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Medrxiv : the Preprint Server for Health Sciences
|
February 19, 2024
Loss-of-function variants in <i>JPH1</i> cause congenital myopathy with prominent facial involvement
Mridul Johari, Ana Topf, Chiara Folland, et al.
Journal of Cellular Physiology
|
May 2, 2017
The skeletal cell-derived molecule sclerostin drives bone marrow adipogenesis
Heather Fairfield, Carolyne Falank, Elizabeth Harris, et al.
The Journal of Allergy and Clinical Immunology
|
January 26, 2019
ADRB2 p.Thr164Ile association with hospitalization depends upon asthma severity
Lynn D Condreay, Mathias N Chiano, Li Li, et al.
Australian Journal of Primary Health
|
September 19, 2024
Codesigning a Community Health Navigator program to assist patients to transition from hospital to community
Mark F Harris, An Tran, Mamta Porwal, et al.
Cell Calcium
|
May 31, 2022
STIM1 and ORAI1 mutations leading to tubular aggregate myopathies are sensitive to the Store-operated Ca<sup>2+</sup>-entry modulators CIC-37 and CIC-39
Beatrice Riva, Emanuela Pessolano, Edoardo Quaglia, et al.
Australian and New Zealand Journal of Public Health
|
June 4, 2014
Characteristics of health impact assessments reported in Australia and New Zealand 2005-2009
Fiona Haigh, Elizabeth Harris, Harrison N G Chok, et al.
International Journal of Molecular Sciences
|
July 27, 2024
An Integrated Transcriptomics and Genomics Approach Detects an X/Autosome Translocation in a Female with Duchenne Muscular Dystrophy
Alba Segarra-Casas, Vicente A Yépez, German Demidov, et al.
BMJ Open
|
February 3, 2024
Community health navigator-assisted transition of care from hospital to community: protocol for a randomised controlled trial
Sharon M Parker, Parisa Aslani, Ben Harris-Roxas, et al.
Ebiomedicine
|
December 22, 2019
A multistage sequencing strategy pinpoints novel candidate alleles for Emery-Dreifuss muscular dystrophy and supports gene misregulation as its pathomechanism
Peter Meinke, Alastair R W Kerr, Rafal Czapiewski, et al.
Neuromuscular Disorders : NMD
|
December 22, 2024
Desmoid tumour: a rare cause of congenital unilateral calf enlargement mimicking calf hypertrophy
Maha Elseed, James N Sampson, Tuomo Polvikoski, et al.
Page
of 18
Search research articles
Search
Showing results (141-150 of 176) with videos related to
Sort By:
Page
of 18
Medrxiv : the Preprint Server for Health Sciences
|
February 19, 2024
Loss-of-function variants in <i>JPH1</i> cause congenital myopathy with prominent facial involvement
Mridul Johari, Ana Topf, Chiara Folland, et al.
Journal of Cellular Physiology
|
May 2, 2017
The skeletal cell-derived molecule sclerostin drives bone marrow adipogenesis
Heather Fairfield, Carolyne Falank, Elizabeth Harris, et al.
The Journal of Allergy and Clinical Immunology
|
January 26, 2019
ADRB2 p.Thr164Ile association with hospitalization depends upon asthma severity
Lynn D Condreay, Mathias N Chiano, Li Li, et al.
Australian Journal of Primary Health
|
September 19, 2024
Codesigning a Community Health Navigator program to assist patients to transition from hospital to community
Mark F Harris, An Tran, Mamta Porwal, et al.
Cell Calcium
|
May 31, 2022
STIM1 and ORAI1 mutations leading to tubular aggregate myopathies are sensitive to the Store-operated Ca<sup>2+</sup>-entry modulators CIC-37 and CIC-39
Beatrice Riva, Emanuela Pessolano, Edoardo Quaglia, et al.
Australian and New Zealand Journal of Public Health
|
June 4, 2014
Characteristics of health impact assessments reported in Australia and New Zealand 2005-2009
Fiona Haigh, Elizabeth Harris, Harrison N G Chok, et al.
International Journal of Molecular Sciences
|
July 27, 2024
An Integrated Transcriptomics and Genomics Approach Detects an X/Autosome Translocation in a Female with Duchenne Muscular Dystrophy
Alba Segarra-Casas, Vicente A Yépez, German Demidov, et al.
BMJ Open
|
February 3, 2024
Community health navigator-assisted transition of care from hospital to community: protocol for a randomised controlled trial
Sharon M Parker, Parisa Aslani, Ben Harris-Roxas, et al.
Ebiomedicine
|
December 22, 2019
A multistage sequencing strategy pinpoints novel candidate alleles for Emery-Dreifuss muscular dystrophy and supports gene misregulation as its pathomechanism
Peter Meinke, Alastair R W Kerr, Rafal Czapiewski, et al.
Neuromuscular Disorders : NMD
|
December 22, 2024
Desmoid tumour: a rare cause of congenital unilateral calf enlargement mimicking calf hypertrophy
Maha Elseed, James N Sampson, Tuomo Polvikoski, et al.
Page
of 18