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Neuromuscular Disorders : NMD
|
October 29, 2000
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)
L V Anderson, R M Harrison, R Pogue, et al.
American Journal of Medical Genetics
|
August 15, 2001
Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy
C A Brown, R W Lanning, K Q McKinney, et al.
Academic Emergency Medicine : Official Journal of the Society for Academic Emergency Medicine
|
December 3, 2014
A research agenda for gender and substance use disorders in the emergency department
Esther K Choo, Gillian Beauchamp, Francesca L Beaudoin, et al.
Journal of Inherited Metabolic Disease
|
November 18, 2016
Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision
Nikolas Boy, Chris Mühlhausen, Esther M Maier, et al.
Gastroenterology
|
December 12, 1997
Risk and significance of endoscopic/radiological evidence of recurrent Crohn's disease
R S McLeod, B G Wolff, A H Steinhart, et al.
Journal of Inherited Metabolic Disease
|
January 5, 2007
Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)
S Kölker, E Christensen, J V Leonard, et al.
Canadian Journal of Gastroenterology = Journal Canadien De Gastroenterologie
|
March 21, 2008
Review and clinical perspectives for the use of infliximab in ulcerative colitis
R Panaccione, R N Fedorak, G Aumais, et al.
Science (New York, N.Y.)
|
January 31, 1992
Lunar impact basins and crustal heterogeneity: new Western limb and far side data from galileo
M J Belton, J W Head, C M Pieters, et al.
Trials
|
December 21, 2017
Establishing core outcome sets for phenylketonuria (PKU) and medium-chain Acyl-CoA dehydrogenase (MCAD) deficiency in children: study protocol for systematic reviews and Delphi surveys
Beth K Potter, Brian Hutton, Tammy J Clifford, et al.
Alimentary Pharmacology & Therapeutics
|
July 16, 2013
Review article: a clinician's guide for therapeutic drug monitoring of infliximab in inflammatory bowel disease
R Khanna, B D Sattin, W Afif, et al.
Page
of 85
Search research articles
Search
Showing results (811-820 of 844) with videos related to
Sort By:
Page
of 85
Neuromuscular Disorders : NMD
|
October 29, 2000
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)
L V Anderson, R M Harrison, R Pogue, et al.
American Journal of Medical Genetics
|
August 15, 2001
Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy
C A Brown, R W Lanning, K Q McKinney, et al.
Academic Emergency Medicine : Official Journal of the Society for Academic Emergency Medicine
|
December 3, 2014
A research agenda for gender and substance use disorders in the emergency department
Esther K Choo, Gillian Beauchamp, Francesca L Beaudoin, et al.
Journal of Inherited Metabolic Disease
|
November 18, 2016
Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision
Nikolas Boy, Chris Mühlhausen, Esther M Maier, et al.
Gastroenterology
|
December 12, 1997
Risk and significance of endoscopic/radiological evidence of recurrent Crohn's disease
R S McLeod, B G Wolff, A H Steinhart, et al.
Journal of Inherited Metabolic Disease
|
January 5, 2007
Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)
S Kölker, E Christensen, J V Leonard, et al.
Canadian Journal of Gastroenterology = Journal Canadien De Gastroenterologie
|
March 21, 2008
Review and clinical perspectives for the use of infliximab in ulcerative colitis
R Panaccione, R N Fedorak, G Aumais, et al.
Science (New York, N.Y.)
|
January 31, 1992
Lunar impact basins and crustal heterogeneity: new Western limb and far side data from galileo
M J Belton, J W Head, C M Pieters, et al.
Trials
|
December 21, 2017
Establishing core outcome sets for phenylketonuria (PKU) and medium-chain Acyl-CoA dehydrogenase (MCAD) deficiency in children: study protocol for systematic reviews and Delphi surveys
Beth K Potter, Brian Hutton, Tammy J Clifford, et al.
Alimentary Pharmacology & Therapeutics
|
July 16, 2013
Review article: a clinician's guide for therapeutic drug monitoring of infliximab in inflammatory bowel disease
R Khanna, B D Sattin, W Afif, et al.
Page
of 85