Gabreels FJ - Search Results

1

Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathies.

Korenke GC, Bentlage HA, Ruitenbeek W, Sengers RC, Sperl W, Trijbels JM, Gabreels FJ, Wijburg FA, Wiedermann V, Hanefeld F, et al. Korenke GC, et al. Among authors: gabreels fj. Eur J Pediatr. 1990 Dec;150(2):104-8. doi: 10.1007/BF02072049. Eur J Pediatr. 1990. PMID: 2279503

2

Successful treatment of pure myopathy, associated with complex I deficiency, with riboflavin and carnitine.

Bernsen PL, Gabreëls FJ, Ruitenbeek W, Sengers RC, Stadhouders AM, Renier WO. Bernsen PL, et al. Among authors: gabreels fj. Arch Neurol. 1991 Mar;48(3):334-8. doi: 10.1001/archneur.1991.00530150106028. Arch Neurol. 1991. PMID: 1900413

3

Congenital muscular dystrophy.

Leyten QH, Gabreëls FJ, Renier WO, Ter Laak HJ, Sengers RC, Mullaart RA. Leyten QH, et al. Among authors: gabreels fj. J Pediatr. 1989 Aug;115(2):214-21. doi: 10.1016/s0022-3476(89)80068-x. J Pediatr. 1989. PMID: 2754551

4

Clinical heterogeneity in respiratory chain complex III deficiency in childhood.

Mourmans J, Wendel U, Bentlage HA, Trijbels JM, Smeitink JA, de Coo IF, Gabreëls FJ, Sengers RC, Ruitenbeek W. Mourmans J, et al. Among authors: gabreels fj. J Neurol Sci. 1997 Jul;149(1):111-7. doi: 10.1016/s0022-510x(97)05379-3. J Neurol Sci. 1997. PMID: 9168175

5

MELAS syndrome. Report of two patients, and comparison with data of 24 patients derived from the literature.

van Hellenberg Hubar JL, Gabreëls FJ, Ruitenbeek W, Sengers RC, Renier WO, Thijssen HO, ter Laak HJ. van Hellenberg Hubar JL, et al. Among authors: gabreels fj. Neuropediatrics. 1991 Feb;22(1):10-4. doi: 10.1055/s-2008-1071408. Neuropediatrics. 1991. PMID: 1903852 Review.

6

A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscle.

Van Erven PM, Gabreëls FJ, Ruitenbeek W, Renier WO, Ter Laak HJ, Stadhouders AM. Van Erven PM, et al. Among authors: gabreels fj. J Neurol Neurosurg Psychiatry. 1988 May;51(5):704-8. doi: 10.1136/jnnp.51.5.704. J Neurol Neurosurg Psychiatry. 1988. PMID: 2841425 Free PMC article.

7

Estimation of pyruvate dehydrogenase (E1) activity in human skeletal muscle; three cases with E1 deficiency.

van Laack HL, Ruitenbeek W, Trijbels JM, Sengers RC, Gabreëls FJ, Janssen AJ, Kerkhof CM. van Laack HL, et al. Among authors: gabreels fj. Clin Chim Acta. 1988 Jan 15;171(1):109-18. doi: 10.1016/0009-8981(88)90296-3. Clin Chim Acta. 1988. PMID: 3127087

8

[Clinical symptoms of mitochondrial myopathies].

Gabreëls FJ, Sengers RC. Gabreëls FJ, et al. Ned Tijdschr Geneeskd. 1988 Jun 4;132(23):1058-61. Ned Tijdschr Geneeskd. 1988. PMID: 3386766 Dutch. No abstract available.

9

A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q.

Fischer JC, Ruitenbeek W, Gabreëls FJ, Janssen AJ, Renier WO, Sengers RC, Stadhouders AM, ter Laak HJ, Trijbels JM, Veerkamp JH. Fischer JC, et al. Among authors: gabreels fj. Eur J Pediatr. 1986 Feb;144(5):441-4. doi: 10.1007/BF00441735. Eur J Pediatr. 1986. PMID: 3956532

10

Treatment of complex I deficiency with riboflavin.

Bernsen PL, Gabreëls FJ, Ruitenbeek W, Hamburger HL. Bernsen PL, et al. Among authors: gabreels fj. J Neurol Sci. 1993 Sep;118(2):181-7. doi: 10.1016/0022-510x(93)90108-b. J Neurol Sci. 1993. PMID: 8229067

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