Výsledky vyhledávání - "L. C. Rossetti"

Factor VIII genotype characterization of haemophilia A affected patients with transient and permanent inhibitors: a comprehensive Argentine study of inhibitor risks

Autor: I. Szurkalo, L. C. Rossetti, Miguel Martin Abelleyro, Raúl Pérez Bianco, L. Primiani, C. P. Radic, M. de Tezanos Pinto, D. Neme, M. Candela, I. B. Larripa, C. D. De Brasi

Publikováno v: Haemophilia : the official journal of the World Federation of Hemophilia. 19(4)

Inhibitor development against exogenous factor VIII is a severe impairment of replacement therapy affecting 18% of Argentine patients with severe haemophilia A (HA). To study the molecular predisposition for inhibitor development, we genotyped 260 HA

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c3daf13ecd950a5567d813fb2e38aa1
https://pubmed.ncbi.nlm.nih.gov/23534532

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Isolation and phenotypic characterization of Lactobacillus casei and Lactobacillus paracasei bacteriophage-resistant mutants

Autor: M L, Capra, D J, Mercanti, L C, Rossetti, J A, Reinheimer, A, Quiberoni

Publikováno v: Journal of applied microbiology. 111(2)

To isolate and characterize bacterial strains derived from Lactobacillus casei and Lactobacillus paracasei strains and resistant to phage MLC-A.Two of nine assayed strains rendered resistant mutants with recovery efficiencies of 83% (Lact. paracasei

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1c4f774758989f26f9565670c4fec7a3
https://pubmed.ncbi.nlm.nih.gov/21599814

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[Molecular genetics of the thalassemias in Argentina]

Autor: V, Varela, L C, Rossetti, A, Binaghi, H M, Targovnik, M S, Abreu

Publikováno v: Sangre. 44(3)

Was to establish the molecular genetics of thalassemias in Argentina.Genomic DNA was amplified by PCR and six point mutations in the beta-globin gene were investigated by Dot Blot hybridization using oligonucleotide probes. The most frequent alpha-th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f86e1031e706aa988f651f1919fa3e0c
https://pubmed.ncbi.nlm.nih.gov/10481583

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[Most frequent beta-thalassemia mutations in the Argentinian population]

Autor: V, Varela, S, Abreu, L C, Rossetti, H, Targovnik

Publikováno v: Sangre. 41(2)

Identification of the beta-thalassemic alleles of higher incidence in our populations.A total of 10 families (40 subjects) were analyzed. All families consisted of one son affected by beta-thalassaemia major (10 patients) and their parents and brothe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fd707b1b642e9a69c31ebff538a6dd4e
https://pubmed.ncbi.nlm.nih.gov/9045354

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