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Journal of Neurosurgery. Case Lessons|April 7, 2025
Concurrent glial tumors in the setting of a nonsyndromic adjacent/colliding meningioma: illustrative casesAhmad Pour-Rashidi, Fada Hossein Nahang, Peyman Gookizadeh, et al.
Clinical Case Reports|August 24, 2023
Co-occurrence of celiac disease and glycogen storage disease in a five-year-old patient with diabetes mellitus; a case reportSina Khani, Amirali Soheili, Seyed Mohammad Vahabi, et al.
Muscle & Nerve|September 21, 2016
Late-onset pompe disease in Iran: A clinical and genetic reportFerdos Nazari, Farnaz Sinaei, Yalda Nilipour, et al.
Neuromuscular Disorders : NMD|January 9, 2024
Neutral lipid storage disease with myopathy: clinicopathological and genetic features of nine Iranian patientsHamed Shahriyari, Mahtab Ramezani, Yalda Nilipour, et al.
Neuromuscular Disorders : NMD|January 15, 2026
Clinical and molecular spectrum of an Iranian Charcot-Marie-Tooth 2T cohort, and the diagnostic importance of whole exome sequencing in identifying co-occurrence inherited disordersZahra Salami, Mahsa Mohammadi, Aida Ghasemi, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|June 26, 2024
Phenotypic and genotyping spectrum of two Iranian cases with RBCK1-associated polyglucosan body myopathyMarzieh Babaee, Yalda Nilipour, Sahar Alijanpour, et al.
Expert Review of Neurotherapeutics|December 13, 2019
An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophiesMahmoud Reza Ashrafi, Man Amanat, Masoud Garshasbi, et al.
Basic and Clinical Neuroscience|November 22, 2017
A Mitochondrial Disorder in a Middle Age Iranian Patient: Report of a Rare CaseMostafa Almasi, Mohammad Reza Motamed, Masoud Mehrpour, et al.
Iranian Journal of Child Neurology|September 21, 2020
A dermatopathic Juvenile Dermatomyositis; An Unexpected Case in ChildhoodMehrnoush Hassas Yeganeh, Pooria Ahmadi, Yalda Nilipour, et al.
BMC Musculoskeletal Disorders|March 28, 2024
A novel homozygous variant (c.5876T > C: p. Leu1959Pro) in DYSF segregates with limb-girdle muscular dystrophy: a case reportHamed Hesami, Serwa Ghasemi, Golnaz Houshmand, et al.
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