-transparent.png){kind=logo}
A family in whom two brothers, a sister and the father presented a long QT interval is reported. The father died suddenly at the age of 37. The opportunity of a more careful research of the syndrome, now underdiagnosed, is underlined in view of the curability such disease.
Related Publications
A Androsoni, and
A Dolara, and
A Manetti, and
G Santoro, and
F Cecchi
December 1998,
Journal of clinical pathology,
A Androsoni, and
A Dolara, and
A Manetti, and
G Santoro, and
F Cecchi
April 2020,
JAMA cardiology,
A Androsoni, and
A Dolara, and
A Manetti, and
G Santoro, and
F Cecchi
May 1979,
Circulation,
A Androsoni, and
A Dolara, and
A Manetti, and
G Santoro, and
F Cecchi
September 1982,
Circulation,
A Androsoni, and
A Dolara, and
A Manetti, and
G Santoro, and
F Cecchi
September 1975,
Acta paediatrica Scandinavica,
A Androsoni, and
A Dolara, and
A Manetti, and
G Santoro, and
F Cecchi
March 2010,
Revista espanola de cardiologia,
A Androsoni, and
A Dolara, and
A Manetti, and
G Santoro, and
F Cecchi
April 1986,
Archives of disease in childhood,
A Androsoni, and
A Dolara, and
A Manetti, and
G Santoro, and
F Cecchi
April 2008,
Prescrire international,
A Androsoni, and
A Dolara, and
A Manetti, and
G Santoro, and
F Cecchi
July 1978,
American journal of diseases of children (1960),
A Androsoni, and
A Dolara, and
A Manetti, and
G Santoro, and
F Cecchi
January 1989,
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke,
