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Høyer, Helle
113
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Online (113)
Mediatypes
Articles (Online) (45)
OpenAccess-fulltext (68)
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1
Repeat expansions in AR, ATXN1, ATXN2 and HTT in Norwegian ..:
Novy, Camilla
;
Busk, Øyvind L
;
Tysnes, Ole-Bjørn
...
Brain Communications. 6 (2024) 2 - p. , 2024
Link:
https://doi.org/10.1093/..
?
2
A Novel SPAST Variant Associated with Isolated Spastic Para..:
Høyer, Helle
;
Nakken, Ola
;
Holmøy, Trygve
.
Case Reports in Genetics. 2023 (2023) - p. 1-5 , 2023
Link:
https://doi.org/10.1155/..
?
3
Genetic overlap between ALS and other neurodegenerative or ..:
Olsen, Cathrine Goberg
;
Busk, Øyvind Løvold
;
Holla, Øystein Lunde
...
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 25 (2023) 1-2 - p. 177-187 , 2023
Link:
https://doi.org/10.1080/..
?
4
Late-onset sensory-motor axonal neuropathy, a novelSLC12A6-..:
Løseth, Sissel
;
Høyer, Helle
;
Le, Kim-Mai
...
Brain. 146 (2022) 3 - p. 912-922 , 2022
Link:
https://doi.org/10.1093/..
?
5
A polymorphic AT-repeat causes frequent allele dropout for ..:
Høyer, Helle
;
Hilmarsen, Hilde T
;
Sunder-Plassmann, Raute
...
Journal of Medical Genetics. 59 (2022) 10 - p. 1024-1026 , 2022
Link:
https://doi.org/10.1136/..
?
6
Genetic Epidemiology of Amyotrophic Lateral Sclerosis in No..:
Olsen, Cathrine Goberg
;
Busk, Øyvind Løvold
;
Aanjesen, Tori Navestad
...
Neuroepidemiology. 56 (2022) 4 - p. 271-282 , 2022
Link:
https://doi.org/10.1159/..
?
7
Clinical characteristics and proteome modifications in two ..:
Høyer, Helle
;
Busk, Øyvind L.
;
Esbensen, Q. Ying.
...
BMC Neurology. 22 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/..
?
8
Clinical trials in pediatric ALS: a TRICALS feasibility stu..:
Kliest, Tessa
;
Van Eijk, Ruben P.A.
;
Al-Chalabi, Ammar
...
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 23 (2022) 7-8 - p. 481-488 , 2022
Link:
https://doi.org/10.1080/..
?
9
HINT1 neuropathy in Norway: clinical, genetic and functiona..:
Amor-Barris, Silvia
;
Høyer, Helle
;
Brauteset, Lin V.
...
Orphanet Journal of Rare Diseases. 16 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
?
10
The genetic landscape of axonal neuropathies in the middle-..:
Senderek, Jan
;
Lassuthova, Petra
;
Kabzińska, Dagmara
...
Neurology. 95 (2020) 24 - p. , 2020
Link:
https://doi.org/10.1212/..
?
11
Inherited motor-sensory neuropathy with upper limb predomin..:
Fabrizi, Gian Maria
;
Høyer, Helle
;
Taioli, Federica
...
Neuromuscular Disorders. 30 (2020) 3 - p. 227-231 , 2020
Link:
https://doi.org/10.1016/..
?
12
Charcot–Marie–Tooth disease type 4C in Norway: Clinical cha..:
Arntzen, Kjell Arne
;
Høyer, Helle
;
Ørstavik, Kristin
...
Neuromuscular Disorders. 28 (2018) 8 - p. 639-645 , 2018
Link:
https://doi.org/10.1016/..
?
13
Variants in Four Genes on Chromosome 12 Is Associated with ..:
Braathen, Geir
;
Høyer, Helle
;
Busk, Øyvind
...
Neurology. 86 (2016) 16_supplement - p. , 2016
Link:
https://doi.org/10.1212/..
?
14
Diagnosing Hereditary Neuropathies in the Clinic with Next-..:
Braathen, Geir
;
Høyer, Helle
;
Busk, Øyvind
...
Neurology. 86 (2016) 16_supplement - p. , 2016
Link:
https://doi.org/10.1212/..
?
15
Corrigendum to "Genetic Diagnosis of Charcot-Marie-Tooth Di..:
Høyer, Helle
;
Braathen, Geir J.
;
Busk, Øyvind L.
...
BioMed Research International. 2015 (2015) - p. 1-2 , 2015
Link:
https://doi.org/10.1155/..
1-15