Jaeken J - Search Results

1

4-Hydroxybutyric aciduria: application of a fluorometric assay to the determination of succinic semialdehyde dehydrogenase activity in extracts of cultured human lymphoblasts.

Gibson KM, Lee CF, Chambliss KL, Kamali V, Francois B, Jaeken J, Jakobs C. Gibson KM, et al. Among authors: jaeken j. Clin Chim Acta. 1991 Feb 15;196(2-3):219-21. doi: 10.1016/0009-8981(91)90076-o. Clin Chim Acta. 1991. PMID: 2029787 No abstract available.

2

Further evaluation of Vigabatrin therapy in 4-hydroxybutyric aciduria.

Jakobs C, Michael T, Jaeger E, Jaeken J, Gibson KM. Jakobs C, et al. Among authors: jaeken j. Eur J Pediatr. 1992 Jun;151(6):466. doi: 10.1007/BF01959366. Eur J Pediatr. 1992. PMID: 1628679 No abstract available.

3

Inherited disorders of GABA metabolism.

Jakobs C, Jaeken J, Gibson KM. Jakobs C, et al. Among authors: jaeken j. J Inherit Metab Dis. 1993;16(4):704-15. doi: 10.1007/BF00711902. J Inherit Metab Dis. 1993. PMID: 8412016 Review.

4

Vigabatrin in the treatment of glutaric aciduria type I.

Francois B, Jaeken J, Gillis P. Francois B, et al. Among authors: jaeken j. J Inherit Metab Dis. 1990;13(3):352-4. doi: 10.1007/BF01799393. J Inherit Metab Dis. 1990. PMID: 2122100 No abstract available.

5

Inborn errors of GABA metabolism.

Gibson KM, Nyhan WL, Jaeken J. Gibson KM, et al. Among authors: jaeken j. Bioessays. 1986 Jan;4(1):24-7. doi: 10.1002/bies.950040107. Bioessays. 1986. PMID: 3790108 No abstract available.

6

4-Aminobutyrate aminotransferase (GABA-transaminase) deficiency.

Medina-Kauwe LK, Tobin AJ, De Meirleir L, Jaeken J, Jakobs C, Nyhan WL, Gibson KM. Medina-Kauwe LK, et al. Among authors: jaeken j. J Inherit Metab Dis. 1999 Jun;22(4):414-27. doi: 10.1023/a:1005500122231. J Inherit Metab Dis. 1999. PMID: 10407778 Review.

7

Vigabatrin in GABA metabolism disorders.

Jaeken J, Casaer P, de Cock P, Francois B. Jaeken J, et al. Lancet. 1989 May 13;1(8646):1074. doi: 10.1016/s0140-6736(89)92466-5. Lancet. 1989. PMID: 2566018 No abstract available.

8

L-2-hydroxyglutaric acidaemia: clinical and biochemical findings in 12 patients and preliminary report on L-2-hydroxyacid dehydrogenase.

Barth PG, Hoffmann GF, Jaeken J, Wanders RJ, Duran M, Jansen GA, Jakobs C, Lehnert W, Hanefeld F, Valk J, et al. Barth PG, et al. Among authors: jaeken j. J Inherit Metab Dis. 1993;16(4):753-61. doi: 10.1007/BF00711907. J Inherit Metab Dis. 1993. PMID: 8412018

9

Congenital nephrotic syndrome: a novel phenotype of type I carbohydrate-deficient glycoprotein syndrome.

van der Knaap MS, Wevers RA, Monnens L, Jakobs C, Jaeken J, van Wijk JA. van der Knaap MS, et al. Among authors: jaeken j. J Inherit Metab Dis. 1996;19(6):787-91. doi: 10.1007/BF01799174. J Inherit Metab Dis. 1996. PMID: 8982953

10

Increased alpha3-fucosylation of alpha(1)-acid glycoprotein in patients with congenital disorder of glycosylation type IA (CDG-Ia).

Van Dijk W, Koeleman C, Van het Hof B, Poland D, Jakobs C, Jaeken J. Van Dijk W, et al. Among authors: jaeken j. FEBS Lett. 2001 Apr 13;494(3):232-5. doi: 10.1016/s0014-5793(01)02349-3. FEBS Lett. 2001. PMID: 11311246 Free article.

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