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Author

Hossein Yousefimanesh

ORCID: 0009-0005-1829-5972
Observed ORCID: 0009-0005-1829-5972
OpenAlex ID: A5110540875
Distal Spinal Muscular Atrophy: An Overlooked Etiology of Weaning Failure in Children with Respiratory Insufficiency
2018 · Asgar Eghbalkhah, Kamyar Kamrani, et al. · Journal of Pediatric Intensive Care · 4
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A case of a 6-year-old girl with a rare compound heterozygous mutation of KCTD7 presenting with progressive myoclonic epilepsy
2024 · Reza Shervin Badv, Fakhreddin Shariatmadari, et al. · Egyptian Journal of Medical Human Genetics · 2
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Novel co-occurrence of SLC26A4 and KCTD7 variants in a pediatric patient with syndromic hearing loss and myoclonic epilepsy
2025 · Fakhreddin Shariatmadari, Amir Mahdi Mohamadi Kamal, et al. · Egyptian Journal of Medical Human Genetics · 1
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Progressive multifocal leukoencephalopathy in a 15-year-old boy with X-linked hyper-IgM syndrome: a case report
2026 · Saeedeh Delavari, Ali Pourvali, et al. · Journal of Medical Case Reports
Differentiation of Comorbid Neurodevelopmental Conditions in Pediatric Speech Delay: A Cross-Sectional Study
2026 · Mahmoud Reza Ashrafi, Morteza Heidari, et al. · Advances in Neurodevelopmental Disorders
Ataxia Telangiectasia with Giant Suprasellar Arachnoid Cyst - A Case Report and a Brief Review.
2025 · Mahmoud Reza Ashrafi, Ali Nikkhah, et al. · Iranian journal of child neurology.
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Brown-Vialetto-Van Laere Syndrome: Case Report of Dramatic Response to Riboflavin.
2025 · Morteza Heidari, Masood Ghahvechi Akbari, et al. · Iranian journal of child neurology.
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Exploring the Immunomics of Pediatric Glioma: Implications for Immune-based Therapeutics
2024 · Azadeh Kiumarsi, Mohamad Taha Ranji, et al.
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Works count: 8
Citation count: 7
H-index: 2
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