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1دورية أكاديمية
المؤلفون: Abhishek Goyal, Varun Loomba, Naved Aslam, Bishav Mohan, Gurpreet Singh Wander
المصدر: Journal of Clinical and Diagnostic Research, Vol 11, Iss 9, p OJ01 (2017)
مصطلحات موضوعية: brugada ecg types, hereditary channelopathies, spontaneous variation, Medicine
وصف الملف: electronic resource
العلاقة: https://jcdr.net/articles/PDF/10640/29327_180917_29327_CETest(RA1)_F(T)PF1-(VJ_PY)_PFA(VJ_SS).pdf; https://doaj.org/toc/2249-782XTest; https://doaj.org/toc/0973-709XTest
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2
المؤلفون: Gurpreet Singh Wander, Bishav Mohan, Naved Aslam, Varun Loomba, Abhishek Goyal
المصدر: Journal of Clinical and Diagnostic Research, Vol 11, Iss 9, p OJ01 (2017)
مصطلحات موضوعية: medicine.medical_specialty, hereditary channelopathies, Internal Medicine Section, business.industry, lcsh:R, Clinical Biochemistry, lcsh:Medicine, General Medicine, medicine.disease, brugada ecg types, spontaneous variation, Internal medicine, medicine, Cardiology, business, Brugada syndrome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9b3e2b54485a946c8eb9bf10ec10e5eTest
https://europepmc.org/articles/PMC5713791Test/ -
3
المؤلفون: Valeria A. Sansone, E. Mancinelli, G. Rotondo, Giovanni Meola
المصدر: European Journal of Histochemistry, Vol 47, Iss 1 (2009)
Europe PubMed Centralمصطلحات موضوعية: Adult, Male, Pathology, medicine.medical_specialty, Histology, Biopsy, Biophysics, Muscle histopathology, Settore BIO/09 - Fisiologia, Ion Channels, Hypokalemic periodic paralysis, medicine, Humans, Point Mutation, Hyperkalemic periodic paralysis, Muscle, Skeletal, lcsh:QH301-705.5, Cells, Cultured, Aged, Potassium-aggravated myotonia, CLCN1, biology, Histocytochemistry, business.industry, Myotonia congenita, Muscle histochemistry, Skeletal muscle, Periodic paralysis, Cell Biology, Middle Aged, medicine.disease, Cell cultures, Hereditary channelopathies, Muscle biopsy, Voltage-gated ion channels, medicine.anatomical_structure, lcsh:Biology (General), Potassium Channels, Voltage-Gated, Paramyotonia congenita, biology.protein, Female, Settore MED/26 - Neurologia, business, Ion Channel Gating, Metabolism, Inborn Errors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00889c6c1554a49c477543f98c499d19Test
https://www.ejh.it/index.php/ejh/article/view/803Test