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Blood|January 1, 1995
Glucose-6 phosphate dehydrogenase mutations and haplotypes in various ethnic groupsW Xu, B Westwood, C S Bartsocas, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|July 1, 1996
Development of cladribine treatment in multiple sclerosisJ C Sipe, J S Romine, J A Koziol, et al.Biodrugs : Clinical Immunotherapeutics, Biopharmaceuticals and Gene Therapy|May 1, 1997
CladribineJ S Romine, J C Sipe, J A Koziol, et al.Blood|February 1, 1985
Inherited phosphofructokinase deficiency in dogs with hyperventilation-induced hemolysis: increased in vitro and in vivo alkaline fragility of erythrocytesU Giger, J W Harvey, R A Yamaguchi, et al.Blood|August 15, 1993
Home treatment with intravenous enzyme replacement therapy for Gaucher disease: an international collaborative study of 33 patientsA Zimran, C E Hollak, A Abrahamov, et al.Lancet (London, England)|July 2, 1994
Cladribine in treatment of chronic progressive multiple sclerosisJ C Sipe, J S Romine, J A Koziol, et al.American Journal of Hematology|December 1, 1995
Triosephosphate isomerase deficiency: repetitive occurrence of point mutation in amino acid 104 in multiple apparently unrelated familiesA Schneider, B Westwood, C Yim, et al.Annals of Hematology|December 29, 2000
Coincidence of Gaucher's disease due to a 1226G/1448C mutation and of an immunoglobulin G lambda multiple myeloma with Bence-Jones proteinuriaH Harder, J Eucker, C Zang, et al.American Journal of Hematology|September 2, 1998
Coincidence of Gaucher's disease due to a private mutation and Ph' positive chronic myeloid leukemiaP E Petrides, P leCoutre, J Müller-Höcker, et al.Journal of Consulting and Clinical Psychology|April 1, 1991
Predictors of differential response to cognitive, experiential, and self-directed psychotherapeutic proceduresL E Beutler, D Engle, D Mohr, et al.Pageof 42