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E Beutler

Showing results (341-350 of 405) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|October 1, 1976
Characterization of heteropolymeric hexosaminidase A in human X mouse hybrid cellsJ Chern, E Beutler, W Kuhl, et al.
Pain|January 1, 1988
Family dynamics and emotional expression among patients with chronic pain and depressionLarry E Beutler, Roger Daldrup, David Engle, et al.
Blood|December 9, 2000
Molecular characterization of a case of atransferrinemiaE Beutler, T Gelbart, P Lee, et al.
Blood Cells, Molecules & Diseases|January 1, 1995
The clinical course of treated and untreated Gaucher disease. A study of 45 patientsE Beutler, A Demina, K Laubscher, et al.
Blood|July 1, 1992
New glucose-6-phosphate dehydrogenase mutations from various ethnic groupsE Beutler, B Westwood, J T Prchal, et al.
The Journal of Clinical Investigation|August 1, 1983
Metabolic compensation for profound erythrocyte adenylate kinase deficiency. A hereditary enzyme defect without hemolytic anemiaE Beutler, D Carson, H Dannawi, et al.
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|September 1, 1991
Enzyme replacement therapy for Gaucher diseaseE Beutler, A Kay, A Saven, 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.
Pageof 41

Showing results (341-350 of 405) with videos related to

Sort By:
Pageof 41
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1976
Characterization of heteropolymeric hexosaminidase A in human X mouse hybrid cellsJ Chern, E Beutler, W Kuhl, et al.
Pain|January 1, 1988
Family dynamics and emotional expression among patients with chronic pain and depressionLarry E Beutler, Roger Daldrup, David Engle, et al.
Blood|December 9, 2000
Molecular characterization of a case of atransferrinemiaE Beutler, T Gelbart, P Lee, et al.
Blood Cells, Molecules & Diseases|January 1, 1995
The clinical course of treated and untreated Gaucher disease. A study of 45 patientsE Beutler, A Demina, K Laubscher, et al.
Blood|July 1, 1992
New glucose-6-phosphate dehydrogenase mutations from various ethnic groupsE Beutler, B Westwood, J T Prchal, et al.
The Journal of Clinical Investigation|August 1, 1983
Metabolic compensation for profound erythrocyte adenylate kinase deficiency. A hereditary enzyme defect without hemolytic anemiaE Beutler, D Carson, H Dannawi, et al.
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|September 1, 1991
Enzyme replacement therapy for Gaucher diseaseE Beutler, A Kay, A Saven, 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.
Pageof 41