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The Turkish Journal of Pediatrics|February 24, 2001
Triosephosphate isomerase deficiency with elevated sweat chloride test: report of a caseI Yenicesu, O Kalayci, E Semizel, et al.
Blood|October 9, 1998
The relationship of the -5, -8, and -24 variant alleles in African Americans to triosephosphate isomerase (TPI) enzyme activity and to TPI deficiencyA Schneider, L Forman, B Westwood, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 20, 1996
The treatment of chronic progressive multiple sclerosis with cladribineE Beutler, J C Sipe, J S Romine, et al.
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.
Archives of Internal Medicine|February 25, 1999
Mastocytosis: diverse presentations and outcomesJ D Pauls, J Brems, P J Pockros, et al.
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