François B - Search Results

1

Neuropsychological outcome of NTBC-treated patients with tyrosinaemia type 1.

De Laet C, Munoz VT, Jaeken J, François B, Carton D, Sokal EM, Dan B, Goyens PJ. De Laet C, et al. Among authors: francois b. Dev Med Child Neurol. 2011 Oct;53(10):962-4. doi: 10.1111/j.1469-8749.2011.04048.x. Epub 2011 Jul 11. Dev Med Child Neurol. 2011. PMID: 21745202 Free article. Clinical Trial. No abstract available.

2

Vigabatrin in the treatment of glutaric aciduria type I.

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

3

Vigabatrin in GABA metabolism disorders.

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

4

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: francois b. 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.

5

Localized brain proton NMR spectroscopy in young adult phenylketonuria patients.

Johannik K, Van Hecke P, François B, Marchal G, Smet MH, Jaeken J, Breysem L, Wilms G, Baert AL. Johannik K, et al. Among authors: francois b. Magn Reson Med. 1994 Jan;31(1):53-7. doi: 10.1002/mrm.1910310108. Magn Reson Med. 1994. PMID: 8121269

6

Nutritional value of essential amino acids in the treatment of adults with phenylketonuria.

Dotremont H, François B, Diels M, Gillis P. Dotremont H, et al. Among authors: francois b. J Inherit Metab Dis. 1995;18(2):127-30. doi: 10.1007/BF00711746. J Inherit Metab Dis. 1995. PMID: 7564226 No abstract available.

7

Iatrogenic skin lesions in phenylketonuric children due to a low tyrosine intake.

François B, Diels M, de la Brassinne M. François B, et al. J Inherit Metab Dis. 1989;12 Suppl 2:332-4. doi: 10.1007/BF03335414. J Inherit Metab Dis. 1989. PMID: 2512437 No abstract available.

8

Rapid identification of PKU-associated mutations by multiplex DGGE analysis of the PAH gene.

Michiels L, François B, Raus J, Vandevyver C. Michiels L, et al. Among authors: francois b. J Inherit Metab Dis. 1996;19(6):735-8. doi: 10.1007/BF01799164. J Inherit Metab Dis. 1996. PMID: 8982945 No abstract available.

9

Heterogeneity of phenylketonuria in Belgium at the genotype-phenotype level.

Francois B, Vandevyver C, Verelst P, Phillippaert L, Raus J. Francois B, et al. J Inherit Metab Dis. 1994;17(3):369-70. doi: 10.1007/BF00711833. J Inherit Metab Dis. 1994. PMID: 7807956 No abstract available.

10

Mutation analysis in families with discordant phenotypes of phenylalanine hydroxylase deficiency. Inheritance and expression of the hyperphenylalaninaemias.

Guldberg P, Levy HL, Koch R, Berlin CM Jr, Francois B, Henriksen KF, Güttler F. Guldberg P, et al. Among authors: francois b. J Inherit Metab Dis. 1994;17(6):645-51. doi: 10.1007/BF00712004. J Inherit Metab Dis. 1994. PMID: 7707686

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