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Authors: ROTTEM M MIRON D SHILOAH E HOROVITZ Y SCHLEZINGER M
Citation: M. Rottem et al., PROPERDIN DEFICIENCY - RARE PRESENTATION WITH MENINGOCOCCAL BONE AND JOINT INFECTIONS, The Pediatric infectious disease journal, 17(4), 1998, pp. 356-358

Authors: SHOHAT M LOTAN R MAGAL N OGUR G TOKGUZ G SCHWABE A FISCHELGHODSIAN N KASTNER D ROTTER JI SCHLEZINGER M DANON Y
Citation: M. Shohat et al., AMYLOIDOSIS IN FMF IS ASSOCIATED WITH A SPECIFIC CORE HAPLOTYPE IN THE MEFV LOCUS, American journal of human genetics, 61(4), 1997, pp. 258-258

Authors: DAGAN T LOTAN R DANON Y MAGAL N OGUR G TOKGUZ G SCHWABE A FISCHELGHODSIAN N ROTTER JI SCHLEZINGER M HALPERN GJ SHOHAT M
Citation: T. Dagan et al., THE VARIOUS FMF CORE HAPLOTYPES IN THE MEFV LOCUS AND THEIR CORRELATION WITH FMF SYMPTOMS, American journal of human genetics, 61(4), 1997, pp. 1136-1136

Authors: LANDAU D OHALI M SHALEV H SCHLEZINGER M MAOR E CARMI R
Citation: D. Landau et al., IMMUNE-MEDIATED PATHOGENESIS OF FAMILIAL HYPOCOMPLEMENTEMIC HEMOLYTIC-UREMIC SYNDROME (HUS), Journal of the American Society of Nephrology, 7(9), 1996, pp. 1837-1837

Authors: ROTTEM M SHILOACH E SCHLEZINGER M
Citation: M. Rottem et al., PROPERDIN DEFICIENCY - RARE PRESENTATION WITH MENINGOCOCCAL OSTEOMYELITIS AND ARTHRITIS, Journal of allergy and clinical immunology, 97(1), 1996, pp. 879-879
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