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Bruton tyrosine kinase gene mutations in Argentina.
Danielian S, El-Hakeh J, Basílico G, Oleastro M, Rosenzweig S, Feldman G, Berozdnik L, Galicchio M, Gallardo A, Giraudi V, Liberatore D, Rivas EM, Zelazko M. Danielian S, et al. Among authors: rosenzweig s. Hum Mutat. 2003 Apr;21(4):451. doi: 10.1002/humu.9131. Hum Mutat. 2003. PMID: 12655572
Efficacy and tolerability of an argentine intravenous immunoglobulin in pediatric patients with primary immunodeficiency diseases.
Krasovec S, Ornani A, Oleastro M, Rosenzweig S, Roy A, Perez L, Campos G, Marín N, Martinez A, Mahieu C, Manfredi MJ, Sisti A, Zelazko M. Krasovec S, et al. Among authors: rosenzweig s. J Clin Immunol. 2007 Mar;27(2):227-32. doi: 10.1007/s10875-006-9055-x. Epub 2007 Jan 19. J Clin Immunol. 2007. PMID: 17235689 Clinical Trial.
A 475 years-old founder effect involving IL12RB1: a highly prevalent mutation conferring Mendelian Susceptibility to Mycobacterial Diseases in European descendants.
Yancoski J, Rocco C, Bernasconi A, Oleastro M, Bezrodnik L, Vrátnica C, Haerynck F, Rosenzweig SD. Yancoski J, et al. Among authors: rosenzweig sd. Infect Genet Evol. 2009 Jul;9(4):574-80. doi: 10.1016/j.meegid.2009.02.010. Epub 2009 Mar 9. Infect Genet Evol. 2009. PMID: 19460324 Free PMC article.
Germline hypomorphic CARD11 mutations in severe atopic disease.
Ma CA, Stinson JR, Zhang Y, Abbott JK, Weinreich MA, Hauk PJ, Reynolds PR, Lyons JJ, Nelson CG, Ruffo E, Dorjbal B, Glauzy S, Yamakawa N, Arjunaraja S, Voss K, Stoddard J, Niemela J, Zhang Y, Rosenzweig SD, McElwee JJ, DiMaggio T, Matthews HF, Jones N, Stone KD, Palma A, Oleastro M, Prieto E, Bernasconi AR, Dubra G, Danielian S, Zaiat J, Marti MA, Kim B, Cooper MA, Romberg N, Meffre E, Gelfand EW, Snow AL, Milner JD. Ma CA, et al. Among authors: rosenzweig sd. Nat Genet. 2017 Aug;49(8):1192-1201. doi: 10.1038/ng.3898. Epub 2017 Jun 19. Nat Genet. 2017. PMID: 28628108 Free PMC article.
509 results