Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing. - Test2 - elhamkhani - TriplyDB

Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing.

Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing.

http://www.wikidata.org/entity/Q34921220

about

Succinate Dehydrogenase Loss in Familial Paraganglioma: Biochemistry, Genetics, and Epigenetics Tumors of the neural crest: Common themes in development and cancer A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes.Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma.Genotype-Phenotype Correlation in Patients With Germline Mutations of VHL, RET, SDHB, and SDHD Genes: Thai Experience.Pheochromocytoma in a Twelve-Year-Old Girl with SDHB-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome.Whole-exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas.Pheochromocytoma/Paraganglioma: Review of perioperative management of blood pressure and update on genetic mutations associated with pheochromocytoma.Leptomeningeal dissemination of a low-grade lumbar paraganglioma: case report.Diagnosis and management of pheochromocytoma: a practical guide to clinicians.Genitourinary paraganglioma: Demographic, pathologic, and clinical characteristics in the surveillance, epidemiology, and end results database (2000-2012).Routine genetic screening with a multi-gene panel in patients with pheochromocytomas.Diagnosing endocrine hypertension: a practical approach.Genotype-Phenotype Correlation in Indian Patients with MEN2-Associated Pheochromocytoma and Comparison of Clinico-Pathological Attributes with Apparently Sporadic Adrenal Pheochromocytoma.Review of Pediatric Pheochromocytoma and Paraganglioma.Multiple retroperitoneal paragangliomas.Impact of surgical resection for subdiaphragmatic paragangliomas.Trends of genetic screening in patients with pheochromocytoma and paraganglioma: 15-year experience in a high-volume tertiary referral center.Von Hippel-Lindau Disease.A Novel RET D898Y Germline Mutation in a Patient with Pheochromocytoma.Pheochromocytoma and Paraganglioma in Neurofibromatosis type 1: frequent surgeries and cardiovascular crises indicate the need for screening.

P2860

Q26796203-D80A323E-2522-4DF8-96CF-5B6FF1E6F2D0 Q26864763-3792773B-16DB-433E-AE9C-8AB6DA3B2734 Q30252766-8400D9D2-E58A-4351-A316-EFF81FF806A5 Q33570108-12B4D96C-2662-4290-9830-1321DA477DF8 Q33602864-446B9E0A-9FF3-4005-801F-8190F8C8FE24 Q34145968-F597FC52-7893-4E10-A788-E8D493ED28AC Q34998940-D3496D6C-619A-4C65-A391-7BC39C3D0CF9 Q36090002-9597E307-1702-44C1-8A9E-716FC18BAA5A Q37735985-48F98793-758B-4FB9-A8A1-68EAAAE3B02B Q38208963-445A71F3-E7F9-4D58-AA45-D43DA10723C5 Q38741943-3AC48ABA-B042-4240-BB72-C28E33D01594 Q38801071-C44522E9-61BD-44A6-AF2A-8FB1105C8C10 Q39337899-553A86B4-89C9-4668-8510-9EEB3E8C13E6 Q40465055-FEFCF726-BB14-48C2-9D86-5DB779E14266 Q40999640-293B0523-1C08-4BE2-B47A-772CF1566227 Q41845048-D8C96DDC-9D71-459C-8DCB-17427869F951 Q45058521-29A830CC-4F68-4089-AF97-38EAE1A3FEB2 Q48283123-616CECA9-D52C-48B7-8825-E8D32663F295 Q55110633-A429662C-BF6A-41D9-BB76-6BD15A28DC9B Q55113665-94377EC5-75DF-448F-9A83-6AE3B916236F Q55446242-87F5F675-E8FC-40E4-B789-A2C8FCDC34D5

P2860

Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing.

http://www.wikidata.org/entity/Q34921220

description

2013 nî lūn-bûn

@nan

2013 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի մարտին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

Inherited mutations in pheochr ...... ld be offered genetic testing.

@ast

Inherited mutations in pheochr ...... ld be offered genetic testing.

@en

Inherited mutations in pheochr ...... ld be offered genetic testing.

@nl

type

label

Inherited mutations in pheochr ...... ld be offered genetic testing.

@ast

Inherited mutations in pheochr ...... ld be offered genetic testing.

@en

Inherited mutations in pheochr ...... ld be offered genetic testing.

@nl

prefLabel

Inherited mutations in pheochr ...... ld be offered genetic testing.

@ast

Inherited mutations in pheochr ...... ld be offered genetic testing.

@en

Inherited mutations in pheochr ...... ld be offered genetic testing.

@nl

P1433

Q34921220-A3088B64-4191-40DC-BCBD-2CAFBDD1B558

P1476

Q34921220-7B3CEE13-E18F-422D-ACD4-F81735E0E23F

P2093

Q34921220-06F8AE7D-AC47-460C-BD3A-55FCB3B4022A

Q34921220-732DD01D-FAF7-43AF-8195-7C46CBF23D5A

Q34921220-EDEB31BD-C17A-444F-AE49-A59091AE0B9D

Q34921220-FF97D543-EBE1-4CB2-8159-C48ACCB897C2

P2860

Q34921220-04EA625C-9848-4DAC-BD2A-D7E5410F2951

Q34921220-05A97E1B-723E-4F07-BB79-27AC2038CB9D

Q34921220-0CB7781D-FD53-4ABC-ACFD-7D122ABEEDC9

Q34921220-0D39FA12-937C-42D8-A438-7ED98935649E

Q34921220-0E5BC7F6-535A-4BC3-AB1A-94109ADBEA4C

Q34921220-1ADA6E81-51FF-4AAC-8A30-98EFC0264F61

Q34921220-1FC80F94-57EB-4AFA-904A-F62C108AC5D5

Q34921220-228CEA74-D542-49D8-99AF-2B1CC7AE631F

Q34921220-2323B37A-E143-4B35-8E3A-00088C027392

Q34921220-277BDE14-FB54-4C25-A180-5E4F1862FA3E

P2888

Q34921220-61249E76-3E65-4CD9-BC2C-719C90F6B8F1

P304

Q34921220-951CC0E2-9A19-4797-8806-76F659D0BE7C

P31

Q34921220-66914D6B-D873-49CA-BEE5-A3DFAC86800D

P356

Q34921220-13992FDF-94DE-4E41-ADD8-3CCCE00F5F01

P433

Q34921220-2040CEB7-E452-4F10-BD25-817C9EF7FFC8

P478

Q34921220-BA07DD45-171B-47B5-8AEB-6E1286E205BC

P50

Q34921220-70ACC722-345B-41F9-A386-7AD7D63985A6

P577

Q34921220-20FD6E0F-163C-4A52-A9F1-0EB7CC9F5BC3

P6179

Q34921220-A2B3900A-6E12-44E0-809E-A012757CDA25

P698

Q34921220-52F4CEE8-D852-4C7F-939B-70868FF5BFFA

P921

Q34921220-546222A8-06F4-4476-B98D-A6E04466A7D3

P932

Q34921220-F987B136-3706-4E80-80C9-FF50ACA6E980

P356

S10434-013-2942-5

P1433

Annals of Surgical Oncology

P1476

Inherited mutations in pheochr ...... ld be offered genetic testing.

@en

P2093

Debbie L Cohen

http://www.w3.org/2001/XMLSchema#string

Douglas L Fraker

http://www.w3.org/2001/XMLSchema#string

Lauren Fishbein

http://www.w3.org/2001/XMLSchema#string

Shana Merrill

http://www.w3.org/2001/XMLSchema#string

P2860

Germline mutations in TMEM127 confer susceptibility to pheochromocytoma

SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing

Immunohistochemistry for SDHB divides gastrointestinal stromal tumors (GISTs) into 2 distinct types

Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD.

SDHA is a tumor suppressor gene causing paraganglioma.

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma.

P2888

s10434-013-2942-5

P304

1444-1450

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1245/S10434-013-2942-5

http://www.w3.org/2001/XMLSchema#string

P433

5

http://www.w3.org/2001/XMLSchema#string

P478

20

http://www.w3.org/2001/XMLSchema#string

P50

Katherine L Nathanson

P577

2013-03-20T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P6179

1030166040

http://www.w3.org/2001/XMLSchema#string

P698

23512077

http://www.w3.org/2001/XMLSchema#string

P921

phaeochromocytoma

P932

4291281

http://www.w3.org/2001/XMLSchema#string