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Journal of the Neurological Sciences|May 9, 2009
Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegiaKirsten Svenstrup, Peter Bross, Pernille Koefoed, et al.
American Journal of Human Genetics|January 20, 2015
CLPB variants associated with autosomal-recessive mitochondrial disorder with cataract, neutropenia, epilepsy, and methylglutaconic aciduriaCarol Saunders, Laurie Smith, Flemming Wibrand, et al.
Journal of Inherited Metabolic Disease|September 4, 2010
A comprehensive HADHA c.1528G>C frequency study reveals high prevalence of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency in PolandDorota Piekutowska-Abramczuk, Rikke K J Olsen, Jolanta Wierzba, et al.
Oncogene|December 17, 2024
Mitochondrial unfolded protein response-dependent β-catenin signaling promotes neuroendocrine prostate cancerJordan Alyse Woytash, Rahul Kumar, Ajay K Chaudhary, et al.
American Journal of Infection Control|November 15, 2021
Clinical characteristics and symptom duration among outpatients with COVID-19Alexandra Lane, Krystal Hunter, Elizabeth Leilani Lee, et al.
Journal of Medical Virology|March 3, 2025
Genetic Landscape and Mitochondrial Metabolic Dysregulation in Patients Suffering From Severe Long COVIDKristoffer Skaalum Hansen, Sofie Eg Jørgensen, Cagla Cömert, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 23, 2025
FDA approval summary: Lifileucel for unresectable or metastatic melanoma previously treated with an anti-PD-1 based immunotherapyLianne Hu, Chaohong Fan, Peter Bross, et al.
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