Items where Author is "Amiri, N."

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Ghosh, S. G. and Becker, K. and Huang, H. and Dixon-Salazar, T. and Chai, G. and Salpietro, V. and Al-Gazali, L. and Waisfisz, Q. and Wang, H. and Vaux, K. K. and Stanley, V. and Manole, A. and Akpulat, U. and Weiss, M. M. and Efthymiou, S. and Hanna, M. G. and Minetti, C. and Striano, P. and Pisciotta, L. and De Grandis, E. and Altmüller, J. and Nürnberg, P. and Thiele, H. and Yis, U. and Okur, T. D. and Polat, A. I. and Amiri, N. and Doosti, M. and Karimani, E. G. and Toosi, M. B. and Haddad, G. and Karakaya, M. and Wirth, B. and van Hagen, J. M. and Wolf, N. I. and Maroofian, R. and Houlden, H. and Cirak, S. and Gleeson, J. G. (2018) Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome. American Journal of Human Genetics, 103 (3). pp. 431-439.

Vahabzadeh, M. and Amiri, N. and Karimi, G. (2018) Effects of silymarin on metabolic syndrome: a review. Journal of the Science of Food and Agriculture, 98 (13). pp. 4816-4823.

Vona, B. and Maroofian, R. and Bellacchio, E. and Najafi, M. and Thompson, K. and Alahmad, A. and He, L. and Ahangari, N. and Rad, A. and Shahrokhzadeh, S. and Bahena, P. and Mittag, F. and Traub, F. and Movaffagh, J. and Amiri, N. and Doosti, M. and Boostani, R. and Shirzadeh, E. and Haaf, T. and Diodato, D. and Schmidts, M. and Taylor, R. W. and Karimiani, E. G. (2018) Expanding the clinical phenotype of IARS2-related mitochondrial disease. BMC medical genetics, 19 (1). p. 196.

This list was generated on Wed Aug 12 02:16:06 2020 EDT.