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Author/Creator Futema, Marta

1. Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy. (15th July 2021)

Authors:
Lopes, Luis R; Garcia-Hernández, Soledad; Lorenzini, Massimiliano; Futema, Marta; Chumakova, Olga; Zateyshchikov, Dmitry; Isidoro-Garcia, Maria; Villacorta, Eduardo; Escobar-Lopez, Luis; Garcia-Pavia, Pablo; Bilbao, Raquel; Dobarro, David; Sandin-Fuentes, Maria; Catalli, Claudio; Gener Querol, Bl...
Journal:
European heart journal
Issue:
Volume 42:Number 32(2021)
Page Start:
3063
Record Type:
Journal Article
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4. Comparison of the characteristics at diagnosis and treatment of children with heterozygous familial hypercholesterolaemia (FH) from eight European countries. (January 2020)

Authors:
Ramaswami, Uma; Futema, Marta; Bogsrud, Martin P.; Holven, Kirsten B.; Roeters van Lennep, Jeanine; Wiegman, Albert; Descamps, Olivier S.; Vrablik, Michal; Freiberger, Tomas; Dieplinger, Hans; Greber-Platzer, Susanne; Hanauer-Mader, Gabriele; Bourbon, Mafalda; Drogari, Euridiki; Humphries, Steve E.
Journal:
Atherosclerosis
Issue:
Volume 292(2020)
Page Start:
178
Record Type:
Journal Article
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5. Comparison of the mutation spectrum and association with pre and post treatment lipid measures of children with heterozygous familial hypercholesterolaemia (FH) from eight European countries. (February 2021)

Authors:
Futema, Marta; Ramaswami, Uma; Tichy, Lukas; Bogsrud, Martin P.; Holven, Kirsten B.; Roeters van Lennep, Jeanine; Wiegman, Albert; Descamps, Olivier S.; De Leener, Anne; Fastre, Elodie; Vrablik, Michal; Freiberger, Tomas; Esterbauer, Harald; Dieplinger, Hans; Greber-Platzer, Susanne; Medeiros, An...
Journal:
Atherosclerosis
Issue:
Volume 319(2021)
Page Start:
108
Record Type:
Journal Article
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6. Cryptic Splice-Altering Variants in MYBPC3 Are a Prevalent Cause of Hypertrophic Cardiomyopathy. (June 2020)

Authors:
Lopes, Luis R.; Barbosa, Pedro; Torrado, Mario; Quinn, Ellie; Merino, Ana; Ochoa, Juan Pablo; Jager, Joanna; Futema, Marta; Carmo-Fonseca, Maria; Monserrat, Lorenzo; Syrris, Petros; Elliott, Perry M.
Journal:
Circulation
Issue:
Volume 13:Number 3(2020)
Page Start:
Record Type:
Journal Article
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7. Efficacy of clinical diagnostic criteria for familial hypercholesterolemia genetic testing in Poland. (June 2016)

Authors:
Mickiewicz, Agnieszka; Chmara, Magdalena; Futema, Marta; Fijalkowski, Marcin; Chlebus, Krzysztof; Galaska, Rafał; Bandurski, Tomasz; Pajkowski, Marcin; Zuk, Monika; Wasag, Bartosz; Limon, Janusz; Rynkiewicz, Andrzej; Gruchala, Marcin
Journal:
Atherosclerosis
Issue:
Volume 249(2016)
Page Start:
52
Record Type:
Journal Article
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8. Filamin C variants are associated with a distinctive clinical and immunohistochemical arrhythmogenic cardiomyopathy phenotype. (15th May 2020)

Authors:
Hall, Charlotte L.; Akhtar, Mohammed M.; Sabater-Molina, Maria; Futema, Marta; Asimaki, Angeliki; Protonotarios, Alexandros; Dalageorgou, Chrysoula; Pittman, Alan M.; Suarez, Mari Paz; Aguilera, Beatriz; Molina, Pilar; Zorio, Esther; Hernández, Juan Pedro; Pastor, Francisco; Gimeno, Juan R.; Syrr...
Journal:
International journal of cardiology
Issue:
Volume 307(2020)
Page Start:
101
Record Type:
Journal Article
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9. Greater preclinical atherosclerosis in treated monogenic familial hypercholesterolemia vs. polygenic hypercholesterolemia. (August 2017)

Authors:
Sharifi, Mahtab; Higginson, Elizabeth; Bos, Sven; Gallivan, Angela; Harvey, Darren; Li, Ka Wah; Abeysekera, Amali; Haddon, Angela; Ashby, Helen; Shipman, Kate E.; Cooper, Jackie A.; Futema, Marta; Roeters van Lennep, Jeanine E.; Sijbrands, Eric J.G.; Labib, Mourad; Nair, Devaki; Humphries, Steve E.
Journal:
Atherosclerosis
Issue:
Volume 263(2017)
Page Start:
405
Record Type:
Journal Article
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