Ruitenbeek W[au] - Search Results

Year	Number of Results
1976	1
1978	1
1979	3
1980	1
1981	1
1982	2
1983	2
1984	5
1985	5
1986	5
1987	9
1988	6
1989	6
1990	5
1991	5
1992	18
1993	13
1994	6
1995	7
1996	8
1997	8
1998	12
1999	5
2000	1
2001	1
2002	2
2003	1
2006	7
2007	1
2008	3
2024	0

1

Importance of mitochondrial transmembrane processes in human mitochondriopathies.

Huizing M, DePinto V, Ruitenbeek W, Trijbels FJ, van den Heuvel LP, Wendel U. Huizing M, et al. Among authors: ruitenbeek w. J Bioenerg Biomembr. 1996 Apr;28(2):109-14. doi: 10.1007/BF02110640. J Bioenerg Biomembr. 1996. PMID: 9132408 Review.

2

Genetic counselling and prenatal diagnosis in disorders of the mitochondrial energy metabolism.

Ruitenbeek W, Wendel U, Hamel BC, Trijbels JM. Ruitenbeek W, et al. J Inherit Metab Dis. 1996;19(4):581-7. doi: 10.1007/BF01799118. J Inherit Metab Dis. 1996. PMID: 8884581 Review.

3

Problems with the biochemical diagnosis in mitochondrial (encephalo-)myopathies.

Trijbels JM, Scholte HR, Ruitenbeek W, Sengers RC, Janssen AJ, Busch HF. Trijbels JM, et al. Among authors: ruitenbeek w. Eur J Pediatr. 1993 Mar;152(3):178-84. doi: 10.1007/BF01956139. Eur J Pediatr. 1993. PMID: 8444240 Review.

4

Mitochondrial myopathies involving the respiratory chain: a biochemical analysis.

Takamiya S, Yanamura W, Capaldi RA, Kennaway NG, Bart R, Sengers RC, Trijbels JM, Ruitenbeek W. Takamiya S, et al. Among authors: ruitenbeek w. Ann N Y Acad Sci. 1986;488:33-43. doi: 10.1111/j.1749-6632.1986.tb46546.x. Ann N Y Acad Sci. 1986. PMID: 3034117 Review. No abstract available.

5

Leigh syndrome, a mitochondrial encephalo(myo)pathy. A review of the literature.

van Erven PM, Cillessen JP, Eekhoff EM, Gabreëls FJ, Doesburg WH, Lemmens WA, Slooff JL, Renier WO, Ruitenbeek W. van Erven PM, et al. Among authors: ruitenbeek w. Clin Neurol Neurosurg. 1987;89(4):217-30. doi: 10.1016/s0303-8467(87)80020-3. Clin Neurol Neurosurg. 1987. PMID: 3319345 Review.

6

Deficiency of the alpha and beta subunits of pyruvate dehydrogenase in a patient with lactic acidosis and unexpected sudden death.

Sperl W, Ruitenbeek W, Kerkhof CM, Sengers RC, Trijbels JM, Guggenbichler JP, Janssen AJ, Bakkeren JA. Sperl W, et al. Among authors: ruitenbeek w. Eur J Pediatr. 1990 Apr;149(7):487-92. doi: 10.1007/BF01959401. Eur J Pediatr. 1990. PMID: 2189731 Review.

7

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: ruitenbeek w. Neuropediatrics. 1991 Feb;22(1):10-4. doi: 10.1055/s-2008-1071408. Neuropediatrics. 1991. PMID: 1903852 Review.

8

Pontocerebellar hypoplasia associated with respiratory-chain defects.

de Koning TJ, de Vries LS, Groenendaal F, Ruitenbeek W, Jansen GH, Poll-The BT, Barth PG. de Koning TJ, et al. Among authors: ruitenbeek w. Neuropediatrics. 1999 Apr;30(2):93-5. doi: 10.1055/s-2007-973467. Neuropediatrics. 1999. PMID: 10401692

9

Adenine nucleotide translocator 1 deficiency associated with Sengers syndrome.

Jordens EZ, Palmieri L, Huizing M, van den Heuvel LP, Sengers RC, Dörner A, Ruitenbeek W, Trijbels FJ, Valsson J, Sigfusson G, Palmieri F, Smeitink JA. Jordens EZ, et al. Among authors: ruitenbeek w. Ann Neurol. 2002 Jul;52(1):95-9. doi: 10.1002/ana.10214. Ann Neurol. 2002. PMID: 12112053

10

[Encephalomyelopathy, cardiomyopathy, cataract and changes in the retinal pigment epithelium resulting from a cytochrome c oxidase deficiency].

Sieverding L, Schmaltz AA, Apitz J, Sengers CA, Ruitenbeek W, Trijbels JM, Schroth G. Sieverding L, et al. Among authors: ruitenbeek w. Klin Padiatr. 1988 Sep-Oct;200(5):381-7. doi: 10.1055/s-2008-1033738. Klin Padiatr. 1988. PMID: 2846943 Review. German.

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