M. Redal

发表

Characterization and Elemental Composition of Atmospheric Aerosol Loads during Springtime Dust Storm in Western Saudi Arabia

M. Khoder, M. Almazroui, M. Alghamdi, 2015 .

Prevalence of CYP2C9 and VKORC1 alleles in the Argentine population and implications for prescribing dosages of anticoagulants.

P. Argibay, W. Belloso, J. Arbelbide, 2012, Genetics and molecular research : GMR.

Editorial: Pharmacogenetics and Pharmacogenomics in Latin America: Ethnic Variability, New Insights in Advances and Perspectives: A RELIVAF-CYTED Initiative

M. J. Fresnadillo Martínez, L. Quiñones, A. López-Cortés, 2022, Frontiers in Pharmacology.

Influence of CYP3A5 polymorphism on tacrolimus maintenance doses and serum levels after renal transplantation: Age dependency and pharmacological interaction with steroids

P. Argibay, W. Belloso, P. Coccia, 2011, Pediatric transplantation.

[Non invasive prenatal genetic diagnosis of fetal RhD and sex through the analysis of free fetal DNA in maternal plasma].

P. Argibay, M. Redal, H. Aiello, 2009, Archivos argentinos de pediatria.

Microorganisms associated particulate matter: a preliminary study.

M. Khoder, M. Alghamdi, M. Shamy, 2014, The Science of the total environment.

Microchimerism and blocking activity in women with recurrent spontaneous abortion (RSA) after alloimmunization with the partner's lymphocytes.

R. Testa, R. Nicholson, M. Redal, 1999, Journal of reproductive immunology.

Human Leukocyte Antigen Matching, Radiographic Score, and Histologic Findings in Massive Frozen Bone Allografts

D. Muscolo, M. Ayerza, E. S. Araujo, 1996, Clinical orthopaedics and related research.

Preliminary Pharmacogenomic-Based Predictive Models of Tamoxifen Response in Hormone-dependent Chilean Breast Cancer Patients

L. Quiñones, D. Cáceres, N. Varela, 2021, Frontiers in Pharmacology.

Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer.

B. Fernandez, D. Huntsman, P. Pharoah, 2007, JAMA.

Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individuals

D. Carraro, C. Vaccaro, Mev Dominguez Valentin, 2011, Familial Cancer.

Effects of airborne particulate matter on alternative pre-mRNA splicing in colon cancer cells.

M. Alló, A. Kornblihtt, M. Khoder, 2015, Environmental research.

[Hereditary diffuse gastric cancer (HDGC): presentation of a family with a new mutation of the CDH1 gene].

D. Huntsman, J. Senz, H. Lynch, 2007, Acta gastroenterologica Latinoamericana.

Clinical utility of pharmacogenomics in the management of hepatitis C

D. Flichman, J. Trinks, M. Redal, 2014, Pharmacogenomics and personalized medicine.

Soluble HLA class I antigens in pediatric patients with renal transplants from related living donors without acute rejection and treated with triple therapy.

M. Redal, J. Ferraris, N. Prigoshin, 1996, Human immunology.

Influence of 5-HTTLPR and 5-HTTVNTR polymorphisms of the serotonin transporter gene (SLC6A4) on major depressive disorder in a sample of Argentinean population.

P. Argibay, M. Redal, Lucas Costa, 2012, Psychiatric genetics.

Perception of the usefulness of drug/gene pairs and barriers for pharmacogenomics in Latin America.

J. Eslava-Schmalbach, A. Roco, L. Quiñones, 2014, Current drug metabolism.

State of Art of Cancer Pharmacogenomics in Latin American Populations

L. Quiñones, A. López-Cortés, M. Redal, 2017, International journal of molecular sciences.

Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome) in Argentina: Report from a Referral Hospital Register

H. Lynch, S. Bala, J. Lynch, 2007, Diseases of the colon and rectum.

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.

Genetics of IL 28 B : impact and effect on treatment response in HCV patients

D. Flichman, J. Trinks, M. Redal, 2014 .

Pharmacogenetics of immunosuppressant polymorphism of CYP3A5 in renal transplant recipients.

M. Redal, N. Imperiali, J. Larriba, 2010, Transplantation proceedings.

Pharmacogenomics in Gastroenterology

W. Belloso, M. Redal, P. Scibona, 2012 .

10 Pharmacogenomics in Gastroenterology

W. Belloso, M. Redal, P. Scibona, 2018 .

Peptic ulcer disease by Helicobacter pylori infection and gastro esophageal reflux disease

W. Belloso, M. Redal, P. Scibona, 2018 .

Global impact of KRAS mutation patterns in FOLFOX treated metastatic colorectal cancer

M. Redal, Lucas Costa, C. Ramírez, 2015, Front. Genet..

Conversion from azathioprine [correction of azathioprina] to mycophenolate mofetil in pediatric renal transplant recipients with chronic rejection.

M. Redal, J. Ferraris, N. Prigoshin, 2000, Transplantation.

HLA‐DRB1 and multiple sclerosis in Argentina

P. Argibay, E. Cristiano, L. Patrucco, 2009, European journal of neurology.

Aberrant expression of glucagon receptors in adrenal glands of a patient with Cushing's syndrome and ACTH-independent macronodular adrenal hyperplasia.

M. Glerean, A. Beskow, M. Redal, 2010, Medicina.

Immunosuppressive activity of deflazacort in pediatric renal transplantation.

M. Redal, J. Ferraris, N. Prigoshin, 1996, Transplantation.

An updated examination of the perception of barriers for pharmacogenomics implementation and the usefulness of drug/gene pairs in Latin America and the Caribbean

M. J. Fresnadillo Martínez, Camila Calfío, L. Quiñones, 2023, Frontiers in Pharmacology.

Genetics of IL 28 B : impact and effect on treatment response in HCV patients

J. Trinks, M. Redal, D. Flichman, 2014 .

Genetics of IL 28 B : impact and effect on treatment response in HCV patients

D. Flichman, J. Trinks, M. Redal, 2014 .

Pharmacogenomics and Personalized Medicine Dovepress Clinical Utility of Pharmacogenomics in the Management of Hepatitis C

J. Trinks, M. Redal, D. Flichman, 2022 .

CD24 as a genetic modifier of disease progression in multiple sclerosis in Argentinean patients

E. Cristiano, L. Patrucco, S. J. González, 2011, Journal of the Neurological Sciences.