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T R Clarke

Showing results (51-60 of 119) with videos related to

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Human Genetics|June 5, 2004
Gene symbol: ATP7A. Disease: Menkes diseaseZ Tumer, N Horn, T Tonnesen, et al.
Bone Marrow Transplantation|July 3, 2003
Life-threatening pulmonary hemorrhages post bone marrow transplantation in Hurler syndrome. Report of three cases and review of the literatureA Gassas, L Sung, J J Doyle, et al.
Journal of Pediatric Hematology/Oncology|September 19, 2008
Novel mutation of the perforin gene and maternal uniparental disomy 10 in a patient with familial hemophagocytic lymphohistiocytosisFatma Al-Jasmi, Mohamed Abdelhaleem, Tracy Stockley, et al.
Journal of Inherited Metabolic Disease|January 27, 2009
Proposed high-risk screening protocol for Fabry disease in patients with renal and vascular diseaseC Auray-Blais, D S Millington, S P Young, et al.
Steroids|January 1, 1997
The multiple murine 3 beta-hydroxysteroid dehydrogenase isoforms: structure, function, and tissue- and developmentally specific expressionA H Payne, I G Abbaszade, T R Clarke, et al.
The West Indian Medical Journal|March 2, 2011
Disclosure of HIV status among HIV clinic attendees in JamaicaT R Clarke, R Gibson, G Barrow, et al.
Circulation|February 7, 2007
Images in cardiovascular medicine. Left ventricular aneurysm associated with mucopolysaccharidosis type VI syndrome (Maroteaux-Lamy syndrome)Gavin Y Oudit, Jagdish Butany, William G Williams, et al.
Analytical Chemistry|February 8, 2012
Urinary globotriaosylsphingosine-related biomarkers for Fabry disease targeted by metabolomicsChristiane Auray-Blais, Michel Boutin, René Gagnon, et al.
Molecular Endocrinology (Baltimore, Md.)|May 29, 2001
Müllerian inhibiting substance signaling uses a bone morphogenetic protein (BMP)-like pathway mediated by ALK2 and induces SMAD6 expressionT R Clarke, Y Hoshiya, S E Yi, et al.
Clinical Dysmorphology|April 3, 2009
Punctate calcifications in lysosomal storage disordersIda Vanessa Doederlein Schwartz, Osvaldo Artigalás, Markus Ries, et al.
Pageof 12

Showing results (51-60 of 119) with videos related to

Sort By:
Pageof 12
Human Genetics|June 5, 2004
Gene symbol: ATP7A. Disease: Menkes diseaseZ Tumer, N Horn, T Tonnesen, et al.
Bone Marrow Transplantation|July 3, 2003
Life-threatening pulmonary hemorrhages post bone marrow transplantation in Hurler syndrome. Report of three cases and review of the literatureA Gassas, L Sung, J J Doyle, et al.
Journal of Pediatric Hematology/Oncology|September 19, 2008
Novel mutation of the perforin gene and maternal uniparental disomy 10 in a patient with familial hemophagocytic lymphohistiocytosisFatma Al-Jasmi, Mohamed Abdelhaleem, Tracy Stockley, et al.
Journal of Inherited Metabolic Disease|January 27, 2009
Proposed high-risk screening protocol for Fabry disease in patients with renal and vascular diseaseC Auray-Blais, D S Millington, S P Young, et al.
Steroids|January 1, 1997
The multiple murine 3 beta-hydroxysteroid dehydrogenase isoforms: structure, function, and tissue- and developmentally specific expressionA H Payne, I G Abbaszade, T R Clarke, et al.
The West Indian Medical Journal|March 2, 2011
Disclosure of HIV status among HIV clinic attendees in JamaicaT R Clarke, R Gibson, G Barrow, et al.
Circulation|February 7, 2007
Images in cardiovascular medicine. Left ventricular aneurysm associated with mucopolysaccharidosis type VI syndrome (Maroteaux-Lamy syndrome)Gavin Y Oudit, Jagdish Butany, William G Williams, et al.
Analytical Chemistry|February 8, 2012
Urinary globotriaosylsphingosine-related biomarkers for Fabry disease targeted by metabolomicsChristiane Auray-Blais, Michel Boutin, René Gagnon, et al.
Molecular Endocrinology (Baltimore, Md.)|May 29, 2001
Müllerian inhibiting substance signaling uses a bone morphogenetic protein (BMP)-like pathway mediated by ALK2 and induces SMAD6 expressionT R Clarke, Y Hoshiya, S E Yi, et al.
Clinical Dysmorphology|April 3, 2009
Punctate calcifications in lysosomal storage disordersIda Vanessa Doederlein Schwartz, Osvaldo Artigalás, Markus Ries, et al.
Pageof 12