Search research articles
Contact Us
Filters
Showing results (151-160 of 176) with videos related to
Page
of 18
Sort By:
Orphanet Journal of Rare Diseases
|
September 8, 2017
Exome sequences versus sequential gene testing in the UK highly specialised Service for Limb Girdle Muscular Dystrophy
Elizabeth Harris, Ana Topf, Rita Barresi, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
January 10, 2015
Transcriptional corepressor MTG16 regulates small intestinal crypt proliferation and crypt regeneration after radiation-induced injury
Shenika V Poindexter, Vishruth K Reddy, Mukul K Mittal, et al.
Health Promotion International
|
April 24, 2018
Understanding Australian policies on public health using social and political science theories: reflections from an Academy of the Social Sciences in Australia Workshop
Fran Baum, Adam Graycar, Toni Delany-Crowe, et al.
Journal of Medical Genetics
|
August 29, 2024
Loss-of-function variants in <i>JPH1</i> cause congenital myopathy with prominent facial and ocular involvement
Mridul Johari, Ana Topf, Chiara Folland, et al.
Neuromuscular Disorders : NMD
|
June 19, 2017
Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domains
Elizabeth Harris, Umar Burki, Chiara Marini-Bettolo, et al.
Brain Communications
|
August 23, 2021
Identification of <i>LAMA1</i> mutations ends diagnostic odyssey and has prognostic implications for patients with presumed Joubert syndrome
Laura Powell, Eric Olinger, Sarah Wedderburn, et al.
Brain : a Journal of Neurology
|
October 24, 2025
EXOSC10 haploinsufficiency causes primary microcephaly by derepression of Sonic hedgehog signalling
Pauline Antonie Ulmke, M Sadman Sakib, Dang Ton Nguyen, et al.
European Journal of Neurology
|
February 4, 2022
The prevalence and associated factors of motoric cognitive risk syndrome in multiple ethnic middle-aged to older adults in west China: a cross-sectional study
Xuelian Sun, Kiyana Elizabeth Harris, Lisha Hou, et al.
Neurology. Clinical Practice
|
February 18, 2026
Assessing the Relationship of Quality of Life With Functional Status in a Large Cohort of Adult Patients With Neuromuscular Disorders
Karen S W Wong, Anando Sen, Jassi Michell-Sodhi, et al.
Neuromuscular Disorders : NMD
|
June 29, 2025
Levels of exercise exposure among people living with neuromuscular disorders: lessons learned from real-world data
Mark Richardson, Virginie Kinet, Karen Wong, et al.
Page
of 18
Search research articles
Search
Showing results (151-160 of 176) with videos related to
Sort By:
Page
of 18
Orphanet Journal of Rare Diseases
|
September 8, 2017
Exome sequences versus sequential gene testing in the UK highly specialised Service for Limb Girdle Muscular Dystrophy
Elizabeth Harris, Ana Topf, Rita Barresi, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
January 10, 2015
Transcriptional corepressor MTG16 regulates small intestinal crypt proliferation and crypt regeneration after radiation-induced injury
Shenika V Poindexter, Vishruth K Reddy, Mukul K Mittal, et al.
Health Promotion International
|
April 24, 2018
Understanding Australian policies on public health using social and political science theories: reflections from an Academy of the Social Sciences in Australia Workshop
Fran Baum, Adam Graycar, Toni Delany-Crowe, et al.
Journal of Medical Genetics
|
August 29, 2024
Loss-of-function variants in <i>JPH1</i> cause congenital myopathy with prominent facial and ocular involvement
Mridul Johari, Ana Topf, Chiara Folland, et al.
Neuromuscular Disorders : NMD
|
June 19, 2017
Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domains
Elizabeth Harris, Umar Burki, Chiara Marini-Bettolo, et al.
Brain Communications
|
August 23, 2021
Identification of <i>LAMA1</i> mutations ends diagnostic odyssey and has prognostic implications for patients with presumed Joubert syndrome
Laura Powell, Eric Olinger, Sarah Wedderburn, et al.
Brain : a Journal of Neurology
|
October 24, 2025
EXOSC10 haploinsufficiency causes primary microcephaly by derepression of Sonic hedgehog signalling
Pauline Antonie Ulmke, M Sadman Sakib, Dang Ton Nguyen, et al.
European Journal of Neurology
|
February 4, 2022
The prevalence and associated factors of motoric cognitive risk syndrome in multiple ethnic middle-aged to older adults in west China: a cross-sectional study
Xuelian Sun, Kiyana Elizabeth Harris, Lisha Hou, et al.
Neurology. Clinical Practice
|
February 18, 2026
Assessing the Relationship of Quality of Life With Functional Status in a Large Cohort of Adult Patients With Neuromuscular Disorders
Karen S W Wong, Anando Sen, Jassi Michell-Sodhi, et al.
Neuromuscular Disorders : NMD
|
June 29, 2025
Levels of exercise exposure among people living with neuromuscular disorders: lessons learned from real-world data
Mark Richardson, Virginie Kinet, Karen Wong, et al.
Page
of 18