Search research articles
Contact Us
Filters
Showing results (1-10 of 14) with videos related to
Page
of 2
Sort By:
Lancet (London, England)
|
September 20, 1986
Pyridoxine in primary hyperoxaluria type I
E 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 acid
A 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 mother
A Niederwieser, A Matasovic, P Tippett, et al.
Pediatric Nephrology (Berlin, Germany)
|
September 1, 1990
Urinary oxalate and glycolate excretion in healthy infants and children
E 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 population
N 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 hyperphenylalaninemia
H 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 tissue
N Blau, L Kierat, A Matasovic, et al.
The Journal of Biological Chemistry
|
March 5, 1990
7-Substituted pterins. A new class of mammalian pteridines
H 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 PTPS
N 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 families
T Oppliger, B Thöny, C Kluge, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Lancet (London, England)
|
September 20, 1986
Pyridoxine in primary hyperoxaluria type I
E 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 acid
A 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 mother
A Niederwieser, A Matasovic, P Tippett, et al.
Pediatric Nephrology (Berlin, Germany)
|
September 1, 1990
Urinary oxalate and glycolate excretion in healthy infants and children
E 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 population
N 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 hyperphenylalaninemia
H 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 tissue
N Blau, L Kierat, A Matasovic, et al.
The Journal of Biological Chemistry
|
March 5, 1990
7-Substituted pterins. A new class of mammalian pteridines
H 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 PTPS
N 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 families
T Oppliger, B Thöny, C Kluge, et al.
Page
of 2