Frederik Heurlin Aidt
Frederik Heurlin Aidt
Bekræftet mail på sund.ku.dk
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Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish population
CM Hagen, FH Aidt, PL Hedley, MK Jensen, O Havndrup, JK Kanters, ...
PloS one 8 (8), e71904, 2013
442013
Dysfunctional mitochondrial respiration in the striatum of the Huntington’s disease transgenic R6/2 mouse model
FH Aidt, SMB Nielsen, J Kanters, D Pesta, TT Nielsen, A Nørremølle, ...
PLoS currents 5, 2013
402013
The Role of CAV3 in Long–QT Syndrome: Clinical and Functional Assessment of a Caveolin-3/Kv11.1 Double Heterozygote Versus Caveolin-3 Single Heterozygote
PL Hedley, JK Kanters, M Dembic, T Jespersen, L Skibsbye, FH Aidt, ...
Circulation: Cardiovascular Genetics 6 (5), 452-461, 2013
292013
MT‐CYB mutations in hypertrophic cardiomyopathy
CM Hagen, FH Aidt, O Havndrup, PL Hedley, C Jespersgaard, M Jensen, ...
Molecular genetics & genomic medicine 1 (1), 54-65, 2013
272013
Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p. F29L in KCNH2
M Christiansen, PL Hedley, J Theilade, B Stoevring, TP Leren, O Eschen, ...
BMC medical genetics 15 (1), 1-11, 2014
142014
SCA28: novel mutation in the AFG3L2 proteolytic domain causes a mild cerebellar syndrome with selective type-1 muscle fiber atrophy
K Svenstrup, TT Nielsen, F Aidt, N Rostgaard, M Duno, F Wibrand, ...
The Cerebellum 16 (1), 62-67, 2017
122017
Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy
CM Hagen, FH Aidt, O Havndrup, PL Hedley, MK Jensen, JK Kanters, ...
PLoS One 10 (4), e0124540, 2015
112015
The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study
PL Hedley, O Haundrup, PS Andersen, FH Aidt, M Jensen, ...
Journal of negative results in biomedicine 10 (1), 1-5, 2011
112011
Localization of A11‐reactive oligomeric species in prion diseases
FH Aidt, LF Hasholt, M Christiansen, H Laursen
Histopathology 62 (7), 994-1001, 2013
92013
Dysfunctional mitochondrial respiration in the striatum of the Huntington’s disease transgenic R6/2 mouse model. PLoS Curr. 2013; 5
FH Aidt, SM Nielsen, J Kanters, D Pesta, TT Nielsen, A Norremolle, ...
Epub 2013/04/10. https://doi. org/10.1371/currents. hd …, 0
5
The role of CAV3 in long QT: clinical and functional assessment of a caveolin-3/Kc11. 1 compound heterozygote
PL Hedley, JK Kanters, M Dembic, T Jesperson, L Skibsbye, FH Aidt, ...
American Heart Association, 2013
32013
Evolutionary dissection of mtDNA hg H: A susceptibility factor for hypertrophic cardiomyopathy
CM Hagen, JL Elson, PL Hedley, FH Aidt, O Havndrup, MK Jensen, ...
Mitochondrial DNA Part A 31 (6), 238-244, 2020
12020
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