Gutman A - Search Results

1

Recurrent metabolic decompensation in profound carnitine palmitoyltransferase II deficiency.

Elpeleg ON, Joseph A, Branski D, Christensen E, Holme E, Demaugre F, Saudubray JM, Gutman A. Elpeleg ON, et al. Among authors: gutman a. J Pediatr. 1993 Jun;122(6):917-9. doi: 10.1016/s0022-3476(09)90019-1. J Pediatr. 1993. PMID: 8501570

2

Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutation.

Spiegel R, Shaag A, Gutman A, Korman SH, Saada A, Elpeleg O, Shalev SA. Spiegel R, et al. Among authors: gutman a. J Inherit Metab Dis. 2007 Apr;30(2):266. doi: 10.1007/s10545-007-0536-8. Epub 2007 Feb 15. J Inherit Metab Dis. 2007. PMID: 17372854

3

Hypocarnitinemia in lysinuric protein intolerance.

Korman SH, Raas-Rothschild A, Elpeleg O, Gutman A. Korman SH, et al. Among authors: gutman a. Mol Genet Metab. 2002 May;76(1):81-3. doi: 10.1016/s1096-7192(02)00019-7. Mol Genet Metab. 2002. PMID: 12175786

4

Muscle carnitine deficiency in patients using valproic acid.

Shapira Y, Gutman A. Shapira Y, et al. Among authors: gutman a. J Pediatr. 1991 Apr;118(4 Pt 1):646-9. doi: 10.1016/s0022-3476(05)83396-7. J Pediatr. 1991. PMID: 2007943 No abstract available.

5

Propionic acidemia--biochemical studies.

Barash V, Elpeleg O, Amit R, Gottfried S, Yatziv S, Gutman A. Barash V, et al. Among authors: gutman a. Isr J Med Sci. 1989 Feb;25(2):103-6. Isr J Med Sci. 1989. PMID: 2495260

6

Novel metabolic and molecular findings in hepatic carnitine palmitoyltransferase I deficiency.

Korman SH, Waterham HR, Gutman A, Jakobs C, Wanders RJ. Korman SH, et al. Among authors: gutman a. Mol Genet Metab. 2005 Nov;86(3):337-43. doi: 10.1016/j.ymgme.2005.07.022. Epub 2005 Sep 16. Mol Genet Metab. 2005. PMID: 16146704

7

Carnitine palmitoyltransferase deficiency: a common cause of recurrent myoglobinuria.

Sadeh M, Gutman A. Sadeh M, et al. Among authors: gutman a. Isr J Med Sci. 1990 Sep;26(9):510-5. Isr J Med Sci. 1990. PMID: 2228562

8

Familial carnitine deficiency: further evidence for autosomal recessive transmission with variable expression.

Shahar E, Brand N, Shapira Y, Barash V, Gutman A. Shahar E, et al. Among authors: gutman a. J Neurol Neurosurg Psychiatry. 1988 Feb;51(2):298-300. doi: 10.1136/jnnp.51.2.298. J Neurol Neurosurg Psychiatry. 1988. PMID: 3346699 Free PMC article.

9

Muscle carnitine deficiency presenting as familial fatal cardiomyopathy.

Colin AA, Jaffe M, Shapira Y, Ne'eman Z, Gutman A, Korman S. Colin AA, et al. Among authors: gutman a. Arch Dis Child. 1987 Nov;62(11):1170-2. doi: 10.1136/adc.62.11.1170. Arch Dis Child. 1987. PMID: 3688923 Free PMC article.

10

Infantile idiopathic myopathic carnitine deficiency: treatment with L-carnitine.

Shapira Y, Glick B, Harel S, Vattin JJ, Gutman A. Shapira Y, et al. Among authors: gutman a. Pediatr Neurol. 1993 Jan-Feb;9(1):35-8. doi: 10.1016/0887-8994(93)90007-y. Pediatr Neurol. 1993. PMID: 8452598

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