E-LIB Suche - Ergebnisse für: Kierat, L.

1

Interspecific interactions in solitary Aculeata – is the pr..:

Kierat, J. ; Miler, K. ; Celary, W..
Bulletin of Entomological Research. 108 (2017) 1 - p. 35-39 , 2017

Link: https://doi.org/10.1017/..

2

Cerebrospinal fluid pterins and folates in Aicardi-Goutière..:

Blau, N. ; Bonafé, L. ; Krägeloh-Mann, I....
Neurology. 61 (2003) 5 - p. 642-647 , 2003

Link: https://doi.org/10.1212/..

3

Mutations in the pterin-4α-carbinolamine dehydratase ( PCBD..:

Thöny, B. ; Neuheiser, F. ; Kierat, L....
Human Genetics. 103 (1998) 2 - p. 162-167 , 1998

Link: https://doi.org/10.1007/..

4

Tetrahydrobiopterin Loading Test in Xanthine Dehydrogenase ..:

Blau, N. ; de Klerk, J.B.C. ; Thöny, B....
Biochemical and Molecular Medicine. 58 (1996) 2 - p. 199-203 , 1996

Link: https://doi.org/10.1006/..

5

Effects of activating and deactivating cytokines on the fun..:

Walter, R. ; Blau, N. ; Kierat, L...
Immunology Letters. 54 (1996) 1 - p. 25-29 , 1996

Link: https://doi.org/10.1016/..

6

Antenatal diagnosis of tetrahydrobiopterin deficiency by qu..:

Blau, N. ; Kierat, L. ; Matasovic, A....
Clinica Chimica Acta. 226 (1994) 2 - p. 159-169 , 1994

Link: https://doi.org/10.1016/..

7

Tetrahydrobiopterin Is a Secretory Product of Murine Vascul..:

Walter, R. ; Schaffner, A. ; Blau, N...
Biochemical and Biophysical Research Communications. 203 (1994) 3 - p. 1522-1526 , 1994

Link: https://doi.org/10.1006/..

8

Differential diagnosis of hyperphenylalaninaemia by a combi..:

Ponzone, A. ; Guardamagna, O. ; Spada, M....
European Journal of Pediatrics. 152 (1993) 8 - p. 655-661 , 1993

Link: https://doi.org/10.1007/..

9

Hyperphenylalaninemia and pterin metabolism in serum and er..:

Ponzone, A. ; Guardamagna, O. ; Spada, M....
Clinica Chimica Acta. 216 (1993) 1-2 - p. 63-71 , 1993

Link: https://doi.org/10.1016/..

10

Screening for tetrahydrobiopterin deficiency in newborns us..:

Blau, N. ; Kierat, L. ; Heizmann, C. W....
Journal of Inherited Metabolic Disease. 15 (1992) 3 - p. 402-404 , 1992

Link: https://doi.org/10.1007/..

11

Hyperphenylalaninaemia presumably due to carbinolamine dehy..:

Blau, N. ; Kierat, L. ; Curtius, H. ‐Ch...
Journal of Inherited Metabolic Disease. 15 (1992) 3 - p. 409-412 , 1992

Link: https://doi.org/10.1007/..

12

A case of 6‐pyruvoyl‐tetrahydropterin synthase deficiency a..:

Schulpis, K. H. ; Covanis, A. ; Loumakou, M....
Journal of Inherited Metabolic Disease. 14 (1991) 5 - p. 845-846 , 1991

Link: https://doi.org/10.1007/..

13

Prenatal Diagnosis of Dihydropteridine Reductase Deficiency..:

Guardamagna, O. ; Spada, M. ; Ponzone, A....
pteridines. 3 (1991) 1-2 - p. 19-21 , 1991

Link: https://doi.org/10.1515/..

14

Hyperphenylalaninemia caused by dihydropteridine reductase ..:

Blau, N. ; Curtius, H.C. ; Kierat, L...
The Journal of Pediatrics. 115 (1989) 4 - p. 661-662 , 1989

Link: https://doi.org/10.1016/..

15

Prenatal Diagnosis of Atypical Phenylketonuria:

Blau, N. ; Niederwieser, A. ; Curtius, H. Ch....
Journal of Inherited Metabolic Disease. 12 (1989) S2 - p. 295-298 , 1989

Link: https://doi.org/10.1007/..