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Multiple presentation of mitochondrial disorders.
Nissenkorn A, Zeharia A, Lev D, Fatal-Valevski A, Barash V, Gutman A, Harel S, Lerman-Sagie T. Nissenkorn A, et al. Among authors: gutman a. Arch Dis Child. 1999 Sep;81(3):209-14. doi: 10.1136/adc.81.3.209. Arch Dis Child. 1999. PMID: 10451392 Free PMC article.
Neurologic presentations of mitochondrial disorders.
Nissenkorn A, Zeharia A, Lev D, Watemberg N, Fattal-Valevski A, Barash V, Gutman A, Harel S, Lerman-Sagie T. Nissenkorn A, et al. Among authors: gutman a. J Child Neurol. 2000 Jan;15(1):44-8. doi: 10.1177/088307380001500110. J Child Neurol. 2000. PMID: 10641610
Transient 'primary' carnitine deficiency.
Lerman-Sagie T, Meshulach I, Gutman A. Lerman-Sagie T, et al. Among authors: gutman a. J Inherit Metab Dis. 1998 Jun;21(4):425-6. doi: 10.1023/a:1005366927461. J Inherit Metab Dis. 1998. PMID: 9700601 No abstract available.
Glycogen storage disease type II in Israel.
Bashan N, Potashnik R, Barash V, Gutman A, Moses SW. Bashan N, et al. Among authors: gutman a. Isr J Med Sci. 1988 Apr-May;24(4-5):224-7. Isr J Med Sci. 1988. PMID: 3132435
390 results