Clinical presentations of mitochondrial cardiomyopathies von Lev, D, Nissenkorn, A, Leshinsky-Silver, E, Sadeh, M, Zeharia, A, Garty, B-Z, Blieden, L, Barash, V, Lerman-Sagie, T

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Critical phenomena in complex contagions von Barash, Vladimir, Cameron, Christopher, Macy, Michael

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Reduced body fat and increased hepatic lipid synthesis in mice bearing interleukin-6-secreting tumor von Metzger, S, Hassin, T, Barash, V, Pappo, O, Chajek-Shaul, T

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A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletion von Leshinsky-Silver, E, Michelson, M, Cohen, S, Ginsberg, M, Sadeh, M, Barash, V, Lerman-Sagie, T, Lev, D

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Neonatal liver failure and Leigh syndrome possibly due to CoQ-responsive OXPHOS deficiency von Leshinsky-Silver, E, Levine, A, Nissenkorn, A, Barash, V, Perach, M, Buzhaker, E, Shahmurov, M, Polak-Charcon, S, Lev, D, Lerman-Sagie, T

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Multiple presentation of mitochondrial disorders von Nissenkorn, Andreea, Zeharia, Avraham, Lev, Dorit, Fatal-Valevski, Aviva, Barash, Varda, Gutman, Alisa, Harel, Shaul, Lerman-Sagie, Tally

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Magneto-optical current sensor by domain wall motion in orthoferrites von Didosyan, Y.S., Hauser, H., Nicolics, J., Barash, V.Y., Fulmek, P.L.

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Identification of a common mutation (Gly194Cys) in both Arab Moslem and Ashkenazi Jewish patients with dihydrolipoamide dehydrogenase (E3) deficiency: Possible beneficial effect of... von Hong, Y. S., Korman, S. H., Lee, J., Ghoshal, P., Wu, Q., Barash, V., Kang, S., Oh, S., Kwon, M., Gutman, A., Rachmel, A., Patel, M. S.

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Insulin resistance in the NIDDM model Psammomys obesus in the normoglycaemic, normoinsulinaemic state von ZIV, E, KALMAN, R, HERSHKOP, K, BARASH, V, SHAFRIR, E, BAR-ON, H

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Interleukin-6 secretion in mice is associated with reduced glucose-6-phosphatase and liver glycogen levels von Metzger, S, Goldschmidt, N, Barash, V, Peretz, T, Drize, O, Shilyansky, J, Shiloni, E, Chajek-Shaul, T

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Hereditary branching enzyme dysfunction in adult polyglucosan body disease: A possible metabolic cause in two patients von Lossos, A., Barash, V., Soffer, D., Argov, Z., Gomori, M., Ben-Nariah, Z., Abramsky, O., Steiner, I.

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Complex I deficiency with diabetes, Fanconi syndrome and mtDNA deletion von Luder, A., Barash, V.

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The frequency of the C854 mutation in the aspartoacylase gene in Ashkenazi Jews in Israel von ELPELEG, O. N, ANIKSTER, Y, BARASH, V, BRANSKI, D, SHAAG, A

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Congenital lacticacidemia caused by lipoamide dehydrogenase deficiency with favorable outcome von Elpeleg, O.N., Ruitenbeek, W., Jakobs, C., Barash, V., De Vivo, D.C., Amir, N.

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Faraday effect in yttrium orthoferrite in the range 1280–1600 nm von Didosyan, Y.S., Barash, V.Y.

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Magnetic field sensor by orthoferrites von Didosyan, Y.S., Barash, V.Y., Bovarin, N.A., Hauser, H., Fulmek, P.

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Subsonic domain wall dynamics in yttrium orthoferrite von Didosyan, Y.S., Hauser, H., Barash, V.Y., Fulmek, P.L.

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Physical exercise enhances hepatic insulin signaling and inhibits phosphoenolpyruvate carboxykinase activity in diabetes-prone Psammomys obesus von Heled, Yuval, Shapiro, Yair, Shani, Yoav, Moran, Daniel S, Langzam, Lea, Barash, Varda, Sampson, Sanford R, Meyerovitch, Joseph

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Metabolic effects of nicotine on human adipose tissue in organ culture von Chajek-Shaul, T., Scherer, G., Barash, V., Shiloni, E., Caine, Y., Steins, O., Stein, Y.

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Neurologic Presentations of Mitochondrial Disorders von Nissenkorn, Andreea, Zeharia, Avraham, Lev, Dorit, Watemberg, Nathan, Fattal-Valevski, Aviva, Barash, Varda, Gutman, Alisa, Harel, Shaul, Lerman-Sagie, Tally

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