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Scholar Results 1 - 10 of 11 citing Cascon: Molecular characterization of a common SDHB deletion in paraganglioma patients. (0.06 sec) 

SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the …

- prsjournal.com
B Pasini, CA Stratakis - Journal of Internal Medicine, 2009 - prsjournal.com
A genetic predisposition for paragangliomas and adrenal or extra-adrenal
phaeochromocytomas was recognized years ago. Beside the well-known syndromes
associated with an increased risk of adrenal phaeochromocytoma, Von Hippel ...
Cited by 3 - Related articles - Cached - All 3 versions

Clinical predictors for germline mutations in head and neck paraganglioma patients: cost …


HPH Neumann, Z Erlic, CC Boedeker, LA … - Cancer Research, 2009 - AACR
Multiple genes and their variants that lend susceptibility to many diseases will
play a major role in the future. Successful genetics-based medicine must not
only serve the patients and families but also be fiscally responsible to ...
Cited by 3 - Related articles - All 3 versions

Genetics of pheochromocytoma and paraganglioma in Spanish patients


A Cascon, G Pita, N Burnichon, I Landa, E … - Journal of Clinical Endocrinology & Metabolism, 2009 - Endocrine Soc
Context: The presence of familial history in pheochromocytoma/paraganglioma
patients, including syndromic antecedents, leads in the majority of cases to a
positive genetic testing for mutations in one of the major susceptibility ...
Cited by 2 - Related articles - All 3 versions

Succinate dehydrogenase subunit B (SDHB) gene deletion associated with a composite …


R Armstrong, KL Greenhalgh, E Rattenberry, … - British Medical Journal, 2009 - jmg.bmj.com
Recently we detected an SDHB deletion in a 13-year-old girl with a composite
paraganglioma/neuroblastoma. The girl had consulted her general practitioner for
dysmenorrhoea, and during the examination had been found to have high blood ...
Cited by 2 - Related articles - All 2 versions

The first Dutch SDHB founder deletion in paraganglioma–pheochromocytoma patients


JP Bayley, AEM Grimbergen, PA van Bunderen, … - BMC Medical Genetics, 2009 - ukpmc.ac.uk
Germline mutations of the tumor suppressor genes SDHB, SDHC and SDHD play a
major role in hereditary paraganglioma and pheochromocytoma. These three genes
encode subunits of succinate dehydrogenase (SDH), the mitochondrial ...

[PDF] Hereditary Paraganglioma-Pheochromocytoma Syndromes


RV Lloyd, WF Young - domex.nps.edu
[Includes:SDHD-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome
(Paragangliomas 1), SDHB-Related Hereditary Paraganglioma-Pheochromocytoma
Syndrome (Paragangliomas 4), SDHC-Related Hereditary Paraganglioma- ...
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SDH MUTATIONS IN TUMOURIGENESIS AND INHERITED ENDOCRINE TUMOURS: …


P Barbara, CA Stratakis, P Barbara - interscience.wiley.com
A genetic predisposition for paragangliomas and adrenal or extra-adrenal
pheochromocytomas was recognized years ago. Beside the well known syndromes
associated with an increased risk of adrenal pheochromocytoma, Von Hippel ...
Related articles

Penetrance and clinical consequences of a gross SDHB deletion in a large family


DC Solis, N Burnichon, H Timmers, MJ … - Clinical Genetics, 2009 - interscience.wiley.com
Mutations in the gene encoding subunit B of the mitochondrial enzyme succinate
dehydrogenase (SDHB) are inherited in an autosomal dominant manner and are
associated with hereditary paraganglioma (PGL) and pheochromocytoma. The ...
Related articles - All 2 versions

The succinate dehydrogenase genetic testing in a large prospective series of patients with …


N Burnichon, V Rohmer, L Amar, P Herman, S … - Journal of Clinical Endocrinology & Metabolism, 2009 - Endocrine Soc
Design: A total of 445 patients with head and neck and/or thoracic-abdominal or
pelvic paragan- gliomas were recruited over 5 yr in 20 referral centers. In
addition to classical direct sequencing of the SDHB, SDHC, and SDHD genes, ...
Related articles - All 3 versions

SDHB 蛋白的表达, 纯化及多克隆抗体制备


雷翠华, 李芳, 万永奇, 莫小阳, 邓云, 吴秀山 … - 激光生物学报, 2009 - cqvip.com
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