Found: 18
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Tissue Doppler echocardiography in patients with long QT syndrome.
- Published in:
- European Journal of Echocardiography, 2003, v. 4, n. 3, p. 209, doi. 10.1016/S1525-2167(03)00011-8
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- Publication type:
- Article
Platelet serotonin content and plasma tryptophan in peri- and postmenopausal women: variations with plasma oestrogen levels and depressive symptoms.
- Published in:
- European Journal of Clinical Investigation, 1988, v. 18, n. 3, p. 297, doi. 10.1111/j.1365-2362.1988.tb01262.x
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- Publication type:
- Article
Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 974, doi. 10.1038/sj.ejhg.5201866
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- Publication type:
- Article
KCNQ1 AND ISK MUTATIONS IN LQTS.
- Published in:
- 1999
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- Publication type:
- Abstract
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization.
- Published in:
- Neuropathology & Applied Neurobiology, 2011, v. 37, n. 3, p. 271, doi. 10.1111/j.1365-2990.2010.01149.x
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- Publication type:
- Article
Low incidence of cardiac events with β-blocking therapy in children with long QT syndrome.
- Published in:
- European Heart Journal, 2004, v. 25, n. 16, p. 1405, doi. 10.1016/j.ehj.2004.06.016
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- Publication type:
- Article
Familial hypertrophic cardiomyopathy. Cardiac ultrasonic abnormalities in genetically affected subjects without echocardiographic evidence of left ventricular hypertrophy.
- Published in:
- European Heart Journal, 1998, v. 19, n. 3, p. 490
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- Publication type:
- Article
Diagnostic performance of QT interval variables from 24-h electrocardiography in the long QT syndrome.
- Published in:
- European Heart Journal, 1998, v. 19, n. 1, p. 158, doi. 10.1053/euhj.1997.0730
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- Publication type:
- Article
QUANTITATIVE AUTORADIOGRAPHIC DETERMINATION OF BINDING SITES FOR A PERIPHERAL BENZODIAZEPINE LIGAND ([<sup>3</sup>H]PK 11195) IN HUMAN IRIS.
- Published in:
- Fundamental & Clinical Pharmacology, 1987, v. 1, n. 3, p. 161, doi. 10.1111/j.1472-8206.1987.tb00555.x
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- Publication type:
- Article
Ex vivo correction of selenoprotein N deficiency in rigid spine muscular dystrophy caused by a mutation in the selenocysteine codon.
- Published in:
- Nucleic Acids Research, 2008, v. 36, n. 1, p. 237, doi. 10.1093/nar/gkm1033
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- Publication type:
- Article
P128Recovery of Scn5a-deficient mice cardiac conduction using AAVs.
- Published in:
- 2018
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- Publication type:
- Abstract
P371 Role of the N- and distal C-terminal domains in Nav1.5 alpha-subunit interaction.
- Published in:
- Cardiovascular Research, 2014, v. 103, n. suppl_1, p. S68, doi. 10.1093/cvr/cvu091.54
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- Publication type:
- Article
C-terminal titin deletions cause a novel early-onset myopathy with fatal cardiomyopathy.
- Published in:
- 2007
- By:
- Publication type:
- journal article
SEPN1: associated with congenital fiber-type disproportion and insulin resistance.
- Published in:
- 2006
- By:
- Publication type:
- Journal Article
COL6A1 genomic deletions in Bethlem myopathy and Ullrich muscular dystrophy.
- Published in:
- 2006
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- Publication type:
- Journal Article
Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy.
- Published in:
- 2005
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- Publication type:
- Journal Article
Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N gene.
- Published in:
- 2004
- By:
- Publication type:
- Journal Article
Partial laminin alpha2 chain deficiency in a patient with myopathy resembling inclusion body myositis.
- Published in:
- 2000
- By:
- Publication type:
- journal article