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H NEUMANN

Showing results (371-380 of 418) with videos related to

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Journal of Medical Genetics|December 7, 2007
Molecular characterisation of a common SDHB deletion in paraganglioma patientsA Cascón, I Landa, E López-Jiménez, et al.
Surgery|December 26, 2006
Posterior retroperitoneoscopic adrenalectomy--results of 560 procedures in 520 patientsMartin K Walz, Piero F Alesina, Frank A Wenger, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 16, 2004
Phase III trial of gemcitabine plus tipifarnib compared with gemcitabine plus placebo in advanced pancreatic cancerE Van Cutsem, H van de Velde, P Karasek, et al.
Environmental Pollution (Barking, Essex : 1987)|July 3, 2010
Variability of sediment-contact tests in freshwater sediments with low-level anthropogenic contamination--determination of toxicity thresholdsS Höss, W Ahlf, C Fahnenstich, et al.
Nephron. Clinical Practice|June 12, 2013
Autosomal dominant polycystic kidney disease: prevalence of renal neoplasias in surgical kidney specimensCordula A Jilg, Vanessa Drendel, Janina Bacher, et al.
Journal of Medical Genetics|September 8, 2019
Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma-paragangliomaJean Pierre Bayley, Birke Bausch, Johannes Adriaan Rijken, et al.
JAMA|August 26, 2004
Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutationsHartmut P H Neumann, Christian Pawlu, Mariola Peczkowska, et al.
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.
Journal of Medical Genetics|September 10, 2003
Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countriesH P H Neumann, M Salzmann, B Bohnert-Iwan, et al.
Pageof 42

Showing results (371-380 of 418) with videos related to

Sort By:
Pageof 42
Journal of Medical Genetics|December 7, 2007
Molecular characterisation of a common SDHB deletion in paraganglioma patientsA Cascón, I Landa, E López-Jiménez, et al.
Surgery|December 26, 2006
Posterior retroperitoneoscopic adrenalectomy--results of 560 procedures in 520 patientsMartin K Walz, Piero F Alesina, Frank A Wenger, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 16, 2004
Phase III trial of gemcitabine plus tipifarnib compared with gemcitabine plus placebo in advanced pancreatic cancerE Van Cutsem, H van de Velde, P Karasek, et al.
Environmental Pollution (Barking, Essex : 1987)|July 3, 2010
Variability of sediment-contact tests in freshwater sediments with low-level anthropogenic contamination--determination of toxicity thresholdsS Höss, W Ahlf, C Fahnenstich, et al.
Nephron. Clinical Practice|June 12, 2013
Autosomal dominant polycystic kidney disease: prevalence of renal neoplasias in surgical kidney specimensCordula A Jilg, Vanessa Drendel, Janina Bacher, et al.
Journal of Medical Genetics|September 8, 2019
Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma-paragangliomaJean Pierre Bayley, Birke Bausch, Johannes Adriaan Rijken, et al.
JAMA|August 26, 2004
Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutationsHartmut P H Neumann, Christian Pawlu, Mariola Peczkowska, et al.
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.
Journal of Medical Genetics|September 10, 2003
Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countriesH P H Neumann, M Salzmann, B Bohnert-Iwan, et al.
Pageof 42