Search Results - "Tajaddini, Mohamadhasan"
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Investigation of Chemokine Receptor CCR2V64Il Gene Polymorphism and Migraine without Aura in the Iranian Population
Published in TheScientificWorld (01-01-2013)“…Background and Objectives. Migraine is a multifactorial common neurovascular disease with a polygenic inheritance. Inflammation plays an important part in…”
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The Mutation of Dual Oxidase 2 (DUOX2) Gene among Patients with Permanent and Transient Congenital Hypothyroidism
Published in Majallah-i dānishkadah-i pizishkī-i Iṣfahān. (Online) (01-07-2011)“…Background: Considering the high prevalence of congenital hypothyroidism (CH) in Isfahan and its different etiologies comparing with other countries, the high…”
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Association of the long pentraxin PTX3 gene polymorphism (rs3816527) with migraine in an Iranian population
Published in Journal of the neurological sciences (15-02-2015)“…Abstract Background Migraine is a common neurovascular disorder with multifactorial and polygenic inheritance. It has been shown that migraine may be a form of…”
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Association of the Long Pentraxin PTX3 Gene Polymorphism (rs3815627) with Migraine in Iranian Population (P6.206)
Published in Neurology (08-04-2014)“…Abstract only…”
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Investigation of Chemokine Receptor CCR2V64Il Gene Polymorphism and Migraine in Iranian Population (P6.208)
Published in Neurology (08-04-2014)“…Abstract only…”
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Association between promoter region of the uPAR (rs344781) gene polymorphism in genetic susceptibility to migraine without aura in three Iranian hospitals
Published in Clinical neurology and neurosurgery (01-05-2014)“…Abstract Introduction Migraine is a chronic neurological disorder. Inflammation has a key role in migraine pathophysiology. Urokinase plasminogen activator…”
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بررسی پلیمورفیسم ژنتیکی C677T در ژن MTHFR در بیماران مبتلا به میگرن در مقایسه با گروه شاهد
Published in Majallah-i dānishkadah-i pizishkī-i Iṣfahān. (Online) (01-01-2013)“…مقدمه: میگرن به عنوان فنوتیپی از اختلالات پلیژنی در نظر گرفته میشود و منعکسکنندهی اثر چندین جایگاه ژنی میباشد که فرایندهای پاتوفیزیولوژیکی متفاوتی را…”
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Association between Ala379Val polymorphism of lipoprotein-associated phospholipase A2 and migraine without aura in Iranian population
Published in Iranian journal of neurology (03-04-2016)“…Background: Migraine is a common neurovascular disorder with multifactorial and polygenic inheritance. The aim of this study was to investigate the association…”
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