نتایج جستجو برای: potassium channelopathy

تعداد نتایج: 77926  

Journal: :iranian journal of chemistry and chemical engineering (ijcce) 2008
gholam hossein nazeri ramin mastour mohammad fayaznia parviz keyghobadi

nitration of potassium sulphamate was carried out using a mixture of sulphuric and nitric acid at -30 °c. the reaction time was optimized at the mole ratio of sulphuric to nitric acid of (1:3.5). the difference in product yield by changing the potassium to ammonium sulphamate was studied throughly. it was found that both the yield and purity of the product is better starting with potassium sulp...

Journal: :علوم باغبانی 0
مهنا ملاولی صاحبعلی بلندنظر سیدجلال طباطبایی

abstract nitrogen is a key nutrient in plant growth and it is necessary for amino acid synthesis. sulfur has very important role in the biosynthesis of the alliums flavor and pungency precursors and potassium improve crop yield and quality. in order to study the effect of ammonium nitrate and potassium sulfate on concentration some of the mineral elements in onion (allium cepa l. azar shahr cv....

Journal: :Brain : a journal of neurology 2002
Ian K Hart Paul Maddison John Newsom-Davis Angela Vincent Kerry R Mills

Clinicians use many terms including undulating myokymia, neuromyotonia, Isaacs' syndrome and Cramp-Fasciculation Syndrome to describe the motor manifestations of generalized peripheral nerve hyperexcitability (PNH). Our previous findings in a selected group of patients with undulating myokymia or neuromyotonia, and EMG doublet or multiplet ('myokymic') motor unit discharges, indicated that an a...

2014
Andreas C Themistocleous Juan D Ramirez Jordi Serra David L H Bennett

Small fibre neuropathy (SFN) is characterised by structural injury selectively affecting small diameter sensory and/or autonomic axons. The clinical presentation is dominated by pain. SFN complicates a number of common diseases such as diabetes mellitus and is likely to be increasingly encountered. The diagnosis of SFN is demanding as clinical features can be vague and nerve conduction studies ...

Journal: :Clinical genetics 2012
J G J Hoeijmakers I S J Merkies M M Gerrits S G Waxman C G Faber

Small fiber neuropathy (SFN) is a disorder typically dominated by neuropathic pain and autonomic dysfunction, in which the thinly myelinated Aδ-fibers and unmyelinated C-fibers are selectively injured. The diagnosis SFN is based on a reduced intraepidermal nerve fiber density and/or abnormal thermal thresholds in quantitative sensory testing. The etiologies of SFN are diverse, although no appar...

Journal: :Brain : a journal of neurology 2009
Stephanie Schorge Dimitri M Kullmann

Among proteins involved in neurological disease ion channels are amenable to the most detailed characterisation: patch-clamp methods allow the opening and closing of individual channels to be documented at millisecond resolution in response to precisely delivered stimuli (whether electrical or pharmacological). In theory, therefore, inherited disorders of ion channels should be ideal candidates...

Journal: :The Journal of Experimental Medicine 2005
Vanda A. Lennon Thomas J. Kryzer Sean J. Pittock A.S. Verkman Shannon R. Hinson

Neuromyelitis optica (NMO) is an inflammatory demyelinating disease that selectively affects optic nerves and spinal cord. It is considered a severe variant of multiple sclerosis (MS), and frequently is misdiagnosed as MS, but prognosis and optimal treatments differ. A serum immunoglobulin G autoantibody (NMO-IgG) serves as a specific marker for NMO. Here we show that NMO-IgG binds selectively ...

2008
Cliona Murphy

Long-QT syndrome (LQTS) is an inherited ion channelopathy resulting in abnormal ventricular repolarization and abnormal prolongation of the QT interval on the electrocardiogram. Clinical features vary, from asymptomatic individuals to those with presyncope, life threatening ventricular arrhythmias and sudden cardiac death (SCD). This case report describes a family with a mutation of the KCNH2 g...

2012
Andrew R. Segerdahl Jingyi Xie Kathryn Paterson Juan D. Ramirez Irene Tracey David L.H. Bennett

We identified a patient with severe inherited erythromelalgia secondary to an L858F mutation in the voltage-gated sodium channel Na(v)1.7. The patient reported severe ongoing foot pain, which was exquisitely sensitive to limb cooling. We confirmed this heat hypersensitivity using quantitative sensory testing. Additionally, we employed a novel perfusion imaging technique in a simple block design...

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