Busch HF - Search Results

1

Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotype.

Scholte HR, Van Coster RN, de Jonge PC, Poorthuis BJ, Jeneson JA, Andresen BS, Gregersen N, de Klerk JB, Busch HF. Scholte HR, et al. Among authors: busch hf. Neuromuscul Disord. 1999 Jul;9(5):313-9. doi: 10.1016/s0960-8966(99)00032-2. Neuromuscul Disord. 1999. PMID: 10407852

2

Increased risk for cardiorespiratory failure associated with the A3302G mutation in the mitochondrial DNA encoded tRNALeu(UUR) gene.

van den Bosch BJ, de Coo IF, Hendrickx AT, Busch HF, de Jong G, Scholte HR, Smeets HJ. van den Bosch BJ, et al. Among authors: busch hf. Neuromuscul Disord. 2004 Oct;14(10):683-8. doi: 10.1016/j.nmd.2004.06.004. Neuromuscul Disord. 2004. PMID: 15351426

3

Vitamin-responsive pyruvate dehydrogenase deficiency in a young girl with external ophthalmoplegia, myopathy and lactic acidosis.

Scholte HR, Busch HF, Luyt-Houwen IE. Scholte HR, et al. Among authors: busch hf. J Inherit Metab Dis. 1992;15(3):331-4. doi: 10.1007/BF02435969. J Inherit Metab Dis. 1992. PMID: 1405466 No abstract available.

4

Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells.

Scholte HR, Busch HF, Luyt-Houwen IE, Vaandrager-Verduin MH, Przyrembel H, Arts WF. Scholte HR, et al. Among authors: busch hf. J Inherit Metab Dis. 1987;10 Suppl 1:81-97. doi: 10.1007/BF01812849. J Inherit Metab Dis. 1987. PMID: 2824921

5

Carnitine deficiency, mitochondrial dysfunction and the heart. Identical defect of oxidative phosphorylation in muscle mitochondria in cardiomyopathy due to carnitine loss and in Duchenne muscular dystrophy.

Scholte HR, Rodrigues Pereira R, Busch HF, Jennekens FG, Luyt-Houwen IE, Vaandrager-Verduin MH. Scholte HR, et al. Among authors: busch hf. Wien Klin Wochenschr. 1989 Jan 6;101(1):12-7. Wien Klin Wochenschr. 1989. PMID: 2913721

6

Exercise responses in patients with an enzyme deficiency in the mitochondrial respiratory chain.

Bogaard JM, Busch HF, Scholte HR, Stam H, Versprille A. Bogaard JM, et al. Among authors: busch hf. Eur Respir J. 1988 May;1(5):445-52. Eur Respir J. 1988. PMID: 3139446

7

Riboflavin-responsive complex I deficiency.

Scholte HR, Busch HF, Bakker HD, Bogaard JM, Luyt-Houwen IE, Kuyt LP. Scholte HR, et al. Among authors: busch hf. Biochim Biophys Acta. 1995 May 24;1271(1):75-83. doi: 10.1016/0925-4439(95)00013-t. Biochim Biophys Acta. 1995. PMID: 7599230 Free article.

8

Vitamin-responsive complex I deficiency in a myopathic patient with increased activity of the terminal respiratory chain and lactic acidosis.

Bakker HD, Scholte HR, Jeneson JA, Busch HF, Abeling NG, van Gennip AH. Bakker HD, et al. Among authors: busch hf. J Inherit Metab Dis. 1994;17(2):196-204. doi: 10.1007/BF00711617. J Inherit Metab Dis. 1994. PMID: 7967474

9

Rapid isolation of muscle and heart mitochondria, the lability of oxidative phosphorylation and attempts to stabilize the process in vitro by taurine, carnitine and other compounds.

Scholte HR, Yu Y, Ross JD, Oosterkamp II, Boonman AM, Busch HF. Scholte HR, et al. Among authors: busch hf. Mol Cell Biochem. 1997 Sep;174(1-2):61-6. Mol Cell Biochem. 1997. PMID: 9309666 Free article.

10

Oxidative phosphorylation in human muscle in patients with ocular myopathy and after general anaesthesia.

Scholte HR, Agsteribbe E, Busch HF, Hoogenraad TU, Jennekens FG, van Linge B, Luyt-Houwen IE, Ross JD, Ruiters MH, Verduin MH. Scholte HR, et al. Among authors: busch hf. Biochim Biophys Acta. 1990 Jul 25;1018(2-3):211-6. doi: 10.1016/0005-2728(90)90251-x. Biochim Biophys Acta. 1990. PMID: 2118384

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