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M Stone

Showing results (1251-1260 of 2,138) with videos related to

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American Journal of Ophthalmology|December 10, 2002
A case-control comparison of the clinical characteristics of glaucoma and ocular hypertensive patients with and without the myocilin Gln368Stop mutationThomas A Graul, Young H Kwon, M Bridget Zimmerman, et al.
Global Advances in Health and Medicine|September 2, 2021
Incorporating Acupuncture Into American Healthcare: Initiating a Discussion on Implementation Science, the Status of the Field, and Stakeholder ConsiderationsDavid W Miller, Eric J Roseen, Jennifer A M Stone, et al.
American Journal of Clinical Oncology|April 16, 1998
Prognostic value of K-ras mutations, ras oncoprotein, and c-erb B-2 oncoprotein expression in adenocarcinoma of the lungJ Nemunaitis, S Klemow, A Tong, et al.
Pharmacogenetics|July 27, 2001
N-Acetyltransferases, sulfotransferases and heterocyclic amine activation in the breastJ A Williams, E M Stone, G Fakis, et al.
Biomaterials|July 8, 1999
Preventing bacterial adhesion onto surfaces: the low-surface-energy approachJ Tsibouklis, M Stone, A A Thorpe, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 10, 2008
Association of a novel mutation in the retinol dehydrogenase 12 (RDH12) gene with autosomal dominant retinitis pigmentosaJohn H Fingert, Kean Oh, Mina Chung, et al.
American Journal of Ophthalmology|March 17, 2007
Familial cavitary optic disk anomalies: clinical features of a large family with examples of progressive optic nerve head cuppingRobert A Honkanen, Lee M Jampol, John H Fingert, et al.
Investigative Ophthalmology & Visual Science|August 1, 2013
Subretinal gene therapy of mice with Bardet-Biedl syndrome type 1Seongjin Seo, Robert F Mullins, Alina V Dumitrescu, et al.
Human Molecular Genetics|April 1, 1997
Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase geneA Nystuen, H Costeff, O N Elpeleg, et al.
Community Mental Health Journal|August 1, 2024
Effects of Texas State Agency Integration on Mental Health Service Use Among Individuals with Co-occurring Cognitive Disabilities and Mental Health ConditionsElizabeth M Stone, Andrew D Jopson, Nicholas J Seewald, et al.
Pageof 214

Showing results (1251-1260 of 2,138) with videos related to

Sort By:
Pageof 214
American Journal of Ophthalmology|December 10, 2002
A case-control comparison of the clinical characteristics of glaucoma and ocular hypertensive patients with and without the myocilin Gln368Stop mutationThomas A Graul, Young H Kwon, M Bridget Zimmerman, et al.
Global Advances in Health and Medicine|September 2, 2021
Incorporating Acupuncture Into American Healthcare: Initiating a Discussion on Implementation Science, the Status of the Field, and Stakeholder ConsiderationsDavid W Miller, Eric J Roseen, Jennifer A M Stone, et al.
American Journal of Clinical Oncology|April 16, 1998
Prognostic value of K-ras mutations, ras oncoprotein, and c-erb B-2 oncoprotein expression in adenocarcinoma of the lungJ Nemunaitis, S Klemow, A Tong, et al.
Pharmacogenetics|July 27, 2001
N-Acetyltransferases, sulfotransferases and heterocyclic amine activation in the breastJ A Williams, E M Stone, G Fakis, et al.
Biomaterials|July 8, 1999
Preventing bacterial adhesion onto surfaces: the low-surface-energy approachJ Tsibouklis, M Stone, A A Thorpe, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 10, 2008
Association of a novel mutation in the retinol dehydrogenase 12 (RDH12) gene with autosomal dominant retinitis pigmentosaJohn H Fingert, Kean Oh, Mina Chung, et al.
American Journal of Ophthalmology|March 17, 2007
Familial cavitary optic disk anomalies: clinical features of a large family with examples of progressive optic nerve head cuppingRobert A Honkanen, Lee M Jampol, John H Fingert, et al.
Investigative Ophthalmology & Visual Science|August 1, 2013
Subretinal gene therapy of mice with Bardet-Biedl syndrome type 1Seongjin Seo, Robert F Mullins, Alina V Dumitrescu, et al.
Human Molecular Genetics|April 1, 1997
Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase geneA Nystuen, H Costeff, O N Elpeleg, et al.
Community Mental Health Journal|August 1, 2024
Effects of Texas State Agency Integration on Mental Health Service Use Among Individuals with Co-occurring Cognitive Disabilities and Mental Health ConditionsElizabeth M Stone, Andrew D Jopson, Nicholas J Seewald, et al.
Pageof 214