Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Hartmut P H Neumann

Showing results (81-90 of 132) with videos related to

Pageof 14
Sort By:
World Journal of Surgery|November 2, 2004
Partial versus total adrenalectomy by the posterior retroperitoneoscopic approach: early and long-term results of 325 consecutive procedures in primary adrenal neoplasiasMartin K Walz, Klaus Peitgen, Daniela Diesing, et al.
Annals of the New York Academy of Sciences|November 15, 2006
Genetic and clinical investigation of pheochromocytoma: a 22-year experience, from Freiburg, Germany to international effortBirke Bausch, Carsten C Boedeker, Ansgar Berlis, et al.
Nephron|October 29, 2018
Co-Inheritance of Autosomal Dominant Polycystic Kidney Disease and Naevoid Basal Cell Carcinoma Syndrome: Effects on Renal ProgressionMaria Florencia Martínez, Luis Daniel Mazzuoccolo, Elisabet Mónica Oddo, et al.
Endocrine-Related Cancer|February 22, 2012
Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3Angelica Malinoc, Maren Sullivan, Thorsten Wiech, et al.
Journal of the American Society of Nephrology : JASN|August 4, 2006
Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting ciliaManfred Fliegauf, Judit Horvath, Christian von Schnakenburg, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|July 28, 2012
Correlation of the genotype of paragangliomas and pheochromocytomas with their metabolic phenotype on 3,4-dihydroxy-6-18F-fluoro-L-phenylalanin PETH Christian Rischke, Matthias R Benz, Damian Wild, et al.
The Journal of Clinical Endocrinology and Metabolism|May 27, 2011
Germline mutations of the TMEM127 gene in patients with paraganglioma of head and neck and extraadrenal abdominal sitesHartmut P H Neumann, Maren Sullivan, Aurelia Winter, et al.
Endocrine-Related Cancer|May 24, 2008
Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastomaCaroline D E Margetts, Mark Morris, Dewi Astuti, et al.
Annals of Human Genetics|January 12, 2010
Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndromeMaren Sullivan, Zoran Erlic, Michael M Hoffmann, et al.
Human Mutation|March 19, 2005
Thirty-four novel mutations of the GLA gene in 121 patients with Fabry diseaseEllen Schäfer, Karin Baron, Urs Widmer, et al.
Pageof 14

Showing results (81-90 of 132) with videos related to

Sort By:
Pageof 14
World Journal of Surgery|November 2, 2004
Partial versus total adrenalectomy by the posterior retroperitoneoscopic approach: early and long-term results of 325 consecutive procedures in primary adrenal neoplasiasMartin K Walz, Klaus Peitgen, Daniela Diesing, et al.
Annals of the New York Academy of Sciences|November 15, 2006
Genetic and clinical investigation of pheochromocytoma: a 22-year experience, from Freiburg, Germany to international effortBirke Bausch, Carsten C Boedeker, Ansgar Berlis, et al.
Nephron|October 29, 2018
Co-Inheritance of Autosomal Dominant Polycystic Kidney Disease and Naevoid Basal Cell Carcinoma Syndrome: Effects on Renal ProgressionMaria Florencia Martínez, Luis Daniel Mazzuoccolo, Elisabet Mónica Oddo, et al.
Endocrine-Related Cancer|February 22, 2012
Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3Angelica Malinoc, Maren Sullivan, Thorsten Wiech, et al.
Journal of the American Society of Nephrology : JASN|August 4, 2006
Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting ciliaManfred Fliegauf, Judit Horvath, Christian von Schnakenburg, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|July 28, 2012
Correlation of the genotype of paragangliomas and pheochromocytomas with their metabolic phenotype on 3,4-dihydroxy-6-18F-fluoro-L-phenylalanin PETH Christian Rischke, Matthias R Benz, Damian Wild, et al.
The Journal of Clinical Endocrinology and Metabolism|May 27, 2011
Germline mutations of the TMEM127 gene in patients with paraganglioma of head and neck and extraadrenal abdominal sitesHartmut P H Neumann, Maren Sullivan, Aurelia Winter, et al.
Endocrine-Related Cancer|May 24, 2008
Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastomaCaroline D E Margetts, Mark Morris, Dewi Astuti, et al.
Annals of Human Genetics|January 12, 2010
Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndromeMaren Sullivan, Zoran Erlic, Michael M Hoffmann, et al.
Human Mutation|March 19, 2005
Thirty-four novel mutations of the GLA gene in 121 patients with Fabry diseaseEllen Schäfer, Karin Baron, Urs Widmer, et al.
Pageof 14