IJ Radiology
An Innovative Journal in the Field of Radiology
Outlines
New Mutation of Pelizaeus-Merzbacher-Like Disease; A Report from Iran
Abstract
References
- 1.The references are available in PDF file.
Copyright
© 2014, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.
Similar Articles
Novel Gene LAMA2 Mutation and Exonic Deletion Underline Merosin-Deficient Congenital Muscular Dystrophy 1A in a Chinese Family
Liang L, Zhang Q, Gu X. Novel Gene LAMA2 Mutation and Exonic Deletion Underline Merosin-Deficient Congenital Muscular Dystrophy 1A in a Chinese Family. Inn J Pediatr. 2017;27(2):e1884. doi: https://doi.org/10.5812/ijp.1884
Identification of Two Siblings with PMM2-Congenital Disorder of Glycosylation Using Exome Sequencing in South East of Iran: Clinical and Genetic Findings
Mir A, Khajeh A, Song Y, Lee H, Tabatabaifar MA. Identification of Two Siblings with PMM2-Congenital Disorder of Glycosylation Using Exome Sequencing in South East of Iran: Clinical and Genetic Findings. Zahedan J Res Med Sci. 2026;28(2):e167519. doi: https://doi.org/10.5812/zjrms-167519
Pathological Variants of Aminoacyl-tRNA-synthetase-Interacting Multifunctional Protein 1 Gene in an Iranian Consanguineous Family With Autosomal Recessive Intellectual Disability
Cheraghee S, Moghbelinejad S, Najafipour R. Pathological Variants of Aminoacyl-tRNA-synthetase-Interacting Multifunctional Protein 1 Gene in an Iranian Consanguineous Family With Autosomal Recessive Intellectual Disability. J Inflamm Dis. 2024;23(6):e156189. doi:
Seizure as the Early and Main Manifestation of Infantile Vanishing White Matter Disease: A Case Report
Rezaei N, Nikbakht S, Ashrafi M, Rezaei Z, Mahdieh N, et al. Seizure as the Early and Main Manifestation of Infantile Vanishing White Matter Disease: A Case Report. Inn J Pediatr. 2018;28(2):e65620. doi: https://doi.org/10.5812/ijp.65620
An Asymptomatic Case of Megalencephalic Leukoencephalopathy with Subcortical Cysts
Kameli R, Barzegar M, Alizadeh H, Ashrafi MR, Sadeghvand S, et al. An Asymptomatic Case of Megalencephalic Leukoencephalopathy with Subcortical Cysts. Inn J Pediatr. 2019;29(4):e91110. doi: https://doi.org/10.5812/ijp.91110
Crossmark
Checking
- Scopus by DOI: 5
Last Update: 1 month ago
- Scopus by Title: 5
Last Update: 1 month ago
- Scopus by Title (Ref): 5
Last Update: 1 month ago
- CrossRef: 4
Last Update: 2 days ago
Ordering Reprints
Articles are published under the Creative Commons license stated on each article. No permission or royalty fee is required for uses permitted by that license. CCC handles optional bulk and customized reprint orders. Any quotation covers production and delivery services only, not copyright permission. > Request Reprints from CCC
Author(s):