(Q37860128)

24 August 2017

1 reference

title

Familial thyroid cancer: a review (English)

1 reference

24 August 2017

1 reference

Vânia Nosé

1

1 reference

24 August 2017

publication date

1 April 2011

1 reference

24 August 2017

1 reference

24 August 2017

volume

24 Suppl 2

1 reference

24 August 2017

page(s)

S19-33

1 reference

https://scigraph.springernature.com/pub.10.1038/modpathol.2010.147

24 August 2017

exact match

0 references

cites work

Familial non-medullary thyroid carcinoma: an update

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial thyroid carcinoma: a diagnostic algorithm

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Increasing incidence of thyroid cancer in the United States, 1973-2002

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Increased incidence of thyroid carcinoma in france: a true epidemic or thyroid nodule management effects? Report from the French Thyroid Cancer Committee

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

A National Cancer Data Base report on 53,856 cases of thyroid carcinoma treated in the U.S., 1985-1995 [see commetns]

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Difference between familial and sporadic medullary thyroid carcinomas

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial medullary thyroid carcinoma and C cell hyperplasia

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Physiologic versus neoplastic C-cell hyperplasia of the thyroid: separation of distinct histologic and biologic entities

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Analysis of RET proto-oncogene abnormalities in patients with MEN 2A, MEN 2B, familial or sporadic medullary thyroid carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Seminars in medicine of the Beth Israel Hospital, Boston. The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Analysis of RET protooncogene point mutations distinguishes heritable from nonheritable medullary thyroid carcinomas

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

RET protooncogene analysis in the diagnosis of medullary thyroid carcinoma and multiple endocrine neoplasia type II

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinomas

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Prognostic significance of somatic RET oncogene mutations in sporadic medullary thyroid cancer: a 10-year follow-up study.

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Medullary thyroid carcinoma: clinical characteristics, treatment, prognostic factors, and a comparison of staging systems

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Early Malignant Progression of Hereditary Medullary Thyroid Cancer

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial thyroid cancer

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

On the prevalence of familial nonmedullary thyroid cancer in multiply affected kindreds

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial risks for nonmedullary thyroid cancer.

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial non-medullary thyroid carcinoma: pathology review in 27 affected cases from 13 French families

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial papillary thyroid carcinoma: genetics, criteria for diagnosis, clinical features, and surgical treatment

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial Nonmedullary Thyroid Cancer

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial nonmedullary thyroid cancer

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial nonmedullary thyroid carcinoma characterized by multifocality and a high recurrence rate in a large study population

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Is familial non-medullary thyroid carcinoma more aggressive than sporadic thyroid cancer? A multicenter series

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial nonmedullary thyroid cancer. An emerging entity that warrants aggressive treatment.

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial papillary thyroid microcarcinoma: a new clinical entity

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial nonmedullary thyroid carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial papillary thyroid carcinoma is genetically distinct from familial adenomatous polyposis coli

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial nonmedullary thyroid cancer: an emerging entity that warrants aggressive treatment

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Does familial non-medullary thyroid cancer adversely affect survival?

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial adenomatous polyposis associated thyroid carcinoma: a distinct type of follicular cell neoplasm

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial adenomatous polyposis-associated thyroid cancer: a clinical, pathological, and molecular genetics study

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Prevalence of thyroid cancer in familial adenomatous polyposis syndrome and the role of screening ultrasound examinations.

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Case records of the Massachusetts General Hospital. Case 37-2006. A 19-year-old woman with thyroid cancer and lower gastrointestinal bleeding

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Mutational analysis of the APC gene in cribriform-morula variant of papillary thyroid carcinoma.

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Cribriform-morular variant of papillary thyroid carcinoma: a pathological and molecular genetic study with evidence of frequent somatic mutations in exon 3 of the beta-catenin gene

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Cancer phenomics: RET and PTEN as illustrative models

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

PTEN: one gene, many syndromes

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndrome

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Abnormal distribution and hyperplasia of thyroid C-cells in PTEN-associated tumor syndromes

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Thyroid gland abnormalities in patients with the syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas (Carney complex)

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Carney Complex, Peutz-Jeghers Syndrome, Cowden Disease, and Bannayan-Zonana Syndrome Share Cutaneous and Endocrine Manifestations, But Not Genetic Loci

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Unusual features of thyroid carcinomas in Japanese patients with Werner syndrome and possible genotype-phenotype relations to cell type and race

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

The Werner syndrome. A model for the study of human aging.

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Simultaneous occurrence of medullary carcinoma and papillary microcarcinoma of thyroid in a patient with MEN 2A syndrome. report of a case

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Medullary and papillary tumors are frequently associated in the same thyroid gland without evidence of reciprocal influence in their biologic behavior

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

A new form of familial multi-nodular goitre with progression to differentiated thyroid cancer.

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

A Comprehensive Analysis ofMNG1,TCO1,fPTC,PTEN,TSHR, and TRKA in Familial Nonmedullary Thyroid Cancer: Confirmation of Linkage to TCO1

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Two families with an autosomal dominant inheritance pattern for papillary carcinoma of the thyroid

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2.

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Solitary, multiple, and familial oxyphil tumours of the thyroid gland

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

At least three genes account for familial papillary thyroid carcinoma: TCO and MNG1 excluded as susceptibility loci from a large Tasmanian family

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial nonmedullary thyroid neoplasia

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

The T1799A BRAF mutation is not a germline mutation in familial nonmedullary thyroid cancer.

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Familial nonmedullary thyroid cancer: a review of the genetics

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

Clinical features and genetic predisposition to hereditary nonmedullary thyroid cancer

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2010.147

7 January 2021

10.1038/MODPATHOL.2010.147

Identifiers

DOI

1 reference

24 August 2017

1 reference