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The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
October 16, 2020
Newborn Screening for Spinal Muscular Atrophy: Ontario Testing and Follow-up Recommendations
Hugh J McMillan, Kristin D Kernohan, Ed Yeh, et al.
Journal of Molecular Histology
|
November 25, 2020
NAIP expression increases in a rat model of liver mass restoration
Julio Plaza-Díaz, Ana I Álvarez-Mercado, Cándido Robles-Sánchez, et al.
Water Research
|
October 6, 2024
Urban wastewater contains a functional human antibody repertoire of mucosal origin
Sean Stephenson, Walaa Eid, Chandler Hayyin Wong, et al.
Plos One
|
March 9, 2018
Inhibitor of apoptosis proteins, NAIP, cIAP1 and cIAP2 expression during macrophage differentiation and M1/M2 polarization
Virginia Morón-Calvente, Salvador Romero-Pinedo, Sofía Toribio-Castelló, et al.
Paediatrics & Child Health
|
February 27, 2018
The Canadian Neuromuscular Disease Registry: Connecting patients to national and international research opportunities
Yi Wei, Anna McCormick, Alex MacKenzie, et al.
Muscle & Nerve
|
September 24, 2025
Feasibility of a Home-Based Exergaming Intervention for Youth With Spinal Muscular Atrophy
Ihsane Iraqi, Pamela Ng, Xing Chen, et al.
Orphanet Journal of Rare Diseases
|
November 28, 2012
Specific combination of compound heterozygous mutations in 17β-hydroxysteroid dehydrogenase type 4 (HSD17B4) defines a new subtype of D-bifunctional protein deficiency
Hugh J McMillan, Thea Worthylake, Jeremy Schwartzentruber, et al.
European Journal of Human Genetics : EJHG
|
November 26, 2015
DNM1L-related mitochondrial fission defect presenting as refractory epilepsy
Jason R Vanstone, Amanda M Smith, Skye McBride, et al.
Genetics
|
October 25, 2017
Pyridoxine-Dependent Epilepsy in Zebrafish Caused by Aldh7a1 Deficiency
Izabella A Pena, Yann Roussel, Kate Daniel, et al.
Annals of the American Thoracic Society
|
August 2, 2017
An Official American Thoracic Society Workshop Report: Translational Research in Rare Respiratory Diseases
Arnold S Kristof, Basil J Petrof, Qutayba Hamid, et al.
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of 5
Search research articles
Search
Showing results (31-40 of 48) with videos related to
Sort By:
Page
of 5
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
October 16, 2020
Newborn Screening for Spinal Muscular Atrophy: Ontario Testing and Follow-up Recommendations
Hugh J McMillan, Kristin D Kernohan, Ed Yeh, et al.
Journal of Molecular Histology
|
November 25, 2020
NAIP expression increases in a rat model of liver mass restoration
Julio Plaza-Díaz, Ana I Álvarez-Mercado, Cándido Robles-Sánchez, et al.
Water Research
|
October 6, 2024
Urban wastewater contains a functional human antibody repertoire of mucosal origin
Sean Stephenson, Walaa Eid, Chandler Hayyin Wong, et al.
Plos One
|
March 9, 2018
Inhibitor of apoptosis proteins, NAIP, cIAP1 and cIAP2 expression during macrophage differentiation and M1/M2 polarization
Virginia Morón-Calvente, Salvador Romero-Pinedo, Sofía Toribio-Castelló, et al.
Paediatrics & Child Health
|
February 27, 2018
The Canadian Neuromuscular Disease Registry: Connecting patients to national and international research opportunities
Yi Wei, Anna McCormick, Alex MacKenzie, et al.
Muscle & Nerve
|
September 24, 2025
Feasibility of a Home-Based Exergaming Intervention for Youth With Spinal Muscular Atrophy
Ihsane Iraqi, Pamela Ng, Xing Chen, et al.
Orphanet Journal of Rare Diseases
|
November 28, 2012
Specific combination of compound heterozygous mutations in 17β-hydroxysteroid dehydrogenase type 4 (HSD17B4) defines a new subtype of D-bifunctional protein deficiency
Hugh J McMillan, Thea Worthylake, Jeremy Schwartzentruber, et al.
European Journal of Human Genetics : EJHG
|
November 26, 2015
DNM1L-related mitochondrial fission defect presenting as refractory epilepsy
Jason R Vanstone, Amanda M Smith, Skye McBride, et al.
Genetics
|
October 25, 2017
Pyridoxine-Dependent Epilepsy in Zebrafish Caused by Aldh7a1 Deficiency
Izabella A Pena, Yann Roussel, Kate Daniel, et al.
Annals of the American Thoracic Society
|
August 2, 2017
An Official American Thoracic Society Workshop Report: Translational Research in Rare Respiratory Diseases
Arnold S Kristof, Basil J Petrof, Qutayba Hamid, et al.
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of 5