About: Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma

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About: Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma Goto Sponge NotDistinct Permalink

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scientific article published on 01 December 1995

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1995 (uk) article scientifique publié en 1995 (fr) im Dezember 1995 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'avientu de 1995 (ast) scientific article published on 01 December 1995 (en)
publication date	wds:Q71568237-6943C01C-6D57-4BCB-AA16-C1433F0FCF3A
publication date	1995-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q71568237-96340B02-B1EB-42BD-A090-30E8B6BCE0DD
language of work or name	English
cites work	wds:Q71568237-1BE7ECC1-559A-4445-9684-5025DED09DBF wds:Q71568237-2922BF22-3C45-49BB-AB46-E2382D76BB78 wds:Q71568237-39C557C3-FB37-42A0-BA87-175B09D48FE8 wds:Q71568237-4179163B-6741-44BB-BC4B-9006EC2C0F11 wds:Q71568237-43D7DFA8-87C9-464C-9E07-70E7CE246329 wds:Q71568237-480F1C6A-7F48-4428-BA8D-48F2999A017E wds:Q71568237-5B3544DC-A962-4D9D-88E1-F5737CE561E3 wds:Q71568237-854D3D6A-34A1-4563-B4D7-A0A0C551661F wds:Q71568237-9F87E0BD-91EE-465E-BBAB-406CE3E662EC wds:Q71568237-A5C4E1AB-28EE-47C4-898D-2600E441BF98 wds:Q71568237-A647F77C-439B-40F0-B17D-E7D883AD5354 wds:Q71568237-AD808AC0-7336-49DD-B1A9-7C45E08D500E wds:Q71568237-B98956B6-C1B2-49E2-800D-DF0475986C61 wds:Q71568237-BB2291DB-02E5-4347-9AB9-CD8185B9C8D0 wds:Q71568237-DE0A5F20-7136-47A2-9BD3-F8330389E038 wds:Q71568237-EED030A0-E680-454F-BDDD-A2C697B31E38 wds:Q71568237-F4D19F39-3AD4-4617-8E78-219554C6DF46
cites work	A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10 Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene. Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours. Risk estimation and screening in families of patients with medullary thyroid carcinoma Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage The clinical outcome of prospective screening for multiple endocrine neoplasia type 2a. An 18-year experience Presymptomatic screening for multiple endocrine neoplasia type 2A with linked DNA markers. The MEN 2A International Collaborative Group Linkage of the multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A. Genetic testing in the diagnosis and management of multiple endocrine neoplasia type II. Clinical screening as compared with DNA analysis in families with multiple endocrine neoplasia type 2A Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinoma Mutation of theRET protooncogene in sporadic medullary thyroid carcinoma Predictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2A
author name string	wds:Q71568237-0FBAC379-6B82-45C3-8549-ADA8B7CCB483 wds:Q71568237-10D23318-99CF-4E01-84A0-4810AD506746 wds:Q71568237-6F995E92-D4AF-41D9-99A2-26A3C0BB6AC8 wds:Q71568237-B2F1284B-9146-46AB-B469-711EC1438F4E
author name string	C Eng H Dralle A Frilling F Raue
rdfs:label	Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma (en) Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma (nl)
skos:prefLabel	Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma (en) Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma (nl)
name	Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma (en) Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma (nl)
author	wds:Q71568237-C3FE8592-4DCE-4587-99B2-02E7E8612135
author	Christoph Broelsch
title	wds:Q71568237-B0EEBAEC-F182-4615-AC73-67CFCC56BFE8
title	Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma (en)
page(s)	wds:Q71568237-819CC677-840F-4152-A3D6-F7D7C520E86C
page(s)	1099-103; discussion 1103-4
instance of	wds:Q71568237-64A0A597-2233-41EB-AF28-30540E29143E
instance of	scholarly article
main subject	wds:Q71568237-169166E0-DAA5-437E-A1AB-078B3774151B wds:Q71568237-20236D27-384F-473C-A575-9F97365A8B54
main subject	familial medullary thyroid carcinoma multiple endocrine neoplasia type 2
PubMed ID	wds:Q71568237-B5146D4B-FECE-4C64-A8E5-BC15D7F85055
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7491529
PubMed ID	7491529
published in	wds:Q71568237-99681A16-1DC3-4019-BFA5-0C388C8FCA9B
published in	Surgery
issue	wds:Q71568237-0FC320B7-93FB-48E1-BCAA-B83443529896
volume	wds:Q71568237-7A502D56-BBEE-4E65-8181-E6497147729D
issue	6
volume	118
DOI	wds:Q71568237-5C1F5BD5-0D33-49F3-AF2C-535480BD32E0
DOI	http://dx.doi.org/10.1016/S0039-6060(05)80120-5
DOI	10.1016/S0039-6060(05)80120-5
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71568237
is cites work of	RET gene mutations and polymorphisms in medullary thyroid carcinomas in Indian patients. Multiple endocrine neoplasia type 2-associated RET proto-oncogene mutations do not contribute to the pathogenesis of sporadic parathyroid tumors RET proto-oncogene mutations in thyroid carcinomas: clinical relevance Hereditary endocrinopathies Personalized medicine: caught between hope, hype and the real world [Prophylactic thyroid surgery]. Video-assisted central compartment lymphadenectomy in a patient with a positive RET oncogene: initial experience Management of the Parathyroid Glands During Preventive Thyroidectomy in Patients With Multiple Endocrine Neoplasia Type 2 Different mutations of the RET gene cause different human tumoral diseases. Surgery for lymph node metastases of medullary thyroid carcinoma: A review Video assisted prophylactic thyroidectomy and central compartment nodes clearance in two RET gene mutation adult carriers Presymptomatic detection and treatment of Japanese carriers of the multiple endocrine neoplasia type 2A gene
is cites work of	wds:Q38010031-A5639665-A933-45E2-9242-EFD931C6B7A3 wds:Q38625926-1AB6334E-70F1-47E7-8593-BB2F802CF47D wds:Q45271002-D4C9BBB7-1234-4B30-987B-DE2C012E33AF wds:Q36696653-10DB3BA9-E814-45C3-B26A-308905A38B47

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