Detalhe da pesquisa
1.
Head-and-neck paragangliomas are associated with sleep-related complaints, especially in the presence of carotid body tumors.
Sleep Breath
; 16(2): 527-34, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21614574
2.
SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma.
Lancet Oncol
; 11(4): 366-72, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20071235
3.
Quantification of sequence exchange events between PMS2 and PMS2CL provides a basis for improved mutation scanning of Lynch syndrome patients.
Hum Mutat
; 31(5): 578-87, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20186688
4.
Low penetrance of a SDHB mutation in a large Dutch paraganglioma family.
BMC Med Genet
; 11: 92, 2010 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-20540712
5.
Psychological distress and use of psychosocial support in familial adenomatous polyposis.
Psychooncology
; 19(3): 289-98, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19382100
6.
Prognostic factors for hereditary cancer distress six months after BRCA1/2 or HNPCC genetic susceptibility testing.
Eur J Cancer
; 43(1): 71-7, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17045473
7.
Comparison of individuals opting for BRCA1/2 or HNPCC genetic susceptibility testing with regard to coping, illness perceptions, illness experiences, family system characteristics and hereditary cancer distress.
Patient Educ Couns
; 65(1): 58-68, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-16872788
8.
Microsatellite instability, immunohistochemistry, and additional PMS2 staining in suspected hereditary nonpolyposis colorectal cancer.
Clin Cancer Res
; 10(3): 972-80, 2004 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-14871975
9.
Genetic testing in Li-Fraumeni syndrome: uptake and psychosocial consequences.
J Clin Oncol
; 28(18): 3008-14, 2010 Jun 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-20479422
10.
Risks of Lynch syndrome cancers for MSH6 mutation carriers.
J Natl Cancer Inst
; 102(3): 193-201, 2010 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-20028993
11.
Molecular characterization of novel germline deletions affecting SDHD and SDHC in pheochromocytoma and paraganglioma patients.
Endocr Relat Cancer
; 16(3): 929-37, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19546167
12.
The common sense model of self-regulation and psychological adjustment to predictive genetic testing: a prospective study.
Psychooncology
; 16(12): 1121-9, 2007 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17328098
13.
A prospective study of the impact of genetic susceptibility testing for BRCA1/2 or HNPCC on family relationships.
Psychooncology
; 16(4): 320-8, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-16909428
14.
Diagnostic approach and management of Lynch syndrome (hereditary nonpolyposis colorectal carcinoma): a guide for clinicians.
CA Cancer J Clin
; 56(4): 213-25, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16870997
15.
Bleeding in carriers of hemophilia.
Blood
; 108(1): 52-6, 2006 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-16551972
16.
Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome).
Gastroenterology
; 130(2): 312-22, 2006 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-16472587
17.
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance.
Gastroenterology
; 127(1): 17-25, 2004 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15236168