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Results: 1-12 |
Results: 12
Frequency of recent retrotransposition events in the human factor IX gene
Authors: Li, XM Scaringe, WA Hill, KA Roberts, S Mengos, A Careri, D Pinto, MT Kasper, CK Sommer, SS
Citation: Xm. Li et al., Frequency of recent retrotransposition events in the human factor IX gene, HUM MUTAT, 17(6), 2001, pp. 511-519
Genetic diagnosis of haemophilia a and B
Authors: Kasper, CK
Citation: Ck. Kasper, Genetic diagnosis of haemophilia a and B, HAEMOPHILIA, 6, 2000, pp. 3-4
Hereditary plasma clotting factor disorders and their management
Authors: Kasper, CK
Citation: Ck. Kasper, Hereditary plasma clotting factor disorders and their management, HAEMOPHILIA, 6, 2000, pp. 13-27
Novel hotspot detector software reveals a non-CpG hotspot of germline mutation in the factor IX gene (F9) in Latin Americans
Authors: Drost, JB Scaringe, WA Jaloma-Cruz, AR Li, XM Ossa, DF Kasper, CK Sommer, SS
Citation: Jb. Drost et al., Novel hotspot detector software reveals a non-CpG hotspot of germline mutation in the factor IX gene (F9) in Latin Americans, HUM MUTAT, 16(3), 2000, pp. 203-210
Kinetics of factor IX activity differ from that of factor IX antigen in patients with haemophilia B receiving high-purity factor IX replacement
Authors: Liebman, HA Rosenwald-Zuckerman, T Retzios, A Yasmin, S Kasper, CK
Citation: Ha. Liebman et al., Kinetics of factor IX activity differ from that of factor IX antigen in patients with haemophilia B receiving high-purity factor IX replacement, HAEMOPHILIA, 5(3), 1999, pp. 174-180
Human recombinant DNA-derived antihaemophilic factor (factor VIII) in the treatment of haemophilia A: conclusions of a 5-year study of home therapy
Authors: Seremetis, S Lusher, JM Abildgaard, CF Kasper, CK Allred, R Hurst, D
Citation: S. Seremetis et al., Human recombinant DNA-derived antihaemophilic factor (factor VIII) in the treatment of haemophilia A: conclusions of a 5-year study of home therapy, HAEMOPHILIA, 5(1), 1999, pp. 9-16
Haemophilia B Brandenberg-type promoter mutation
Authors: Heit, JA Ketterling, RP Zapata, RE Ordonez, SM Kasper, CK Sommer, SS
Citation: Ja. Heit et al., Haemophilia B Brandenberg-type promoter mutation, HAEMOPHILIA, 5(1), 1999, pp. 73-75
Articular contractures in haemophilia - Foreword
Authors: Kasper, CK
Citation: Ck. Kasper, Articular contractures in haemophilia - Foreword, HAEMOPHILIA, 5, 1999, pp. IV-IV
Reported in vivo splice-site mutations in the factor IX gene: Severity of splicing defects and a hypothesis for predicting deleterious splice donor mutations
Authors: Ketterling, RP Drost, JB Scaringe, WA Liao, DZ Liu, JZ Kasper, CK Sommer, SS
Citation: Rp. Ketterling et al., Reported in vivo splice-site mutations in the factor IX gene: Severity of splicing defects and a hypothesis for predicting deleterious splice donor mutations, HUM MUTAT, 13(3), 1999, pp. 221-231
Germline origins in the human F9 gene: frequent G : C--> A : T mosaicism and increased mutations with advanced maternal age
Authors: Ketterling, RP Vielhaber, E Li, XM Drost, J Schaid, DJ Kasper, CK Phillips, JA Koerper, MA Kim, H Sexauer, C Gruppo, R Ambriz, R Paredes, R Sommer, SS
Citation: Rp. Ketterling et al., Germline origins in the human F9 gene: frequent G : C--> A : T mosaicism and increased mutations with advanced maternal age, HUM GENET, 105(6), 1999, pp. 629-640
Human factor VIII for bleeding in patients with inhibitors
Authors: Kasper, CK
Citation: Ck. Kasper, Human factor VIII for bleeding in patients with inhibitors, VOX SANGUIN, 77, 1999, pp. 47-48
A randomized, double-blind comparison of two dosage levels of recombinant factor VIIa in the treatment of joint, muscle and mucocutaneous haemorrhages in persons with haemophilia A and B, with and without inhibitors
Authors: Lusher, JM Roberts, HR Davignon, G Joist, JH Smith, H Shapiro, A Laurian, Y Kasper, CK Mannucci, PM
Citation: Jm. Lusher et al., A randomized, double-blind comparison of two dosage levels of recombinant factor VIIa in the treatment of joint, muscle and mucocutaneous haemorrhages in persons with haemophilia A and B, with and without inhibitors, HAEMOPHILIA, 4(6), 1998, pp. 790-798
Risultati: 1-12 |