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Showing 1 to 12 of 14 entries
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Griscelli syndrome: a case report.

Iranian journal of child neurology

Mansouri Nejad SE, Yazdan Panah MJ, Tayyebi Meibodi N, Ashraf Zadeh F, Akhondian J, Beiraghi Toosi M, Eslamieh H.
PMID: 25657774
Iran J Child Neurol. 2014;8(4):72-5.

OBJECTIVE: Griscelli syndrome (GS) is a rare autosomal recessive immune deficiency disorder that presents with pigmentary dilution of the skin and hair, recurrent skin and pulmonary infections, neurologic problems, hypogammaglobulinemia, and variable cellular immunodeficiency. Three mutations have been described...

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Mansouri Nejad SE, Yazdan Panah MJ, Tayyebi Meibodi N, et al. Griscelli syndrome: a case report. Iran J Child Neurol. 2014;8(4):72-5
Mansouri Nejad, S. E., Yazdan Panah, M. J., Tayyebi Meibodi, N., Ashraf Zadeh, F., Akhondian, J., Beiraghi Toosi, M., & Eslamieh, H. (2014). Griscelli syndrome: a case report. Iranian journal of child neurology, 8(4), 72-5.
Mansouri Nejad, Seyed Ebrahim, et al. "Griscelli syndrome: a case report." Iranian journal of child neurology vol. 8,4 (2014): 72-5.
Mansouri Nejad SE, Yazdan Panah MJ, Tayyebi Meibodi N, Ashraf Zadeh F, Akhondian J, Beiraghi Toosi M, Eslamieh H. Griscelli syndrome: a case report. Iran J Child Neurol. 2014;8(4):72-5. PMID: 25657774; PMCID: PMC4307372.
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Homocystinuria: A Rare Disorder Presenting as Cerebral Sinovenous Thrombosis.

Iranian journal of child neurology

Eslamiyeh H, Ashrafzadeh F, Akhondian J, Beiraghi Toosi M.
PMID: 26221164
Iran J Child Neurol. 2015;9(2):53-7.

Objective Homocystinuria is an inborn error of amino acid metabolism caused by cystathionine beta-synthase deficiency that affects methionine metabolism. The clinical features are heterogeneous ranging from mental retardation, ectopia lentis, and osteoporosis to vascular events such as deep vein...

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Eslamiyeh H, Ashrafzadeh F, Akhondian J, et al. Homocystinuria: A Rare Disorder Presenting as Cerebral Sinovenous Thrombosis. Iran J Child Neurol. 2015;9(2):53-7
Eslamiyeh, H., Ashrafzadeh, F., Akhondian, J., & Beiraghi Toosi, M. (2015). Homocystinuria: A Rare Disorder Presenting as Cerebral Sinovenous Thrombosis. Iranian journal of child neurology, 9(2), 53-7.
Eslamiyeh, Hossein, et al. "Homocystinuria: A Rare Disorder Presenting as Cerebral Sinovenous Thrombosis." Iranian journal of child neurology vol. 9,2 (2015): 53-7.
Eslamiyeh H, Ashrafzadeh F, Akhondian J, Beiraghi Toosi M. Homocystinuria: A Rare Disorder Presenting as Cerebral Sinovenous Thrombosis. Iran J Child Neurol. 2015;9(2):53-7. PMID: 26221164; PMCID: PMC4515342.
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Psychological Signs as the Only Presentation of Wilson's Disease in an 11-Year-Old Boy.

Iranian journal of child neurology

Beiraghi Toosi M, Akhondian J, Ashraf Zadeh F, Donyadideh N, Javid A.
PMID: 29696053
Iran J Child Neurol. 2018;12(2):113-116.

Wilson's disease (WD) is a rare autosomal recessive disease due to copper metabolism disturbance. The clinical presentation spectrum of Wilson's disease is wide and initial findings of the disease depend on the organ involved. Neurologic disorders can develop insidiously...

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Beiraghi Toosi M, Akhondian J, Ashraf Zadeh F, et al. Psychological Signs as the Only Presentation of Wilson's Disease in an 11-Year-Old Boy. Iran J Child Neurol. 2018;12(2):113-116
Beiraghi Toosi, M., Akhondian, J., Ashraf Zadeh, F., Donyadideh, N., & Javid, A. (2018). Psychological Signs as the Only Presentation of Wilson's Disease in an 11-Year-Old Boy. Iranian journal of child neurology, 12(2), 113-116.
Beiraghi Toosi, Mehran, et al. "Psychological Signs as the Only Presentation of Wilson's Disease in an 11-Year-Old Boy." Iranian journal of child neurology vol. 12,2 (2018): 113-116.
Beiraghi Toosi M, Akhondian J, Ashraf Zadeh F, Donyadideh N, Javid A. Psychological Signs as the Only Presentation of Wilson's Disease in an 11-Year-Old Boy. Iran J Child Neurol. 2018;12(2):113-116. PMID: 29696053; PMCID: PMC5904746.
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Levetiracetam (levebel) Versus Carbamazepine Monotherapy for Focal Epilepsy in Children: A randomized clinical trial.

Iranian journal of child neurology

Akhondian J, Ashrafzadeh F, Eslamiyeh H.
PMID: 32256625
Iran J Child Neurol. 2020;14(2):69-77.

OBJECTIVE: This study aimed at comparing the effect of a newly approved drug leveitiracetam (LEV) versus carbamazepine (CBZ) in the treatment of childhood focal epilepsy.METHODS & MATERIALS: The study population included newly diagnosed children with focal epilepsy (1-16 years...

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Akhondian J, Ashrafzadeh F, Eslamiyeh H. Levetiracetam (levebel) Versus Carbamazepine Monotherapy for Focal Epilepsy in Children: A randomized clinical trial. Iran J Child Neurol. 2020;14(2):69-77
Akhondian, J., Ashrafzadeh, F., & Eslamiyeh, H. (2020). Levetiracetam (levebel) Versus Carbamazepine Monotherapy for Focal Epilepsy in Children: A randomized clinical trial. Iranian journal of child neurology, 14(2), 69-77.
Akhondian, Javad, et al. "Levetiracetam (levebel) Versus Carbamazepine Monotherapy for Focal Epilepsy in Children: A randomized clinical trial." Iranian journal of child neurology vol. 14,2 (2020): 69-77.
Akhondian J, Ashrafzadeh F, Eslamiyeh H. Levetiracetam (levebel) Versus Carbamazepine Monotherapy for Focal Epilepsy in Children: A randomized clinical trial. Iran J Child Neurol. 2020;14(2):69-77. PMID: 32256625; PMCID: PMC7085127.
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Joubert syndrome in three children in a family: a case series.

Iranian journal of child neurology

Akhondian J, Ashrafzadeh F, Beiraghi Toosi M, Moazen N, Mohammadpoor T, Karami R.
PMID: 24665289
Iran J Child Neurol. 2013;7(1):39-42.

Joubert syndrome (JS) is a rare autosomal recessive central nervous system malformation characterized by hypoplasia of the cerebellar vermis, hypotonia and abnormal psychomotor development, along with altered respiratory pattern and various ophthalmologic features. Here, we describe three children with...

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Akhondian J, Ashrafzadeh F, Beiraghi Toosi M, et al. Joubert syndrome in three children in a family: a case series. Iran J Child Neurol. 2013;7(1):39-42
Akhondian, J., Ashrafzadeh, F., Beiraghi Toosi, M., Moazen, N., Mohammadpoor, T., & Karami, R. (2013). Joubert syndrome in three children in a family: a case series. Iranian journal of child neurology, 7(1), 39-42.
Akhondian, Javad, et al. "Joubert syndrome in three children in a family: a case series." Iranian journal of child neurology vol. 7,1 (2013): 39-42.
Akhondian J, Ashrafzadeh F, Beiraghi Toosi M, Moazen N, Mohammadpoor T, Karami R. Joubert syndrome in three children in a family: a case series. Iran J Child Neurol. 2013;7(1):39-42. PMID: 24665289; PMCID: PMC3943079.
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Angelman Syndrome: A Case Report.

Iranian journal of child neurology

Ashrafzadeh F, Sadrnabavi A, Akhondian J, Beiraghi Toosi M, Mohammadi M, Hassanpour K.
PMID: 27247589
Iran J Child Neurol. 2016;10(2):86-9.

Objective Angelman syndrome (AS) is a neurodevelopmental disorder presented by jerky movement, speech delay and cognitive disability epilepsy as well as dysmorphic features. It occurs due to an expression deletion in 15q11-q13 chromosome. In this article, we present an...

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Ashrafzadeh F, Sadrnabavi A, Akhondian J, et al. Angelman Syndrome: A Case Report. Iran J Child Neurol. 2016;10(2):86-9
Ashrafzadeh, F., Sadrnabavi, A., Akhondian, J., Beiraghi Toosi, M., Mohammadi, M., & Hassanpour, K. (2016). Angelman Syndrome: A Case Report. Iranian journal of child neurology, 10(2), 86-9.
Ashrafzadeh, Farah, et al. "Angelman Syndrome: A Case Report." Iranian journal of child neurology vol. 10,2 (2016): 86-9.
Ashrafzadeh F, Sadrnabavi A, Akhondian J, Beiraghi Toosi M, Mohammadi M, Hassanpour K. Angelman Syndrome: A Case Report. Iran J Child Neurol. 2016;10(2):86-9. PMID: 27247589; PMCID: PMC4885160.
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Epstein-barr virus encephalitis: a case report.

Iranian journal of child neurology

Hashemian S, Ashrafzadeh F, Akhondian J, Beiraghi Toosi M.
PMID: 25767548
Iran J Child Neurol. 2015;9(1):107-10.

Many neurologic manifestations of Epstein-Barr virus (EBV) infection have been documented, including encephalitis, aseptic meningitis, transverse myelitis, and Guillain-Barre syndrome. These manifestations can occur alone or coincidentally with the clinical picture of infectious mononucleosis. EBV encephalitis is rare and...

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Hashemian S, Ashrafzadeh F, Akhondian J, et al. Epstein-barr virus encephalitis: a case report. Iran J Child Neurol. 2015;9(1):107-10
Hashemian, S., Ashrafzadeh, F., Akhondian, J., & Beiraghi Toosi, M. (2015). Epstein-barr virus encephalitis: a case report. Iranian journal of child neurology, 9(1), 107-10.
Hashemian, Somayh, et al. "Epstein-barr virus encephalitis: a case report." Iranian journal of child neurology vol. 9,1 (2015): 107-10.
Hashemian S, Ashrafzadeh F, Akhondian J, Beiraghi Toosi M. Epstein-barr virus encephalitis: a case report. Iran J Child Neurol. 2015;9(1):107-10. PMID: 25767548; PMCID: PMC4322508.
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Comparative Study of Hearing Impairment among Healthy and Intensive Care unit Neonates in Mashhad, North East Iran.

Iranian journal of otorhinolaryngology

Farhat A, Ghasemi MM, Akhondian J, Mohammadzadeh A, Esmaeili H, Amiri R, Raoof Saeb AA, Tale MR, Madani Sani F.
PMID: 26788475
Iran J Otorhinolaryngol. 2015 Jul;27(81):273-7.

INTRODUCTION: According to World Health Organization (WHO) 2001 statistics, hearing disorders are the most common congenital disease, and the incidence rate among high-risk newborns is as much as ten times as high as that in healthy neonates. However, 78%...

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Farhat A, Ghasemi MM, Akhondian J, et al. Comparative Study of Hearing Impairment among Healthy and Intensive Care unit Neonates in Mashhad, North East Iran. Iran J Otorhinolaryngol. 2015;27(81):273-7
Farhat, A., Ghasemi, M. M., Akhondian, J., Mohammadzadeh, A., Esmaeili, H., Amiri, R., Raoof Saeb, A. A., Tale, M. R., & Madani Sani, F. (2015). Comparative Study of Hearing Impairment among Healthy and Intensive Care unit Neonates in Mashhad, North East Iran. Iranian journal of otorhinolaryngology, 27(81), 273-7.
Farhat, Ahmadshah, et al. "Comparative Study of Hearing Impairment among Healthy and Intensive Care unit Neonates in Mashhad, North East Iran." Iranian journal of otorhinolaryngology vol. 27,81 (2015): 273-7.
Farhat A, Ghasemi MM, Akhondian J, Mohammadzadeh A, Esmaeili H, Amiri R, Raoof Saeb AA, Tale MR, Madani Sani F. Comparative Study of Hearing Impairment among Healthy and Intensive Care unit Neonates in Mashhad, North East Iran. Iran J Otorhinolaryngol. 2015 Jul;27(81):273-7. PMID: 26788475; PMCID: PMC4710879.
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Evidence based medicine in pediatric practice: brief review.

Iranian journal of pediatrics

Kianifar HR, Akhondian J, Najafi-Sani M, Sadeghi R.
PMID: 23056715
Iran J Pediatr. 2010 Sep;20(3):261-8.

Practicing medicine according to the best evidence is gaining popularity in the medical societies. Although this concept, which is usually called Evidence Based Medicine (EBM) has been explained in many resources, it has not been addressed enough in pediatrics....

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Kianifar HR, Akhondian J, Najafi-Sani M, et al. Evidence based medicine in pediatric practice: brief review. Iran J Pediatr. 2010;20(3):261-8
Kianifar, H. R., Akhondian, J., Najafi-Sani, M., & Sadeghi, R. (2010). Evidence based medicine in pediatric practice: brief review. Iranian journal of pediatrics, 20(3), 261-8.
Kianifar, Hamid-Reza, et al. "Evidence based medicine in pediatric practice: brief review." Iranian journal of pediatrics vol. 20,3 (2010): 261-8.
Kianifar HR, Akhondian J, Najafi-Sani M, Sadeghi R. Evidence based medicine in pediatric practice: brief review. Iran J Pediatr. 2010 Sep;20(3):261-8. PMID: 23056715; PMCID: PMC3446038.
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Prevalence and risk factors of seizure in children with acute bacterial meningitis: updating previous evidence using an epidemiological design.

Iranian journal of child neurology

Ataei Nakhaei A, Bakhtiari E, Ghahremani S, Akhondian J, Sasan MS, Movahed M, Aelami MH.
PMID: 34282362
Iran J Child Neurol. 2021;15(3):47-54. doi: 10.22037/ijcn.v15i2.22250.

OBJECTIVE: The current study aimed to investigate the prevalence and risk factors of seizure in acute bacterial meningitis.MATERIALS & METHODS: In the present study, a total of 180 children (age range, 2 months to 14 years) with acute bacterial...

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Ataei Nakhaei A, Bakhtiari E, Ghahremani S, et al. Prevalence and risk factors of seizure in children with acute bacterial meningitis: updating previous evidence using an epidemiological design. Iran J Child Neurol. 2021;15(3):47-54doi: 10.22037/ijcn.v15i2.22250.
Ataei Nakhaei, A., Bakhtiari, E., Ghahremani, S., Akhondian, J., Sasan, M. S., Movahed, M., & Aelami, M. H. (2021). Prevalence and risk factors of seizure in children with acute bacterial meningitis: updating previous evidence using an epidemiological design. Iranian journal of child neurology, 15(3), 47-54. https://doi.org/10.22037/ijcn.v15i2.22250
Ataei Nakhaei, Alireza, et al. "Prevalence and risk factors of seizure in children with acute bacterial meningitis: updating previous evidence using an epidemiological design." Iranian journal of child neurology vol. 15,3 (2021): 47-54. doi: https://doi.org/10.22037/ijcn.v15i2.22250
Ataei Nakhaei A, Bakhtiari E, Ghahremani S, Akhondian J, Sasan MS, Movahed M, Aelami MH. Prevalence and risk factors of seizure in children with acute bacterial meningitis: updating previous evidence using an epidemiological design. Iran J Child Neurol. 2021;15(3):47-54. doi: 10.22037/ijcn.v15i2.22250. PMID: 34282362; PMCID: PMC8272553.
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Extensive cerebral Sinovenous Thrombosis in a 5 Year Old Girl, Following Mild Dehydration. (Case Report and Review of Literature).

Iranian Red Crescent medical journal

Ashrafzadeh F, Akhondian J, Beiraghi Toosi M, Hashemi N.
PMID: 24693409
Iran Red Crescent Med J. 2013 Dec;15(12):e6418. doi: 10.5812/ircmj.6418. Epub 2013 Dec 05.

Cerebral sinovenous thrombosis (CSVT) in children has rarely been reported in the literature, especially without underlying disorder. It has increasingly been diagnosed due to clinical awareness and sensitive neuroimaging techniques. The aim of this article was to report a...

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Ashrafzadeh F, Akhondian J, Beiraghi Toosi M, et al. Extensive cerebral Sinovenous Thrombosis in a 5 Year Old Girl, Following Mild Dehydration. (Case Report and Review of Literature). Iran Red Crescent Med J. 2013;15(12):e6418doi: 10.5812/ircmj.6418.
Ashrafzadeh, F., Akhondian, J., Beiraghi Toosi, M., & Hashemi, N. (2013). Extensive cerebral Sinovenous Thrombosis in a 5 Year Old Girl, Following Mild Dehydration. (Case Report and Review of Literature). Iranian Red Crescent medical journal, 15(12), e6418. https://doi.org/10.5812/ircmj.6418
Ashrafzadeh, Farah, et al. "Extensive cerebral Sinovenous Thrombosis in a 5 Year Old Girl, Following Mild Dehydration. (Case Report and Review of Literature)." Iranian Red Crescent medical journal vol. 15,12 (2013): e6418. doi: https://doi.org/10.5812/ircmj.6418
Ashrafzadeh F, Akhondian J, Beiraghi Toosi M, Hashemi N. Extensive cerebral Sinovenous Thrombosis in a 5 Year Old Girl, Following Mild Dehydration. (Case Report and Review of Literature). Iran Red Crescent Med J. 2013 Dec;15(12):e6418. doi: 10.5812/ircmj.6418. Epub 2013 Dec 05. PMID: 24693409; PMCID: PMC3955524.
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Hypoparathyroidism as the first manifestation of kearns-sayre syndrome: a case report.

Iranian journal of child neurology

Ashrafzadeh F, Ghaemi N, Akhondian J, Beiraghi Toosi M, Elmi S.
PMID: 24665319
Iran J Child Neurol. 2013;7(4):53-7.

OBJECTIVE: Kearns-Sayre syndrome is a mitochondrial myopathy, which was first described by Tomas Kearn in 1958. Diagnostic symptoms include retinitis pigmentosa, chronic and progressive external ophthalmoplegia plus one or more of following factors: heart conduction system disorders, cerebellar ataxia,...

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Ashrafzadeh F, Ghaemi N, Akhondian J, et al. Hypoparathyroidism as the first manifestation of kearns-sayre syndrome: a case report. Iran J Child Neurol. 2013;7(4):53-7
Ashrafzadeh, F., Ghaemi, N., Akhondian, J., Beiraghi Toosi, M., & Elmi, S. (2013). Hypoparathyroidism as the first manifestation of kearns-sayre syndrome: a case report. Iranian journal of child neurology, 7(4), 53-7.
Ashrafzadeh, Farah, et al. "Hypoparathyroidism as the first manifestation of kearns-sayre syndrome: a case report." Iranian journal of child neurology vol. 7,4 (2013): 53-7.
Ashrafzadeh F, Ghaemi N, Akhondian J, Beiraghi Toosi M, Elmi S. Hypoparathyroidism as the first manifestation of kearns-sayre syndrome: a case report. Iran J Child Neurol. 2013;7(4):53-7. PMID: 24665319; PMCID: PMC3943048.
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Showing 1 to 12 of 14 entries