Search research articles
Contact Us
Filters
Showing results (291-300 of 300) with videos related to
Page
of 30
Sort By:
You have reached the last page of results.
This site can display upto 300 results.
Brain : a Journal of Neurology
|
February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutations
P Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
Biorxiv : the Preprint Server for Biology
|
February 8, 2024
A Novel Pan-RAS Inhibitor with a Unique Mechanism of Action Blocks Tumor Growth in Mouse Models of GI Cancer
Jeremy B Foote, Tyler E Mattox, Adam B Keeton, et al.
Journal of Medical Genetics
|
April 1, 2018
Retrospective natural history of thymidine kinase 2 deficiency
Caterina Garone, Robert W Taylor, Andrés Nascimento, et al.
Nature Communications
|
February 19, 2021
POLRMT mutations impair mitochondrial transcription causing neurological disease
Monika Oláhová, Bradley Peter, Zsolt Szilagyi, et al.
American Journal of Human Genetics
|
July 31, 2018
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder
Carol-Anne Martin, Kata Sarlós, Clare V Logan, et al.
American Journal of Human Genetics
|
May 3, 2024
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder
Carol-Anne Martin, Kata Sarlós, Clare V Logan, et al.
American Journal of Human Genetics
|
September 8, 2018
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder
Carol-Anne Martin, Kata Sarlós, Clare V Logan, et al.
Human Mutation
|
April 23, 2013
ANO5 gene analysis in a large cohort of patients with anoctaminopathy: confirmation of male prevalence and high occurrence of the common exon 5 gene mutation
Anna Sarkozy, Debbie Hicks, Judith Hudson, et al.
Neurology
|
January 30, 2025
Characterization of Factors Associated With Death in Deceased Patients With Mitochondrial Disorders: A Multicenter Cross-Sectional Survey
Alina Ivaniuk, Irina A Anselm, Aaron Bowen, et al.
The New England Journal of Medicine
|
November 10, 2021
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report
, Damian Smedley, Katherine R Smith, et al.
Page
of 30
Search research articles
Search
Showing results (291-300 of 300) with videos related to
Sort By:
Page
of 30
You have reached the last page of results.
This site can display upto 300 results.
Brain : a Journal of Neurology
|
February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutations
P Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
Biorxiv : the Preprint Server for Biology
|
February 8, 2024
A Novel Pan-RAS Inhibitor with a Unique Mechanism of Action Blocks Tumor Growth in Mouse Models of GI Cancer
Jeremy B Foote, Tyler E Mattox, Adam B Keeton, et al.
Journal of Medical Genetics
|
April 1, 2018
Retrospective natural history of thymidine kinase 2 deficiency
Caterina Garone, Robert W Taylor, Andrés Nascimento, et al.
Nature Communications
|
February 19, 2021
POLRMT mutations impair mitochondrial transcription causing neurological disease
Monika Oláhová, Bradley Peter, Zsolt Szilagyi, et al.
American Journal of Human Genetics
|
July 31, 2018
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder
Carol-Anne Martin, Kata Sarlós, Clare V Logan, et al.
American Journal of Human Genetics
|
May 3, 2024
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder
Carol-Anne Martin, Kata Sarlós, Clare V Logan, et al.
American Journal of Human Genetics
|
September 8, 2018
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder
Carol-Anne Martin, Kata Sarlós, Clare V Logan, et al.
Human Mutation
|
April 23, 2013
ANO5 gene analysis in a large cohort of patients with anoctaminopathy: confirmation of male prevalence and high occurrence of the common exon 5 gene mutation
Anna Sarkozy, Debbie Hicks, Judith Hudson, et al.
Neurology
|
January 30, 2025
Characterization of Factors Associated With Death in Deceased Patients With Mitochondrial Disorders: A Multicenter Cross-Sectional Survey
Alina Ivaniuk, Irina A Anselm, Aaron Bowen, et al.
The New England Journal of Medicine
|
November 10, 2021
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report
, Damian Smedley, Katherine R Smith, et al.
Page
of 30