Bentlage HA - Search Results

1

Sudden infant death associated with defective oxidative phosphorylation.

Smeitink JA, Fischer JC, Ruitenbeek W, Duran M, Hofkamp M, Bentlage HA, Poll-The BT. Smeitink JA, et al. Among authors: bentlage ha. Lancet. 1993 Jun 19;341(8860):1601. doi: 10.1016/0140-6736(93)90741-x. Lancet. 1993. PMID: 8099679 No abstract available.

2

Favourable clinical course in an infant with severe deficiency of complex III of the respiratory chain combined with less severe deficiencies of complexes I, II and IV.

Rubio-Gozalbo ME, Ruitenbeek W, Bentlage HA, Schägger H, Sengers RC, Trijbels JM, ter Laak HJ, Mariman EC, Bakker MM, de Jager J, Smeitink JA. Rubio-Gozalbo ME, et al. Among authors: bentlage ha. Eur J Pediatr. 1997 Dec;156(12):931-4. doi: 10.1007/s004310050745. Eur J Pediatr. 1997. PMID: 9453375

3

Human diseases with defects in oxidative phosphorylation. 1. Decreased amounts of assembled oxidative phosphorylation complexes in mitochondrial encephalomyopathies.

Bentlage H, de Coo R, ter Laak H, Sengers R, Trijbels F, Ruitenbeek W, Schlote W, Pfeiffer K, Gencic S, von Jagow G, et al. Bentlage H, et al. Eur J Biochem. 1995 Feb 1;227(3):909-15. doi: 10.1111/j.1432-1033.1995.tb20218.x. Eur J Biochem. 1995. PMID: 7867654 Free article.

4

Electrophoretic separation of multiprotein complexes from blood platelets and cell lines: technique for the analysis of diseases with defects in oxidative phosphorylation.

Schägger H, Bentlage H, Ruitenbeek W, Pfeiffer K, Rotter S, Rother C, Böttcher-Purkl A, Lodemann E. Schägger H, et al. Electrophoresis. 1996 Apr;17(4):709-14. doi: 10.1002/elps.1150170415. Electrophoresis. 1996. PMID: 8738332

5

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: bentlage ha. J Neurol Sci. 1997 Jul;149(1):111-7. doi: 10.1016/s0022-510x(97)05379-3. J Neurol Sci. 1997. PMID: 9168175

6

Neonatal De Toni-Debré-Fanconi syndrome due to a defect in complex III of the respiratory chain.

Wendel U, Ruitenbeek W, Bentlage HA, Sengers RC, Trijbels JM. Wendel U, et al. Among authors: bentlage ha. Eur J Pediatr. 1995 Nov;154(11):915-8. doi: 10.1007/BF01957505. Eur J Pediatr. 1995. PMID: 8582406

7

Combined deficiencies of the pyruvate dehydrogenase complex and enzymes of the respiratory chain in mitochondrial myopathies.

Sperl W, Ruitenbeek W, Sengers RC, Trijbels JM, Bentlage H, Wraith JE, Heilmann C, Stöckler S, Binder C, Korenke GC, et al. Sperl W, et al. Eur J Pediatr. 1992 Mar;151(3):192-5. doi: 10.1007/BF01954382. Eur J Pediatr. 1992. PMID: 1601011

8

Extreme variability of clinical symptoms among sibs in a MELAS family correlated with heteroplasmy for the mitochondrial A3243G mutation.

de Vries D, de Wijs I, Ruitenbeek W, Begeer J, Smit P, Bentlage H, van Oost B. de Vries D, et al. J Neurol Sci. 1994 Jun;124(1):77-82. doi: 10.1016/0022-510x(94)90014-0. J Neurol Sci. 1994. PMID: 7931425

9

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: bentlage ha. Eur J Pediatr. 1990 Dec;150(2):104-8. doi: 10.1007/BF02072049. Eur J Pediatr. 1990. PMID: 2279503

10

New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiency.

Dionisi-Vici C, Ruitenbeek W, Fariello G, Bentlage H, Wanders RJ, Schägger H, Bosman C, Piantadosi C, Sabetta G, Bertini E. Dionisi-Vici C, et al. Ann Neurol. 1997 Oct;42(4):661-5. doi: 10.1002/ana.410420419. Ann Neurol. 1997. PMID: 9382480 Free article.

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