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Occupational and Environmental Medicine
|
August 6, 2013
Lung cancer risk among bakers, pastry cooks and confectionary makers: the SYNERGY study
Thomas Behrens, Benjamin Kendzia, Tabea Treppmann, et al.
Journal of Occupational and Environmental Medicine
|
February 6, 2015
Lung cancer risk among cooks when accounting for tobacco smoking: a pooled analysis of case-control studies from Europe, Canada, New Zealand, and China
Carolina Bigert, Per Gustavsson, Kurt Straif, et al.
Journal of the American Society of Nephrology : JASN
|
April 5, 2017
Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2
Oscar Rubio Cabezas, Sarah E Flanagan, Horia Stanescu, et al.
American Journal of Epidemiology
|
September 27, 2013
Lung cancer risk among hairdressers: a pooled analysis of case-control studies conducted between 1985 and 2010
Ann C Olsson, Yiwen Xu, Joachim Schüz, et al.
Nature
|
June 21, 2019
Noncoding deletions reveal a gene that is critical for intestinal function
Danit Oz-Levi, Tsviya Olender, Ifat Bar-Joseph, et al.
Molecular Psychiatry
|
February 17, 2010
A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication
M Arcos-Burgos, M Jain, M T Acosta, et al.
Journal of the American Society of Nephrology : JASN
|
February 12, 2022
A Founder Mutation in <i>EHD1</i> Presents with Tubular Proteinuria and Deafness
Naomi Issler, Sara Afonso, Irith Weissman, et al.
International Journal of Cancer
|
May 28, 2014
Lung cancer risk among bricklayers in a pooled analysis of case-control studies
Dario Consonni, Sara De Matteis, Angela C Pesatori, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 20, 2020
Pseudouridylation defect due to <i>DKC1</i> and <i>NOP10</i> mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis
Eszter Balogh, Jennifer C Chandler, Máté Varga, et al.
Journal of the American Society of Nephrology : JASN
|
April 15, 2018
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure
Markus Reichold, Enriko D Klootwijk, Joerg Reinders, et al.
Page
of 94
Search research articles
Search
Showing results (701-710 of 940) with videos related to
Sort By:
Page
of 94
Occupational and Environmental Medicine
|
August 6, 2013
Lung cancer risk among bakers, pastry cooks and confectionary makers: the SYNERGY study
Thomas Behrens, Benjamin Kendzia, Tabea Treppmann, et al.
Journal of Occupational and Environmental Medicine
|
February 6, 2015
Lung cancer risk among cooks when accounting for tobacco smoking: a pooled analysis of case-control studies from Europe, Canada, New Zealand, and China
Carolina Bigert, Per Gustavsson, Kurt Straif, et al.
Journal of the American Society of Nephrology : JASN
|
April 5, 2017
Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2
Oscar Rubio Cabezas, Sarah E Flanagan, Horia Stanescu, et al.
American Journal of Epidemiology
|
September 27, 2013
Lung cancer risk among hairdressers: a pooled analysis of case-control studies conducted between 1985 and 2010
Ann C Olsson, Yiwen Xu, Joachim Schüz, et al.
Nature
|
June 21, 2019
Noncoding deletions reveal a gene that is critical for intestinal function
Danit Oz-Levi, Tsviya Olender, Ifat Bar-Joseph, et al.
Molecular Psychiatry
|
February 17, 2010
A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication
M Arcos-Burgos, M Jain, M T Acosta, et al.
Journal of the American Society of Nephrology : JASN
|
February 12, 2022
A Founder Mutation in <i>EHD1</i> Presents with Tubular Proteinuria and Deafness
Naomi Issler, Sara Afonso, Irith Weissman, et al.
International Journal of Cancer
|
May 28, 2014
Lung cancer risk among bricklayers in a pooled analysis of case-control studies
Dario Consonni, Sara De Matteis, Angela C Pesatori, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 20, 2020
Pseudouridylation defect due to <i>DKC1</i> and <i>NOP10</i> mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis
Eszter Balogh, Jennifer C Chandler, Máté Varga, et al.
Journal of the American Society of Nephrology : JASN
|
April 15, 2018
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure
Markus Reichold, Enriko D Klootwijk, Joerg Reinders, et al.
Page
of 94