Search research articles
Contact Us
Filters
Showing results (91-100 of 198) with videos related to
Page
of 20
Sort By:
Journal of Biomolecular Structure & Dynamics
|
October 1, 1995
Conformational preferences of the calliFMRFamides and their free-acid analogues
J C Sewell, H Duve, A Thorpe, et al.
Irish Journal of Medical Science
|
December 8, 2010
Administering intravenous immunoglobulin during infection is associated with infusion reactions in selected patients
S Khan, M Abuzakouk, P C Doré, et al.
Medical Hypotheses
|
August 1, 2007
Abnormal O-glycosylation of CD43 may account for some features of Wiskott-Aldrich syndrome
S Khan, S Holding, P C Doré, et al.
Journal of Inherited Metabolic Disease
|
September 3, 1999
Reversible dementia in an adolescent with cblC disease: clinical heterogeneity within the same family
P Augoustides-Savvopoulou, I Mylonas, A C Sewell, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Galactose increase in an infant whose mother is heterozygous for peripheral uridine diphosphate galactose-4-epimerase deficiency
K M Keller, S Wirth, A C Sewell, et al.
Journal of Clinical Gastroenterology
|
June 1, 1990
Abdominal pain from intestinal duplication
B D Cecil, G M Larson, C Sewell, et al.
AIDS Patient Care and Stds
|
May 22, 2001
Antiretroviral medication compliance in patients with AIDS
P A Frick, P Gal, T W Lane, et al.
Health Care Management Science
|
August 1, 2000
An integer programming model for vaccine procurement and delivery for childhood immunization: a pilot study
S H Jacobson, E C Sewell, R Deuson, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1981
Aspartylglycosaminuria in an Italian family: clinical and biochemical characteristics
J Gehler, A C Sewell, C Becker, et al.
Helvetica Paediatrica Acta
|
January 1, 1981
Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian family
J Gehler, A C Sewell, C Becker, et al.
Page
of 20
Search research articles
Search
Showing results (91-100 of 198) with videos related to
Sort By:
Page
of 20
Journal of Biomolecular Structure & Dynamics
|
October 1, 1995
Conformational preferences of the calliFMRFamides and their free-acid analogues
J C Sewell, H Duve, A Thorpe, et al.
Irish Journal of Medical Science
|
December 8, 2010
Administering intravenous immunoglobulin during infection is associated with infusion reactions in selected patients
S Khan, M Abuzakouk, P C Doré, et al.
Medical Hypotheses
|
August 1, 2007
Abnormal O-glycosylation of CD43 may account for some features of Wiskott-Aldrich syndrome
S Khan, S Holding, P C Doré, et al.
Journal of Inherited Metabolic Disease
|
September 3, 1999
Reversible dementia in an adolescent with cblC disease: clinical heterogeneity within the same family
P Augoustides-Savvopoulou, I Mylonas, A C Sewell, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Galactose increase in an infant whose mother is heterozygous for peripheral uridine diphosphate galactose-4-epimerase deficiency
K M Keller, S Wirth, A C Sewell, et al.
Journal of Clinical Gastroenterology
|
June 1, 1990
Abdominal pain from intestinal duplication
B D Cecil, G M Larson, C Sewell, et al.
AIDS Patient Care and Stds
|
May 22, 2001
Antiretroviral medication compliance in patients with AIDS
P A Frick, P Gal, T W Lane, et al.
Health Care Management Science
|
August 1, 2000
An integer programming model for vaccine procurement and delivery for childhood immunization: a pilot study
S H Jacobson, E C Sewell, R Deuson, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1981
Aspartylglycosaminuria in an Italian family: clinical and biochemical characteristics
J Gehler, A C Sewell, C Becker, et al.
Helvetica Paediatrica Acta
|
January 1, 1981
Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian family
J Gehler, A C Sewell, C Becker, et al.
Page
of 20