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H Neumann

Showing results (611-620 of 650) with videos related to

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Clinical and Translational Allergy|November 25, 2023
The South African Pollen Monitoring Network: Insights from 2 years of national aerospora sampling (2019-2021)Nanike Esterhuizen, Dilys M Berman, Frank H Neumann, et al.
The Journal of Clinical Endocrinology and Metabolism|November 13, 2009
Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndromeZoran Erlic, Michael M Hoffmann, Maren Sullivan, et al.
International Urology and Nephrology|February 28, 2012
Adult patients with sporadic polycystic kidney disease: the importance of screening for mutations in the PKD1 and PKD2 genesHartmut P H Neumann, Janina Bacher, Zinaida Nabulsi, et al.
Journal of the National Cancer Institute|October 8, 2013
Screening for cervical cancer precursors with p16/Ki-67 dual-stained cytology: results of the PALMS studyHans Ikenberg, Christine Bergeron, Dietmar Schmidt, et al.
The Journal of Clinical Endocrinology and Metabolism|October 2, 2008
Impact of screening kindreds for SDHD p.Cys11X as a common mutation associated with paraganglioma syndrome type 1Mariola Peczkowska, Zoran Erlic, Michael M Hoffmann, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 20, 2007
[Von Hippel-Lindau disease. Interdisciplinary patient care]H P H Neumann, M Cybulla, S Gläsker, et al.
Digestive Endoscopy : Official Journal of the Japan Gastroenterological Endoscopy Society|February 20, 2026
Endoscopist and Patients' Values and Preferences on Artificial Intelligence in Endoscopy: An Intercontinental Opinion Survey by the World Endoscopy OrganizationO F Ahmad, A de Groof, A Ali, et al.
Cerebrovascular Diseases Extra|November 10, 2012
Characteristics of intracranial aneurysms in the else kröner-fresenius registry of autosomal dominant polycystic kidney diseaseHartmut P H Neumann, Angelica Malinoc, Janina Bacher, et al.
American Journal of Human Genetics|December 20, 2003
Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paragangliomaSakari Vanharanta, Mary Buchta, Sarah R McWhinney, et al.
Endocrine-Related Cancer|September 17, 2008
Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC>TGG) mutationIoana N Milos, Karin Frank-Raue, Nelson Wohllk, et al.
Pageof 65

Showing results (611-620 of 650) with videos related to

Sort By:
Pageof 65
Clinical and Translational Allergy|November 25, 2023
The South African Pollen Monitoring Network: Insights from 2 years of national aerospora sampling (2019-2021)Nanike Esterhuizen, Dilys M Berman, Frank H Neumann, et al.
The Journal of Clinical Endocrinology and Metabolism|November 13, 2009
Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndromeZoran Erlic, Michael M Hoffmann, Maren Sullivan, et al.
International Urology and Nephrology|February 28, 2012
Adult patients with sporadic polycystic kidney disease: the importance of screening for mutations in the PKD1 and PKD2 genesHartmut P H Neumann, Janina Bacher, Zinaida Nabulsi, et al.
Journal of the National Cancer Institute|October 8, 2013
Screening for cervical cancer precursors with p16/Ki-67 dual-stained cytology: results of the PALMS studyHans Ikenberg, Christine Bergeron, Dietmar Schmidt, et al.
The Journal of Clinical Endocrinology and Metabolism|October 2, 2008
Impact of screening kindreds for SDHD p.Cys11X as a common mutation associated with paraganglioma syndrome type 1Mariola Peczkowska, Zoran Erlic, Michael M Hoffmann, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 20, 2007
[Von Hippel-Lindau disease. Interdisciplinary patient care]H P H Neumann, M Cybulla, S Gläsker, et al.
Digestive Endoscopy : Official Journal of the Japan Gastroenterological Endoscopy Society|February 20, 2026
Endoscopist and Patients' Values and Preferences on Artificial Intelligence in Endoscopy: An Intercontinental Opinion Survey by the World Endoscopy OrganizationO F Ahmad, A de Groof, A Ali, et al.
Cerebrovascular Diseases Extra|November 10, 2012
Characteristics of intracranial aneurysms in the else kröner-fresenius registry of autosomal dominant polycystic kidney diseaseHartmut P H Neumann, Angelica Malinoc, Janina Bacher, et al.
American Journal of Human Genetics|December 20, 2003
Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paragangliomaSakari Vanharanta, Mary Buchta, Sarah R McWhinney, et al.
Endocrine-Related Cancer|September 17, 2008
Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC>TGG) mutationIoana N Milos, Karin Frank-Raue, Nelson Wohllk, et al.
Pageof 65