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1.
Juvenile polyposis syndrome might be misdiagnosed as familial adenomatous polyposis: a case report and literature review.
BMC Gastroenterol
; 20(1): 167, 2020 Jun 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32487124
2.
Early screening the small bowel is key to protect Peutz-Jeghers syndrome patients from surgery: a novel mutation c.243delG in STK11 gene.
BMC Gastroenterol
; 19(1): 70, 2019 May 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-31072341
3.
The altered activity of P53 signaling pathway by STK11 gene mutations and its cancer phenotype in Peutz-Jeghers syndrome.
BMC Med Genet
; 19(1): 141, 2018 08 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-30092773
4.
Close and regular surveillance is key to prevent severe complications for Peutz-Jeghers syndrome patients without gastrointestinal polyps: case report of a novel STK11 mutation (c.471_472delCT) in a Chinese girl.
BMC Surg
; 18(1): 24, 2018 Apr 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-29685139
5.
Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient.
BMC Med Genet
; 18(1): 130, 2017 11 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-29141581
6.
A 23-Nucleotide Deletion in STK11 Gene Causes Peutz-Jeghers Syndrome and Malignancy in a Chinese Patient Without a Positive Family History.
Dig Dis Sci
; 62(11): 3014-3020, 2017 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-28986664
7.
Colonoscopic diagnosis of rectal endometriosis without obvious or exact mucosa-infiltrated signs: A Video Vignette.
Colorectal Dis
; 23(6): 1593-1594, 2021 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-33751772
8.
Drugs for Neuropathic Pain Are Promising in Treating Feed-induced Dystonia in Central Nervous System Disabled Children.
J Pediatr Gastroenterol Nutr
; 66(1): e25, 2018 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-28902092
9.
Efficacy of cecal retroflexion observed on adenoma missing of ascending colon during colonoscopy: A prospective, randomized, pilot trial.
Medicine (Baltimore)
; 102(34): e34806, 2023 Aug 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-37653767
10.
Re-recognition of BMPR1A-related polyposis: beyond juvenile polyposis and hereditary mixed polyposis syndrome.
Gastroenterol Rep (Oxf)
; 11: goac082, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-36632626
11.
Delayed diagnosis of Peutz-Jeghers syndrome due to pathological information loss or mistake in family/personal history.
Orphanet J Rare Dis
; 16(1): 261, 2021 06 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-34103092
12.
STK11 gene analysis reveals a significant number of splice mutations in Chinese PJS patients.
Cancer Genet
; 230: 47-57, 2019 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30528796
13.
Adenoma miss rate determined by very shortly repeated colonoscopy: Retrospective analysis of data from a single tertiary medical center in China.
Medicine (Baltimore)
; 97(38): e12297, 2018 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-30235675
14.
Recurrent sigmoid volvulus relieved by transanal ileus tube implantation.
Gastroenterol Rep (Oxf)
; 10: goac030, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35785265
15.
A novel germline mutation (c.A527G) in STK11 gene causes Peutz-Jeghers syndrome in a Chinese girl: A case report.
Medicine (Baltimore)
; 96(49): e8591, 2017 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-29245219
16.
Detection and miss rates of autofluorescence imaging of adenomatous and polypoid lesions during colonoscopy: a systematic review and meta-analysis.
Endosc Int Open
; 3(3): E226-35, 2015 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-26171435
17.
[Primary coloduodenal fistula].
Zhonghua Wei Chang Wai Ke Za Zhi
; 16(12): 1230-3, 2013 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-24369408
18.
A novel mutation (c.855delG) in STK11 gene is associated with Peutz-Jeghers syndrome in a Chinese family.
Dig Liver Dis
; 50(3): 312-314, 2018 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-29301733
19.
A novel STK11 missense mutation (c.346Gâ¯>â¯T) causing Peutz-Jeghers syndrome in a Chinese male with a negative family history.
Dig Liver Dis
; 50(8): 864-866, 2018 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-29921539
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