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Ylikallio, Emil
115
results:
Search for persons
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Format
Online (115)
Mediatypes
Articles (Online) (32)
Bookchapter (Online) (2)
OpenAccess-fulltext (81)
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english (97)
finnish (3)
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1
Variants in tropomyosins TPM2 and TPM3 causing muscle hyper..:
Wallgren-Pettersson, Carina
;
Jokela, Manu
;
Lehtokari, Vilma-Lotta
...
Neuromuscular Disorders. 35 (2024) - p. 29-32 , 2024
Link:
https://doi.org/10.1016/..
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2
Rare PMP22 variants in mild to severe neuropathy uncorrelat..:
Palu, Edouard
;
Järvilehto, Julius
;
Pennonen, Jana
...
neurogenetics. 24 (2023) 4 - p. 291-301 , 2023
Link:
https://doi.org/10.1007/..
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3
Human IP3 receptor triple knockout stem cells remain plurip..:
Rönkkö, Julius
;
Rodriguez, Yago
;
Rasila, Tiina
...
Cell Calcium. 114 (2023) - p. 102782 , 2023
Link:
https://doi.org/10.1016/..
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4
Lowered oxidative capacity in spinal muscular atrophy, Joke..:
Ratia, Nadja
;
Palu, Edouard
;
Lantto, Hanna
...
Frontiers in Neurology. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
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5
Structural insights into Charcot–Marie–Tooth disease‐linked..:
Sutinen, Aleksi
;
Nguyen, Giang Thi Tuyet
;
Raasakka, Arne
...
FEBS Open Bio. 12 (2022) 7 - p. 1306-1324 , 2022
Link:
https://doi.org/10.1002/..
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6
Neurofilament Light Regulates Axon Caliber, Synaptic Activi..:
Sainio, Markus T.
;
Rasila, Tiina
;
Molchanova, Svetlana M.
...
Frontiers in Cell and Developmental Biology. 9 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
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7
Serum Creatine, Not Neurofilament Light, Is Elevated in CHC..:
Järvilehto, Julius
;
Harjuhaahto, Sandra
;
Palu, Edouard
...
Frontiers in Neurology. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
8
Threshold of heteroplasmic truncating MT-ATP6 mutation in r..:
Kenvin, Sebastian
;
Torregrosa-Muñumer, Ruben
;
Reidelbach, Marco
...
Human Molecular Genetics. 31 (2021) 6 - p. 958-974 , 2021
Link:
https://doi.org/10.1093/..
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9
Bi-allelic loss-of-function OBSCN variants predispose indiv..:
Cabrera-Serrano, Macarena
;
Caccavelli, Laure
;
Savarese, Marco
...
Brain. 145 (2021) 11 - p. 3985-3998 , 2021
Link:
https://doi.org/10.1093/..
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10
Attitudes towards genetic testing and information: does par..:
Saastamoinen, Antti
;
Hyttinen, Virva
;
Kortelainen, Mika
...
Journal of Community Genetics. 11 (2020) 4 - p. 461-473 , 2020
Link:
https://doi.org/10.1007/..
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11
Distinct effects on mRNA export factor GANP underlie neurol..:
Tyynismaa, Henna
;
Ylikallio, Emil
;
Stewart, Murray
...
Human Molecular Genetics. 29 (2020) 9 - p. 1426-1439 , 2020
Link:
https://doi.org/10.1093/..
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12
LATE BREAKING NEWS E-POSTER PRESENTATION:
Rönkkö, Julius
;
Molchanova, Svetlana
;
Revah-Politi, Anya
...
Neuromuscular Disorders. 30 (2020) - p. S167-S168 , 2020
Link:
https://doi.org/10.1016/..
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13
De novo SPTAN1mutation in axonal sensorimotor neuropathy an..:
Ylikallio, Emil
;
Ritari, Niina
;
Sainio, Markus
...
Brain. 143 (2020) 12 - p. e104-e104 , 2020
Link:
https://doi.org/10.1093/..
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14
Dominant mutations in ITPR3 cause Charcot‐Marie‐Tooth disea..:
Rönkkö, Julius
;
Molchanova, Svetlana
;
Revah‐Politi, Anya
...
Annals of Clinical and Translational Neurology. 7 (2020) 10 - p. 1962-1972 , 2020
Link:
https://doi.org/10.1002/..
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15
ALS and Parkinson's disease genes CHCHD10 and CHCHD2 modify..:
Harjuhaahto, Sandra
;
Rasila, Tiina S.
;
Molchanova, Svetlana M.
...
Neurobiology of Disease. 141 (2020) - p. 104940 , 2020
Link:
https://doi.org/10.1016/..
1-15