Search Results - "Bandipalliam, Prathap"
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Aberrant DNA Methylation in Hereditary Nonpolyposis Colorectal Cancer Without Mismatch Repair Deficiency
Published in Gastroenterology (New York, N.Y. 1943) (01-05-2010)“…Background & Aims Approximately half of the families that fulfill Amsterdam criteria for Lynch syndrome or hereditary nonpolyposis colorectal cancer (HNPCC) do…”
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Calculation of Risk of Colorectal and Endometrial Cancer Among Patients With Lynch Syndrome
Published in Gastroenterology (New York, N.Y. 1943) (01-11-2009)“…Background & Aims Lynch syndrome is the most common hereditary colorectal cancer (CRC) syndrome. Some previous estimates of lifetime risk for CRC and…”
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Risk of Pancreatic Cancer in Families With Lynch Syndrome
Published in JAMA : the journal of the American Medical Association (28-10-2009)“…CONTEXT Lynch syndrome is an inherited cause of colorectal cancer caused by mutations of DNA mismatch repair (MMR) genes. A number of extracolonic tumors have…”
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Syndrome of early onset colon cancers, hematologic malignancies & features of neurofibromatosis in HNPCC families with homozygous mismatch repair gene mutations
Published in Familial cancer (01-11-2005)“…Hereditary nonpolyposis colon cancer (HNPCC) is the most common hereditary colon cancer syndrome. It is characterized by multiple colon as well as extracolonic…”
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Variability in the clinical phenotype among families with HNPCC—The potential importance of the location of the mutation in the gene
Published in International journal of cancer (15-05-2007)Get full text
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Desmoid Tumors and Familial Adenomatous Polyposis: A Tale of Two Syndromes
Published in Journal of clinical gastroenterology (01-03-2007)Get full text
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MALT lymphomas--a closer look in the genomics era
Published in Southern medical journal (Birmingham, Ala.) (01-12-2006)Get full text
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Gynecologic Cancer as a “Sentinel Cancer” for Women With Hereditary Nonpolyposis Colorectal Cancer Syndrome
Published in Obstetrics and gynecology (New York. 1953) (01-03-2005)“…OBJECTIVE:Women with hereditary nonpolyposis colorectal cancer syndrome have a 40–60% lifetime risk for colon cancer, a 40–60% lifetime risk for endometrial…”
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Comprehensive Molecular Analysis of Mismatch Repair Gene Defects in Suspected Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) Cases
Published in Cancer research (Chicago, Ill.) (01-09-2009)“…An accurate algorithm is essential for effective molecular diagnosis of hereditary colorectal cancer (CRC). Here, we have extended the analysis of 71 CRC cases…”
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Intraductal Papillary Mucinous Neoplasm of the Pancreas With Loss of Mismatch Repair in a Patient With Lynch Syndrome
Published in The American journal of surgical pathology (01-02-2009)“…Intraductal papillary mucinous neoplasm (IPMN) of the pancreas is a precancerous lesion with a well-described progression to carcinoma. This case report…”
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Correlation of polyp number and family history of colon cancer with germline MYH mutations
Published in Clinical gastroenterology and hepatology (01-10-2005)“…Affected individuals with biallelic MYH mutations are believed to display multiple adenomatous polyps without evidence of vertical transmission. Our goal was…”
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Aberrant DNA Methylation in Hereditary Non-Polyposis Colorectal Cancer without Mismatch Repair Deficiency
Published in Gastroenterology (New York, N.Y. 1943) (25-01-2010)Get full text
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Comprehensive genetic and endoscopic evaluation may be necessary to distinguish sporadic versus familial adenomatous polyposis–associated abdominal desmoid tumors
Published in Surgery (01-06-2004)“…There are limited data regarding how many patients with desmoid tumors actually represent cases with underlying familial adenomatous polyposis. A proband…”
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Clinical presentation correlates with the type of mismatch repair gene involved in hereditary nonpolyposis colon cancer
Published in Gastroenterology (New York, N.Y. 1943) (01-03-2004)Get full text
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Surveillance of patients at high risk for colorectal cancer
Published in The Medical clinics of North America (01-01-2005)“…Colorectal cancer (CRC) mortality may be greatly reduced by clinically feasible screening programs. The benefits of surveillance of high-risk programs are…”
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