Börnstein B - Search Results

1

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.

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

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

8

The pathogenic role of point mutations affecting the translational initiation codon of mitochondrial genes.

Fernández-Moreno MA, Bornstein B, Campos Y, Arenas J, Garesse R. Fernández-Moreno MA, et al. Among authors: bornstein b. Mol Genet Metab. 2000 Jul;70(3):238-40. doi: 10.1006/mgme.2000.3005. Mol Genet Metab. 2000. PMID: 10924280

9

Myocardial carnitine and carnitine palmitoyltransferase deficiencies in patients with severe heart failure.

Martín MA, Gómez MA, Guillén F, Börnstein B, Campos Y, Rubio JC, de la Calzada CS, Arenas J. Martín MA, et al. Among authors: bornstein b. Biochim Biophys Acta. 2000 Nov 15;1502(3):330-6. doi: 10.1016/s0925-4439(00)00061-2. Biochim Biophys Acta. 2000. PMID: 11068176 Free article.

10

Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II gene.

Campos Y, García-Redondo A, Fernández-Moreno MA, Martínez-Pardo M, Goda G, Rubio JC, Martín MA, del Hoyo P, Cabello A, Bornstein B, Garesse R, Arenas J. Campos Y, et al. Among authors: bornstein b. Ann Neurol. 2001 Sep;50(3):409-13. doi: 10.1002/ana.1141. Ann Neurol. 2001. PMID: 11558799

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