Infantile Spasm: A Review Article

por TAGHDIRI, Mohammad Mahdi, NEMATI, Hamid
Publicado 2014

Causes and Factors Associated with Neonatal Seizure and its Short-term Outcome: A Retrospective Prognostic Cohort Study

por NEMATI, Hamid, KARIMZADEH, Parvaneh, FALLAHI, Minoo
Publicado 2018

Language development in Iranian children with epilepsy

por Nemati, Hamid, Jalalipour, Maryam, Niliyeh, Shadi, Maneshian, Behjat
Publicado 2020

Autistic feature as a presentation of Inborn Errors of Metabolism

por AHMADABADI, Farzad, NEMATI, Hamid, ABDOLMOHAMMADZADEH, Amirmohammad, AHADI, Adel
Publicado 2020

Cost-Effectiveness Analysis of Topiramate versus Phenobarbital in the Treatment of Children with Febrile Seizure

por NEMATI, Hamid, TALEBIANPOUR, Hamid, LOTFI, Farhad, SEPEHRI, Nazanin Zahra, KESHAVARZ, Khosro
Publicado 2019

Treatment of Child Gratification Disorder

por NEMATI, Hamid, AHMADABADI, Farzad, SHAHISAVANDI, Mina, FARJOUD KOUHANJANI, Mohsen, ROSTAMIHOSSEINKHANI, Mahtab
Publicado 2022

Pediatric Stroke in the Southern Region of Iran: A Retrospective Prognostic Cohort Study

por Nemati, Hamid, BEHRAD, Leila, Esmaeil Zadeh, Hossein, Mahdizadegan, Nima, Paktinat, Mohammad
Publicado 2023

Epidemiology of Severe Cutaneous Adverse Drug Reaction and Its HLA Association among Pediatrics

por Esmaeilzadeh, Hossein, Farjadian, Shirin, Alyasin, Soheila, Nemati, Hamid, Nabavizadeh, Hesamodin, Esmaeilzadeh, Elmira
Publicado 2019

Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports

por Dastsooz, Hassan, Nemati, Hamid, Fard, Mohammad Ali Farazi, Fardaei, Majid, Faghihi, Mohammad Ali
Publicado 2017

Evaluation of The Metabolic Syndrome Criteria And Body Composition in Ambulatory Children with Epilepsy UsingSodium Valproate and Carbamazepine In Southern Iran: A Case-Control Stu...

por INALOO, Soroor, SAKI, Forough, PAKTINAT, Mohammad, KATIBEH, Pegah, NEMATI, Hamid, RANJBAR OMRANI, Gholamhossein
Publicado 2020

A follow-up study of patients with COVID-19 presenting with seizures

por Asadi-Pooya, Ali A., Kouhanjani, Mohsen Farjoud, Nemati, Hamid, Emami, Amir, Javanmardi, Fatemeh
Publicado 2021

COVID-19 vaccine-related frequently asked questions (FAQs) by people with epilepsy and carers in Iran; educational video is included

por Asadi-Pooya, Ali A., Karimi, Afrooz, Razavizadegan, Seyed Mohammad Ali, Ashjazadeh, Nahid, Nemati, Hamid
Publicado 2022

The Effect of Family Empowerment Model on Quality of Life in Children with Epilepsy in South of Iran, 2018: A Randomized Controlled Clinical Trial

por NEMATI, Hamid, MAHDAVI KHANOUKI, Zahra, GHASEMPOUR, Mohammad, AMIRIFAR, Ahmad Ali, ALAEI KARAHROUDI, Fatemeh, GHOLAMI, Maryam
Publicado 2021

The relationship between maternal mental health and communication skills in children in Shiraz, Iran

por Maharlouei, Najmeh, Alibeigi, Hossein, Rezaianzadeh, Abbas, Keshavarz, Pedram, Raeisi Shahraki, Hadi, Nemati, Hamid, B. lankarani, Kamran
Publicado 2019

Case Report of RANBP2 Mutation and Familial Acute Necrotizing Encephalopathy

por Paktinat, Mohamad, Hessami, Kamran, Inaloo, Soroor, Nemati, Hamid, Katibeh, Pegah, Nejabat, Marzieh, Darabi, Mohammad Hassan, Bereshneh, Ali Hosseini
Publicado 2021

The Clinical Features and Diagnosis of Canavan’s Disease: A Case Series of Iranian Patients

por KARIMZADEH, Parvaneh, JAFARI, Narjes, NEJAD BIGLARI, Habibe, RAHIMIAN, Elham, AHMADABADI, Farzad, NEMATI, Hamid, NASEHI, Mohamad Mehdi, GHOFRANI, Mohammad, MOLLAMOHAMMADI, Mohsen
Publicado 2014

Case reports of juvenile GM1 gangliosidosisis type II caused by mutation in GLB1 gene

por Karimzadeh, Parvaneh, Naderi, Samaneh, Modarresi, Farzaneh, Dastsooz, Hassan, Nemati, Hamid, Farokhashtiani, Tayebeh, Shamsian, Bibi Shahin, Inaloo, Soroor, Faghihi, Mohammad Ali
Publicado 2017

Study on MRI Changes in Phenylketonuria in Patients Referred to Mofid Hospital/Iran

por KARIMZADEH, Parveneh, AHMADABADI, Farzad, JAFARI, Narjes, SHARIATMADARI, Fakhreddin, NEMATI, Hamid, AHADI, Adel, KARIMI DARDASHTI, Sanaz, MIRZARAHIMI, Mehrdad, DASTBORHAN, Zahra, ZARE NOGHABI, Javad
Publicado 2014

Genetic Testing in Various Neurodevelopmental Disorders Which Manifest as Cerebral Palsy: A Case Study From Iran

por Nejabat, Marzieh, Inaloo, Soroor, Sheshdeh, Afsaneh Taghipour, Bahramjahan, Shima, Sarvestani, Fatima Masoomi, Katibeh, Pegah, Nemati, Hamid, Tabei, Seyed Mohammad Bagher, Faghihi, Mohammad Ali
Publicado 2021

A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case report

por Ziyaee, Fateme, Shorafa, Eslam, Dastsooz, Hassan, Habibzadeh, Parham, Nemati, Hamid, Saeed, Amir, Silawi, Mohammad, Farazi Fard, Mohammad Ali, Faghihi, Mohammad Ali, Dastgheib, Seyed Alireza
Publicado 2019