Zobrazeno 1 - 10
of 195
pro vyhledávání: '"Ghaffarpour, M."'
Autor:
Pakdaman H, Amini Harandi A, Gharagozli K, Abbasi M, Ghaffarpour M, Ashrafi F, Delavar Kasmaei H
Publikováno v:
Neuropsychiatric Disease and Treatment, Vol Volume 13, Pp 2551-2557 (2017)
Hossein Pakdaman,1 Ali Amini Harandi,1 Koroush Gharagozli,1 Mehdi Abbasi,1 Majid Ghaffarpour,2 Farzad Ashrafi,1 Hosein Delavar Kasmaei,1 Asghar Amini Harandi3 1Brain Mapping Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Ira
Externí odkaz:
https://doaj.org/article/91caa645e2fd48818289c375e4b2a375
Autor:
Aghamollaii, V., Harirchian, M.H., Modabbernia, A., Ghaffarpour, M., Mousavi, M., Tafakhori, A.
Publikováno v:
In Neurophysiologie Clinique / Clinical Neurophysiology October 2011 41(4):161-171
Publikováno v:
Tehran University Medical Journal, Vol 66, Iss 10, Pp 714-720 (2009)
"nBackground: Many studies have shown that about 45-65% of multiple sclerosis (M.S) patients suffer from cognitive impairments. Semantic memory as one of the subcategories of cognition is quite important for effective communication. In the present st
Externí odkaz:
https://doaj.org/article/fa7a185d2a204ecd9dd4e2fbfe8243d9
Publikováno v:
Tehran University Medical Journal, Vol 66, Iss 1, Pp 1-6 (2008)
Background: Multiple sclerosis (MS) is an inflammatory disease of the central nervous system with multifocal areas of demyelination. Despite an increased understanding of the mechanisms causing MS, immunological factors that indicate disease activity
Externí odkaz:
https://doaj.org/article/2870651df53c4720a22d4c1ed9619e3e
Publikováno v:
Acta Medica Iranica, Vol 42, Iss 4, Pp 259-262 (2004)
Lamotrigine has been used widely in the treatment of partial and secondary generalized seizures. In this study use of lamotrigine as monotherapy for the newly diagnosed primary generalized tonic–clonic seizure has been investigated and compared wit
Externí odkaz:
https://doaj.org/article/b38ab021ab5649b5b9444549b16f74b5
Publikováno v:
Acta Medica Iranica, Vol 41, Iss 4, Pp 244-247 (2003)
Primary hypokalemic periodic paralysis is a familial channelopathy inherited as an autosomal dominant trait. The first attack of paralysis may be evolved at any age, but has been reported to be most common in the second decade, so that some authoriti
Externí odkaz:
https://doaj.org/article/af9df1020c8d40a381a4d419de0e08cc
Publikováno v:
Acta Medica Iranica, Vol 40, Iss 4, Pp 214-218 (2002)
Footdrop is a relatively common deficit among the neurological disorders, which has different causes with various levels of involvement in neuromuscular system, including central nervous system (brain cortex, spinal cord), fifth lumbar root, peripher
Externí odkaz:
https://doaj.org/article/5a51aca9296543d0b59664e7b0e541db
Publikováno v:
Acta Medica Iranica, Vol 40, Iss 3, Pp 198-202 (2002)
This case series reports 100 patients with lung cancer and their presenting neurologic symptoms and sings. 78% of patients were maleand 22% were female. Mean age was 62±1.04 years with a peak age between 65 and 75 years. Most patients presented with
Externí odkaz:
https://doaj.org/article/53d7d37496074cab91a3c2cf3bd1b73d
Autor:
Ghabaee M, Ghaffarpour M "
Publikováno v:
Acta Medica Iranica, Vol 39, Iss 3, Pp 153-158 (2001)
est (RST) is the most commonly used electrodiagnostic test to asses the defect of neuromuscular transmission, which is reported to be positive in the diffuse and restricted ocular forms 60-95% and 14-50%, respectively. In a cross-sectional study, to
Externí odkaz:
https://doaj.org/article/144ef7a3215d4a4b92d2f681130a1a98
Autor:
Zarif Yeganeh, M., Ghaffarpour, M., Farhud, D.D., Karimlou, M., Ghabaee, M., Haghighi Nazari, A., Najmabadi, H., Ohadi, M.
Publikováno v:
In Journal of Neuroimmunology 2009 216(1):103-107