Cargando…

We need well-designed multicenter studies to investigate neurologic manifestations of coronavirus disease 2019

Detalles Bibliográficos
Autores principales:	Ashrafi, Mahmoud Reza, Mohammadi, Mahmoud, Zamani, Gholamreza, Khosroshahi, Nahid, Badv, Reza Shervin, Tavasoli, Alireza, Heidari, Morteza, Yarali, Bahram, Azizimalamiri, Reza
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Tehran University of Medical Sciences 2020
Materias:	Letter to Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8185591/ http://dx.doi.org/10.18502/cjn.v19i3.5429

Ejemplares similares

The quality of life in children with spinal muscular atrophy: a case–control study
por: Zamani, Gholamreza, et al.
Publicado: (2022)

Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophy
por: Zamani, Gholamreza, et al.
Publicado: (2022)

Clonidine Versus Chloral Hydrate for Recording Sleep EEG in Children
por: ASHRAFI, Mahmoud Reza, et al.
Publicado: (2020)

Neurological and Vascular Manifestations of Ethylmalonic Encephalopathy
por: TAVASOLI, Ali Reza, et al.
Publicado: (2017)

Epilepsia Partialis Continua a Clinical Feature of a Missense Variant in the ADCK3 Gene and Poor Response to Therapy
por: Ashrafi, Mahmoud Reza, et al.
Publicado: (2022)

Childhood Guillain–Barre syndrome in the SARS‐CoV‐2 era: Is there any causative relation?
por: Pourbakhtyaran, Elham, et al.
Publicado: (2022)

Bilateral horizontal gaze palsy in an 8‐year‐old girl: A rare case with NDUFS4 gene mutation
por: Vafaee‐Shahi, Mohammad, et al.
Publicado: (2021)

Clinical and Paraclinical Screening for Celiac Disease in Children with Intractable Epilepsy
por: Ghazizadeh Esslami, Golnaz, et al.
Publicado: (2021)

Clinical and imaging outcomes after intrathecal injection of umbilical cord tissue mesenchymal stem cells in cerebral palsy: a randomized double-blind sham-controlled clinical trial
por: Amanat, Man, et al.
Publicado: (2021)

The Efficacy of the Ketogenic Diet in Improving Seizures and EEG Findings in Patients with Refractory Infantile Spasms
por: HANIFIHA, Melika, et al.
Publicado: (2022)

Downward Vertical Gaze Palsy As A Prominent Manifestation Of Episodic Ataxia Type 2: A Case Report
por: SHERVIN BADV, Reza, et al.
Publicado: (2013)

Expanding the genetic spectrum of giant axonal neuropathy: Two novel variants in Iranian families
por: Ashrafi, Mahmoud Reza, et al.
Publicado: (2023)

Neuralgic Amyotrophy with Cervical Root and Cranial Nerves Involvement in a Child
por: ASHRAFI shrafi, Mahmoud Reza, et al.
Publicado: (2019)

Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy (SMA-PME): three new cases and review of the mutational spectrum
por: Najafi, Ali, et al.
Publicado: (2023)

Hemi-ESES associated with agenesis of the corpus callosum and normal cognition
por: Mohammadi, Mahmoud, et al.
Publicado: (2019)

Sleep Inducing for EEG Recording in Children: A Comparison between Oral Midazolam and Chloral Hydrate
por: ASHRAFI, Mahmoud Reza, et al.
Publicado: (2013)

Comparison of Serum Zinc and Copper levels in Children and adolescents with Intractable and Controlled Epilepsy
por: KHERADMAND, Zeynab, et al.
Publicado: (2014)

CNS Structural Anomalies in Iranian Children with Global Developmental Delay
por: ZAMANI, Gholam Reza, et al.
Publicado: (2013)

Alexander Disease: Report of Two Unrelated Infantile Form Cases, Identified by GFAP Mutation Analysis and Review of Literature; The First Report from Iran
por: Ashrafi, Mahmoud-Reza, et al.
Publicado: (2013)

Diagnosis of an Abnormality in Brain MRI
por: Hosseini, Seyed-Ahmad, et al.
Publicado: (2014)

Cytomegalovirus Infection and Guillain-Barré Syndrome: The First Case-Control Study in Iran
por: Mamishi, Setareh, et al.
Publicado: (2021)

ACER3-related leukoencephalopathy: expanding the clinical and imaging findings spectrum due to novel variants
por: Dehnavi, Ali Zare, et al.
Publicado: (2021)

Tumefactive Multiple Sclerosis Variants: Report of Two Cases of Schilder and Balo Diseases
por: ASHRAFI, Mahmoud Reza, et al.
Publicado: (2017)

Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutations
por: Tavasoli, Ali Reza, et al.
Publicado: (2018)

Novel homozygous frameshift variant in the ATCAY gene in an Iranian patient with Cayman cerebellar ataxia; expanding the neuroimaging and clinical features: a case report
por: Siavashani, Elham Salehi, et al.
Publicado: (2023)

The Impact of Manual Ability Level on Participation of Children with Cerebral Palsy in Life Areas: A Cross-Sectional Study
por: PASHMDARFARD, Marzieh, et al.
Publicado: (2019)

The safety and efficacy of umbilical cord blood mononuclear cells in individuals with spastic cerebral palsy: a randomized double-blind sham-controlled clinical trial
por: Zarrabi, Morteza, et al.
Publicado: (2022)

Genetic testing of leukodystrophies unraveling extensive heterogeneity in a large cohort and report of five common diseases and 38 novel variants
por: Mahdieh, Nejat, et al.
Publicado: (2021)

Follow‐up of 25 patients with treatable ataxia: A comprehensive case series study
por: Ashrafi, Mahmoud Reza, et al.
Publicado: (2022)

Neurologic Manifestations of Childhood Rheumatic Diseases
por: SHIARI, Reza
Publicado: (2012)

Patterns of Antiepileptic Drug Reactions in Children: A Multicenter Study
por: SEDIGHI, Parinaz, et al.
Publicado: (2022)

Experimental Therapeutic Strategies in Epilepsies Using Anti-Seizure Medications
por: Rahim, Fakher, et al.
Publicado: (2021)

Differentiating Post–Digital Nannying Autism Syndrome from Autism Spectrum Disorders in Young Children: A Comparative Cross-Sectional Study
por: Pouretemad, Hamid Reza, et al.
Publicado: (2022)

Associations between Symptom Severity of Autism Spectrum Disorder and Screen Time among Toddlers Aged 16 to 36 Months
por: Sadeghi, Saeid, et al.
Publicado: (2023)

Pelizaeus–Merzbacher Disease: the First Genetically Approved Case Report from Iran
por: Ashrafi, Mahmoud-Reza, et al.
Publicado: (2011)

A comprehensive overview of SMN and NAIP copy numbers in Iranian SMA patients
por: Savad, Shahram, et al.
Publicado: (2023)

Vitamin D Supplementation for Premenstrual Syndrome-Related inflammation and antioxidant markers in students with vitamin D deficient: a randomized clinical trial
por: Heidari, Hajar, et al.
Publicado: (2019)

Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients
por: Dehnavi, Ali Zare, et al.
Publicado: (2023)

Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients
por: Dehnavi, Ali Zare, et al.
Publicado: (2023)

Assessment of genetic diversity among Iranian Aegilops triuncialis accessions using ISSR, SCoT, and CBDP markers
por: Khodaee, Lavin, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_phbn399jalffjka8k99jl6vmdq