Epidemiology and genetics of early onset colorectal cancer—African overview with a focus on Ethiopia
Colorectal cancer (CRC) is a common cause of cancer-related death worldwide, with high
rates of late diagnosis and increased mortality in sub-Saharan Africa. Furthermore, there is …
rates of late diagnosis and increased mortality in sub-Saharan Africa. Furthermore, there is …
Do hereditary syndrome-related gynecologic cancers have any specific features?
N Neto, TM Cunha - Insights into Imaging, 2015 - Springer
Hereditary syndromes are responsible for 10% of gynaecologic cancers, among which
hereditary breast-ovarian cancer and hereditary non-polyposis colon cancer syndromes …
hereditary breast-ovarian cancer and hereditary non-polyposis colon cancer syndromes …
Etiology of familial breast cancer with undetected BRCA1 and BRCA2 mutations: clinical implications
E Yiannakopoulou - Cellular oncology, 2014 - Springer
Background Familial breast cancer accounts for 20–30% of all breast cancer cases.
Mutations in the BRCA1 and BRCA2 genes account for the majority of high risk families with …
Mutations in the BRCA1 and BRCA2 genes account for the majority of high risk families with …
[HTML][HTML] Diagnostic difficulty in Peutz-Jeghers syndrome
J Loureiro, GL Menegazzo, L Vergamini… - … of Coloproctology (Rio …, 2015 - SciELO Brasil
A case of diagnostic difficulty facing the patient with colonic polyposis secondary to Peutz-
Jeghers syndrome, but without family history and pathognomonic clinical features of the …
Jeghers syndrome, but without family history and pathognomonic clinical features of the …
Peutz-Jeghers syndrome in pediatric patients: experience in a tertiary care institution in Mexico
R Ortegón-Gallareta, R Vázquez-Frías… - Boletín médico del …, 2022 - scielo.org.mx
Abstract Background: Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant inherited
disease characterized by the development of polyps in the gastrointestinal tract …
disease characterized by the development of polyps in the gastrointestinal tract …
Синдром Пейтца-Егерса: что стало известно за 125 лет изучения?(обзор литературы)
ТА Савельева, ДЮ Пикунов, АМ Кузьминов… - …, 2021 - ruproctology.com
Аннотация Синдром Пейтца-Егерса (СПЕ) является крайне редким аутосомно-
доминантным наследственным заболеванием, которое клинически характеризуется …
доминантным наследственным заболеванием, которое клинически характеризуется …
Prédisposition héréditaire aux cancers digestifs, mammaires, gynécologiques et gonadiques: état des lieux du syndrome de Peutz-Jeghers
A Turpin, S Cattan, J Leclerc, A Wacrenier… - Bulletin du cancer, 2014 - Elsevier
Résumé Le syndrome de Peutz-Jeghers (SPJ) est une affection rare, à transmission
autosomique dominante, liée à des mutations du gène suppresseur de tumeur STK11. Il …
autosomique dominante, liée à des mutations du gène suppresseur de tumeur STK11. Il …
[PDF][PDF] Peutz-Jeghers syndrome: what has been known for 125 years of research?
TA Savelyeva, DY Pikunov, AM Kuzminov… - …, 2021 - researchgate.net
The Peutz-Jeghers syndrome (PJS) is an extremely rare autosomal dominant hereditary
disease characterized by the growth of hamartomatous polyps in the gastrointestinal tract …
disease characterized by the growth of hamartomatous polyps in the gastrointestinal tract …
Masas ováricas de la niña y la adolescente
G De Lambert, B Fresneau, S Chapelière, C Mussini… - EMC-Pediatría, 2018 - Elsevier
Las masas ováricas, tanto si son orgánicas (tumores benignos o malignos) como
funcionales, se diagnostican a cualquier edad durante la infancia o la adolescencia, casi …
funcionales, se diagnostican a cualquier edad durante la infancia o la adolescencia, casi …
Peutz-Jeghers 综合征研究进展
张世玉， 范媛 - 口腔医学杂志, 2015 - stomatology.cn
Peutz-Jeghers 综合征(Peutz-Jeghers syndrome, PJS) 又叫色素沉着息肉综合征,
伴有口腔黏膜, 口周皮肤等部位色素斑及胃肠道错构瘤性息肉, 是一种由丝氨酸/苏氨酸蛋白激酶 …
伴有口腔黏膜, 口周皮肤等部位色素斑及胃肠道错构瘤性息肉, 是一种由丝氨酸/苏氨酸蛋白激酶 …