相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Surgical Outcomes After Pancreatic Resection of Screening-Detected Lesions in Individuals at High Risk for Developing Pancreatic Cancer
Marcia Irene Canto et al.
JOURNAL OF GASTROINTESTINAL SURGERY (2020)
Management of patients with increased risk for familial pancreatic cancer: updated recommendations from the International Cancer of the Pancreas Screening (CAPS) Consortium
Michael Goggins et al.
GUT (2020)
Low-level parental mosaicism in an apparent de novo case of Peutz-Jeghers syndrome
G. I. Butel-Simoes et al.
FAMILIAL CANCER (2019)
Novel germline STK11 variants and breast cancer phenotype identified in an Indian cohort of Peutz-Jeghers syndrome
Anuja Lipsa et al.
HUMAN MOLECULAR GENETICS (2019)
Deleterious Germline Mutations Are a Risk Factor for Neoplastic Progression Among High-Risk Individuals Undergoing Pancreatic Surveillance
Toshiya Abe et al.
JOURNAL OF CLINICAL ONCOLOGY (2019)
Endoscopic management of polyposis syndromes: European Society of Gastrointestinal Endoscopy (ESGE) Guideline
Monique E. van Leerdam et al.
ENDOSCOPY (2019)
Long-Term Outcome in Patients with a Solitary Peutz-Jeghers Polyp
Masaya Iwamuro et al.
GASTROENTEROLOGY RESEARCH AND PRACTICE (2019)
Clinical and Genetic Study of Children With Peutz-Jeghers Syndrome Identifies a High Frequency of STK11 De Novo Mutation
Hong-Mei Zhao et al.
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION (2019)
Management of Peutz-Jeghers Syndrome in Children and Adolescents: A Position Paper From the ESPGHAN Polyposis Working Group
Andrew Latchford et al.
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION (2019)
STK11 gene analysis reveals a significant number of splice mutations in Chinese PJS patients
Yu-Liang Jiang et al.
CANCER GENETICS (2019)
Appropriateness of pancreatic resection in high-risk individuals for familial pancreatic ductal adenocarcinoma: a patient-level meta-analysis and proposition of the Beaujon score
Louis de Mestier et al.
UNITED EUROPEAN GASTROENTEROLOGY JOURNAL (2019)
Surveillance for pancreatic cancer in high-risk individuals
I. C. A. W. Konings et al.
BJS OPEN (2019)
Development of a high risk pancreatic screening clinic using 3.0 T MRI
Chad A. Barnes et al.
FAMILIAL CANCER (2018)
Prenatal diagnosis in a hereditary Peutz-Jeghers syndrome family with high cancer risk
Zhiqing Wang et al.
BMC MEDICAL GENETICS (2018)
Risk of Neoplastic Progression in Individuals at High Risk for Pancreatic Cancer Undergoing Long-term Surveillance
Marcia Irene Canto et al.
GASTROENTEROLOGY (2018)
Pancreatic cancer screening in high-risk individuals: Ready for prime time?
Marco J. Bruno
GASTROINTESTINAL ENDOSCOPY (2018)
Screening/surveillance programs for pancreatic cancer in familial high-risk individuals: A systematic review and proportion meta-analysis of screening results
Salvatore Paiella et al.
PANCREATOLOGY (2018)
Genetic analysis and clinical description of Greek patients with Peutz-Jeghers syndrome: Creation of a National Registry
Florentia Fostira et al.
CANCER GENETICS (2018)
Results of surveillance in individuals at high-risk of pancreatic cancer: A systematic review and meta-analysis
Marianna Signoretti et al.
UNITED EUROPEAN GASTROENTEROLOGY JOURNAL (2018)
Clinical manifestations and STK11 germline mutations in Taiwanese patients with Peutz-Jeghers syndrome
Jy-Ming Chiang et al.
ASIAN JOURNAL OF SURGERY (2018)
High Prevalence of Hereditary Cancer Syndromes and Outcomes in Adults with Early-Onset Pancreatic Cancer
Sarah A. Bannon et al.
CANCER PREVENTION RESEARCH (2018)
Screening and surveillance in hereditary gastrointestinal cancers: Recommendations from the European Society of Digestive Oncology (ESDO) expert discussion at the 20th European Society for Medical Oncology (ESMO)/World Congress on Gastrointestinal Cancer, Barcelona, June 2018
Deepak B. Vangala et al.
EUROPEAN JOURNAL OF CANCER (2018)
The role of STK 11 gene testing in individuals with oral pigmentation
Bich-Thu Duong et al.
AUSTRALASIAN JOURNAL OF DERMATOLOGY (2017)
Prevalence and Progression of Pancreatic Cystic Precursor Lesions Differ Between Groups at High Risk of Developing Pancreatic Cancer
Ingrid C. A. W. Konings et al.
PANCREAS (2017)
Cancer risk in patients with Peutz-Jeghers syndrome: A retrospective cohort study of 336 cases
Hong-Yu Chen et al.
TUMOR BIOLOGY (2017)
First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndrome
Victoria McKay et al.
FAMILIAL CANCER (2016)
A multicentre comparative prospective blinded analysis of EUS and MRI for screening of pancreatic cancer in high-risk individuals
F. Harinck et al.
GUT (2016)
Disease pattern in Danish patients with Peutz-Jeghers syndrome
A. M. Jelsig et al.
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE (2016)
Updates on breast cancer genetics: Clinical implications of detecting syndromes of inherited increased susceptibility to breast cancer
Erin F. Cobain et al.
SEMINARS IN ONCOLOGY (2016)
Update on our investigation of malignant tumors associated with Peutz-Jeghers syndrome in Japan
Hideyuki Ishida et al.
SURGERY TODAY (2016)
Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome
Zhiheng Huang et al.
BMC GASTROENTEROLOGY (2015)
STK11 Domain XI Mutations: Candidate Genetic Drivers Leading to the Development of Dysplastic Polyps in Peutz-Jeghers Syndrome
Zhiqing Wang et al.
HUMAN MUTATION (2014)
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
Pawel Borun et al.
BMC MEDICAL GENETICS (2013)
Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: Results of an Italian multicenter study
Nicoletta Resta et al.
DIGESTIVE AND LIVER DISEASE (2013)
International Cancer of the Pancreas Screening (CAPS) Consortium summit on the management of patients with increased risk for familial pancreatic cancer
Marcia Irene Canto et al.
GUT (2013)
Pancreatic cancer risk in Peutz-Jeghers syndrome patients: a large cohort study and implications for surveillance
Susanne E. Korsse et al.
JOURNAL OF MEDICAL GENETICS (2013)
Peutz-Jeghers syndrome and family planning: the attitude towards prenatal diagnosis and pre-implantation genetic diagnosis
Margot G. F. van Lier et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2012)
Frequent Detection of Pancreatic Lesions in Asymptomatic High-Risk Individuals
Marcia Irene Canto et al.
GASTROENTEROLOGY (2012)
High Cumulative Risk of Intussusception in Patients With Peutz-Jeghers Syndrome: Time to Update Surveillance Guidelines?
M. G. F. van Lier et al.
AMERICAN JOURNAL OF GASTROENTEROLOGY (2011)
Peutz-Jeghers Syndrome: Intriguing Suggestion of Gastrointestinal Cancer Prevention From Surveillance
A. R. Latchford et al.
DISEASES OF THE COLON & RECTUM (2011)
High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome
Margot G. F. van Lier et al.
GUT (2011)
Update on Screening Breast MRI in High-Risk Women
C. Boetes
OBSTETRICS AND GYNECOLOGY CLINICS OF NORTH AMERICA (2011)
High Cancer Risk in Peutz-Jeghers Syndrome: A Systematic Review and Surveillance Recommendations
M. G. F. van Lier et al.
AMERICAN JOURNAL OF GASTROENTEROLOGY (2010)
High prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers Syndrome patients
Janos Papp et al.
BMC MEDICAL GENETICS (2010)
Familial pancreatic Cancer in Italy. Risk assessment, screening programs and clinical approach: A position paper from the Italian Registry
Marco Del Chiaro et al.
DIGESTIVE AND LIVER DISEASE (2010)
Germline Mutation Analysis of STK11 Gene Using Direct Sequencing and Multiplex Ligation-Dependent Probe Amplification Assay in Korean Children with Peutz-Jeghers Syndrome
Hye Ran Yang et al.
DIGESTIVE DISEASES AND SCIENCES (2010)
Peutz-Jeghers syndrome: a systematic review and recommendations for management
A. D. Beggs et al.
GUT (2010)
Truncating mutations in Peutz-Jeghers syndrome are associated with more polyps, surgical interventions and cancers
Heidi Salloch et al.
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE (2010)
Psychosocial impact of Peutz-Jeghers Syndrome
Alice Woo et al.
FAMILIAL CANCER (2009)
Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates
Wendy W. J. de Leng et al.
CLINICAL GENETICS (2007)
An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus
E. Chow et al.
CLINICAL GENETICS (2006)
A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients
Nikita Thakur et al.
BMC MEDICAL GENETICS (2006)
Cancer risks in LKB1 germline mutation carriers
H Mehenni et al.
GUT (2006)
Screening for early pancreatic neoplasia in high-risk individuals: A prospective controlled study
Marcia Irene Canto et al.
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY (2006)
Frequency and spectrum of cancers in the Peutz-Jeghers syndrome
Nicholas Hearle et al.
CLINICAL CANCER RESEARCH (2006)
LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome
E Volikos et al.
JOURNAL OF MEDICAL GENETICS (2006)
Peutz-Jeghers syndrome and management recommendations
FM Giardiello et al.
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY (2006)
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome
S Aretz et al.
HUMAN MUTATION (2005)
Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADα, and MO25α, in Peutz-Jeghers syndrome
P Alhopuro et al.
BRITISH JOURNAL OF CANCER (2005)
Genotype-phenotype correlations in Peutz-Jeghers syndrome
CI Amos et al.
JOURNAL OF MEDICAL GENETICS (2004)
A new indication for pancreas transplantation: high grade pancreatic dysplasia
KP Charpentier et al.
CLINICAL TRANSPLANTATION (2004)
Relative frequency and morphology of cancers in STK11 mutation carriers
W Lim et al.
GASTROENTEROLOGY (2004)
Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome
W Lim et al.
BRITISH JOURNAL OF CANCER (2003)
Long-term results of polyp clearance by intraoperative enteroscopy in the Peutz-Jeghers syndrome
DP Edwards et al.
DISEASES OF THE COLON & RECTUM (2003)
Course and follow-up of solitary Peutz-Jeghers polyps: a case series
M Oncel et al.
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE (2003)
Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients
RJ Scott et al.
CLINICAL GENETICS (2002)
Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2
K Buchet-Poyau et al.
CYTOGENETIC AND GENOME RESEARCH (2002)
Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma
S Olschwang et al.
JOURNAL OF MEDICAL GENETICS (2001)
CDX2 mutations do not account for juvenile polyposis or Peutz-Jeghers syndrome and occur infrequently in sporadic colorectal cancers
KL Woodford-Richens et al.
BRITISH JOURNAL OF CANCER (2001)
Gene for the human transmembrane-type protein tyrosine phosphatase H (PTPRH): genomic structure, fine-mapping and its exclusion as a candidate for Peutz-Jeghers syndrome
AG Marneros et al.
CYTOGENETICS AND CELL GENETICS (2001)
Inherited pancreatic cancer: Surveillance and treatment strategies for affected families
SJ Rulyak et al.
PANCREATOLOGY (2001)
Timing and extent of surgical intervention in patients from hereditary pancreatic cancer kindreds
PB Kekis et al.
PANCREATOLOGY (2001)
Very high risk of cancer in familial Peutz-Jeghers syndrome
FM Giardiello et al.
GASTROENTEROLOGY (2000)