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World Journal of Pediatrics : WJP
|
May 4, 2017
Newborn screening for Duchenne muscular dystrophy in China: follow-up diagnosis and subsequent treatment
Qing Ke, Zheng-Yan Zhao, Robert Griggs, et al.
Journal of Neuromuscular Diseases
|
January 8, 2024
The Early Care (0-3 Years) In Duchenne Muscular Dystrophy Meeting Report
Niki Armstrong, Susan Apkon, Kiera N Berggren, et al.
Annals of Neurology
|
December 15, 2015
MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs
Obaid M Albulym, Marina L Kennerson, Matthew B Harms, et al.
Journal of Neuromuscular Diseases
|
April 5, 2018
Treatment Algorithm for Infants Diagnosed with Spinal Muscular Atrophy through Newborn Screening
Jacqueline Glascock, Jacinda Sampson, Amanda Haidet-Phillips, et al.
Neuromuscular Disorders : NMD
|
October 2, 2009
DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy
Kevin M Flanigan, Diane M Dunn, Andrew von Niederhausern, et al.
Sexually Transmitted Infections
|
March 27, 2023
Sexual and reproductive health in Britain during the first year of the COVID-19 pandemic: cross-sectional population survey (Natsal-COVID-Wave 2) and national surveillance data
Kirstin R Mitchell, Malachi Willis, Emily Dema, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
April 13, 2023
Standardising outcome reporting for clinical trials of interventions for heavy menstrual bleeding: Development of a core outcome set
Natalie A M Cooper, Carol Rivas, Malcolm G Munro, et al.
Muscle & Nerve
|
June 22, 2020
The CINRG Becker Natural History Study: Baseline characteristics
Paula R Clemens, Gabriela Niizawa, Jia Feng, et al.
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of 4
Search research articles
Search
Showing results (31-40 of 38) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 38 results.
World Journal of Pediatrics : WJP
|
May 4, 2017
Newborn screening for Duchenne muscular dystrophy in China: follow-up diagnosis and subsequent treatment
Qing Ke, Zheng-Yan Zhao, Robert Griggs, et al.
Journal of Neuromuscular Diseases
|
January 8, 2024
The Early Care (0-3 Years) In Duchenne Muscular Dystrophy Meeting Report
Niki Armstrong, Susan Apkon, Kiera N Berggren, et al.
Annals of Neurology
|
December 15, 2015
MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs
Obaid M Albulym, Marina L Kennerson, Matthew B Harms, et al.
Journal of Neuromuscular Diseases
|
April 5, 2018
Treatment Algorithm for Infants Diagnosed with Spinal Muscular Atrophy through Newborn Screening
Jacqueline Glascock, Jacinda Sampson, Amanda Haidet-Phillips, et al.
Neuromuscular Disorders : NMD
|
October 2, 2009
DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy
Kevin M Flanigan, Diane M Dunn, Andrew von Niederhausern, et al.
Sexually Transmitted Infections
|
March 27, 2023
Sexual and reproductive health in Britain during the first year of the COVID-19 pandemic: cross-sectional population survey (Natsal-COVID-Wave 2) and national surveillance data
Kirstin R Mitchell, Malachi Willis, Emily Dema, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
April 13, 2023
Standardising outcome reporting for clinical trials of interventions for heavy menstrual bleeding: Development of a core outcome set
Natalie A M Cooper, Carol Rivas, Malcolm G Munro, et al.
Muscle & Nerve
|
June 22, 2020
The CINRG Becker Natural History Study: Baseline characteristics
Paula R Clemens, Gabriela Niizawa, Jia Feng, et al.
Page
of 4