Malignant tumors associated with juvenile polyposis syndrome in Japan.
- Published in:
- Surgery Today, 2018, v. 48, n. 3, p. 253, doi. 10.1007/s00595-017-1538-2
- By:
- Publication type:
- Article
Works matching DE "JUVENILE polyposis syndrome"
Results: 14
1
2
Colocolic Intussusception in a Child with Pathologic Lead Point Along with Intestinal Malrotation-A Rare Case Report and Brief Review.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
3
Carcinosarcoma with choriocarcinomatous and osteosarcomatous differentiation in a patient with juvenile polyposis syndrome.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
4
JP-HHT phenotype in Danish patients with SMAD4 mutations.
- Published in:
- Clinical Genetics, 2016, v. 90, n. 1, p. 55, doi. 10.1111/cge.12693
- By:
- Publication type:
- Article
5
The gastrointestinal manifestation of constitutional mismatch repair deficiency syndrome: from a single adenoma to polyposis-like phenotype and early onset cancer.
- Published in:
- Clinical Genetics, 2015, v. 88, n. 5, p. 474, doi. 10.1111/cge.12518
- By:
- Publication type:
- Article
6
Gastrointestinal Manifestations of Hereditary Hemorrhagic Telangiectasia (HHT): A Systematic Review of the Literature.
- Published in:
- 2017
- By:
- Publication type:
- journal article
7
Correction to: Gastrointestinal juvenile-like (inflammatory/hyperplastic) mucosal polyps in neurofibromatosis type 1 with no concurrent genetic or clinical evidence of other syndromes.
- Published in:
- 2019
- By:
- Publication type:
- corrected article
8
Gastrointestinal juvenile-like (inflammatory/hyperplastic) mucosal polyps in neurofibromatosis type 1 with no concurrent genetic or clinical evidence of other syndromes.
- Published in:
- Virchows Archiv: European Journal of Pathology, 2019, v. 474, n. 2, p. 259, doi. 10.1007/s00428-018-2462-6
- By:
- Publication type:
- Article
9
Issue Information.
- Published in:
- Histopathology, 2017, v. 70, n. 6, p. 843, doi. 10.1111/his.13222
- Publication type:
- Article
10
Massive gastric juvenile-type polyposis: a clinicopathological analysis of 22 cases.
- Published in:
- Histopathology, 2017, v. 70, n. 6, p. 918, doi. 10.1111/his.13149
- By:
- Publication type:
- Article
11
Juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia caused by the SMAD4 gene mutation in a paediatric patient - a case report and a review of the literature.
- Published in:
- Polish Journal of Pediatrics / Pediatria Polska, 2021, v. 96, n. 1, p. 71, doi. 10.5114/POLP.2021.104832
- By:
- Publication type:
- Article
12
A Novel SMAD4 Mutation Causing Severe Juvenile Polyposis Syndrome with Protein Losing Enteropathy, Immunodeficiency, and Hereditary Haemorrhagic Telangiectasia.
- Published in:
- Case Reports in Gastrointestinal Medicine, 2015, v. 2015, p. 1, doi. 10.1155/2015/140616
- By:
- Publication type:
- Article
13
Corrigendum to “Nonfamilial Juvenile Polyposis Syndrome with Exon 5 Novel Mutation in SMAD 4 Gene”.
- Published in:
- 2017
- By:
- Publication type:
- Correction Notice
14
Germline variants in Hamartomatous Polyposis Syndrome-associated genes from patients with one or few hamartomatous polyps.
- Published in:
- Scandinavian Journal of Gastroenterology, 2016, v. 51, n. 9, p. 1118, doi. 10.1080/00365521.2016.1174880
- By:
- Publication type:
- Article