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1 Ergebnisse
1
Parálisis periódica hipocalémica: reporte de caso y revisió..:
Rojas García, William
;
Flórez Romero, Andrés
;
Pinzón Rincón, Diana
Statland J, Phillips L, Triverdi J. Muscle channelopathies. Neurol Clin. 2014;32:801–15. 2. Fontaine B. Periodic paralysis. Adv Genet. 2008;63:3–23. 3. Statland J, Barohn R. Muscle channelopathies: The nondystrophic myotonias and periodic paralyses. Continuum (Minneap Minn). 2014;19:1598–614. 4. Imbrici P, Liantonio A, Camerino G, de Bellis M, Camerino C, Mele A, et al. Therapeutic approaches to genetic ion channelopathies and perspectives in drug discovery. Front Pharmacol. 2016;7:121. 5. Ke T, Gomez CR, Mateus HE, Castano JA, Wang QK. Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family. J Hum Genet. 2009;54:60–4. 6. Zheng J, Liang Z, Hou Y, Liu F, Hu Y, Lin P, et al. A novel Kir2.6 mutation associated with hypokalemic periodic paralysis. Clin Nuerophysiol. 2016;127:2503–8. 7. Burge JA, Hanna MG. Novel insights into the pathomechanisms of eskeletal muscle channelopathies. Curr Neurol Neur.... , 2022
Link:
https://repositorio.fucsalud.edu.co/handle/001/1997
RT Journal T1
Parálisis periódica hipocalémica: reporte de caso y revisión del tema ; Hypokalemic periodic paralysis: A case report and a topic review
UL https://suche.suub.uni-bremen.de/peid=base-ftfucsalud:oai:repositorio.fucsalud.edu.co:001_1997&Exemplar=1&LAN=DE A1 Rojas García, William A1 Flórez Romero, Andrés A1 Pinzón Rincón, Diana PB Sociedad de Cirugía de Bogotá, Hospital de San José y Fundación Universitaria de Ciencias de la Salud YR 2022 K1 Canalopatías K1 Parálisis periódica familiar K1 Parálisis periódicas K1 Parálisis periódicas hipocalémicas K1 Channel pathology K1 Family periodic paralysis K1 Periodic paralysis K1 Hypokalemic periodic paralysis JF Statland J, Phillips L, Triverdi J. Muscle channelopathies. Neurol Clin. 2014;32:801–15. 2. Fontaine B. Periodic paralysis. Adv Genet. 2008;63:3–23. 3. Statland J, Barohn R. Muscle channelopathies: The nondystrophic myotonias and periodic paralyses. Continuum (Minneap Minn). 2014;19:1598–614. 4. Imbrici P, Liantonio A, Camerino G, de Bellis M, Camerino C, Mele A, et al. Therapeutic approaches to genetic ion channelopathies and perspectives in drug discovery. Front Pharmacol. 2016;7:121. 5. Ke T, Gomez CR, Mateus HE, Castano JA, Wang QK. Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family. J Hum Genet. 2009;54:60–4. 6. Zheng J, Liang Z, Hou Y, Liu F, Hu Y, Lin P, et al. A novel Kir2.6 mutation associated with hypokalemic periodic paralysis. Clin Nuerophysiol. 2016;127:2503–8. 7. Burge JA, Hanna MG. Novel insights into the pathomechanisms of eskeletal muscle channelopathies. Curr Neurol Neur... LK http://dx.doi.org/https://repositorio.fucsalud.edu.co/handle/001/1997 DO https://repositorio.fucsalud.edu.co/handle/001/1997 SF ELIB - SuUB Bremen
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