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