نتایج جستجو برای: hypokalemic paralysis

تعداد نتایج: 20271  

2012
Shinsaku Imashuku Tomoko Teramura-Ikeda Naoko Kudo Shigehiro Kaneda Toshihiro Tajima

A 16-year-old Japanese boy with a history of truancy had been treated at a psychiatric clinic. When the patient was referred to us for hypokalemia-associated paralysis, the diagnosis of thyrotoxic hypokalemic periodic paralysis was made, common in Asian men. Subsequently, the patient was found to have persistently high plasma renin and aldos-terone levels. Thus, solute carrier family 12 member ...

Journal: :The Turkish journal of pediatrics 2010
Faruk Incecik Mihriban Ozlem Hergüner Sakir Altunbaşak Frank Lehman-Horn

Hypokalemic periodic paralysis (HypoPP) is an autosomal dominant disorder characterized by episodic attacks of muscle weakness associated with a decrease in blood potassium levels. Recently, mutations in the gene coding for the skeletal muscle voltage-gated sodium channel alpha subunit (SCN4A) have been reported. We detected the R672H mutation in one HypoPP Turkish family.

2017
Abdelghafour Elkoundi Noureddine Kartite Mustapha Bensghir Nawfal Doghmi Salim Jaafar Lalaoui

In rare cases, patients with Gitelman syndrome may present with hypokalemic paralysis mimicking Guillain-Barré syndrome. The severity of resultant symptoms may be life-threatening. Controversial drugs such as aldactone, amiloride, and eplerenone should be used in this situation despite the lack of safety data.

Journal: :Physical chemistry chemical physics : PCCP 2016
Indre Thiel Alexey Fedorov Rene Verel Sergii Yakunin Maksym V Kovalenko Christophe Copéret

Photoluminescence decay was used as a structure-sensitive method to compare the distribution of emitting sites in periodic mesoporous organosilicates (PMOs) to their respective molecular analogs. The observed close similarity of PL decays confirms the molecular nature of PMOs and high homogeneity of emitting sites.

Journal: :The Cochrane database of systematic reviews 2008
V Sansone G Meola T P Links M Panzeri M R Rose

BACKGROUND Primary periodic paralyses are rare inherited muscle diseases characterised by episodes of flaccid weakness affecting one or more limbs, lasting several hours to several days, caused by mutations in skeletal muscle channel genes. OBJECTIVES The objective of this review was to systematically review treatment of periodic paralyses. SEARCH STRATEGY We searched the Cochrane Neuromusc...

Journal: :Indian Journal of Sexually Transmitted Diseases and AIDS 2015

Journal: :European Journal of Case Reports in Internal Medicine 2015

Journal: :CJEM 2003
Phillip Wong

Hypokalemic periodic paralysis is a rare and dramatic complication of hyperthyroidism. This series summarizes the clinical and metabolic features of 10 patients who presented to the Western and Sunshine hospitals in Melbourne, Australia, between 1997 and 2002 with thyrotoxic periodic paralysis (TPP). TPP classically presents with proximal lower-limb weakness in the setting of a low potassium le...

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