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Journal of Medical Genetics
|
December 7, 2007
Molecular characterisation of a common SDHB deletion in paraganglioma patients
A Cascón, I Landa, E López-Jiménez, et al.
Surgery
|
December 26, 2006
Posterior retroperitoneoscopic adrenalectomy--results of 560 procedures in 520 patients
Martin 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 cancer
E 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 thresholds
S 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 specimens
Cordula 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-paraganglioma
Jean 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 mutations
Hartmut 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 syndrome
Zoran 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 countries
H P H Neumann, M Salzmann, B Bohnert-Iwan, et al.
Page
of 42
Search research articles
Search
Showing results (371-380 of 418) with videos related to
Sort By:
Page
of 42
Journal of Medical Genetics
|
December 7, 2007
Molecular characterisation of a common SDHB deletion in paraganglioma patients
A Cascón, I Landa, E López-Jiménez, et al.
Surgery
|
December 26, 2006
Posterior retroperitoneoscopic adrenalectomy--results of 560 procedures in 520 patients
Martin 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 cancer
E 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 thresholds
S 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 specimens
Cordula 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-paraganglioma
Jean 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 mutations
Hartmut 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 syndrome
Zoran 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 countries
H P H Neumann, M Salzmann, B Bohnert-Iwan, et al.
Page
of 42