Annika Winbo

Pediatrics

Publications

Author

Title

Year sorteringsordning

Fulltext

Winbo, Annika
Stattin, Eva-Lena
Westin, Ida Maria; et al.

Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis
BMC Medical Genetics, 18

2017

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Mann, Stefan A.
Imtiaz, Mohammad
Winbo, Annika; et al.

Convergence of models of human ventricular myocyte electrophysiology after global optimization to recapitulate clinical long QT phenotypes
Journal of Molecular and Cellular Cardiology, 100: 25-34

2016

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Winbo, Annika
Fosdal, Inger
Lindh, Maria; et al.

Third Trimester Fetal Heart Rate Predicts Phenotype and Mutation Burden in the Type 1 Long QT Syndrome
Circulation, 8(4): 806-814

2015

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Winbo, Annika
Rydberg, Annika

Vestibular dysfunction is a clinical feature of the Jervell and Lange-Nielsen Syndrome
Scandinavian Cardiovascular Journal, 49(1): 7-13

2015

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Winbo, Annika
Stattin, Eva-Lena
Nordin, Charlotte; et al.

Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1 families
BMC Cardiovascular Disorders, 14: 22-

2014

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Winbo, Annika
Sandström, Olof
Palmqvist, Richard; et al.

Iron-deficiency anaemia, gastric hyperplasia, and elevated gastrin levels due to potassium channel dysfunction in the Jervell and Lange-Nielsen Syndrome
Cardiology in the Young, 23(3): 325-334

2013

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Diamant, Ulla-Britt
Jensen, Steen M
Winbo, Annika; et al.

Vectorcardiographic recordings of the Q-T interval in a pediatric long Q-T syndrome population
Pediatric Cardiology, 34(2): 245-249

2013

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Diamant, Ulla-Britt
Vahedi, Farzad
Winbo, Annika; et al.

Electrophysiological phenotype in the LQTS mutations Y111C and R518X in the KCNQ1 gene
Journal of applied physiology, 115(10): 1423-1432

2013

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Winbo, Annika

Long QT syndrome in Sweden: founder effects and associated cardiac phenotypes

2012

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Winbo, Annika
Stattin, Eva-Lena
Diamant, Ulla-Britt; et al.

Prevalence, mutation spectrum, and cardiac phenotype of the Jervell and Lange-Nielsen syndrome in Sweden
Europace, 14(12): 1799-1806

2012

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