| scholarly article | Q13442814 |
| review article | Q7318358 |
| P2093 | author name string | Francis M Giardiello | |
| Jill D Trimbath | |||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | management recommendation | Q124146017 |
| Peutz-Jeghers syndrome | Q1544989 | ||
| P304 | page(s) | 408-415 | |
| P577 | publication date | 2006-04-01 | |
| P1433 | published in | Clinical Gastroenterology and Hepatology | Q5133759 |
| P1476 | title | Peutz-Jeghers syndrome and management recommendations. | |
| P478 | volume | 4 |
| Q34325954 | 10 rare tumors that warrant a genetics referral. |
| Q47684546 | A 23-Nucleotide Deletion in STK11 Gene Causes Peutz-Jeghers Syndrome and Malignancy in a Chinese Patient Without a Positive Family History. |
| Q41913623 | A Case of Laugier-Hunziker Syndrome |
| Q41072078 | A Rare Case of Solitary Peutz Jeghers Type Hamartomatous Duodenal Polyp with Dysplasia! |
| Q35919542 | A case of Peutz-Jeghers syndrome associated with high-grade intramucosal neoplasia |
| Q38968577 | A lesson from a reported pathogenic variant in Peutz-Jeghers syndrome: a case report |
| Q46240275 | A novel germline mutation (c.A527G) in STK11 gene causes Peutz-Jeghers syndrome in a Chinese girl: A case report. |
| Q36288945 | A novel mutation in the STK11 gene causes heritable Peutz-Jeghers syndrome - a case report |
| Q39257685 | A tumor of the uterine cervix with a complex histology in a Peutz-Jeghers syndrome patient with genomic deletion of the STK11 exon 1 region. |
| Q36416282 | ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes |
| Q83705852 | Acute malignant intestinal obstruction accompanied by synchronous multifocal intestinal cancer in Peutz-Jeghers syndrome: report of a case |
| Q54420283 | Breakpoint determination of 15 large deletions in Peutz-Jeghers subjects. |
| Q34995365 | Breast ultrasound in the management of gynecomastia in Peutz-Jeghers syndrome in monozygotic twins: two case reports |
| Q40144123 | Cancer risk in patients with Peutz-Jeghers syndrome: A retrospective cohort study of 336 cases |
| Q54384425 | Capsule endoscopy in small-bowel surveillance of patients with hereditary polyposis syndromes. |
| Q47816852 | Case Report: Spleen-preserving Multivisceral Transplant for Peutz-Jeghers Syndrome |
| Q34252517 | Chemopreventive efficacy of rapamycin on Peutz-Jeghers syndrome in a mouse model |
| Q39547521 | Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular characterization of a new contiguous gene syndrome. |
| Q37785236 | Clinical Genetics of Hereditary Colorectal Cancer |
| Q43847583 | Clinical presentations and surgical approach of acute intussusception caused by Peutz-Jeghers syndrome in adults |
| Q52569170 | 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. |
| Q33891853 | Conservative approach in Peutz-Jeghers syndrome: Single-balloon enteroscopy and small bowel polypectomy |
| Q37697666 | Correlation between genotype and phenotype in three families with Peutz-Jeghers Syndrome |
| Q58830522 | Current Approaches to Pediatric Polyposis Syndromes |
| Q34639739 | Current advance in small bowel tumors |
| Q41686937 | Deletion of endothelial cell-specific liver kinase B1 increases angiogenesis and tumor growth via vascular endothelial growth factor |
| Q39918456 | Disease pattern in Danish patients with Peutz-Jeghers syndrome. |
| Q38784244 | Double-balloon endoscopy and Peutz-Jeghers syndrome: a new look at an old disease |
| Q47773920 | Duodenal cancer in a young patient with Peuts-Jeghers syndrome harboring an entire deletion of the STK11 gene |
| Q27014027 | Early diagnosis of pancreatic cancer: challenges and new developments |
| Q91655781 | Early onset Peutz-Jeghers syndrome, the importance of appropriate diagnosis and follow-up: A case report |
| Q64059528 | Early screening the small bowel is key to protect Peutz-Jeghers syndrome patients from surgery: a novel mutation c.243delG in STK11 gene |
| Q37678614 | Endothelial cell-specific liver kinase B1 deletion causes endothelial dysfunction and hypertension in mice in vivo |
| Q34155002 | Epidemiology of pancreatic cancer and the role of family history |
| Q37427872 | Extracolonic manifestations of hereditary colorectal cancer syndromes |
| Q36371610 | Familial Gastric Cancers |
| Q34655489 | Familial colorectal cancer, beyond Lynch syndrome |
| Q37921953 | Gastric tumours in hereditary cancer syndromes: clinical features, molecular biology and strategies for prevention |
| Q47864304 | Gastrointestinal diseases and their oro-dental manifestations: Part 4: Peutz-Jeghers syndrome |
| Q37866697 | Gastrointestinal polyps and cancer in Peutz-Jeghers syndrome: clinical aspects |
| Q37468316 | Genetic risk and gynecologic cancers. |
| Q26744177 | Genetic risks and familial associations of small bowel carcinoma |
| Q38194650 | Genetic testing in inherited polyposis syndromes - how and why? |
| Q87970170 | Giant rectal polyp prolapse in an adult patient with the Peutz-Jeghers syndrome |
| Q26775636 | Hamartomatous Tumors in the Gastrointestinal Tract |
| Q24654006 | Hamartomatous polyposis syndromes |
| Q83767560 | Hamartomatous polyposis syndromes |
| Q34582357 | Hamartomatous polyposis syndromes. |
| Q21202845 | Hamartomatous polyposis syndromes: a review |
| Q38287107 | Hereditary and common familial colorectal cancer: evidence for colorectal screening |
| Q38266306 | Hereditary breast cancer syndromes and genetic testing |
| Q30652890 | Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers |
| Q33916338 | Hereditary hamartomatous polyposis syndromes: understanding the disease risks as children reach adulthood |
| Q34746938 | High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome. |
| Q37820895 | High cumulative risk of intussusception in patients with Peutz-Jeghers syndrome: time to update surveillance guidelines? |
| Q38826581 | Histopathological, Molecular, and Genetic Profile of Hereditary Diffuse Gastric Cancer: Current Knowledge and Challenges for the Future |
| Q38166590 | Hypoxia induced tumor metabolic switch contributes to pancreatic cancer aggressiveness. |
| Q44885579 | Identification of molecular alterations in gastrointestinal carcinomas and dysplastic hamartomas in Peutz-Jeghers syndrome |
| Q54449617 | Immunohistological evidence for Wnt-signaling activation in Peutz-Jeghers polyposis. |
| Q84683717 | Implications of genetic risk factors in breast cancer: culprit genes and associated malignancies |
| Q24628009 | Inherited colorectal cancer syndromes |
| Q37543834 | LKB1 and AMPK family signaling: the intimate link between cell polarity and energy metabolism |
| Q37829489 | LKB1 loss of function studied in vivo |
| Q37333592 | LKB1; linking cell structure and tumor suppression |
| Q37153048 | Lessons from the skin--cutaneous features of familial cancer |
| Q37015068 | Liver kinase b1 is required for white adipose tissue growth and differentiation |
| Q38254792 | MRI of the stomach: a pictorial review with a focus on oncological applications and gastric motility |
| Q37472932 | Management of gastric polyps: a pathology-based guide for gastroenterologists |
| Q46704554 | Management of prepubertal gynecomastia in two monozygotic twins with Peutz-Jeghers syndrome: from aromatase inhibitors to subcutaneous mastectomy |
| Q37685564 | Medical management update: Peutz Jeghers syndrome |
| Q90704103 | Metachronous triple cancer associated with Peutz-Jeghers syndrome treated with curative surgery: a case report |
| Q88619637 | Microsatellite instability in colorectal cancer |
| Q26769935 | Molecular approach to genetic and epigenetic pathogenesis of early-onset colorectal cancer |
| Q42406512 | Molecular genetics of colorectal cancer |
| Q39045050 | Multidetector CT enterography of focal small bowel lesions: a radiological-pathological correlation. |
| Q36693160 | Novel serine/threonine kinase 11 gene mutations in Peutz-Jeghers syndrome patients and endoscopic management |
| Q30465558 | Organ-sparing surgery of the bilateral testicular large cell calcifying sertoli cell tumor in patient with atypical Peutz-Jeghers syndrome |
| Q41982039 | Pancreatic LKB1 deletion leads to acinar polarity defects and cystic neoplasms |
| Q47743285 | Pediatric juvenile polyposis syndromes: an update. |
| Q53130981 | Performance of double-balloon enteroscopy for the management of small bowel polyps in hamartomatous polyposis syndromes. |
| Q41314878 | Peutz-Jeghers syndrome manifested as massive melæna at CHU-JRA Madagascar hospital: a case report |
| Q41916766 | Peutz-Jeghers syndrome with early onset of pre-adolescent gynecomastia: a predigree case report and clinical and molecular genetic analysis |
| Q33773686 | Peutz-Jeghers syndrome with germline mutation of STK11. |
| Q33627030 | Peutz-Jeghers syndrome with intermittent upper intestinal obstruction: A case report and review of the literature |
| Q37423083 | Peutz-Jeghers syndrome with small intestinal malignancy and cervical carcinoma |
| Q36601303 | Peutz-Jeghers syndrome: Four cases in one family. |
| Q84463153 | Peutz-Jeghers syndrome: a study of long-term surgical morbidity and causes of mortality |
| Q37422996 | Peutz-Jeghers syndrome: diagnostic and therapeutic approach. |
| Q90641250 | Peutz-Jeghers syndrome: need for early screening |
| Q40481435 | Peutz-jeghers syndrome with synchronous adenocarcinoma arising from ileal polyps. |
| Q44389089 | Psychosocial impact of Peutz-Jeghers Syndrome |
| Q38808384 | Rare non-epithelial ovarian neoplasms: Pathology, genetics and treatment |
| Q35161917 | Role and regulation of autophagy in cancer |
| Q38214800 | Role of cilia in normal pancreas function and in diseased states |
| Q45363222 | 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. |
| Q38180592 | Small bowel intussusception in a pregnant woman with Peutz-Jeghers Syndrome. |
| Q90656775 | Small bowel polyp resection using device-assisted enteroscopy in Peutz-Jeghers Syndrome: Results of a specialised tertiary care centre |
| Q37907905 | Small bowel polyposis syndromes |
| Q92764264 | Smooth muscle-specific LKB1 deletion exaggerates angiotensin II-induced abdominal aortic aneurysm in mice |
| Q37724721 | Solitary Peutz-Jeghers-type appendiceal hamartomatous polyp growing into the terminal ileum |
| Q24564006 | Strategies for early detection of resectable pancreatic cancer |
| Q37350822 | The LKB1 tumor suppressor differentially affects anchorage independent growth of HPV positive cervical cancer cell lines |
| Q26768191 | The Usefulness of Capsule Endoscopy for Small Bowel Tumors |
| Q58793642 | The altered activity of P53 signaling pathway by STK11 gene mutations and its cancer phenotype in Peutz-Jeghers syndrome |
| Q54222172 | The role of STK 11 gene testing in individuals with oral pigmentation. |
| Q37934215 | The tumor suppressor kinase LKB1: lessons from mouse models |
| Q34263162 | Translational advances regarding hereditary breast cancer syndromes |
| Q54445947 | Trilateral retinoblastoma in a patient with Peutz-Jeghers syndrome. |
| Q51616672 | Truncating mutations in Peutz-Jeghers syndrome are associated with more polyps, surgical interventions and cancers. |
| Q42225489 | Unusually early presentation of small-bowel adenocarcinoma in a patient with Peutz-Jeghers syndrome |
| Q26995167 | Update on imaging of Peutz-Jeghers syndrome |
| Q30251978 | Update on our investigation of malignant tumors associated with Peutz-Jeghers syndrome in Japan |
| Q37785235 | Upper Gastrointestinal Cancer Predisposition Syndromes |
| Q53123915 | [Rare hereditary syndromes associated with polyposis and the development of malignant tumors]. |
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