A. Della Valle

发表

Three new mutations in hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay.

P. Peltomäki, H. Lynch, C. Sarroca, 2003, Cancer genetics and cytogenetics.

Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

Aung Ko Win, M. von Knebel Doeberitz, B. Bonanni, 2021, European journal of cancer.

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Aung Ko Win, P. Møller, E. Hovig, 2019, Genetics in Medicine.

Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

Aung Ko Win, M. von Knebel Doeberitz, B. Bonanni, 2020, Genetics in Medicine.

A snapshot of current genetic testing practice in Lynch syndrome: The results of a representative survey of 33 Latin American existing centres/registries.

P. Møller, E. Hovig, J. C. Bazo-Alvarez, 2019, European journal of cancer.

Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Aung Ko Win, P. Møller, E. Hovig, 2020, Genetics in Medicine.

Hereditary nonpolyposis colorectal cancer (lynch syndrome II) in Uruguay

T. Smyrk, P. Peltomäki, H. Lynch, 2000, Diseases of the colon and rectum.

Genetic and epigenetic characteristics of patients with colorectal cancer from Uruguay.

Florencia Neffa, P. Esperón, Carolina Vergara, 2022, Pathology, research and practice.

Germline Mutations in PALB2, BRCA1, and RAD51C, Which Regulate DNA Recombination Repair, in Patients With Gastric Cancer.

C. Yau, N. Hu, A. Goldstein, 2017, Gastroenterology.

Iron utilization after iron dextran administration for iron deficiency in patients with dialysis-associated anemia: a prospective analysis and comparison of two agents.

T. Wiltbank, D. Roe, P. Zager, 1996, American journal of kidney diseases : the official journal of the National Kidney Foundation.

A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America

P. Møller, E. Hovig, R. Reis, 2017, BMC Cancer.

Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study.

Katherine M. Tucker, Aung Ko Win, Swati G. Patel, 2021, The Lancet. Oncology.

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Aung Ko Win, P. Møller, E. Hovig, 2019, Genetics in Medicine.

Evaluation of MLH1 variants of unclear significance

R. Reis, I. Hinrichsen, G. Plotz, 2018, Genes, chromosomes & cancer.

Evaluation of MLH1 I219V polymorphism in unrelated South American individuals suspected of having Lynch syndrome.

L. Rasmussen, D. Carraro, S. D. da Silva, 2012, Anticancer research.

Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database

Aung Ko Win, M. von Knebel Doeberitz, B. Bonanni, 2023, EClinicalMedicine.

Aggressive mutation in a familial adenomatous polyposis syndrome family: when phenotype guides clinical surveillance.

Florencia Neffa, P. Esperón, A. Della Valle, 2018, Journal of gastrointestinal oncology.