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Results: 1-3 |
Results: 3
Identification of fifteen novel mutations and genotype-phenotype relationship in Fabry disease
Authors: Altarescu, GM Goldfarb, LG Park, KY Kaneski, C Jeffries, N Litvak, S Nagle, JW Schiffmann, R
Citation: Gm. Altarescu et al., Identification of fifteen novel mutations and genotype-phenotype relationship in Fabry disease, CLIN GENET, 60(1), 2001, pp. 46-51
Rapid identification of local T cell expansion in inflammatory organ diseases by flow cytometric T cell receptor V beta analysis
Authors: Muraro, PA Jacobsen, M Necker, A Nagle, JW Gaber, R Sommer, N Oertel, WH Martin, R Hemmer, B
Citation: Pa. Muraro et al., Rapid identification of local T cell expansion in inflammatory organ diseases by flow cytometric T cell receptor V beta analysis, J IMMUNOL M, 246(1-2), 2000, pp. 131-143
Novel exon 3B proteolipid protein gene mutation causing late-onset spasticparaplegia type 2 with variable penetrance in female family members
Authors: Sivakumar, K Sambuughin, N Selenge, B Nagle, JW Baasanjav, D Hudson, LD Goldfarb, LG
Citation: K. Sivakumar et al., Novel exon 3B proteolipid protein gene mutation causing late-onset spasticparaplegia type 2 with variable penetrance in female family members, ANN NEUROL, 45(5), 1999, pp. 680-683
Risultati: 1-3 |