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L. Kierat

Veröffentlichungen von L. Kierat zu Kierat, L. ->
weitere Veröffentlichungen von L. Kierat:
Tetrahydrobiopterin Is a Secretory Product of Murine Vascular Endothelial Cells (1994)
Hyperphenylalaninaemia presumably due to carbinolamine dehydratase deficiency: Loading tests with pterin derivatives (1992)
Screening for tetrahydrobiopterin deficiency in newborns using dried urine on filter paper (1992)
Differential diagnosis of hyperphenylalaninaemia by a combined phenylalanine-tetrahydrobiopterin loading test (1993)
Antenatal diagnosis of tetrahydrobiopterin deficiency by quantification of pterins in amniotic fluid and enzyme activity in fetal and extrafetal tissue (1994)
Solid-phase immunoassay for the vitamin B"1"2-binding protein transcobalamin II in human serum (1982)
Synthesis and secretion of the human vitamin B12-binding protein, transcobalamin II, by cultured skin fibroblasts and by bone marrow cells (1985)
Hyperphenylalaninemia and pterin metabolism in serum and erythrocytes (1993)
A case of 6-pyruvoyl-tetrahydropterin synthase deficiency after screening 1 500 000 newborns in Greece (1991)
Mutations in the pterin-4α-carbinolamine dehydratase (PCBD) gene cause a benign form of hyperphenylalaninemia (1998)
Veröffentlichungen zu Kierat, L.
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1
Walter, R., Schaffner, A., ... Tetrahydrobiopterin Is a Secretory Product of Murine Vascular Endothelial Cells
in: Biochemical and Biophysical Research Communications, in: Biochemical and Biophysical Research Communications . - Amsterdam : Elsevier, ISSN 0006-291X, ZDB-ID 1461396-7 Vol. 203, No. 3 (1994), p. 1522-1526
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1994
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2
Blau, N., Kierat, L., ... Hyperphenylalaninaemia presumably due to carbinolamine dehydratase deficiency: Loading tests with pterin derivatives
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 15 (3. 1992), p. 409-412
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1992
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3
Blau, N., Kierat, L., ... Screening for tetrahydrobiopterin deficiency in newborns using dried urine on filter paper
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 15 (3. 1992), p. 402-404
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1992
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4
Ponzone, A., Guardamagna, O., ... Differential diagnosis of hyperphenylalaninaemia by a combined phenylalanine-tetrahydrobiopterin loading test
in: European journal of pediatrics , ISSN 1432-1076, Vol. 152 (8. 1993), p. 655-661
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1993
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5
Blau, N., Kierat, L., ... Antenatal diagnosis of tetrahydrobiopterin deficiency by quantification of pterins in amniotic fluid and enzyme activity in fetal and extrafetal tissue
in: Clinica Chimica Acta, in: Clinica Chimica Acta . - Amsterdam : Elsevier, ISSN 0009-8981, ZDB-ID 1499920-1 Vol. 226, No. 2 (1994), p. 159-169
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1994
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6
Frater-Schroder, M., Kierat, L., ... Solid-phase immunoassay for the vitamin B"1"2-binding protein transcobalamin II in human serum
in: Analytical Biochemistry, in: Analytical Biochemistry . - Amsterdam : Elsevier, ISSN 0003-2697, ZDB-ID 1461105-3 Vol. 124, No. 1 (1982), p. 92-101
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1982
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7
Frater-Schroder, M., Porck, H.J., ... Synthesis and secretion of the human vitamin B12-binding protein, transcobalamin II, by cultured skin fibroblasts and by bone marrow cells
in: Biochimica et Biophysica Acta (BBA)/Molecular Cell Research, in: Biochimica et Biophysica Acta (BBA)/Molecular Cell Research . - Amsterdam : Elsevier, ISSN 0167-4889, ZDB-ID 2209512-3 Vol. 845, No. 3 (1985), p. 421-427
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1985
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8
Ponzone, A., Guardamagna, O., ... Hyperphenylalaninemia and pterin metabolism in serum and erythrocytes
in: Clinica Chimica Acta, in: Clinica Chimica Acta . - Amsterdam : Elsevier, ISSN 0009-8981, ZDB-ID 1499920-1 Vol. 216, No. 1-2 (1993), p. 63-71
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1993
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9
Schulpis, K. H., Covanis, A., ... A case of 6-pyruvoyl-tetrahydropterin synthase deficiency after screening 1 500 000 newborns in Greece
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 14 (5. 1991), p. 845-846
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1991
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10
Thöny, B., Neuheiser, F., ... Mutations in the pterin-4α-carbinolamine dehydratase (PCBD) gene cause a benign form of hyperphenylalaninemia
in: Human genetics , ISSN 1432-1203, Vol. 103 (2. 1998), p. 162-167
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1998