Last Updated: 09/26/2026
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Found 30 publications
Single-Nuclei Transcriptomic Profiling of Human Myocardium in Long-Chain 3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency.
Journal: Circulation. Heart failure
Published: March 31, 2026
Potential synergistic role of pre-formed GSTT1 antibodies and de novo HLA antibodies in a heart-transplant recipient diagnosed with AMR.
Journal: Human immunology
Published: August 08, 2025
Lethal Neonatal Pulmonary Hypertension in Trisomy 21 (T21) Likely Due to Congenital Portosystemic Shunts.
Journal: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
Published: May 24, 2025
C-terminal frameshift variants in GPKOW are associated with a multisystemic X-linked disorder.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 21, 2024
The Glu86 Residue in TBX4 Proves Critical for Human Lung Development.
Journal: American journal of medical genetics. Part A
Published: September 12, 2024
Intracranial calcifications simulating Aicardi-Goutières syndrome in PARS2-related mitochondrial disease.
Journal: American journal of medical genetics. Part A
Published: November 22, 2023
The Many Faces of Arrhythmogenic Cardiomyopathy: An Overview.
Journal: The application of clinical genetics
Published: June 29, 2023
Atypical infiltrates on endomyocardial biopsy are associated with adverse outcomes in pediatric heart transplantation.
Journal: The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation
Published: December 19, 2022
Arrhythmogenic cardiomyopathy is under-recognized in end-stage pediatric heart failure: A 36-year single-center experience.
Journal: Pediatric transplantation
Published: September 25, 2022
LMOD2-related dilated cardiomyopathy presenting in late infancy.
Journal: American journal of medical genetics. Part A
Published: October 27, 2021
Last Updated: 09/26/2026