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BMC Medical Genetics
|
August 20, 2017
Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports
Hassan Dastsooz, Hamid Nemati, Mohammad Ali Farazi Fard, et al.
Epilepsy & Behavior : E&B
|
June 13, 2022
COVID-19 vaccine-related frequently asked questions (FAQs) by people with epilepsy and carers in Iran; educational video is included
Ali A Asadi-Pooya, Afrooz Karimi, Seyed Mohammad Ali Razavizadegan, et al.
Journal of Autism and Developmental Disorders
|
June 27, 2025
Effects of Citicoline in Children with Autism Spectrum Disorder: A Randomized, Open-label Clinical Trial
Samaneh Zare, Hamid Reihani, Razieh Taghizadeh Sarvestani, et al.
Iranian Journal of Child Neurology
|
November 16, 2021
The Effect of Family Empowerment Model on Quality of Life in Children with Epilepsy in South of Iran, 2018: A Randomized Controlled Clinical Trial
Hamid Nemati, Zahra Mahdavi Khanouki, Mohammad Ghasempour, et al.
Epidemiology and Health
|
July 20, 2019
The relationship between maternal mental health and communication skills in children in Shiraz, Iran
Najmeh Maharlouei, Hossein Alibeigi, Abbas Rezaianzadeh, et al.
Journal of Bone and Mineral Metabolism
|
September 8, 2018
Bone mineral density loss in ambulatory children with epilepsy in spite of using supplemental vitamin D in Southern Iran: a case-control study
Soroor Inaloo, Mohammad Paktinat, Forough Saki, et al.
Pain Practice : the Official Journal of World Institute of Pain
|
September 23, 2022
Application of cinnarizine in migraine prevention: A systematic review and meta-analysis
Mohammad Shafie'ei, Mohsen Farjoud Kouhanjani, Zahra Akbari, et al.
International Journal of Pediatrics
|
March 29, 2021
Case Report of RANBP2 Mutation and Familial Acute Necrotizing Encephalopathy
Mohamad Paktinat, Kamran Hessami, Soroor Inaloo, et al.
BMC Medical Genetics
|
July 19, 2017
Case reports of juvenile GM1 gangliosidosisis type II caused by mutation in GLB1 gene
Parvaneh Karimzadeh, Samaneh Naderi, Farzaneh Modarresi, et al.
Iranian Journal of Child Neurology
|
February 7, 2015
The Clinical Features and Diagnosis of Canavan's Disease: A Case Series of Iranian Patients
Parvaneh Karimzadeh, Narjes Jafari, Habibe Nejad Biglari, et al.
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of 5
Search research articles
Search
Showing results (21-30 of 46) with videos related to
Sort By:
Page
of 5
BMC Medical Genetics
|
August 20, 2017
Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports
Hassan Dastsooz, Hamid Nemati, Mohammad Ali Farazi Fard, et al.
Epilepsy & Behavior : E&B
|
June 13, 2022
COVID-19 vaccine-related frequently asked questions (FAQs) by people with epilepsy and carers in Iran; educational video is included
Ali A Asadi-Pooya, Afrooz Karimi, Seyed Mohammad Ali Razavizadegan, et al.
Journal of Autism and Developmental Disorders
|
June 27, 2025
Effects of Citicoline in Children with Autism Spectrum Disorder: A Randomized, Open-label Clinical Trial
Samaneh Zare, Hamid Reihani, Razieh Taghizadeh Sarvestani, et al.
Iranian Journal of Child Neurology
|
November 16, 2021
The Effect of Family Empowerment Model on Quality of Life in Children with Epilepsy in South of Iran, 2018: A Randomized Controlled Clinical Trial
Hamid Nemati, Zahra Mahdavi Khanouki, Mohammad Ghasempour, et al.
Epidemiology and Health
|
July 20, 2019
The relationship between maternal mental health and communication skills in children in Shiraz, Iran
Najmeh Maharlouei, Hossein Alibeigi, Abbas Rezaianzadeh, et al.
Journal of Bone and Mineral Metabolism
|
September 8, 2018
Bone mineral density loss in ambulatory children with epilepsy in spite of using supplemental vitamin D in Southern Iran: a case-control study
Soroor Inaloo, Mohammad Paktinat, Forough Saki, et al.
Pain Practice : the Official Journal of World Institute of Pain
|
September 23, 2022
Application of cinnarizine in migraine prevention: A systematic review and meta-analysis
Mohammad Shafie'ei, Mohsen Farjoud Kouhanjani, Zahra Akbari, et al.
International Journal of Pediatrics
|
March 29, 2021
Case Report of RANBP2 Mutation and Familial Acute Necrotizing Encephalopathy
Mohamad Paktinat, Kamran Hessami, Soroor Inaloo, et al.
BMC Medical Genetics
|
July 19, 2017
Case reports of juvenile GM1 gangliosidosisis type II caused by mutation in GLB1 gene
Parvaneh Karimzadeh, Samaneh Naderi, Farzaneh Modarresi, et al.
Iranian Journal of Child Neurology
|
February 7, 2015
The Clinical Features and Diagnosis of Canavan's Disease: A Case Series of Iranian Patients
Parvaneh Karimzadeh, Narjes Jafari, Habibe Nejad Biglari, et al.
Page
of 5