Novel etiopathophysiological aspects of thyrotoxic periodic paralysis

RMB Maciel, SC Lindsey… - Nature Reviews …, 2011 - nature.com
Thyrotoxicosis can lead to thyrotoxic periodic paralysis (TPP), an endocrine channelopathy,
and is the most common cause of acquired periodic paralysis. Typically, paralytic attacks …

[HTML][HTML] Mutations in potassium channel Kir2. 6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis

DP Ryan, MRD da Silva, TW Soong, B Fontaine… - Cell, 2010 - cell.com
Thyrotoxic hypokalemic periodic paralysis (TPP) is characterized by acute attacks of
weakness, hypokalemia, and thyrotoxicosis of various etiologies. These transient attacks …

[HTML][HTML] Ion channelopathies in endocrinology: recent genetic findings and pathophysiological insights

ALR Rolim, SC Lindsey, IS Kunii… - … de Endocrinologia & …, 2010 - SciELO Brasil
Ion channels serve diverse cellular functions, mainly in cell signal transduction. In endocrine
cells, these channels play a major role in hormonal secretion, Ca2+-mediated cell signaling …

Thyrotoxic hypokalaemic periodic paralysis in a Turkish population: three new case reports and analysis of the case series

M Cesur, F Bayram, MA Temel, M Ozkaya… - Clinical …, 2008 - Wiley Online Library
Objective Thyrotoxic hypokalaemic periodic paralysis (THPP) is an uncommon condition
with intermittent episodes of muscle weakness and occasionally severe paralysis. THPP is a …

[HTML][HTML] Potassium channel gene mutations rarely cause atrial fibrillation

PT Ellinor, VI Petrov-Kondratov, E Zakharova… - BMC medical …, 2006 - Springer
Background Mutations in several potassium channel subunits have been associated with
rare forms of atrial fibrillation. In order to explore the role of potassium channels in inherited …

[HTML][HTML] Mutation analysis of CACNA1S and SCN4A in patients with hypokalemic periodic paralysis

XY Wang, BW Ren, ZH Yong… - Molecular …, 2015 - spandidos-publications.com
Mutations in CACNA1S (calcium channel, voltage‑dependent, L type, alpha 1S subunit) and
SCN4A (sodium channel, voltage‑gated, type IV, alpha subunit) are associated with …

[HTML][HTML] Etiology of hypokalemic paralysis in Korea: data from a single center

JK Wi, HJ Lee, EY Kim, JH Cho… - Electrolytes & Blood …, 2012 - synapse.koreamed.org
Recognizing the underlying causes of hypokalemic paralysis seems to be essential for the
appropriate management of affected patients and their prevention of recurrent attacks. There …

Association of genetic variants in GABRA3 gene and thyrotoxic hypokalaemic periodic paralysis in Thai population

W Jongjaroenprasert, S Chanprasertyotin… - Clinical …, 2008 - Wiley Online Library
Background Genetic predisposition has been suggested to play role in the pathogenesis of
thyrotoxic hypokalaemic periodic paralysis (THPP). Objectives In this study, we assessed the …

[HTML][HTML] Cervical spinal cord neurapraxia in the setting of Klippel–Feil anomaly: a diagnostic and therapeutic challenge

SN Gupta, JH Piatt, B Belay - Spinal Cord, 2007 - nature.com
Study design: Case report. Setting: Temple University Children's Medical Center in USA.
Objectives: To report a patient whose recurrent and transient episodes of quadriplegia …

[HTML][HTML] Perfil clínico-epidemiológico de pacientes con parálisis periódica tirotóxica en dos hospitales peruanos

JL Paz-Ibarra, SM Sáenz-Bustamante… - Revista Médica del …, 2022 - ncbi.nlm.nih.gov
Resultados: la edad promedio al diagnóstico fue de 35.77±9.6 años, todos de raza mestiza,
en 82% de los pacientes el diagnóstico de hipertiroidismo fue establecido a partir de esta …