RT-225
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Neuronal degeneration localized
in the thoracic spinal cord sympathetic center in a case with prolonged long QT interval
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Lino Rossi, Luigi Matturri.
Institutes of Pathology, University of Milan, IRCCS Ospedale Maggiore, Milan, Italy
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References
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1.
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2.
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Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential
responses to Na+ channels blockade and to increases in heart rate: implications for
gene-specific therapy.
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3.
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Rosen MR:
Long QT syndrome patients with gene mutations.
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4.
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Shimizu W, Antzelevitch C:
Sodium channel block with mexiletine is effective in reducing torsade de pointes in LQT2
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5.
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7.
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Hereditares QT-syndrom: ein weiterer Fall mit grenzstrang-ganglionitis.
Herz Kreislauf 1982; 3: 149-153.
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