Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Ali Ghabeli Juibary"'
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 3, Iss 11, Pp 206-213 (2017)
Background: Among different mechanisms, oxidative stress has a possible role in neural injury in cerebrovascular events. Objectives: Assessment the oxidants-antioxidants imbalance in ischemic and hemorrhagic strokes. Materials and Methods: Serum leve
Externí odkaz:
https://doaj.org/article/c060b9e05ff74345a87bc93249e895b5
Autor:
Karim Nikkhah, Mohammad Taghi Farzadfard, Payam Sasannejad, Ali Ghabeli Juibary, Marzieh Taheri, Samira Aminzadeh
Publikováno v:
Patient Safety and Quality Improvement Journal, Vol 3, Iss 3, Pp 243-246 (2015)
Introduction: Trigeminal Neuralgia (TN) is a unilateral, recurrent, sharp facial pain disorder that is limited to the distribution of divisions of the trigeminal nerve. The aim of this study was to evaluate the efficacy of Botulinum neurotoxin type A
Externí odkaz:
https://doaj.org/article/15c2715c276549d6aeb16a0b8ce7d18a
Autor:
Karim Nikkhah, Payam Sasannejad, Morteza Saeidi, Mohsen Muhebati, Sirus Nekuyi, Farid Chekani, Azadeh Fallah Rastgar, Mohammad Taghi Farzadfard, Ali Ghabeli Juibary, Samira Aminzadeh
Publikováno v:
Patient Safety and Quality Improvement Journal, Vol 3, Iss 2, Pp 211-215 (2015)
Introduction: Subarachnoid Hemorrhage (SAH) which accounts for (5% to 10%) of cerebrovascular accidents is an important cause of mortality and disability. It can be complicated by many neurological and medical conditions including cardiovascular comp
Externí odkaz:
https://doaj.org/article/63391acbb62a47f6aaf767eeda487c01
Publikováno v:
مجله دانشگاه علوم پزشکی گرگان, Vol 10, Iss 3, Pp 38-44 (2008)
Background and Objective: Cystic fibrosis (CF) is the most common inherited disorder in Caucasian populations caused by mutation in cystic fibrosis transmembrane conductance regulator (CFTR). The type of mutations and their distributions varies widel
Externí odkaz:
https://doaj.org/article/f5efc1285a87462b8bdfe1e756898ebf
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 3, Iss 8, Pp 54-59 (2017)
Pompe disease, also termed glycogen storage disease type II or acid maltase deficiency, caused by deficient activity of acid alpha-glucosidase (GAA), the glycogen degrading lysosomal enzyme. As a result, massive lysosomal glycogen deposits in the num
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bea4776851426ba49592de78cb116e58
https://doi.org/10.18869/acadpub.cjns.3.8.54
https://doi.org/10.18869/acadpub.cjns.3.8.54
Publikováno v:
Iranian Journal of Neurology
Background: The human T-cell lymphotropic virus type-I (HTLV-I) is the first identified pathogenic human retrovirus. Breastfeeding has been reported to be the predominant route of vertical transmission of HTLV-I. The objective of this systematic revi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34c947315f007b9e24f6734623c6f7e7
https://doi.org/10.18502/ijnl.v17i4.589
https://doi.org/10.18502/ijnl.v17i4.589
Autor:
Ali Ghabeli Juibary, Mohammad Taghi Farzadfard, Mahmoud Reza Azarpazhooh, Réza Behrouz, Naghmeh Mokhber, Moira K. Kapral, Amanda G. Thrift, Mohammad Sobhan Sheikh Andalibi, Amin Amiri, Negar Morovatdar, Saverio Stranges
Publikováno v:
Epidemiology and Biostatistics Publications
Background Accurate information about disability rate after stroke remains largely unclear in many countries. Population-based studies are necessary to estimate the rate and determinants of disability after stroke. Methods Patients were recruited fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b08d2a212d7e61ce4fdd39abd570725
https://ir.lib.uwo.ca/epidempub/126
https://ir.lib.uwo.ca/epidempub/126
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 2, Iss 5, Pp 50-53 (2016)
We report a rare genetic disorder case of neuroacanthocytosis with clinical profile (oro-lingual-facial abnormal involuntary movements, neuropathy) and typical magnetic resonance findings (cerebral atrophy, bilateral caudate nuclei atrophy with dilat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7501023b4eff3fdc3e3a04cd6b0f1880
http://cjns.gums.ac.ir/browse.php?a_code=A-10-32-39&slc_lang=en&sid=1
http://cjns.gums.ac.ir/browse.php?a_code=A-10-32-39&slc_lang=en&sid=1
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 1, Iss 3, Pp 47-51 (2015)
Sjogren-Larsson Syndrome (SLS) is an inherited autosomal recessive neurocutaneous disorder with congenital ichthyosis, spastic diplegia or quadriplegia and mental retardation. We report a case of Sjogren-Larsson Syndrome with clinical profile (mental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::b6c832e24f1736d68229fb49ff08d3af
http://cjns.gums.ac.ir/browse.php?a_code=A-10-32-25&slc_lang=en&sid=1
http://cjns.gums.ac.ir/browse.php?a_code=A-10-32-25&slc_lang=en&sid=1
Publikováno v:
Journal of Pediatric Neurology. :039-042
Febrile seizure (FS) is the most common neurological disorder in the pediatric population. The clinical characteristics of 630 patients who had episodes of FS were retrospectively reviewed. No preference was seen for either sex (1.2:1). In those case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4094c4ece1822b482b4dfdff76c624e9
https://doi.org/10.1055/s-0035-1557425
https://doi.org/10.1055/s-0035-1557425