Tyler E. Reimschisel

Medical Genetics | Neurology | Pediatrics

11100 Euclid Ave
Cleveland, OH 44106

Last Updated: 09/26/2026

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Found 14 publications

Heart Transplantation in Children with Mitochondrial Disease.

Heart Transplantation in Children with Mitochondrial Disease.

Journal: The Journal of pediatrics

Published: August 05, 2019

Response to Newman et al.

Response to Newman et al.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 08, 2017

A systematic review of the published literature on team-based learning in health professions education.

A systematic review of the published literature on team-based learning in health professions education.

Journal: Medical teacher

Published: July 01, 2017

Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia.

Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia.

Journal: American journal of human genetics

Published: April 25, 2017

Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant.

Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant.

Journal: American journal of medical genetics. Part A

Published: March 02, 2017

Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.

Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: March 01, 2017

Inside the 8p23.1 duplication syndrome; eight microduplications of likely or uncertain clinical significance.

Inside the 8p23.1 duplication syndrome; eight microduplications of likely or uncertain clinical significance.

Journal: American journal of medical genetics. Part A

Published: September 14, 2014

Practice patterns of mitochondrial disease physicians in North America. Part 1: diagnostic and clinical challenges.

Practice patterns of mitochondrial disease physicians in North America. Part 1: diagnostic and clinical challenges.

Journal: Mitochondrion

Published: March 07, 2013

You too can teach clinical reasoning!

You too can teach clinical reasoning!

Journal: Pediatrics

Published: October 24, 2012

Comprehensive assessment of serious adverse events following immunization by health care providers.

Comprehensive assessment of serious adverse events following immunization by health care providers.

Journal: The Journal of pediatrics

Published: August 03, 2012

Novel 9q34.11 gene deletions encompassing combinations of four Mendelian disease genes: STXBP1, SPTAN1, ENG, and TOR1A.

Novel 9q34.11 gene deletions encompassing combinations of four Mendelian disease genes: STXBP1, SPTAN1, ENG, and TOR1A.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: June 23, 2012

Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148.

Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148.

Journal: Human molecular genetics

Published: May 01, 2012

Showing 1-12 of 14

Last Updated: 09/26/2026