Janssen A - Search Results

1

Cerebrotendinous xanthomatosis. Controversies about nerve and muscle: observations in ten patients.

Verrips A, van Engelen BG, ter Laak H, Gabreëls-Festen A, Janssen A, Zwarts M, Wevers RA, Gabreëls FJ. Verrips A, et al. Among authors: janssen a. Neuromuscul Disord. 2000 Aug;10(6):407-14. doi: 10.1016/s0960-8966(00)00112-7. Neuromuscul Disord. 2000. PMID: 10899446 Clinical Trial.

2

Normal carnitine levels in patients with chronic fatigue syndrome.

Soetekouw PM, Wevers RA, Vreken P, Elving LD, Janssen AJ, van der Veen Y, Bleijenberg G, van der Meer JW. Soetekouw PM, et al. Among authors: janssen aj. Neth J Med. 2000 Jul;57(1):20-4. doi: 10.1016/s0300-2977(00)00030-9. Neth J Med. 2000. PMID: 10862998

3

Pyruvate metabolism in Lafora disease.

Busard HL, Renier WO, Gabreëls FJ, Trijbels JM, Janssen AJ, Lamers KJ. Busard HL, et al. Among authors: janssen aj. Epilepsia. 1989 May-Jun;30(3):314-7. doi: 10.1111/j.1528-1157.1989.tb05303.x. Epilepsia. 1989. PMID: 2498072

4

Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscle.

Bentlage HA, Wendel U, Schägger H, ter Laak HJ, Janssen AJ, Trijbels JM. Bentlage HA, et al. Among authors: janssen aj. Neurology. 1996 Jul;47(1):243-8. doi: 10.1212/wnl.47.1.243. Neurology. 1996. PMID: 8710086 Free article.

5

Comparison of 3 instruments to measure muscle strength in children: A prospective study.

Van den Beld WA, Van der Sanden GA, Janssen AJ, Sengers RC, Verbeek AL, Gabreëls FJ. Van den Beld WA, et al. Among authors: janssen aj. Eur J Paediatr Neurol. 2011 Nov;15(6):512-8. doi: 10.1016/j.ejpn.2011.05.006. Epub 2011 Jul 1. Eur J Paediatr Neurol. 2011. PMID: 21723758

6

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: janssen aj. Clin Chim Acta. 1988 Jan 15;171(1):109-18. doi: 10.1016/0009-8981(88)90296-3. Clin Chim Acta. 1988. PMID: 3127087

7

Postnatal development of pyruvate oxidation in quadriceps muscle of the rat.

Sperl W, Sengers RC, Trijbels JM, Ruitenbeek W, De Graaf R, Ter Laak H, Van Lith T, Kerkhoff C, Janssen A. Sperl W, et al. Among authors: janssen a. Biol Neonate. 1992;61(3):188-200. doi: 10.1159/000243742. Biol Neonate. 1992. PMID: 1319216

8

A new motor performance test in a prospective study on children with suspected myopathy.

van den Beld WA, van der Sanden GA, Feuth T, Janssen AJ, Sengers RC, Verbeek AL, Gabreëls FJ. van den Beld WA, et al. Among authors: janssen aj. Dev Med Child Neurol. 2006 Sep;48(9):739-43. doi: 10.1017/S0012162206001587. Dev Med Child Neurol. 2006. PMID: 16904020 Free article.

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: janssen aj. Eur J Pediatr. 1986 Feb;144(5):441-4. doi: 10.1007/BF00441735. Eur J Pediatr. 1986. PMID: 3956532

10

Progressive poliodystrophy (Alpers' disease) with a defect in cytochrome aa3 in muscle: a report of two unrelated patients.

Prick MJ, Gabreëls FJ, Trijbels JM, Janssen AJ, le Coultre R, van Dam K, Jaspar HH, Ebels EJ, Op de Coul AA. Prick MJ, et al. Among authors: janssen aj. Clin Neurol Neurosurg. 1983;85(1):57-70. doi: 10.1016/0303-8467(83)90024-0. Clin Neurol Neurosurg. 1983. PMID: 6303665

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