Bentlage HA - Search Results

1

Multiple deficiencies of mitochondrial DNA- and nuclear-encoded subunits of respiratory NADH dehydrogenase detected with peptide- and subunit-specific antibodies in mitochondrial myopathies.

Bentlage HA, Janssen AJ, Chomyn A, Attardi G, Walker JE, Schägger H, Sengers RC, Trijbels FJ. Bentlage HA, et al. Biochim Biophys Acta. 1995 Mar 8;1234(1):63-73. doi: 10.1016/0005-2736(94)00288-z. Biochim Biophys Acta. 1995. PMID: 7533543 Free article.

2

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

3

Immunoprecipitation of human mitochondrial translation products with peptide-specific antibodies.

Bentlage HA, Chomyn A. Bentlage HA, et al. Methods Enzymol. 1996;264:218-28. doi: 10.1016/s0076-6879(96)64022-1. Methods Enzymol. 1996. PMID: 8965695 No abstract available.

4

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

5

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. Neurology. 1996 Jul;47(1):243-8. doi: 10.1212/wnl.47.1.243. Neurology. 1996. PMID: 8710086 Free article.

6

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

7

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

8

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.

9

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

10

Relationship of genotype to phenotype in fibroblast-derived transmitochondrial cell lines carrying the 3243 mutation associated with the MELAS encephalomyopathy: shift towards mutant genotype and role of mtDNA copy number.

Bentlage HA, Attardi G. Bentlage HA, et al. Hum Mol Genet. 1996 Feb;5(2):197-205. doi: 10.1093/hmg/5.2.197. Hum Mol Genet. 1996. PMID: 8824875

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