The muir-torre syndrome: a rare variant of hereditary nonpolyposis colorectal cancer associated with hmsh2 mutation

No abstract is available for this paper.

• Publication year

  1998

• Venue

  American Journal of Gastroenterology

• Publication date

  1998-09-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1111/j.1572-0241.1998.00487.xPMID 9732950
• 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.

• Genetic testing is important in families with a history suggestive of hereditary non‐olyposis colorectal cancer even if the Amsterdam criteria are not fulfilled

  1997cited by this paper
• Genetic testing is important in families with a history suggestive of hereditary non-polyposis colorectal cancer even if the Amsterdam criteria are not fulfilled.

  1997cited by this paper
• Spontaneous intestinal carcinomas and skin neoplasms in Msh2-deficient mice.

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

  1996cited by this paper
• Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

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

  1996cited by this paper
• Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer.

  1996cited by this paper
• Lessons from Hereditary Review Colorectal Cancer

  1996cited by this paper
• De novo duplication in Charcot-Marie-Tooth type 1A.

  1996cited by this paper
• Molecular mechanisms underlying hereditary nonpolyposis colorectal carcinoma.

  1996cited by this paper
• Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?

  1996cited by this paper
• Genetic linkage analysis in hereditary non-polyposis colon cancer syndrome.

  1995cited by this paper
• Microsatellite instability in human non-melanoma and melanoma skin cancer.

  1995cited by this paper
• In vitro transcription/translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer.

  1995cited by this paper
• Microsatellite Instability in Keratoacanthoma

  1995cited by this paper
• Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage.

  1994cited by this paper
• Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations.

  1994cited by this paper
• Genetic linkage in Muir-Torre syndrome to the same chromosomal region as cancer family syndrome.

  1994cited by this paper
• Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review.

  1993cited by this paper
• Molecular diagnosis of familial adenomatous polyposis.

  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
• Association of sebaceous gland tumors and internal malignancy: the Muir-Torre syndrome.

  1991influential reference
• 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

• Establishment and Characterization of Three Human Ocular Adnexal Sebaceous Carcinoma Cell Lines

  2024cites this paper
• Early age of onset and broad cancer spectrum persist in MSH6- and PMS2-associated Lynch syndrome.

  2022cites this paper
• Cutaneous Sebaceous Carcinoma Presenting as a Large Fungating Breast Tumour in Synchronicity With Primary Carcinomata of the Breasts

  2022cites this paper
• Hereditary nonpolyposis CRC

  2022cites this paper
• NGS Analysis Confirms Common TP53 and RB1 Mutations, and Suggests MYC Amplification in Ocular Adnexal Sebaceous Carcinomas

  2021cites this paper
• Muir-Torre syndrome

  2020cites this paper
• Molecular pathology in real time

  2016cites this paper
• Dermatopathology Primer of Cutaneous Tumors

  2015cites this paper
• Sebaceous Gland carcinoma - Case Report and Literature

  2014cites this paper
• FANCJ localization by mismatch repair is vital to maintain genomic integrity after UV irradiation.

  2014cites this paper
• Juvenile Polyposis ( JP ) Clinical Overview

  2014influential citation
• Investigating Tumor Suppressors in the DNA Damage Response: Caretakers of the Genome and Biomarkers to Predict Therapeutic Response: A Dissertation

  2014cites this paper
• Ultraviolet damage, DNA repair and vitamin D in nonmelanoma skin cancer and in malignant melanoma: an update.

  2014cites this paper
• Identification of Patients at Risk for Hereditary Colorectal Cancer

  2012cites this paper
• Lower gastrointestinal tract cancer predisposition syndromes.

  2010cites this paper
• Genetics and Tumor Genomics in Familial Colorectal Cancer

  2010cites this paper
• “Sporadic” Colorectal Tumors in Multiple Primary Malignancies

  2009cites this paper
• First case report of Muir–Torre syndrome associated with non-small cell lung cancer

  2009cites this paper
• Muir-Torre syndrome – a case report and review of literature

  2008cites this paper
• Sebaceous carcinoma of the skin of the breast: a case report

  2008cites this paper
• UV damage and DNA repair in malignant melanoma and nonmelanoma skin cancer.

  2008cites this paper
• Muir-Torre syndromea case report and review of literature

  2008cites this paper
• Current approaches in familial colorectal cancer: a clinical perspective.

  2006cites this paper
• UV Damage and DNA Repair in Basal Cell and Squamous Cell Carcinomas

  2006cites this paper
• Sebaceous gland tumors and internal malignancy in the context of Muir-Torre syndrome. A case report and review of the literature

  2006cites this paper
• Retrospektive Analyse von Patienten mit kolorektalem Karzinom nach den Amsterdam- und Bethesda-Kriterien

  2006cites this paper
• Polyposis and Familial Cancer Syndromes

  2006cites this paper
• Syndrome of Early Onset Colon Cancers, Hematologic Malignancies & Features of Neurofibromatosis in HNPCC Families with Homozygous Mismatch Repair Gene Mutations

  2005cites this paper
• A skin tumor as a marker for a hereditary cancer syndrome: Muir-Torre syndrome

  2005influential citation
• Endoscopic management of familial colonic neoplasia.

  2005cites this paper
• Muir-Torre Syndrome Associated With Turcot Syndrome

  2004cites this paper
• Muir-Torre Syndrome Presenting with Ileus: a Case Report

  2004cites this paper
• Spectrum of genetic alterations in Muir‐Torre syndrome is the same as in HNPCC

  2004cites this paper
• [Muir-Torre syndrome].

  2002cites this paper
• Genetic insights into familial cancers-- update and recent discoveries.

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

  2002cites this paper
• Mutation detection in colorectal cancers : direct sequencing of DNA mismatch repair genes.

  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
• Reduced human mismatch repair protein expression in the development of precancerous skin lesions to squamous cell carcinoma

  2001cites this paper
• Muir-Torre syndrome.

  2001cites this paper
• [Muir-Torre syndrome].

  2001cites this paper
• Muir-Torre-Syndrom

  2001cites this paper
• Serous retinal detachment caused by leukaemic choroidal infiltration during complete remission

  2000cites this paper
• Sudden bilateral visual loss in acute myeloid leukaemia

  2000cites this paper
• Retinal telangiectasis and angioid streaks

  2000cites this paper
• La bombe n’était pas seulement dans le ventre

  2000cites this paper
• Sclerosing lipid granuloma of the medial canthus 30 years after dacryocystitis

  2000cites this paper
• Therapy of subhyaloidal hemorrhage by intravitreal application of rtPA and SF(6) gas.

  2000cites this paper
• Blunt trauma in Best's vitelliform macular dystrophy

  2000cites this paper
• Ophthalmic features of primary oxalosis after combined liver/kidney transplantation

  2000cites this paper
• Acquired capillary haemangioma of the eyelid in an adult treated with cutting diathermy

  2000cites this paper
• Diplopia, ptosis, and hepatitis as presenting signs and symptoms of giant cell arteritis

  2000cites this paper
• Idiopathic sclerosing inflammation of the orbit: a new finding of calcification

  2000cites this paper
• Treatment of subhyaloid haemorrhage with intravitreal tissue plasminogen activator and C3F8 gas injection

  2000cites this paper
• Observations on time course changes of the cherry red spot in a patient with Tay-Sachs disease

  2000cites this paper
• Epidermoid carcinoma arising in an ocular leishmania lesion

  2000cites this paper
• Sebaceous gland carcinoma of the eyelid and palpebral conjunctiva in a patient with Muir-Torre syndrome

  2000cites this paper
• [The bomb was not only in the abdomen].

  2000cites this paper
• Effects of homozygous apolipoprotein A-1 deficiency on the cornea

  2000cites this paper
• [Diseases associated with adnexal tumors. II--Sebaceous tumors, sudoral tumors].

  1999cites this paper
• Genetic testing in hereditary colorectal cancer: indications and procedures

  1999cites 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