Showing 1 - 19 results of 19 for search 'Najafi, M', query time: 0.07s
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Different presentations of congenital gastrointestinal obstructions: a report of five cases by Najafi M, Abbaslou P
Published 2009-02-01
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Drug withdrawal in patients with epilepsy: Prognostic value of the EEG by Najafi M, Tamizi Far B
Published 2001-10-01
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Tempering of deformed and as-quenched martensite in structural steel by Najafi M., Mirzadeh H., Alibeyki M.
Published 2019-01-01
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CYTOGENETIC FINDINGS IN ACUTE MYELOID LEUKEMIA by Gh. Toogeh, A. H. Najafi M. Keyhani
Published 2003-12-01
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CYTOGENETIC FINDINGS IN ACUTE MYELOID LEUKEMIA by Gh. Toogeh, A. H. Najafi M. Keyhani
Published 2003-08-01
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Similarity learning for dense label transfer by Najafi, M, Kulharia, V, Ajanthan, T, Torr, P
Published 2018Conference item -
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The Mechanisms of Radiation-Induced Bystander Effect by Najafi M, Fardid R, Hadadi Gh, Fardid M
Published 2014-12-01
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Expression levels of the BAK1 and BCL2 genes highlight the role of apoptosis in age-related hearing impairment by Falah M, Najafi M, Houshm, M, Farhadi M
Published 2016-07-01
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Curcumin Protects Against Radiotherapy-Induced Oxidative Injury to the Skin by Shabeeb D, Musa AE, Abd Ali HS, Najafi M
Published 2020-08-01
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Prognostic value of intrathecal IgG synthesis in multiple sclerosis: a study in 54 patients by Aghamohammadi A, Najafi M R, Ghaffarpour M, Najafi F, Saadatnia M H
Published 2008-06-01
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The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusis by Falah M, Houshmand M, Najafi M, Balali M, Mahmoudian S, Asghari A, Emamdjomeh H, Farhadi M
Published 2016-10-01
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Anti-Müllerian hormone as a predictor of IVF treatment by Mehrafza M, Raoufi A, Abdollahian P, Nikpouri Z, Shadmani K, Najafi M, Vojoudi E, Hosseini A
Published 2012-09-01
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Radioactive decays of highly-charged ions by Gao B. S., Najafi M. A., Atanasov D. R., Blaum K., Bosch F., Brandau C., Chen X. C., Dillmann I., Dimopoulou Ch., Faestermann Th., Geissel H., Gernhäuser R., Hillenbrand P.-M., Kovalenko O., Kozhuharov C., Litvinov S. A., Litvinov Yu. A., Maier L., Nolden F., Piotrowski J., Sanjari M. S., Scheidenberger C., Spillmann U., Steck M., Stöhlker Th., Trageser Ch., Tu X. L., Weick H., Winckler N., Xu H. S., Yamaguchi T., Yan X. L., Zhang Y. H., Zhou X. H.
Published 2015-01-01
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Homozygous missense variants in NTNG2, encoding a presynaptic netrin-G2 adhesion protein, lead to a distinct neurodevelopmental disorder by Dias, CM, Punetha, J, Zheng, C, Mazaheri, N, Rad, A, Efthymiou, S, Petersen, A, Dehghani, M, Pehlivan, D, Partlow, JN, Posey, JE, Salpietro, V, Gezdirici, A, Malamiri, RA, Menabawy, NM, Selim, LA, Mehrjardi, MY, Banu, S, Polla, DL, Yang, E, Varaghchi, J, Mitani, T, Van Beusekom, E, Najafi, M, Sedaghat, A, Keller-Ramey, J, Durham, L, Coban-Akdemir, Z, Karaca, E, Orlova, V, Schaeken, LLM, Sherafat, A, Jhangiani, SN, Stanley, V, Shariati, G, Galehdari, H, Gleeson, JG, Walsh, CA, Lupski, JR, Seiradake, E, Houlden, H, Van Bokhoven, H, Maroofian, R
Published 2019Journal article