Thyroid involvement in two patients with Bannayan-Riley-Ruvalcaba syndrome. - Wikidata - awgldk - TriplyDB

Thyroid involvement in two patients with Bannayan-Riley-Ruvalcaba syndrome.

Thyroid involvement in two patients with Bannayan-Riley-Ruvalcaba syndrome.

http://www.wikidata.org/entity/Q37472559

about

Germline TTN variants are enriched in PTEN-wildtype Bannayan-Riley-Ruvalcaba syndrome.Thyroid Pathology Findings in Cowden Syndrome: A Clue for the Diagnosis of the PTEN Hamartoma Tumor Syndrome.

P2860

Q47109102-CACC38D4-D1FA-4131-81CE-AF46C7F23E98 Q53421695-C8420474-0E72-4626-BDAE-D2BBCD7E1073

P2860

Thyroid involvement in two patients with Bannayan-Riley-Ruvalcaba syndrome.

http://www.wikidata.org/entity/Q37472559

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on January 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Thyroid involvement in two patients with Bannayan-Riley-Ruvalcaba syndrome.

@en

Thyroid involvement in two patients with Bannayan-Riley-Ruvalcaba syndrome.

@nl

type

label

Thyroid involvement in two patients with Bannayan-Riley-Ruvalcaba syndrome.

@en

Thyroid involvement in two patients with Bannayan-Riley-Ruvalcaba syndrome.

@nl

prefLabel

Thyroid involvement in two patients with Bannayan-Riley-Ruvalcaba syndrome.

@en

Thyroid involvement in two patients with Bannayan-Riley-Ruvalcaba syndrome.

@nl

P1433

Q37472559-334BF09C-1945-4E20-9D2A-532742CED577

P1476

Q37472559-60C20707-2A13-4658-94F9-F036506F872C

P2093

Q37472559-84B70541-7FEB-4F39-92B8-41C0599AA3C2

Q37472559-9AA43ABC-31E7-4A15-8E7D-0468FB2FBAC9

Q37472559-DDBD1E39-1633-4296-A31B-7B4075178D84

Q37472559-FC563229-92D4-4E22-8F90-B17E54EC52B2

Q37472559-FCF9E9FD-AE74-4B50-972A-E66E149FDAD2

Q37472559-FF3C48F9-924C-4986-A8BC-664318FB0AF8

P2860

Q37472559-0066E930-A9E7-4B26-83E5-D605C2022238

Q37472559-032A6E16-2CA0-48E7-8D2B-6632D708C97B

Q37472559-0D6A6498-0935-4F15-8B44-5D71AB86EF4C

Q37472559-359395C7-0790-4AA2-A373-AE14E6959FEE

Q37472559-4397DB0D-7CF0-43A0-BBE1-AD3B9C0AE186

Q37472559-496425FE-6952-4F8D-A1BE-FAE79DC82F68

Q37472559-4EC1EF3E-631A-42AA-9D8D-49ED1B2C1276

Q37472559-57B9FE54-29E9-4681-A7C5-B7845FCE39E2

Q37472559-67ABF4B7-2AD3-43EA-AC09-47840C67EB85

Q37472559-8A6BE9F1-3CA7-4A42-B8FD-56F66B83A3A2

P304

Q37472559-47D7FDA4-7CDA-49CA-9897-68283D105A1F

P31

Q37472559-233059f6-a1d1-41d6-a69d-f46d96ac3d63

Q37472559-76EDBA8E-77D6-4B29-BEC2-4735B7CBB84F

P356

Q37472559-ACA7F0EF-D852-409C-802C-64F6C6910B75

P433

Q37472559-AAA4D99B-1478-4C4E-BBEE-7CA983813FAC

P478

Q37472559-18E55F26-22B3-45F1-B68F-8E52F5B01E43

P50

Q37472559-3CDF3F06-ECE2-4620-BFB0-833C2AB7A0B7

Q37472559-F1C08BB8-2DEB-49F4-BF8C-900915D36812

P577

Q37472559-A0FBEF54-F7CE-467A-8B77-CC65A81D5DE0

P698

Q37472559-D394A0B1-5BF8-4069-AA7C-41D4E7BB7788

P932

Q37472559-C36A2AFC-5CFD-41A7-A63B-5AED60883BFA

P356

P1433

Journal of clinical research in pediatric endocrinology

P1476

Thyroid involvement in two patients with Bannayan-Riley-Ruvalcaba syndrome

@en

P2093

Andrea Corrias

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

Arianna Santanera

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

Cristina Molinatto

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

Francesca Feyles

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

Gerdi Tuli

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

Valentina Peiretti

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

P2860

Thyroid nodules in pediatrics: which ones can be left alone, which ones must be investigated, when and how

Lipomatosis, angiomatosis, and macrencephalia. A previously undescribed congenital syndrome

Risk of tumorigenesis in overgrowth syndromes: A comprehensive review

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

PTEN hamartoma tumor syndromes.

Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases.

Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterations

Genetic and phenotypic heterogeneity in the PTEN hamartoma tumour syndrome.

Hereditary gastrointestinal polyposis syndromes.

The hamartomatous polyposis syndromes: clinical and radiologic features.

P304

261-265

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

P31

scholarly article

P356

10.4274/JCRPE.984

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

P433

4

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

P478

5

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

P50

Alessandro Mussa

P577

2013-01-01T00:00:00Z

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

P698

24379037

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

P932

3890226

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