Search research articles
Contact Us
Filters
Showing results (81-90 of 119) with videos related to
Page
of 12
Sort By:
The West Indian Medical Journal
|
March 2, 2011
Validation of the Beck Depression Inventory II in HIV-positive patients
G E Lipps, G A Lowe, W De La Haye, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
September 25, 2012
An evaluation framework for funding drugs for rare diseases
Eric Winquist, Chaim M Bell, Joe T R Clarke, et al.
Echocardiography (Mount Kisco, N.Y.)
|
April 14, 2012
Systolic myocardial mechanics in patients with Anderson-Fabry disease with and without left ventricular hypertrophy and in comparison to nonobstructive hypertrophic cardiomyopathy
Christiane Gruner, Flavia Verocai, Shemy Carasso, et al.
Pediatrics
|
October 4, 2006
The natural history of juvenile or subacute GM2 gangliosidosis: 21 new cases and literature review of 134 previously reported
Gustavo H B Maegawa, Tracy Stockley, Michael Tropak, et al.
Analytica Chimica Acta
|
August 28, 2016
UPLC-MS/MS detection of disaccharides derived from glycosaminoglycans as biomarkers of mucopolysaccharidoses
Christiane Auray-Blais, Pamela Lavoie, Shunji Tomatsu, et al.
Molecular Genetics and Metabolism
|
October 12, 2010
Efficient analysis of urinary glycosaminoglycans by LC-MS/MS in mucopolysaccharidoses type I, II and VI
Christiane Auray-Blais, Patrick Bhérer, René Gagnon, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 10, 2017
Long-term outcome of patients with X-linked adrenoleukodystrophy: A retrospective cohort study
Christel Tran, Jaina Patel, Hewson Stacy, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
September 15, 2011
Impact of measures to enhance the value of observational surveys in rare diseases: the Fabry Outcome Survey (FOS)
Joe T R Clarke, Roberto Giugliani, Gere Sunder-Plassmann, et al.
Lancet (London, England)
|
December 5, 2009
Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data
A Mehta, M Beck, P Elliott, et al.
American Journal of Medical Genetics. Part A
|
June 14, 2006
Novel mutations in dihydrolipoamide dehydrogenase deficiency in two cousins with borderline-normal PDH complex activity
Jessie M Cameron, Valeriy Levandovskiy, Neviana Mackay, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 119) with videos related to
Sort By:
Page
of 12
The West Indian Medical Journal
|
March 2, 2011
Validation of the Beck Depression Inventory II in HIV-positive patients
G E Lipps, G A Lowe, W De La Haye, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
September 25, 2012
An evaluation framework for funding drugs for rare diseases
Eric Winquist, Chaim M Bell, Joe T R Clarke, et al.
Echocardiography (Mount Kisco, N.Y.)
|
April 14, 2012
Systolic myocardial mechanics in patients with Anderson-Fabry disease with and without left ventricular hypertrophy and in comparison to nonobstructive hypertrophic cardiomyopathy
Christiane Gruner, Flavia Verocai, Shemy Carasso, et al.
Pediatrics
|
October 4, 2006
The natural history of juvenile or subacute GM2 gangliosidosis: 21 new cases and literature review of 134 previously reported
Gustavo H B Maegawa, Tracy Stockley, Michael Tropak, et al.
Analytica Chimica Acta
|
August 28, 2016
UPLC-MS/MS detection of disaccharides derived from glycosaminoglycans as biomarkers of mucopolysaccharidoses
Christiane Auray-Blais, Pamela Lavoie, Shunji Tomatsu, et al.
Molecular Genetics and Metabolism
|
October 12, 2010
Efficient analysis of urinary glycosaminoglycans by LC-MS/MS in mucopolysaccharidoses type I, II and VI
Christiane Auray-Blais, Patrick Bhérer, René Gagnon, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 10, 2017
Long-term outcome of patients with X-linked adrenoleukodystrophy: A retrospective cohort study
Christel Tran, Jaina Patel, Hewson Stacy, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
September 15, 2011
Impact of measures to enhance the value of observational surveys in rare diseases: the Fabry Outcome Survey (FOS)
Joe T R Clarke, Roberto Giugliani, Gere Sunder-Plassmann, et al.
Lancet (London, England)
|
December 5, 2009
Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data
A Mehta, M Beck, P Elliott, et al.
American Journal of Medical Genetics. Part A
|
June 14, 2006
Novel mutations in dihydrolipoamide dehydrogenase deficiency in two cousins with borderline-normal PDH complex activity
Jessie M Cameron, Valeriy Levandovskiy, Neviana Mackay, et al.
Page
of 12