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A Matasovic

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Lancet (London, England)|September 20, 1986
Pyridoxine in primary hyperoxaluria type IE Leumann, A Matasovic, A Niederwieser
Journal of Chromatography|January 11, 1978
New bromisoval (bromural) metabolites in human urine: alpha-(cystein-S-yl)isovalerylurea, alpha-(N-acetylcystein-S-yl)isovalerylurea and alpha-(cysteamin-S-yl)isovaleric acidA Niederwieser, B Steinmann, A Matasovic
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 2, 1977
A new sulfur amino acid, named hawkinsin, identified in a baby with transient tyrosinemia and her motherA Niederwieser, A Matasovic, P Tippett, et al.
Pediatric Nephrology (Berlin, Germany)|September 1, 1990
Urinary oxalate and glycolate excretion in healthy infants and childrenE P Leumann, A Dietl, A Matasovic
Clinical Chemistry|July 17, 1998
Simultaneous determination of oxalate, glycolate, citrate, and sulfate from dried urine filter paper spots in a pediatric populationN Blau, A Matasovic, A Lukasiewicz-Wedlechowicz, et al.
Biochemical and Biophysical Research Communications|June 16, 1988
Primapterin, anapterin, and 6-oxo-primapterin, three new 7-substituted pterins identified in a patient with hyperphenylalaninemiaH C Curtius, T Kuster, A Matasovic, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 1, 1994
Antenatal diagnosis of tetrahydrobiopterin deficiency by quantification of pterins in amniotic fluid and enzyme activity in fetal and extrafetal tissueN Blau, L Kierat, A Matasovic, et al.
The Journal of Biological Chemistry|March 5, 1990
7-Substituted pterins. A new class of mammalian pteridinesH C Curtius, A Matasovic, G Schoedon, et al.
Human Mutation|June 30, 2000
Isolated central form of tetrahydrobiopterin deficiency associated with hemizygosity on chromosome 11q and a mutant allele of PTPSN Blau, T Scherer-Oppliger, A Baumer, et al.
Human Mutation|January 1, 1997
Identification of mutations causing 6-pyruvoyl-tetrahydropterin synthase deficiency in four Italian familiesT Oppliger, B Thöny, C Kluge, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Lancet (London, England)|September 20, 1986
Pyridoxine in primary hyperoxaluria type IE Leumann, A Matasovic, A Niederwieser
Journal of Chromatography|January 11, 1978
New bromisoval (bromural) metabolites in human urine: alpha-(cystein-S-yl)isovalerylurea, alpha-(N-acetylcystein-S-yl)isovalerylurea and alpha-(cysteamin-S-yl)isovaleric acidA Niederwieser, B Steinmann, A Matasovic
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 2, 1977
A new sulfur amino acid, named hawkinsin, identified in a baby with transient tyrosinemia and her motherA Niederwieser, A Matasovic, P Tippett, et al.
Pediatric Nephrology (Berlin, Germany)|September 1, 1990
Urinary oxalate and glycolate excretion in healthy infants and childrenE P Leumann, A Dietl, A Matasovic
Clinical Chemistry|July 17, 1998
Simultaneous determination of oxalate, glycolate, citrate, and sulfate from dried urine filter paper spots in a pediatric populationN Blau, A Matasovic, A Lukasiewicz-Wedlechowicz, et al.
Biochemical and Biophysical Research Communications|June 16, 1988
Primapterin, anapterin, and 6-oxo-primapterin, three new 7-substituted pterins identified in a patient with hyperphenylalaninemiaH C Curtius, T Kuster, A Matasovic, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 1, 1994
Antenatal diagnosis of tetrahydrobiopterin deficiency by quantification of pterins in amniotic fluid and enzyme activity in fetal and extrafetal tissueN Blau, L Kierat, A Matasovic, et al.
The Journal of Biological Chemistry|March 5, 1990
7-Substituted pterins. A new class of mammalian pteridinesH C Curtius, A Matasovic, G Schoedon, et al.
Human Mutation|June 30, 2000
Isolated central form of tetrahydrobiopterin deficiency associated with hemizygosity on chromosome 11q and a mutant allele of PTPSN Blau, T Scherer-Oppliger, A Baumer, et al.
Human Mutation|January 1, 1997
Identification of mutations causing 6-pyruvoyl-tetrahydropterin synthase deficiency in four Italian familiesT Oppliger, B Thöny, C Kluge, et al.
Pageof 2