المؤلفون: Thomas, LE, Hurley, JJ, Sanchez, AA, Aznarez, MR, Backman, AS, Bjork, J, Capella, G, Clark, SK, Colas, C, Dekker, E, Dolwani, S, Ghorbanoghli, Z, Gonn, M, Romero, SG, Hes, FJ, Jundi, H, Kelland, S, Latchford, AR, Brito, HL, Lynch, PM, Meuser, E, Mork, ME, Mort, M, Garcia, MN, Nielsen, M, Parc, Y, Ricci, MT, Saurin, JC, van der Tuin, K, Vasen, H, Vilar, E, Vinet, O, Vitellaro, M, Walton, SJ, West, HD, Sampson, JR

المصدر: Gastroenterology. 160(3):952

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:146404311

المؤلفون: O’Shea, NR, Hodges, NC, Man, RF, Clark, SK, Roon, ACVon, Latchford, AR

المصدر: Gut; 2017, Vol. 66 Issue: Supplement 2 pA35-A35, 1p

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المؤلفون: Latchford AR; Polyposis Registry, St Mark's Hospital, Harrow, UK; Department of Surgery and Cancer, Imperial College, London, UK. Electronic address: andrew.latchford@nhs.net., Clark SK; Polyposis Registry, St Mark's Hospital, Harrow, UK; Department of Surgery and Cancer, Imperial College, London, UK.

المصدر: Best practice & research. Clinical gastroenterology [Best Pract Res Clin Gastroenterol] 2022 Jun-Aug; Vol. 58-59, pp. 101789. Date of Electronic Publication: 2022 Apr 06.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101120605 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-1916 (Electronic) Linking ISSN: 15216918 NLM ISO Abbreviation: Best Pract Res Clin Gastroenterol Subsets: MEDLINE

مواضيع طبية MeSH: Neoplasms*/complications , Peutz-Jeghers Syndrome*/complications , Peutz-Jeghers Syndrome*/diagnosis, Humans

المؤلفون: Anele CC; The Polyposis Registry, St Mark's Hospital, London North West University Healthcare NHS Trust, Harrow, United Kingdom.; Department of Surgery and Cancer, Imperial College, London, United Kingdom., Martin I; The Polyposis Registry, St Mark's Hospital, London North West University Healthcare NHS Trust, Harrow, United Kingdom.; Department of Surgery and Cancer, Imperial College, London, United Kingdom., McGinty Duggan PM; The Polyposis Registry, St Mark's Hospital, London North West University Healthcare NHS Trust, Harrow, United Kingdom., Chauhan J; The Polyposis Registry, St Mark's Hospital, London North West University Healthcare NHS Trust, Harrow, United Kingdom., Clark SK; The Polyposis Registry, St Mark's Hospital, London North West University Healthcare NHS Trust, Harrow, United Kingdom.; Department of Surgery and Cancer, Imperial College, London, United Kingdom., Faiz OD; The Polyposis Registry, St Mark's Hospital, London North West University Healthcare NHS Trust, Harrow, United Kingdom.; Department of Surgery and Cancer, Imperial College, London, United Kingdom., Latchford AR; The Polyposis Registry, St Mark's Hospital, London North West University Healthcare NHS Trust, Harrow, United Kingdom.; Department of Surgery and Cancer, Imperial College, London, United Kingdom.

المصدر: Diseases of the colon and rectum [Dis Colon Rectum] 2022 Apr 01; Vol. 65 (4), pp. 529-535.

نوع المنشور: Journal Article; Video-Audio Media

بيانات الدورية: Publisher: Lippincott Country of Publication: United States NLM ID: 0372764 Publication Model: Print Cited Medium: Internet ISSN: 1530-0358 (Electronic) Linking ISSN: 00123706 NLM ISO Abbreviation: Dis Colon Rectum Subsets: MEDLINE

مواضيع طبية MeSH: Adenoma* , Adenomatous Polyposis Coli*/diagnosis , Adenomatous Polyposis Coli*/genetics , Adenomatous Polyposis Coli*/surgery , Colorectal Neoplasms*/pathology, Humans ; Phenotype ; Retrospective Studies

SCR Disease Name: Attenuated familial adenomatous polyposis

المؤلفون: Blatter R; Institute for Medical Genetics and Pathology, University Hospital Basel, and Research Group Human Genomics, Department of Research, University of Basel, Basel, Switzerland., Tschupp B; Institute for Medical Genetics and Pathology, University Hospital Basel, and Research Group Human Genomics, Department of Research, University of Basel, Basel, Switzerland., Aretz S; Institute of Human Genetics, University Hospital Bonn, Bonn, Germany.; National Center for Hereditary Tumour Syndromes, University Hospital, Bonn, Germany., Bernstein I; Department of Surgical Gastroenterology, Aalborg University Hospital, Aalborg, and Danish HNPCC Registry, Department of Surgical Gastroenterology, Hvidovre University Hospital, Hvidovre, Denmark., Colas C; Department of Oncogenetics and Angiogenetics, Pitie-Salpetriere Hospital, Sorbonne Université, Paris, France.; Department of Genetics, Institut Curie, Université de Recherche Paris Sciences et Lettres, Paris, France., Evans DG; Department of Genomic Medicine, Manchester Universities NHS Foundation Trust and Division of Evolution and Genomic Sciences, University of Manchester, Manchester, United Kingdom., Genuardi M; Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Genetica Medica, Rome, Italy.; Università Cattolica del Sacro Cuore, Istituto di Medicina Genomica, Rome, Italy., Hes FJ; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands., Hüneburg R; National Center for Hereditary Tumour Syndromes, University Hospital, Bonn, Germany.; Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany., Järvinen H; Department of Surgery, Helsinki University Central Hospital, Helsinki University, Helsinki, Finland., Lalloo F; Department of Genomic Medicine, Manchester Universities NHS Foundation Trust and Division of Evolution and Genomic Sciences, University of Manchester, Manchester, United Kingdom., Moeslein G; Center for Hereditary Tumors, HELIOS Klinikum Wuppertal, University Witten-Herdecke, Wuppertal, Germany., Renkonen-Sinisalo L; Department of Surgery, Helsinki University Central Hospital, Helsinki University, Helsinki, Finland., Resta N; Division of Medical Genetics, Department of Biomedical Sciences and Human Oncology (DIMO), University of Bari 'Aldo Moro', Bari, Italy., Spier I; Institute of Human Genetics, University Hospital Bonn, Bonn, Germany.; National Center for Hereditary Tumour Syndromes, University Hospital, Bonn, Germany., Varvara D; Division of Medical Genetics, Department of Biomedical Sciences and Human Oncology (DIMO), University of Bari 'Aldo Moro', Bari, Italy., Vasen H; Department of Gastroenterology and Hepatology, Leiden University Medical Centre, Leiden, The Netherlands., Latchford AR; Polyposis Registry, St. Mark's Hospital, Harrow, United Kingdom. andrew.latchford@nhs.net., Heinimann K; Institute for Medical Genetics and Pathology, University Hospital Basel, and Research Group Human Genomics, Department of Research, University of Basel, Basel, Switzerland. karl.heinimann@usb.ch.

المصدر: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2020 Sep; Vol. 22 (9), pp. 1524-1532. Date of Electronic Publication: 2020 May 13.

نوع المنشور: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

مواضيع طبية MeSH: Intestinal Polyposis*/congenital , Intestinal Polyposis*/diagnosis , Intestinal Polyposis*/epidemiology , Intestinal Polyposis*/genetics , Neoplastic Syndromes, Hereditary*/epidemiology , Neoplastic Syndromes, Hereditary*/genetics, Adult ; Bone Morphogenetic Protein Receptors, Type I/genetics ; Germ-Line Mutation ; Humans ; Retrospective Studies ; Smad4 Protein/genetics ; Surveys and Questionnaires

SCR Disease Name: Juvenile polyposis syndrome

المؤلفون: Latchford AR; Derriford Hospital, Plymouth, United Kingdom. andylatch@doctors.org.uk, Neale K, Phillips RK, Clark SK

المصدر: Diseases of the colon and rectum [Dis Colon Rectum] 2012 Oct; Vol. 55 (10), pp. 1038-43.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Lippincott Country of Publication: United States NLM ID: 0372764 Publication Model: Print Cited Medium: Internet ISSN: 1530-0358 (Electronic) Linking ISSN: 00123706 NLM ISO Abbreviation: Dis Colon Rectum Subsets: MEDLINE

مواضيع طبية MeSH: Intestinal Polyposis/*congenital , Neoplastic Syndromes, Hereditary/*genetics , Neoplastic Syndromes, Hereditary/*pathology, Adolescent ; Adult ; Aged ; Bone Morphogenetic Protein Receptors, Type I/genetics ; Child ; Child, Preschool ; Disease Progression ; Endoscopy, Gastrointestinal ; Female ; Follow-Up Studies ; Genotype ; Humans ; Intestinal Polyposis/genetics ; Intestinal Polyposis/pathology ; Intestinal Polyposis/surgery ; Male ; Middle Aged ; Mutation ; Neoplastic Syndromes, Hereditary/surgery ; Phenotype ; Registries ; Retrospective Studies ; Smad4 Protein/genetics ; Treatment Outcome

SCR Disease Name: Juvenile polyposis syndrome

المؤلفون: Latchford AR; Department of Gastroenterology, Derriford Hospital, Plymouth, UK. andylatch@doctors.org.uk, Neale K, Phillips RK, Clark SK

المصدر: Diseases of the colon and rectum [Dis Colon Rectum] 2011 Dec; Vol. 54 (12), pp. 1547-51.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Lippincott Country of Publication: United States NLM ID: 0372764 Publication Model: Print Cited Medium: Internet ISSN: 1530-0358 (Electronic) Linking ISSN: 00123706 NLM ISO Abbreviation: Dis Colon Rectum Subsets: MEDLINE

مواضيع طبية MeSH: Population Surveillance*, Gastrointestinal Neoplasms/*prevention & control , Peutz-Jeghers Syndrome/*complications, Adolescent ; Adult ; Child ; Child, Preschool ; Endoscopy, Gastrointestinal ; Female ; Gastrointestinal Neoplasms/etiology ; Humans ; Intestinal Polyps/surgery ; Male ; Middle Aged ; Peutz-Jeghers Syndrome/surgery ; Registries ; Retrospective Studies ; Young Adult

المؤلفون: Latchford AR; Department of Gastroenterology, Derriford Hospital, Plymouth, UK. andylatch@doctors.org.uk, Phillips RK

المصدر: Familial cancer [Fam Cancer] 2011 Sep; Vol. 10 (3), pp. 455-61.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Springer Country of Publication: Netherlands NLM ID: 100898211 Publication Model: Print Cited Medium: Internet ISSN: 1573-7292 (Electronic) Linking ISSN: 13899600 NLM ISO Abbreviation: Fam Cancer Subsets: MEDLINE

مواضيع طبية MeSH: Gastrointestinal Diseases/*etiology , Neoplasms/*etiology , Peutz-Jeghers Syndrome/*complications , Polyps/*etiology, Gastrointestinal Diseases/pathology ; Humans ; Neoplasms/pathology ; Peutz-Jeghers Syndrome/pathology ; Polyps/pathology

المؤلفون: Beggs AD; Department of Clinical Genetics, St Georges, University of London, Cranmer Terrace, London, UK., Latchford AR, Vasen HF, Moslein G, Alonso A, Aretz S, Bertario L, Blanco I, Bülow S, Burn J, Capella G, Colas C, Friedl W, Møller P, Hes FJ, Järvinen H, Mecklin JP, Nagengast FM, Parc Y, Phillips RK, Hyer W, Ponz de Leon M, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Tejpar S, Thomas HJ, Wijnen JT, Clark SK, Hodgson SV

المصدر: Gut [Gut] 2010 Jul; Vol. 59 (7), pp. 975-86.

نوع المنشور: Consensus Development Conference; Journal Article; Systematic Review

بيانات الدورية: Publisher: British Medical Assn Country of Publication: England NLM ID: 2985108R Publication Model: Print Cited Medium: Internet ISSN: 1468-3288 (Electronic) Linking ISSN: 00175749 NLM ISO Abbreviation: Gut Subsets: MEDLINE

مواضيع طبية MeSH: Peutz-Jeghers Syndrome/*diagnosis, Adult ; Aged ; Breast Neoplasms/diagnosis ; Child ; Child, Preschool ; Endoscopy, Gastrointestinal ; Evidence-Based Medicine/methods ; Female ; Gastrointestinal Neoplasms/diagnosis ; Genital Neoplasms, Female/diagnosis ; Genotype ; Humans ; Long-Term Care/methods ; Male ; Mass Screening/methods ; Middle Aged ; Peutz-Jeghers Syndrome/genetics ; Peutz-Jeghers Syndrome/therapy ; Phenotype ; Population Surveillance/methods ; Young Adult