Search Results

Display Settings
Results per page: 10
Sort By: Relevance
Filter
  • 1-10 of  399 results for ""PEUTZ-Jeghers syndrome""

Your Filters

Publisher : biomed central
Reset filters
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

Genetic variation at a splicing branch point in intron 7 of STK11: a rare variant decreasing its expression in a Chinese family with Peutz-Jeghers syndrome.

  • Authors : Wang X; Department of Pain, Tongji Medical College, The Central Hospital of Wuhan, Huazhong University of Science and Technology, Wuhan, Hubei, China.; Li Y

Subjects: Introns*/Introns*/Introns*/genetics ; Pedigree* ; Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/genetics

  • Source: World journal of surgical oncology [World J Surg Oncol] 2024 Jul 30; Vol. 22 (1), pp. 202. Date of Electronic Publication: 2024 Jul 30.Publisher: BioMed Central Country of Publication: England NLM ID: 101170544 Publication Model: Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

When synchronous mucinous metaplasia and neoplasia of the female genital tract and peutz-jeghers syndrome meet: a case report and literature reviews.

  • Authors : Zhou Y; College of Medicine, Cheeloo College of Medicine, Shandong University, 44 Wenhua Xi Road, Jinan, Shandong, People's Republic of China.; Department of Obstetrics and Gynecology, Qilu Hospital of Shandong University, 107 Wenhua Xi Road, Jinan, Shandong, People's Republic of China.

Subjects: Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/complications ; Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/diagnosis ; Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/pathology

  • Source: BMC women's health [BMC Womens Health] 2024 Jun 28; Vol. 24 (1), pp. 375. Date of Electronic Publication: 2024 Jun 28.Publisher: BioMed Central Country of Publication: England NLM ID: 101088690 Publication Model: Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

Peutz-Jeghers syndrome with polyps in the stomach, duodenum, and small and large intestine: a case report.

  • Authors : Shah ZA; Hayatabad Medical Complex Peshawar, Peshawar, Pakistan.; Zeb M

Subjects: Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/complications ; Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/diagnosis ; Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/surgery

  • Source: Journal of medical case reports [J Med Case Rep] 2024 Mar 05; Vol. 18 (1), pp. 86. Date of Electronic Publication: 2024 Mar 05.Publisher: BioMed Central Country of Publication: England NLM ID: 101293382 Publication Model: Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

Changes of gut microbiota and short chain fatty acids in patients with Peutz-Jeghers syndrome.

  • Authors : Zhou A; Department of Gastroenterology, Second Affiliated Hospital, Army Medical University, Chongqing, 400037, China.; Tang B

Subjects: Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/genetics ; Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/pathology ; Gastrointestinal Microbiome*

  • Source: BMC microbiology [BMC Microbiol] 2023 Nov 30; Vol. 23 (1), pp. 373. Date of Electronic Publication: 2023 Nov 30.Publisher: BioMed Central Country of Publication: England NLM ID: 100966981 Publication Model: Electronic Cited Medium:

Record details

Connect Read More Add to Saved list
×
Academic Journal

Intraductal oncocytic papillary neoplasm arising in Peutz-Jeghers Syndrome bile duct: a unique case report.

  • Authors : Liu Q; Department of Pathology, Air Force Medical Center, PLA, Beijing, People's Republic of China.; China Medical University, Shenyang, People's Republic of China.

Subjects: Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/complications ; Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/diagnosis ; Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/genetics

  • Source: Diagnostic pathology [Diagn Pathol] 2022 Dec 28; Vol. 17 (1), pp. 96. Date of Electronic Publication: 2022 Dec 28.Publisher: BioMed Central Country of Publication: England NLM ID: 101251558 Publication Model: Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

A novel missense mutation of the STK11 gene in a Chinese family with Peutz-Jeghers syndrome.

  • Authors : Yu Z; Department of Pediatrics, Qilu Hospital, Shandong University, 107 Wen Hua Xi Road, Jinan, 250012, Shandong, People's Republic of China.; Liu L

Subjects: Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/genetics; Humans ; Male

  • Source: BMC gastroenterology [BMC Gastroenterol] 2022 Dec 22; Vol. 22 (1), pp. 536. Date of Electronic Publication: 2022 Dec 22.Publisher: BioMed Central Country of Publication: England NLM ID: 100968547 Publication Model: Electronic Cited Medium:

Record details

Read Online Read More Add to Saved list
×
Academic Journal

Multidisciplinary management for Peutz-Jeghers syndrome and prevention of vertical transmission to offspring using preimplantation genetic testing.

  • Authors : Xu X; Center for Reproductive Medicine, Henan Key Laboratory of Reproduction and Genetics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, Henan, China.; Henan Key Laboratory of Reproduction and Genetics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Subjects: Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/diagnosis ; Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/genetics ; Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/pathology

  • Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2022 Feb 21; Vol. 17 (1), pp. 64. Date of Electronic Publication: 2022 Feb 21.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

Delayed diagnosis of Peutz-Jeghers syndrome due to pathological information loss or mistake in family/personal history.

  • Authors : Jiang YL; Department of Gastroenterology, Beijing Shijitan Hospital, Capital Medical University, 10 Tieyi Rd., Beijing, 100038, China.; Xu XD

Subjects: Peutz-Jeghers Syndrome*; Delayed Diagnosis ; Family

  • Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2021 Jun 08; Vol. 16 (1), pp. 261. Date of Electronic Publication: 2021 Jun 08.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

Laparoscopic-assisted disinvagination and polypectomy for multiple intussusceptions induced by small intestinal polyps in patients with Peutz-Jeghers syndrome: a case report.

  • Authors : Yamamoto M; Department of Gastroenterological Surgery, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-ku, Osaka, 541-8567, Japan. .; Department of Surgery, JCHO Hoshigaoka Medical Center, 4-8-1, Hoshigaoka, Hirakata, Osaka, 573-8511, Japan. .

Subjects: Intussusception*/Intussusception*/Intussusception*/etiology ; Intussusception*/Intussusception*/Intussusception*/surgery ; Laparoscopy*

  • Source: World journal of surgical oncology [World J Surg Oncol] 2021 Jan 21; Vol. 19 (1), pp. 22. Date of Electronic Publication: 2021 Jan 21.Publisher: BioMed Central Country of Publication: England NLM ID: 101170544 Publication Model: Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

Distinct promoter methylation patterns of LKB1 in the hamartomatous polyps of Peutz-Jeghers syndrome and its potential in gastrointestinal malignancy prediction.

  • Authors : Li T; Department of Pathology, Air Force Medical Center, PLA, Beijing, China.; Lin W

Subjects: Gastrointestinal Neoplasms* ; Hamartoma* ; Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/Peutz-Jeghers Syndrome*/genetics

  • Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2020 Aug 15; Vol. 15 (1), pp. 208. Date of Electronic Publication: 2020 Aug 15.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium:

Record details

Read More Add to Saved list
×
  • 1-10 of  399 results for ""PEUTZ-Jeghers syndrome""