About: Risk estimation and screening in families of patients with medullary thyroid carcinoma

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scientific article published on 01 February 1988

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 1988 (uk) im Februar 1988 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en febreru de 1988 (ast) գիտական հոդված հրատարակված 1988 թվականի փետրվարի 1-ին (hy) artikull shkencor i botuar më 01 shkurt 1988 (sq) scientific article published on 01 February 1988 (en)
publication date	wds:Q69912692-491CB42F-1F23-40C7-9461-DE9D5829FDD4
publication date	1988-02-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q69912692-425EB8EA-D4C7-4369-98C1-46B28D5E7779
language of work or name	English
author name string	wds:Q69912692-052E43D8-D6C8-4BD2-9A3F-BC1EED42F718 wds:Q69912692-05F0BA50-F457-42B9-A680-FDA9EDAF3CAB wds:Q69912692-09177BEC-B819-4417-80A4-0D1EBF3C1167 wds:Q69912692-5D2B743D-7CB0-4F8E-9C0B-5C3DEAD34372 wds:Q69912692-9289389B-11DE-4AF2-86FA-A84B1282D661 wds:Q69912692-C2FCD62C-2839-4DC3-8978-944B0F9BA0DE wds:Q69912692-E17E7591-929D-4A2E-9209-CC5BAEA035B9
author name string	B A Ponder R F Gagel M E Pembrey M A Ponder M Telenius-Berg P Semple R Coffey
rdfs:label	Risk estimation and screening in families of patients with medullary thyroid carcinoma (en) Risk estimation and screening in families of patients with medullary thyroid carcinoma (nl) Risk estimation and screening in families of patients with medullary thyroid carcinoma (sq)
skos:prefLabel	Risk estimation and screening in families of patients with medullary thyroid carcinoma (en) Risk estimation and screening in families of patients with medullary thyroid carcinoma (nl) Risk estimation and screening in families of patients with medullary thyroid carcinoma (sq)
name	Risk estimation and screening in families of patients with medullary thyroid carcinoma (en) Risk estimation and screening in families of patients with medullary thyroid carcinoma (nl) Risk estimation and screening in families of patients with medullary thyroid carcinoma (sq)
author	wds:Q69912692-A1F616B1-198A-401C-B1ED-143D5560E757
author	Douglas F. Easton
title	wds:Q69912692-96D29DAC-F42E-43B2-B0AB-72BB625D10AC
title	Risk estimation and screening in families of patients with medullary thyroid carcinoma (en)
page(s)	wds:Q69912692-8B4CC664-0D5A-4CED-BDA6-183A859E3E13
page(s)	397-401
instance of	wds:Q69912692-029D379E-69BB-464E-A8B4-51E90D763D0E
instance of	scholarly article
main subject	wds:Q69912692-3100CCAB-E0D9-43D6-9624-01BC93231586
main subject	thyroid carcinoma
PubMed ID	wds:Q69912692-AB033EE7-034A-44BF-9876-4BE3E7F2F2E5
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/2893198
PubMed ID	2893198
published in	wds:Q69912692-5DD5B242-272B-4C0C-AFFD-A1AB95ABB6DF
published in	The Lancet
issue	wds:Q69912692-1118F593-3E94-4B4D-87E5-8E2FC8014A42
volume	wds:Q69912692-E8FB5748-20A8-4A22-B534-62209C442B4E
issue	8582
volume	1
DOI	wds:Q69912692-6DDA55DA-D081-4828-931F-40E860BDB932
DOI	http://dx.doi.org/10.1016/S0140-6736(88)91191-9
DOI	10.1016/S0140-6736(88)91191-9
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q69912692
is cites work of	Thyroid cancer Highly penetrant hereditary cancer syndromes. RAS proto-oncogene in medullary thyroid carcinoma Complete penetrance of Creutzfeldt-Jakob disease in Libyan Jews carrying the E200K mutation in the prion protein gene Genetic insights into familial cancers-- update and recent discoveries Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. The clinical and screening age-at-onset distribution for the MEN-2 syndrome Hereditary thyroid cancer Thyroid carcinoma Oncological implications of RET gene mutations in Hirschsprung's disease Mutation of theRET protooncogene in sporadic medullary thyroid carcinoma 10 Multiple endocrine neoplasia Roles of trk family neurotrophin receptors in medullary thyroid carcinoma development and progression RET oncogene in MEN2, MEN2B, MTC and other forms of thyroid cancer Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytoma. Timing and extent of surgery in patients with familial medullary thyroid carcinoma/multiple endocrine neoplasia 2A-related RET mutations not affecting codon 634. Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma Medullary thyroid cancer: RET testing of an archival material Diagnosis and Management of Hereditary Phaeochromocytoma and Paraganglioma. Lessons from genes mutated in multiple endocrine neoplasia (MEN) syndromes. (111)In-octreotide scintigraphy for identification of metastatic medullary thyroid carcinoma in children and adolescents [Usefulness of RET proto-oncogene in the diagnosis of hereditary-type medullary carcinoma of the thyroid. Correlation with surgical findings] Medullary thyroid cancer Multiple endocrine neoplasia type 2. Clinical features and screening. Medullary thyroid cancer: clinico-pathological profile and outcome in a tertiary care center in North India Presymptomatic genetic screening in families with multiple endocrine neoplasia type 2 Germline mutations of the RET proto-oncogene in pedigree with MEN type 2A: DNA analysis and its implications for pediatric surgery The gene for MEN 2A is tightly linked to the centromere of chromosome 10 Presymptomatic screening for medullary thyroid carcinoma in patients with multiple endocrine neoplasia type 2A. Adrenal disorders of pregnancy. RET oncogene mutations in medullary thyroid carcinoma in Mexican families Inheritable forms of medullary thyroid carcinoma Familial pheochromocytoma Genetic analysis of 24 French families with multiple endocrine neoplasia type 2A Medullary carcinoma of the thyroid presenting as multifocal bronchial carcinoid tumour [Progress in the diagnosis and therapy of C cell carcinoma of the thyroid gland] The importance of multiple endocrine neoplasia syndromes in differential diagnosis A Korean family of familial medullary thyroid cancer with Cys618Ser RET germline mutation Presymptomatic detection and treatment of Japanese carriers of the multiple endocrine neoplasia type 2A gene Early diagnosis of multiple endocrine neoplasia type IIa RET mutations in a large indian family with medullary thyroid carcinoma [Molecular diagnosis of hereditary cancer]

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