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H A Simmonds

Showing results (231-240 of 250) with videos related to

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Clinical Nephrology|June 1, 1991
Familial juvenile gouty nephropathy with renal urate hypoexcretion preceding renal diseaseF Moro, C S Ogg, H A Simmonds, et al.
Human Molecular Genetics|October 1, 1996
HPRT-APRT-deficient mice are not a model for lesch-nyhan syndromeS J Engle, D E Womer, P M Davies, 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 conditioningC 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 mediumT 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 featuresM Köhler, B Assmann, C Bräutigam, et al.
Nucleosides, Nucleotides & Nucleic Acids|July 5, 2008
Metabolism of 4-pyridone-3-carboxamide-1-beta-D-ribonucleoside triphosphate and its nucleoside precursor in the erythrocytesE M Slominska, C Orlewska, A Yuen, et al.
Prenatal Diagnosis|October 1, 1987
First trimester diagnosis of adenosine deaminase deficiencyT Dooley, L D Fairbanks, H A Simmonds, et al.
Advances in Experimental Medicine and Biology|May 23, 1998
Efficacy of allopurinol in ameliorating the progressive renal disease in familial juvenile hyperuricaemic nephropathy (FJHN). A six-year updateM B McBride, H A Simmonds, C S Ogg, et al.
Advances in Experimental Medicine and Biology|January 1, 1994
Biochemical and immunological status following gene therapy and PEG-ADA therapy for adenosine deaminase (ADA) deficiencyL D Fairbanks, H A Simmonds, P M Hoogerbrugge, et al.
Nucleosides, Nucleotides & Nucleic Acids|December 2, 2004
Adenylosuccinate lyase deficiency--first British caseA M Marinaki, M Champion, M A Kurian, et al.
Pageof 25

Showing results (231-240 of 250) with videos related to

Sort By:
Pageof 25
Clinical Nephrology|June 1, 1991
Familial juvenile gouty nephropathy with renal urate hypoexcretion preceding renal diseaseF Moro, C S Ogg, H A Simmonds, et al.
Human Molecular Genetics|October 1, 1996
HPRT-APRT-deficient mice are not a model for lesch-nyhan syndromeS J Engle, D E Womer, P M Davies, 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 conditioningC 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 mediumT 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 featuresM Köhler, B Assmann, C Bräutigam, et al.
Nucleosides, Nucleotides & Nucleic Acids|July 5, 2008
Metabolism of 4-pyridone-3-carboxamide-1-beta-D-ribonucleoside triphosphate and its nucleoside precursor in the erythrocytesE M Slominska, C Orlewska, A Yuen, et al.
Prenatal Diagnosis|October 1, 1987
First trimester diagnosis of adenosine deaminase deficiencyT Dooley, L D Fairbanks, H A Simmonds, et al.
Advances in Experimental Medicine and Biology|May 23, 1998
Efficacy of allopurinol in ameliorating the progressive renal disease in familial juvenile hyperuricaemic nephropathy (FJHN). A six-year updateM B McBride, H A Simmonds, C S Ogg, et al.
Advances in Experimental Medicine and Biology|January 1, 1994
Biochemical and immunological status following gene therapy and PEG-ADA therapy for adenosine deaminase (ADA) deficiencyL D Fairbanks, H A Simmonds, P M Hoogerbrugge, et al.
Nucleosides, Nucleotides & Nucleic Acids|December 2, 2004
Adenylosuccinate lyase deficiency--first British caseA M Marinaki, M Champion, M A Kurian, et al.
Pageof 25