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Journal of Inherited Metabolic Disease
|
January 1, 1996
Mitochondrial very long-chain acyl-CoA dehydrogenase deficiency with a mild clinical course
B Merinero, C Pérez-Cerdá, M J Garcia, et al.
Journal of Inherited Metabolic Disease
|
July 13, 2004
Glutathione synthetase deficiency associated with antenatal cerebral bleeding
L W Brüggemann, F Groenendaal, E Ristoff, et al.
American Journal of Translational Research
|
May 22, 2012
Validation of transcatheter left ventricular electromechanical mapping for assessment of cardiac function and targeted transendocardial injection in a porcine ischemia-reperfusion model
Sharven Taghavi, Jason M Duran, Remus M Berretta, et al.
American Heart Journal
|
March 30, 2002
Coronary stent implantation in patients older than 75 years of age: clinical profile and initial and long-term (3 years) outcome
Juan C Muñoz, Joaquín J Alonso, Juan M Duran, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1997
Abnormal glutathione conjugation in patients with tyrosinaemia type I
T M Mulders, D J Bergman, B T Poll-The, et al.
Journal of Inherited Metabolic Disease
|
November 5, 1997
Dihydropyrimidinase deficiency and congenital microvillous atrophy: coincidence or genetic relation?
B Assmann, G F Hoffmann, L Wagner, et al.
The Journal of Cell Biology
|
June 24, 2020
The function of GORASPs in Golgi apparatus organization in vivo
Rianne Grond, Tineke Veenendaal, Juan M Duran, et al.
Pediatric Research
|
February 1, 1987
A new case of purine nucleoside phosphorylase deficiency: enzymologic, clinical, and immunologic characteristics
G Rijksen, W Kuis, S K Wadman, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
July 5, 2008
Identification of two novel mutations C79X and R235Q in the dihydropyrimidine dehydrogenase gene in a patient presenting with hematuria
A B P van Kuilenburg, J Meijer, D Dobritzsch, et al.
Plos One
|
September 14, 2019
Upgraded molecular models of the human KCNQ1 potassium channel
Georg Kuenze, Amanda M Duran, Hope Woods, et al.
Page
of 65
Search research articles
Search
Showing results (491-500 of 646) with videos related to
Sort By:
Page
of 65
Journal of Inherited Metabolic Disease
|
January 1, 1996
Mitochondrial very long-chain acyl-CoA dehydrogenase deficiency with a mild clinical course
B Merinero, C Pérez-Cerdá, M J Garcia, et al.
Journal of Inherited Metabolic Disease
|
July 13, 2004
Glutathione synthetase deficiency associated with antenatal cerebral bleeding
L W Brüggemann, F Groenendaal, E Ristoff, et al.
American Journal of Translational Research
|
May 22, 2012
Validation of transcatheter left ventricular electromechanical mapping for assessment of cardiac function and targeted transendocardial injection in a porcine ischemia-reperfusion model
Sharven Taghavi, Jason M Duran, Remus M Berretta, et al.
American Heart Journal
|
March 30, 2002
Coronary stent implantation in patients older than 75 years of age: clinical profile and initial and long-term (3 years) outcome
Juan C Muñoz, Joaquín J Alonso, Juan M Duran, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1997
Abnormal glutathione conjugation in patients with tyrosinaemia type I
T M Mulders, D J Bergman, B T Poll-The, et al.
Journal of Inherited Metabolic Disease
|
November 5, 1997
Dihydropyrimidinase deficiency and congenital microvillous atrophy: coincidence or genetic relation?
B Assmann, G F Hoffmann, L Wagner, et al.
The Journal of Cell Biology
|
June 24, 2020
The function of GORASPs in Golgi apparatus organization in vivo
Rianne Grond, Tineke Veenendaal, Juan M Duran, et al.
Pediatric Research
|
February 1, 1987
A new case of purine nucleoside phosphorylase deficiency: enzymologic, clinical, and immunologic characteristics
G Rijksen, W Kuis, S K Wadman, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
July 5, 2008
Identification of two novel mutations C79X and R235Q in the dihydropyrimidine dehydrogenase gene in a patient presenting with hematuria
A B P van Kuilenburg, J Meijer, D Dobritzsch, et al.
Plos One
|
September 14, 2019
Upgraded molecular models of the human KCNQ1 potassium channel
Georg Kuenze, Amanda M Duran, Hope Woods, et al.
Page
of 65