A5068247616- Blood groups and transfusion
- Blood disorders and treatments
- Erythrocyte Function and Pathophysiology
- Genetic factors in colorectal cancer
- Colorectal Cancer Screening and Detection
- Cancer Genomics and Diagnostics
- Platelet Disorders and Treatments
- Diabetes and associated disorders
- Tracheal and airway disorders
- Congenital Ear and Nasal Anomalies
- Neonatal Health and Biochemistry
- Mycobacterium research and diagnosis
- Hemoglobinopathies and Related Disorders
- Immunodeficiency and Autoimmune Disorders
- Cystic Fibrosis Research Advances
- Health and Medical Research Impacts
- Helicobacter pylori-related gastroenterology studies
- Colorectal Cancer Treatments and Studies
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Nutrition, Genetics, and Disease
- Pancreatic and Hepatic Oncology Research
Hospital Provincial de Rosario
2017-2018
Centro Científico Tecnólogico - Rosario
2015
Instituto Universitario Italiano de Rosario
2015
Hospital Italiano de Buenos Aires
2006-2009
National University of Rosario
2008
National University of the Littoral
2008
Universidad de Granada
2008
The spectrum of BRCA1/2 genetic variation in breast-ovarian cancer patients has been scarcely investigated outside Europe and North America, with few reports for South where Amerindian founder effects recent multiracial immigration are predicted to result high diversity. We describe here the results BRCA1/BRCA2 germline analysis an Argentinean series breast/ovarian selected young age at diagnosis or family history.The study (134 patients) included 37 cases diagnosed within 40 years no...
Genetic counselling and testing for Lynch syndrome (LS) have recently been introduced in several Latin America countries. We aimed to characterize the clinical, molecular mismatch repair (MMR) variants spectrum of patients with suspected LS America.Eleven hereditary cancer registries 34 published databases were used identify unrelated families that fulfilled Amsterdam II (AMSII) criteria and/or Bethesda guidelines or suggestive a dominant colorectal (CRC) inheritance syndrome.We performed...
summary The frequencies of several human platelet antigens (HPAs) vary between different populations and are a major determinant for the prevalence HPA alloimmunization its clinical associated entities. aim this study was to characterize allele seven systems in two ethnic groups from Argentinean city Rosario, population minority Amerindian group recently arrived north country, Tobas. A total 192 healthy unrelated individuals blood donors hospital staff Hospital Italiano Garibaldi 27 Toba...
Abstract Background Hereditary non-polyposis colon cancer (HNPCC) is an autosomal dominant syndrome predisposing to the early development of various cancers including those colon, rectum, endometrium, ovarium, small bowel, stomach and urinary tract. HNPCC caused by germline mutations in DNA mismatch repair genes, mostly hMSH2 or hMLH1. In this study, we report analysis for genetic counseling three first-degree relatives (the mother two sisters) a male who died colorectal adenocarcinoma at...