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Clinical and Experimental Nephrology
|
May 1, 2017
A randomized, controlled clinical trial to evaluate the immunogenicity of a PreS/S hepatitis B vaccine Sci-B-Vac™, as compared to Engerix B<sup>®</sup>, among vaccine naïve and vaccine non-responder dialysis patients
E Elhanan, M Boaz, I Schwartz, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
May 1, 1989
Hepatic and biliary tract abnormalities in patients with AIDS. Sonographic-pathologic correlation
K Grumbach, B G Coleman, A A Gal, et al.
Human Mutation
|
January 1, 1993
Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase gene
J J Hopwood, S Bunge, C P Morris, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
June 23, 2000
Immunolocalization of activated transforming growth factor beta1 in juvenile nasopharyngeal angiofibroma
D G Dillard, C Cohen, S Muller, et al.
Journal of Biotechnology
|
March 27, 2001
Engineering zucchini yellow mosaic potyvirus as a non-pathogenic vector for expression of heterologous proteins in cucurbits
T Arazi, S G Slutsky, Y M Shiboleth, et al.
The American Journal of Surgical Pathology
|
August 26, 1998
Survival analysis of 200 pulmonary neuroendocrine tumors with clarification of criteria for atypical carcinoid and its separation from typical carcinoid
W D Travis, W Rush, D B Flieder, et al.
The Annals of Thoracic Surgery
|
February 19, 2013
Routine intraoperative frozen section analysis of bronchial margins is of limited utility in lung cancer resection
Rachel M Owen, Seth D Force, Anthony A Gal, et al.
Journal of Inherited Metabolic Disease
|
January 24, 2002
Anderson-Fabry disease: clinical manifestations of disease in female heterozygotes
C Whybra, C Kampmann, I Willers, et al.
Advances in Oto-Rhino-Laryngology
|
June 27, 2000
Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3
H S Scott, S E Antonarakis, L Mittaz, et al.
American Journal of Medical Genetics
|
April 1, 1990
Gene of type II autosomal dominant retinitis pigmentosa maps on the long arm of chromosome 3
J E Olsson, C Samanns, J Jimenez, et al.
Page
of 49
Search research articles
Search
Showing results (361-370 of 488) with videos related to
Sort By:
Page
of 49
Clinical and Experimental Nephrology
|
May 1, 2017
A randomized, controlled clinical trial to evaluate the immunogenicity of a PreS/S hepatitis B vaccine Sci-B-Vac™, as compared to Engerix B<sup>®</sup>, among vaccine naïve and vaccine non-responder dialysis patients
E Elhanan, M Boaz, I Schwartz, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
May 1, 1989
Hepatic and biliary tract abnormalities in patients with AIDS. Sonographic-pathologic correlation
K Grumbach, B G Coleman, A A Gal, et al.
Human Mutation
|
January 1, 1993
Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase gene
J J Hopwood, S Bunge, C P Morris, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
June 23, 2000
Immunolocalization of activated transforming growth factor beta1 in juvenile nasopharyngeal angiofibroma
D G Dillard, C Cohen, S Muller, et al.
Journal of Biotechnology
|
March 27, 2001
Engineering zucchini yellow mosaic potyvirus as a non-pathogenic vector for expression of heterologous proteins in cucurbits
T Arazi, S G Slutsky, Y M Shiboleth, et al.
The American Journal of Surgical Pathology
|
August 26, 1998
Survival analysis of 200 pulmonary neuroendocrine tumors with clarification of criteria for atypical carcinoid and its separation from typical carcinoid
W D Travis, W Rush, D B Flieder, et al.
The Annals of Thoracic Surgery
|
February 19, 2013
Routine intraoperative frozen section analysis of bronchial margins is of limited utility in lung cancer resection
Rachel M Owen, Seth D Force, Anthony A Gal, et al.
Journal of Inherited Metabolic Disease
|
January 24, 2002
Anderson-Fabry disease: clinical manifestations of disease in female heterozygotes
C Whybra, C Kampmann, I Willers, et al.
Advances in Oto-Rhino-Laryngology
|
June 27, 2000
Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3
H S Scott, S E Antonarakis, L Mittaz, et al.
American Journal of Medical Genetics
|
April 1, 1990
Gene of type II autosomal dominant retinitis pigmentosa maps on the long arm of chromosome 3
J E Olsson, C Samanns, J Jimenez, et al.
Page
of 49