(Q37302842)

19 August 2017

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title

Familial non-medullary thyroid carcinoma: an update (English)

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19 August 2017

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Vânia Nosé

1

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19 August 2017

1 January 2008

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19 August 2017

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19 August 2017

19

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19 August 2017

4

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19 August 2017

226-240

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https://scigraph.springernature.com/pub.10.1007/s12022-008-9045-z

19 August 2017

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cites work

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

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https://api.crossref.org/works/10.1007%2FS12022-008-9045-Z

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

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12022-008-9045-Z

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

21 January 2018

1 reference

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https://api.crossref.org/works/10.1007%2FS12022-008-9045-Z

Familial nonmedullary thyroid neoplasia

21 January 2018

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12 December 2020

Does familial non-medullary thyroid cancer adversely affect survival?

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Molecular genetics of thyroid cancer: implications for diagnosis, treatment and prognosis

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12 December 2020

Somatic mutations of the ret protooncogene in sporadic medullary thyroid carcinoma are not restricted to exon 16 and are associated with tumor recurrence

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12 December 2020

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

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12 December 2020

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

1 reference

12 December 2020

PAX8-PPARgamma rearrangement in thyroid tumors: RT-PCR and immunohistochemical analyses

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12 December 2020

Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic loci.

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12 December 2020

Familial Occurrence of Differentiated (Non-Medullary) Thyroid Cancer

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12 December 2020

Molecular profile and clinical-pathologic features of the follicular variant of papillary thyroid carcinoma. An unusually high prevalence of ras mutations

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12 December 2020

RET/PTC rearrangement in thyroid tumors

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12 December 2020

Pathologic diagnosis of papillary thyroid carcinoma: today and tomorrow

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12 December 2020

Familial nonmedullary thyroid cancer

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12 December 2020

Histology of familial thyroid tumours linked to a gene mapping to chromosome 19p13.2.

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Prophylactic thyroidectomy in multiple endocrine neoplasia type 2A.

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12 December 2020

Thyroid pathologic findings in patients with Cowden disease

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12 December 2020

Papillary thyroid carcinoma associated with papillary renal neoplasia: genetic linkage analysis of a distinct heritable tumor syndrome

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12 December 2020

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

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12 December 2020

RET/PTC rearrangements and BRAF mutations in thyroid tumorigenesis

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12 December 2020

Alterations of the BRAF gene in thyroid tumors.

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12 December 2020

Familial Nonmedullary Thyroid Cancer

1 reference

12 December 2020

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

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12 December 2020

Familial thyroid cancer

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12 December 2020

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

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12 December 2020

Familial multiple endocrine neoplasia: the first 100 years

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12 December 2020

RAS point mutations and PAX8-PPAR gamma rearrangement in thyroid tumors: evidence for distinct molecular pathways in thyroid follicular carcinoma.

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12 December 2020

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

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12 December 2020

Cribriform-morular variant of papillary carcinoma: a distinctive variant representing the sporadic counterpart of familial adenomatous polyposis-associated thyroid carcinoma?

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12 December 2020

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

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12 December 2020

Familial risks for nonmedullary thyroid cancer.

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12 December 2020

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

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12 December 2020

Carcinoma of the thyroid and other diseases of the thyroid in identical twins

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12 December 2020

Difference between familial and sporadic medullary thyroid carcinomas

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Familial papillary thyroid microcarcinoma: a new clinical entity

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12 December 2020

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

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12 December 2020

Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinoma

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12 December 2020

Familial nonmedullary thyroid carcinoma

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12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

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12 December 2020

Chromosomal aberrations by comparative genomic hybridization in thyroid tumors in patients with familial nonmedullary thyroid cancer

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12 December 2020

Excess of rare cancers in Werner syndrome (adult progeria)

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12 December 2020

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

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12 December 2020

Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriers

1 reference

12 December 2020

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

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12 December 2020

Cancer phenomics: RET and PTEN as illustrative models

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

High prevalence of BRAF mutations in thyroid cancer: genetic evidence for constitutive activation of the RET/PTC-RAS-BRAF signaling pathway in papillary thyroid carcinoma

1 reference

12 December 2020

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

1 reference

12 December 2020

Enhanced B-Raf protein expression is independent of V600E mutant status in thyroid carcinomas

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial medullary thyroid carcinoma and C cell hyperplasia

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic heterogeneity in familial nonmedullary thyroid carcinoma: exclusion of linkage to RET, MNG1, and TCO in 56 families. NMTC Consortium.

1 reference

12 December 2020

BRAF mutations in thyroid tumors are restricted to papillary carcinomas and anaplastic or poorly differentiated carcinomas arising from papillary carcinomas

1 reference

12 December 2020

Pathogenetic mechanisms in thyroid follicular-cell neoplasia

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

PTEN: one gene, many syndromes

1 reference

12 December 2020

Occult papillary thyroid carcinoma in the young and the aged

1 reference

12 December 2020

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

1 reference

12 December 2020

The role of PTEN, a phosphatase gene, in inherited and sporadic nonmedullary thyroid tumors

1 reference

12 December 2020

Pathology and genetics of thyroid carcinoma

1 reference

12 December 2020

C cell hyperplasia/neoplasia

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Microcarcinoma of the thyroid

1 reference

12 December 2020

BRAF in papillary thyroid carcinoma of ovary (struma ovarii)

1 reference

12 December 2020

Early Malignant Progression of Hereditary Medullary Thyroid Cancer

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Germline mutations of the APC gene in patients with familial adenomatous polyposis-associated thyroid carcinoma: results from a European cooperative study

1 reference

12 December 2020

Occult papillary carcinoma of the thyroid. A "normal" finding in Finland. A systematic autopsy study

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S12022-008-9045-Z

Identifiers

DOI

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19 August 2017

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PubMed ID

18931957