Zobrazeno 1 - 10
of 660
pro vyhledávání: '"juvenile polyposis syndrome"'
Publikováno v:
Gastroenterology Insights, Vol 15, Iss 1, Pp 122-144 (2024)
Multiple gastric polyps are observed in various polyposis syndromes and conditions associated with polypoid lesion development in the stomach. Polyposis syndromes often occur concurrently with specific malignant tumors and can manifest at any point i
Externí odkaz:
https://doaj.org/article/8b747844c6674121b63d271279cc9db0
Autor:
Kenya Nakamura, Koji Kubota, Akira Shimizu, Tsuyoshi Notake, Tomohiko Ikehara, Kentaro Umemura, Atsushi Kamachi, Takamune Goto, Hidenori Tomida, Yoshiyuki Takahashi, Tadanobu Nagaya, Takeji Umemura, Yuji Soejima
Publikováno v:
Surgical Case Reports, Vol 10, Iss 1, Pp 1-7 (2024)
Abstract Background Juvenile polyposis syndrome (JPS) is an autosomal dominant, inherited disorder characterized by multiple hyperproliferative polyps of the gastrointestinal tract, particularly of the colon, rectum, and stomach. SMAD4 mutations are
Externí odkaz:
https://doaj.org/article/7791600a5f3a41b9b51dfc536f3730fb
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 21, Iss 1, Pp 1-64 (2023)
Abstract Background Juvenile polyposis syndrome (JPS), a rare autosomal dominant syndrome, affects one per 100 000 births, increasing lifetime cancer risk by 9 – 50%. Around 40–60% of JPS cases are caused by disease-causing variants (DCV) in SMAD
Externí odkaz:
https://doaj.org/article/113d8f99c31e4f2883f0ce8ac868cc90
Autor:
Giovanna Forte, Antonia Lucia Buonadonna, Candida Fasano, Paola Sanese, Filomena Cariola, Andrea Manghisi, Anna Filomena Guglielmi, Martina Lepore Signorile, Katia De Marco, Valentina Grossi, Vittoria Disciglio, Cristiano Simone
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 14, p 7939 (2024)
Juvenile polyposis syndrome (JPS) is an inherited autosomal dominant condition that predisposes to the development of juvenile polyps throughout the gastrointestinal (GI) tract, and it poses an increased risk of GI malignancy. Germline causative vari
Externí odkaz:
https://doaj.org/article/997e30fbf6b448178cbf5ce9f1180fff
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 21, Iss 1, Pp 1-10 (2023)
Abstract Background Juvenile Polyposis Syndrome (JPS) is an autosomal dominant condition with hamartomatous polyps in the gastrointestinal tract, associated with an increased risk of gastrointestinal malignancy. Disease causing variants (DCVs) in BMP
Externí odkaz:
https://doaj.org/article/b4f69321faa4438e8279f2b74536f2de
Autor:
Gonzalez, Raul S1, Adsay, Volkan2, Graham, Rondell P3, Shroff, Stuti G4, Feely, Michael M5, Drage, Michael G6, Lewin, David N7, Swanson, Eric A8, Yantiss, Rhonda K9, Bağci, Pelin2, Krasinskas, Alyssa M2 akrasin@emory.edu
Publikováno v:
Histopathology. May2017, Vol. 70 Issue 6, p918-928. 11p. 2 Color Photographs, 1 Chart, 1 Graph.
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 11, p 5812 (2024)
Juvenile polyposis syndrome (JPS) is a rare autosomal dominant disorder characterized by multiple juvenile polyps in the gastrointestinal tract, often associated with mutations in genes such as Smad4 and BMPR1A. This study explores the impact of Smad
Externí odkaz:
https://doaj.org/article/11bd462604e94358bd4b4cb93f8cc996
Autor:
Takayuki Matsumoto, Junji Umeno, Keisuke Jimbo, Masami Arai, Itaru Iwama, Hiroshi Kashida, Takahiro Kudo, Koichi Koizumi, Yasushi Sato, Shigeki Sekine, Shinji Tanaka, Kohji Tanakaya, Kazuo Tamura, Keiji Hirata, Suguru Fukahori, Motohiro Esaki, Hideki Ishikawa, Takeo Iwama, Yasushi Okazaki, Yutaka Saito, Nariaki Matsuura, Michihiro Mutoh, Naohiro Tomita, Takashi Akiyama, Toshiki Yamamoto, Hideyuki Ishida, Yoshiko Nakayama
Publikováno v:
Journal of the Anus, Rectum and Colon, Vol 7, Iss 2, Pp 115-125 (2023)
Juvenile polyposis syndrome (JPS) is a rare disease characterized by multiple hamartomatous polyps within the gastrointestinal tract. SMAD4 or BMPR1A is known as a causative gene of JPS. Approximately 75% of newly diagnosed cases have an autosomal-do
Externí odkaz:
https://doaj.org/article/4303d107d2664da9b1128f48062decc5
Autor:
Johansson, Joel1 joejo597@student.liu.se, Sahin, Christofer1 chrsa265@student.liu.se, Pestoff, Rebecka2 rebecka.pestoff@lio.se, Ignatova, Simone2 simone.ignatova@lio.se, Forsberg, Pia3 pia.forsberg@liu.se, Edsjö, Anders4 anders.edsjo@gu.se, Ekstedt, Mattias1 mattias.ekstedt@lio.se, Stenmark Askmalm, Marie2 mariestenmark@icloud.com
Publikováno v:
Case Reports in Gastrointestinal Medicine. 2/1/2015, Vol. 2015, p1-5. 5p.
Publikováno v:
Cancer Management and Research, Vol Volume 14, Pp 2953-2969 (2022)
Jessica M Long,1,* Jessica Ebrahimzadeh,1,* Peter P Stanich,2 Bryson W Katona3 1Division of Hematology and Oncology, Penn Medicine, Philadelphia, PA, USA; 2Division of Gastroenterology, Hepatology & Nutrition, The Ohio State University, Wexne
Externí odkaz:
https://doaj.org/article/013d4fa538bf4f78a15f0059b473b0a7