Colorectal Cancer and the Muir-Torre Syndrome in a Gypsy Family: A Review

No abstract is available for this paper.

• Publication year

  1999

• Venue

  American Journal of Gastroenterology

• Publication date

  1999-03-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1111/j.1572-0241.1999.00575.xPMID 10086635
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Colorectal

  2020cited by this paper
• Colorectal carcinoma survival among hereditary nonpolyposis colorectal carcinoma family members

  1998cited by this paper
• Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria.

  1998cited by this paper
• Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer

  1997cited by this paper
• Muir‐Torre syndrome: clinical features and molecular genetic analysis

  1997cited by this paper
• Cancer risk associated with germline DNA mismatch repair gene mutations.

  1997cited by this paper
• Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?

  1996cited by this paper
• The genetic basis of Muir-Torre syndrome includes the hMLH1 locus.

  1996cited by this paper
• Hereditary nonpolyposis colorectal cancer (Lynch syndrome): An updated review

  1996cited by this paper
• Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients

  1996cited by this paper
• Isolated expression of the Muir‐Torre phenotype in a member of a family with hereditary non‐polyposis colorectal cancer

  1995cited by this paper
• Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability

  1995cited by this paper
• Life‐time risk of different cancers in hereditary non‐polyposis colorectal cancer (hnpcc) syndrome

  1995cited by this paper
• Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations.

  1994cited by this paper
• hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds.

  1994cited by this paper
• Muir-Torre syndrome: Heterogeneity, natural history, diagnosis, and management

  1993cited by this paper
• Association of sebaceous gland tumors and internal malignancy: the Muir-Torre syndrome.

  1991cited by this paper
• The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)

  1991cited by this paper
• Muir‐Torre syndrome in several members of a family with a variant of the Cancer Family Syndrome

  1985cited by this paper
• The cancer family syndrome. Rare cutaneous phenotypic linkage of Torre's syndrome.

  1981cited by this paper
• Multiple sebaceous tumors.

  1968cited by this paper
• Multiple primary carcinomata of the colon, duodenum, and larynx associated with kerato‐acanthomata of the face

  1967cited by this paper

• Muir-Torre Syndrome and founder mismatch repair gene mutations: A long gone historical genetic challenge.

  2016cites this paper
• Dermatology clinics: what's new in dermatopathology: news in nonmelanocytic neoplasia.

  2012cites this paper
• Hereditary cancer syndromes: a radiologist's perspective.

  2011cites this paper
• A Case of Muir-Torre Syndrome

  2011cites this paper
• Genes are more than skin deep: a case of Muir-Torre syndrome.

  2008cites this paper
• Muir-Torre syndrome: a rare but important disorder.

  2008cites this paper
• The frequency of Muir-Torre syndrome among Lynch syndrome families.

  2008cites this paper
• Lessons learned from DNA repair defective syndromes

  2007cites this paper
• Penile keratoacanthoma associated with urothelial carcinoma of the bladder in Muir-Torre syndrome.

  2007cites this paper
• Syndrome mit genetischer Instabilität: Modellerkrankungen für die (Haut‐) Kanzerogenese

  2006cites this paper
• Syndromes with genetic instability: Model diseases for (skin) cancerogenesis

  2006cites this paper
• Hereditary colorectal cancer-part II.

  2005cites this paper
• DNA mismatch repair and the significance of a sebaceous skin tumor for visceral cancer prevention.

  2004cites this paper
• Inherited predisposition to cancer: A historical overview

  2004cites this paper
• Muir-Torre Syndrome: Role of the Dermatopathologist in Diagnosis

  2004influential citation
• Lynch Syndrome: History and Current Status

  2004cites this paper
• Colon cancer screening practices following genetic testing for hereditary nonpolyposis colon cancer (HNPCC) mutations.

  2004cites this paper
• Hereditary nonpolyposis colorectal carcinoma (HNPCC) and HNPCC‐like families: Problems in diagnosis, surveillance, and management

  2004cites this paper
• Haploinsufficiency for tumour suppressor genes: when you don't need to go all the way.

  2004cites this paper
• Inherited Disorders of Genomic Instability and Cancer Susceptibility

  2004cites this paper
• The clinical importance and prognostic implications of microsatellite instability in sporadic cancer.

  2003cites this paper
• Multiple Primary Cancer, Including Transitional Cell Carcinoma of the Upper Uroepithelial Tract in a Multigeneration HNPCC Family: Molecular Genetic, Diagnostic, and Management Implications

  2003cites this paper
• Frequency of microsatellite instability in unselected sebaceous gland neoplasias and hyperplasias.

  2003cites this paper
• Hereditary nonpolyposis colorectal cancer and related conditions

  2003influential citation
• Roma health issues: a review of the literature and discussion

  2003cites this paper
• Three new mutations in hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay.

  2003cites this paper
• Pathogenesis and clinical management of hereditary non‐polyposis colorectal cancer

  2002cites this paper
• Muir-Torre Syndrome: A Case for Surveillance of the Ampulla of Vater

  2002cites this paper
• [Muir-Torre syndrome].

  2002cites this paper
• Loss of DNA Mismatch Repair Proteins in Skin Tumors From Patients With Muir–Torre Syndrome and MSH2 or MLH1 Germline Mutations: Establishment of Immunohistochemical Analysis as a Screening Test

  2002cites this paper
• Microsatellite instability and its relevance to cutaneous tumorigenesis

  2002cites this paper
• "Second hit" in sebaceous tumors from Muir-Torre patients with germline mutations in MSH2: allele loss is not the preferred mode of inactivation.

  2001cites this paper
• Multiple Sebaceous Adenomas and Extraocular Sebaceous Carcinoma in a Patient with Multiple Sclerosis: Case Report and Review of Literature

  2001cites this paper
• Molecular Pathologic Analysis Enhances the Diagnosis and Management of Muir-Torre Syndrome and Gives Insight Into Its Underlying Molecular Pathogenesis

  2001cites this paper
• Muir-Torre syndrome: case report of a patient with concurrent jejunal and ureteral cancer and a review of the literature.

  1999cites this paper
• The Muir-Torre syndrome in kindreds with hereditary nonpolyposis colorectal cancer (Lynch syndrome): A classic obligation in preventive medicine.

  1999cites this paper