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The Journal of Pediatrics
|
December 1, 1979
3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency: postnatal management following prenatal diagnosis by analysis of maternal urine
M Duran, R B Schutgens, A Ketel, et al.
European Journal of Immunology
|
April 1, 1986
Functional and mechanistic studies on the toxicity of deoxyguanosine for the in vitro proliferation and differentiation of human peripheral blood B lymphocytes
J G Scharenberg, L J Spaapen, G T Rijkers, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 15, 1985
Octanoylglucuronide excretion in patients with a defective oxidation of medium-chain fatty acids
M Duran, D Ketting, R van Vossen, et al.
Microbiology Spectrum
|
December 12, 2022
Staphylococcus aureus Breast Implant Infection Isolates Display Recalcitrance To Antibiotic Pocket Irrigants
Jesus M Duran Ramirez, Jana Gomez, Blake M Hanson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 1, 1980
Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor
J L Johnson, W R Waud, K V Rajagopalan, et al.
Journal of Neurosurgery
|
April 7, 2010
Intracerebral hemorrhage and seizures
Andrew M Naidech, Isis M Duran, Storm Liebling, et al.
The Annals of Thoracic Surgery
|
May 1, 1981
Heart valve replacement with the Hancock bioprosthesis: a 6-year review
J I Gallo, B Ruiz, M F Carrion, et al.
European Journal of Pediatrics
|
August 1, 1998
Late-onset holocarboxylase synthetase-deficiency: pre- and post-natal diagnosis and evaluation of effectiveness of antenatal biotin therapy
T Suormala, B Fowler, C Jakobs, et al.
Journal of Inherited Metabolic Disease
|
August 13, 1998
The effect of fasting, long-chain triglyceride load and carnitine load on plasma long-chain acylcarnitine levels in mitochondrial very long-chain acyl-CoA dehydrogenase deficiency
C G Costa, L Dorland, I T de Almeida, et al.
Journal of Inherited Metabolic Disease
|
October 14, 2000
Isolated and contiguous glycerol kinase gene disorders: a review
D R Sjarif, J K Ploos van Amstel, M Duran, et al.
Page
of 65
Search research articles
Search
Showing results (331-340 of 646) with videos related to
Sort By:
Page
of 65
The Journal of Pediatrics
|
December 1, 1979
3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency: postnatal management following prenatal diagnosis by analysis of maternal urine
M Duran, R B Schutgens, A Ketel, et al.
European Journal of Immunology
|
April 1, 1986
Functional and mechanistic studies on the toxicity of deoxyguanosine for the in vitro proliferation and differentiation of human peripheral blood B lymphocytes
J G Scharenberg, L J Spaapen, G T Rijkers, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 15, 1985
Octanoylglucuronide excretion in patients with a defective oxidation of medium-chain fatty acids
M Duran, D Ketting, R van Vossen, et al.
Microbiology Spectrum
|
December 12, 2022
Staphylococcus aureus Breast Implant Infection Isolates Display Recalcitrance To Antibiotic Pocket Irrigants
Jesus M Duran Ramirez, Jana Gomez, Blake M Hanson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 1, 1980
Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor
J L Johnson, W R Waud, K V Rajagopalan, et al.
Journal of Neurosurgery
|
April 7, 2010
Intracerebral hemorrhage and seizures
Andrew M Naidech, Isis M Duran, Storm Liebling, et al.
The Annals of Thoracic Surgery
|
May 1, 1981
Heart valve replacement with the Hancock bioprosthesis: a 6-year review
J I Gallo, B Ruiz, M F Carrion, et al.
European Journal of Pediatrics
|
August 1, 1998
Late-onset holocarboxylase synthetase-deficiency: pre- and post-natal diagnosis and evaluation of effectiveness of antenatal biotin therapy
T Suormala, B Fowler, C Jakobs, et al.
Journal of Inherited Metabolic Disease
|
August 13, 1998
The effect of fasting, long-chain triglyceride load and carnitine load on plasma long-chain acylcarnitine levels in mitochondrial very long-chain acyl-CoA dehydrogenase deficiency
C G Costa, L Dorland, I T de Almeida, et al.
Journal of Inherited Metabolic Disease
|
October 14, 2000
Isolated and contiguous glycerol kinase gene disorders: a review
D R Sjarif, J K Ploos van Amstel, M Duran, et al.
Page
of 65