Showing 1-12 of 19

Last Updated: 09/26/2026