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Archives of Disease in Childhood
|
January 1, 1979
Complete deficiency of adenine phosphoribosyltransferase: a third case presenting as renal stones in a young child
T M Barratt, H A Simmonds, J S Cameron, et al.
Clinical and Experimental Medicine
|
January 12, 2008
4-pyridone-3-carboxamide ribonucleoside triphosphate accumulating in erythrocytes in end stage renal failure originates from tryptophan metabolism
A Laurence, S M Edbury, A M Marinaki, et al.
Journal of Clinical Epidemiology
|
January 1, 1988
A comparison of problems reported by persons with cancer and their same sex siblings
P S Houts, J M Yasko, M A Simmonds, et al.
Clinical Nephrology
|
June 1, 1991
Familial juvenile gouty nephropathy with renal urate hypoexcretion preceding renal disease
F Moro, C S Ogg, H A Simmonds, et al.
Medical Interface
|
December 8, 1996
Pain management guidelines: implications for managed care--a roundtable discussion
A Brady, C Cleeland, G Goldstein, et al.
Human Molecular Genetics
|
October 1, 1996
HPRT-APRT-deficient mice are not a model for lesch-nyhan syndrome
S J Engle, D E Womer, P M Davies, et al.
Human Vaccines & Immunotherapeutics
|
November 21, 2018
Are we speaking the same language? an argument for the consistent use of terminology and definitions for childhood vaccination indicators
Shannon E MacDonald, Margaret L Russell, Xianfang C Liu, et al.
Bone Marrow Transplantation
|
August 11, 2001
Successful HLA-identical bone marrow transplantation in a patient with PNP deficiency using busulfan and fludarabine for conditioning
C F Classen, A S Schulz, M Sigl-Kraetzig, et al.
Metabolic Brain Disease
|
June 13, 2000
Adenoviruses encoding HPRT correct biochemical abnormalities of HPRT-deficient cells and allow their survival in negative selection medium
T D Southgate, D Bain, L D Fairbanks, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 22, 2000
Adenylosuccinase deficiency: possibly underdiagnosed encephalopathy with variable clinical features
M Köhler, B Assmann, C Bräutigam, et al.
Page
of 41
Search research articles
Search
Showing results (361-370 of 401) with videos related to
Sort By:
Page
of 41
Archives of Disease in Childhood
|
January 1, 1979
Complete deficiency of adenine phosphoribosyltransferase: a third case presenting as renal stones in a young child
T M Barratt, H A Simmonds, J S Cameron, et al.
Clinical and Experimental Medicine
|
January 12, 2008
4-pyridone-3-carboxamide ribonucleoside triphosphate accumulating in erythrocytes in end stage renal failure originates from tryptophan metabolism
A Laurence, S M Edbury, A M Marinaki, et al.
Journal of Clinical Epidemiology
|
January 1, 1988
A comparison of problems reported by persons with cancer and their same sex siblings
P S Houts, J M Yasko, M A Simmonds, et al.
Clinical Nephrology
|
June 1, 1991
Familial juvenile gouty nephropathy with renal urate hypoexcretion preceding renal disease
F Moro, C S Ogg, H A Simmonds, et al.
Medical Interface
|
December 8, 1996
Pain management guidelines: implications for managed care--a roundtable discussion
A Brady, C Cleeland, G Goldstein, et al.
Human Molecular Genetics
|
October 1, 1996
HPRT-APRT-deficient mice are not a model for lesch-nyhan syndrome
S J Engle, D E Womer, P M Davies, et al.
Human Vaccines & Immunotherapeutics
|
November 21, 2018
Are we speaking the same language? an argument for the consistent use of terminology and definitions for childhood vaccination indicators
Shannon E MacDonald, Margaret L Russell, Xianfang C Liu, et al.
Bone Marrow Transplantation
|
August 11, 2001
Successful HLA-identical bone marrow transplantation in a patient with PNP deficiency using busulfan and fludarabine for conditioning
C F Classen, A S Schulz, M Sigl-Kraetzig, et al.
Metabolic Brain Disease
|
June 13, 2000
Adenoviruses encoding HPRT correct biochemical abnormalities of HPRT-deficient cells and allow their survival in negative selection medium
T D Southgate, D Bain, L D Fairbanks, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 22, 2000
Adenylosuccinase deficiency: possibly underdiagnosed encephalopathy with variable clinical features
M Köhler, B Assmann, C Bräutigam, et al.
Page
of 41