Bornstein B - Search Results

1

A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibers.

Arenas J, Campos Y, Bornstein B, Ribacoba R, Martín MA, Rubio JC, Santorelli FM, Zeviani M, DiMauro S, Garesse R. Arenas J, et al. Among authors: bornstein b. Neurology. 1999 Jan 15;52(2):377-82. doi: 10.1212/wnl.52.2.377. Neurology. 1999. PMID: 9932960

2

Arylsulfatase A in urine of patients with urothelial tumors.

Arenas J, Mayor J, Gella FJ, Fraile B, Bornstein B, Jarillo MD, Martinez A, Santos I. Arenas J, et al. Among authors: bornstein b. Clin Biochem. 1988 Jan;21(1):73-7. doi: 10.1016/s0009-9120(88)80116-4. Clin Biochem. 1988. PMID: 2894259

3

[Recurrent myoglobinuria in a girl due to carnitine palmitoyltransferase deficiency].

Carrasco Marina LL, Ramos Lizana J, Vázquez López M, Garrote de Marcos JM, Arregui Sierra A, Bornstein B, Arenas J. Carrasco Marina LL, et al. Among authors: bornstein b. An Esp Pediatr. 1996 Jan;44(1):67-9. An Esp Pediatr. 1996. PMID: 8849066 Review. Spanish. No abstract available.

4

Cyclosporine nephrotoxicity and rejection crisis: diagnosis by urinary enzyme excretion.

Bornstein B, Arenas J, Morales JM, Praga M, Rodicio JL, Martinez A, Valdivieso L. Bornstein B, et al. Nephron. 1996;72(3):402-6. doi: 10.1159/000188903. Nephron. 1996. PMID: 8852487

5

Effects of L-carnitine on erythrocyte acyl-CoA, free CoA, and glycerophospholipid acyltransferase in uremia.

de los Reyes B, Navarro JA, Pérez-García R, Liras A, Campos Y, Bornstein B, Arenas J. de los Reyes B, et al. Among authors: bornstein b. Am J Clin Nutr. 1998 Mar;67(3):386-90. doi: 10.1093/ajcn/67.3.386. Am J Clin Nutr. 1998. PMID: 9497180 Clinical Trial.

6

Mitochondrial gene expression and respiratory enzyme activities in cardiac diseases.

Bornstein B, Huertas R, Ochoa P, Campos Y, Guillen F, Garesse R, Arenas J. Bornstein B, et al. Biochim Biophys Acta. 1998 Feb 27;1406(1):85-90. doi: 10.1016/s0925-4439(97)00076-8. Biochim Biophys Acta. 1998. PMID: 9545545 Free article.

7

[Human mitochondrial genetic system].

Enríquez JA, Martínez-Azorín F, Garesse R, López-Pérez MJ, Pérez-Martos A, Bornstein B, Montoya J. Enríquez JA, et al. Among authors: bornstein b. Rev Neurol. 1998 Apr;26 Suppl 1:S21-6. Rev Neurol. 1998. PMID: 9810587 Review. Spanish.

8

[Studies of pathogenicity and characterization of molecular phenotype caused by mutations in human mitochondrial DNA].

Bornstein B, Enríquez JA, Montoya J, Garesse R. Bornstein B, et al. Rev Neurol. 1998 Apr;26 Suppl 1:S36-43. Rev Neurol. 1998. PMID: 9810589 Review. Spanish.

9

Molecular analysis in Spanish patients with muscle carnitine palmitoyltransferase deficiency.

Martín MA, Rubio JC, De Bustos F, Del Hoyo P, Campos Y, García A, Börnstein B, Cabello A, Arenas J. Martín MA, et al. Among authors: bornstein b. Muscle Nerve. 1999 Jul;22(7):941-3. doi: 10.1002/(sici)1097-4598(199907)22:7<941::aid-mus20>3.0.co;2-z. Muscle Nerve. 1999. PMID: 10398215 Clinical Trial.

10

Structure and regulated expression of the delta-aminolevulinate synthase gene from Drosophila melanogaster.

Ruiz de Mena I, Fernández-Moreno MA, Bornstein B, Kaguni LS, Garesse R. Ruiz de Mena I, et al. Among authors: bornstein b. J Biol Chem. 1999 Dec 24;274(52):37321-8. doi: 10.1074/jbc.274.52.37321. J Biol Chem. 1999. PMID: 10601299 Free article.

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