P Karimzadeh
Shahid Beheshti University of Medical Sciences
H-index: 19
Asia-Iran
Top articles of P Karimzadeh
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Psychometric Properties of the Persian Version of the Dizziness Handicap Inventory for Patient Caregivers in Children | BMC Pregnancy and Childbirth | Aazam Shakarami Mina Iravani Mojgan Mirghafourvand Mohammad Asghari Jafarabadi | 2021/12 |
GM1 and GM2-Gangliosidosis: Clinical Features, Neuroimaging Findings and electroencephalography | Iranian Journal of Child Neurology | Parvaneh Karimzadeh Masoomah Ebrahimi Korosh Etemad Farzad Ahmad Abadi Zahra Hosseini Nezhad | 2024/3/12 |
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population | Thyroid | Lucy X Ma Osvaldo Espin-Garcia Philippe L Bedard Tracy Stockley Rebecca Prince | 2022/6/1 |
Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review | Mohammad-Reza Ghasemi Sahand Tehrani Fateh Aysan Moeinafshar Hossein Sadeghi Parvaneh Karimzadeh | 2024/2/13 | |
Ophthalmic manifestations of biotinidase deficiency: report of a case and review of literature | Fatemeh Abdi Sadaf Parvin Vahid Zare Hosseinabadi Maryam Kachuei Arzhang Gordiz | 2024/1/26 | |
P604: Diagnostic utility of NGS testing in a highly consanguineous population: Findings from 1400+ Iranian patients with Mendelian disorders | Genetics in Medicine Open | Ayda Abolhassani Zohreh Fattahi Maryam Beheshtian Mahsa Fadaee Raheleh Vazehan | 2024/1/1 |
Identification of novel mutations in TPK1 and SLC19A3 genes in families exhibiting thiamine metabolism dysfunction syndrome | Heliyon | Fatemeh Norouzi Rostami Hossein Sadeghi Farzad Hashemi-Gorji Sahand Tehrani Fateh Reza Mirfakhraie | 2024/3/30 |
Neuropsychiatric Manifestations of COVID-19 in Hospitalized Pediatrics: A Multicenter Cross-sectional Study | Archives of Pediatric Infectious Diseases | Ghazal Zahed Parvaneh Karimzadeh Lawrence Sagin Wissow Soroor Arman Marzieh Babaee | 2023/1/31 |
Comparing Pregabalin and Sodium Valproate in Pediatric Migraine Prophylaxis: A Randomized Clinical Trial | Iranian Journal of Child Neurology | Narjes Jafari Mohammad Mehdi Nasehi Aiden Nasiri Eghbali Mohammad Mahdi Taghdiri Parvaneh Karimzadeh | 2023 |
The The Prevalence of Serum Anti Nuclear Antibodies in Children Treated With Anti-Epileptics | Acta Medica Iranica | Parvaneh Karimzadeh Reza Shiari Masoud Hassanvand Amouzadeh Samane Rahimi Shaghayegh Sadat Esmail Nejad | 2023/12/24 |
Evaluation of clinical and paraclinical findings in children with autoimmune encephalitis | Javad Mahdavi Seyedmousa Motavallihaghi Reza Ghasemikhah | 2022/12/1 | |
Alopecia areata-like pattern of baldness: the most recent update and the expansion of novel phenotype and genotype in the CTNNB1 gene | Neurological Sciences | Aysan Moeinafshar Sahand Tehrani Fateh Hossein Sadeghi Parvaneh Karimzadeh Reza Mirfakhraie | 2023/11 |
Clinical and genetic characterization of neuronal ceroid lipofuscinoses (NCLs) in 29 Iranian patients: identification of 11 novel mutations | Human Genetics | Samareh Panjeshahi Parvaneh Karimzadeh Abolfazl Movafagh Farzad Ahmadabadi Elham Rahimian | 2023/8 |
Megaconial congenital muscular dystrophy due to CHKB gene variants, the first report of thirteen Iranian patients | Neuromuscular Disorders | Fariba Zemorshidi Shahriar Nafissi Reza Boostani Ehsan Ghayoor Karimiani Bahram Haghi Ashtiani | 2023/7/1 |
A girl with myelopathy and vision loss, misdiagnosis as neuromyelitis optica spectrum disorder: the first Iranian case report on biotinidase deficiency | Iranian Journal of Pediatrics | Mohammadmahdi Nasehi Parvaneh Karimzadeh Aidin Tabrizi Meisam Babaei | 2022/8/31 |
Neuroimaging Findings of the High-risk Neonates and Infants Referred to Mofid Children’s Hospital | Iranian Journal of Child Neurology | Sasan Saket Parvaneh Karimzadeh Mohammad Mehdi Nasehi Mohammad Mehdi Taghdiri Minoo Falahi | 2022 |
Neurodegenerative disorder and diffuse brain calcifications due to FARSB mutation in two siblings | Clinical Case Reports | Parvaneh Karimzadeh Sepideh Rezakhani Mohammad Miryounesi Sahar Alijanpour | 2022/8 |
Babaei Z.(2022)“Adenylosuccinate lyase Deficiency (ADSL) and Report the First Case from Iran” | International Surgery Case Reports | P Karimzadeh Zahra H Nezhad M Keramatipour A Heidari M Khalili | 2022 |
Guillain-Barre syndrome in a child infected with COVID-19 | Archives of Pediatric Infectious Diseases | Sedigheh Rafiei Tabatabaei Ghazal Shariatpanahi Romina Azadkiya Parvaneh Karimzadeh Abdollah Karimi | 2022/4/30 |
Characterizing Genotypes and Phenotypes Associated with Dysfunction of Channel-Encoding Genes in a Cohort of Patients with Intellectual Disability | Archives of Iranian medicine | Naeim Ehtesham Meysam Mosallaei Maryam Beheshtian Shahrouz Khoshbakht Mahsa Fadaee | 2022/12 |
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