Search research articles
Contact Us
Filters
Showing results (341-350 of 405) with videos related to
Page
of 41
Sort By:
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 cells
J Chern, E Beutler, W Kuhl, et al.
Pain
|
January 1, 1988
Family dynamics and emotional expression among patients with chronic pain and depression
Larry E Beutler, Roger Daldrup, David Engle, et al.
Blood
|
December 9, 2000
Molecular characterization of a case of atransferrinemia
E 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 patients
E Beutler, A Demina, K Laubscher, et al.
Blood
|
July 1, 1992
New glucose-6-phosphate dehydrogenase mutations from various ethnic groups
E 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 anemia
E 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 case
I Yenicesu, O Kalayci, E Semizel, et al.
Blood
|
September 1, 1991
Enzyme replacement therapy for Gaucher disease
E 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 deficiency
A 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 cladribine
E Beutler, J C Sipe, J S Romine, et al.
Page
of 41
Search research articles
Search
Showing results (341-350 of 405) with videos related to
Sort By:
Page
of 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 cells
J Chern, E Beutler, W Kuhl, et al.
Pain
|
January 1, 1988
Family dynamics and emotional expression among patients with chronic pain and depression
Larry E Beutler, Roger Daldrup, David Engle, et al.
Blood
|
December 9, 2000
Molecular characterization of a case of atransferrinemia
E 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 patients
E Beutler, A Demina, K Laubscher, et al.
Blood
|
July 1, 1992
New glucose-6-phosphate dehydrogenase mutations from various ethnic groups
E 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 anemia
E 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 case
I Yenicesu, O Kalayci, E Semizel, et al.
Blood
|
September 1, 1991
Enzyme replacement therapy for Gaucher disease
E 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 deficiency
A 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 cladribine
E Beutler, J C Sipe, J S Romine, et al.
Page
of 41