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Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen
|
April 7, 2012
[Genetics of pheochromocytoma]
B Bausch, A Malinoc, L Maruschke, et al.
Endocrine-Related Cancer
|
March 25, 2005
Epigenetic analysis of HIC1, CASP8, FLIP, TSP1, DCR1, DCR2, DR4, DR5, KvDMR1, H19 and preferential 11p15.5 maternal-allele loss in von Hippel-Lindau and sporadic phaeochromocytomas
C D E Margetts, D Astuti, D C Gentle, et al.
Clinical Genetics
|
August 4, 2016
Simple and rapid characterization of novel large germline deletions in SDHB, SDHC and SDHD-related paraganglioma
A S Hoekstra, B van den Ende, X P Julià, et al.
British Journal of Cancer
|
October 27, 2004
Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastoma
D Astuti, M Morris, C Krona, et al.
Journal of Neuro-Oncology
|
April 22, 2024
Screening and surveillance recommendations for central nervous system hemangioblastomas in pediatric patients with Von Hippel-Lindau disease
Anna Laura Knoblauch, B-I Blaß, C Steiert, et al.
Journal of the American Society of Nephrology : JASN
|
October 24, 2008
Increased expression of secreted frizzled-related protein 4 in polycystic kidneys
Daniel Romaker, Michael Puetz, Sven Teschner, et al.
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.
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.
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.
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of 3
Search research articles
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Showing results (21-30 of 29) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 29 results.
Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen
|
April 7, 2012
[Genetics of pheochromocytoma]
B Bausch, A Malinoc, L Maruschke, et al.
Endocrine-Related Cancer
|
March 25, 2005
Epigenetic analysis of HIC1, CASP8, FLIP, TSP1, DCR1, DCR2, DR4, DR5, KvDMR1, H19 and preferential 11p15.5 maternal-allele loss in von Hippel-Lindau and sporadic phaeochromocytomas
C D E Margetts, D Astuti, D C Gentle, et al.
Clinical Genetics
|
August 4, 2016
Simple and rapid characterization of novel large germline deletions in SDHB, SDHC and SDHD-related paraganglioma
A S Hoekstra, B van den Ende, X P Julià, et al.
British Journal of Cancer
|
October 27, 2004
Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastoma
D Astuti, M Morris, C Krona, et al.
Journal of Neuro-Oncology
|
April 22, 2024
Screening and surveillance recommendations for central nervous system hemangioblastomas in pediatric patients with Von Hippel-Lindau disease
Anna Laura Knoblauch, B-I Blaß, C Steiert, et al.
Journal of the American Society of Nephrology : JASN
|
October 24, 2008
Increased expression of secreted frizzled-related protein 4 in polycystic kidneys
Daniel Romaker, Michael Puetz, Sven Teschner, et al.
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.
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.
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.
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of 3