Items where Author is "Ashrafzadeh, F."

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Number of items: 11.

Article

Scala, M. and Chua, G. L. and Chin, C. F. and Alsaif, H. S. and Borovikov, A. and Riazuddin, S. and Riazuddin, S. and Chiara Manzini, M. and Severino, M. and Kuk, A. and Fan, H. and Jamshidi, Y. and Toosi, M. B. and Doosti, M. and Karimiani, E. G. and Salpietro, V. and Dadali, E. and Baydakova, G. and Konovalov, F. and Lozier, E. and O’Connor, E. and Sabr, Y. and Alfaifi, A. and Ashrafzadeh, F. and Striano, P. and Zara, F. and Alkuraya, F. S. and Houlden, H. and Maroofian, R. and Silver, D. L. (2020) Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features. European Journal of Human Genetics.

Rymen, D. and Lindhout, M. and Spanou, M. and Ashrafzadeh, F. and Benkel, I. and Betzler, C. and Coubes, C. and Hartmann, H. and Kaplan, J. D. and Ballhausen, D. and Koch, J. and Lotte, J. and Mohammadi, M. H. and Rohrbach, M. and Dinopoulos, A. and Wermuth, M. and Willis, D. and Brugger, K. and Wevers, R. A. and Boltshauser, E. and Bierau, J. and Mayr, J. A. and Wortmann, S. B. (2020) Expanding the clinical and genetic spectrum of CAD deficiency: an epileptic encephalopathy treatable with uridine supplementation. Genetics in Medicine.

Lekszas, C. and Nanda, I. and Vona, B. and Böck, J. and Ashrafzadeh, F. and Donyadideh, N. and Ebrahimzadeh, F. and Ahangari, N. and Maroofian, R. and Karimiani, E. G. and Haaf, T. (2019) Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: A case report. BMC Medical Genomics, 12 (1).

Ghaemi, N. and Hasanabadi, H. and Ashrafzadeh, F. and Sarvari, S. and Rahimi, H. and Hashemian, S. (2018) Peripheral neuropathy in children and adolescents with insulin-dependent diabetes mellitus. Iranian Journal of Child Neurology, 12 (2). pp. 83-90.

Boskabadi, H. and Ashrafzadeh, F. and Doosti, H. and Zakerihamidi, M. (2015) Assessment of risk factors and prognosis in asphyxiated infants. Iranian Journal of Pediatrics, 25 (4).

Boskabadi, H. and Ashrafzadeh, F. and Azarkish, F. and Khakshour, A. (2015) Complications of neonatal jaundice and the predisposing factors in newborns. Journal of Babol University of Medical Sciences, 17 (9). pp. 7-13.

Hashemian, S. and Ashrafzadeh, F. and Akhondian, J. and Beiraghi Toosi, M. (2015) Epstein-barr virus encephalitis: A case report. Iranian Journal of Child Neurology, 9 (1). pp. 107-110.

Hojjati, M. and Bejestani, G. S. and Ashrafzadeh, F. (2015) Investigation on the effectiveness of Holistic Multi-Dimensional Treatment Model (HMTM) in improvement of CARS test indicators in children suffering from autism spectrum disorder. International Journal of Pediatrics, 3 (2). pp. 543-553.

Livani, F. and Meibodi, N. and Rajabi, O. and Ashrafzadeh, F. and Layegh, P. (2013) Trichothiodystrophy: Role of a dermato-trchologist. International Journal of Trichology, 5 (2). pp. 102-103.

Ghandehari, K. and Ashrafzadeh, F. and Mood, Z. I. and Ebrahimzadeh, S. and Arabikhan, K. (2012) Development and validation of the Asian Migraine Criteria (AMC). Journal of Clinical Neuroscience, 19 (2). pp. 224-228.

Behmanesh, F. and Ashrafzadeh, F. and Varasteh, A. and Shakeri, A. and Shahsavand, S. (2012) Evaluation of Interleukin 1 β in febrile convulsion. Iranian Journal of Allergy, Asthma and Immunology, 11 (4). pp. 336-339.

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