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Clinics (Sao Paulo, Brazil)
|
May 16, 2012
Head and neck paragangliomas: clinical and molecular genetic classification
Christian Offergeld, Christoph Brase, Svetlana Yaremchuk, 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 study
Hans Ikenberg, Christine Bergeron, Dietmar Schmidt, 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 genes
Hartmut P H Neumann, Janina Bacher, Zinaida Nabulsi, 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 1
Mariola 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 Organization
O 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 disease
Hartmut 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 paraganglioma
Sakari 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) mutation
Ioana N Milos, Karin Frank-Raue, Nelson Wohllk, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 30, 2012
The endemic paraganglioma syndrome type 1: origin, spread, and clinical expression
Francesca Schiavi, Serena Demattè, Maria Enrica Cecchini, et al.
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of 42
Search research articles
Search
Showing results (381-390 of 418) with videos related to
Sort By:
Page
of 42
Clinics (Sao Paulo, Brazil)
|
May 16, 2012
Head and neck paragangliomas: clinical and molecular genetic classification
Christian Offergeld, Christoph Brase, Svetlana Yaremchuk, 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 study
Hans Ikenberg, Christine Bergeron, Dietmar Schmidt, 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 genes
Hartmut P H Neumann, Janina Bacher, Zinaida Nabulsi, 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 1
Mariola 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 Organization
O 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 disease
Hartmut 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 paraganglioma
Sakari 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) mutation
Ioana N Milos, Karin Frank-Raue, Nelson Wohllk, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 30, 2012
The endemic paraganglioma syndrome type 1: origin, spread, and clinical expression
Francesca Schiavi, Serena Demattè, Maria Enrica Cecchini, et al.
Page
of 42