FGF21 is a biomarker for mitochondrial translation and mtDNA maintenance disorders

Jenni M. Lehtonen, Saara Forsstrom, Emanuela Bottani, Carlo Viscomi, Olivier R. Baris, Helena Isoniemi, Krister Hockerstedt, Pia Osterlund, Mikko Hurme, Juulia Jylhava, Sirpa Leppa, Ritva Markkula, Tiina Helio, Giuliana Mombelli, Johanna Uusimaa, Reijo Laaksonen, Hannu Laaksovirta, Mari Auranen, Massimo Zeviani, Jan SmeitinkRudolf J. Wiesner, Kazuto Nakada, Pirjo Isohanni, Anu Suomalainen

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Originalspråkengelska
TidskriftNeurology
Volym87
Utgåva22
Sidor (från-till)2290-2299
Antal sidor10
ISSN0028-3878
DOI
StatusPublicerad - 29 nov 2016
MoE-publikationstypA1 Tidskriftsartikel-refererad

Vetenskapsgrenar

  • 3124 Neurologi och psykiatri
  • 3111 Biomedicinska vetenskaper

Citera det här

Lehtonen, Jenni M. ; Forsstrom, Saara ; Bottani, Emanuela ; Viscomi, Carlo ; Baris, Olivier R. ; Isoniemi, Helena ; Hockerstedt, Krister ; Osterlund, Pia ; Hurme, Mikko ; Jylhava, Juulia ; Leppa, Sirpa ; Markkula, Ritva ; Helio, Tiina ; Mombelli, Giuliana ; Uusimaa, Johanna ; Laaksonen, Reijo ; Laaksovirta, Hannu ; Auranen, Mari ; Zeviani, Massimo ; Smeitink, Jan ; Wiesner, Rudolf J. ; Nakada, Kazuto ; Isohanni, Pirjo ; Suomalainen, Anu. / FGF21 is a biomarker for mitochondrial translation and mtDNA maintenance disorders. I: Neurology. 2016 ; Vol. 87, Nr. 22. s. 2290-2299.
@article{950093afc5254067b6e31a56958438bf,
title = "FGF21 is a biomarker for mitochondrial translation and mtDNA maintenance disorders",
keywords = "GROWTH, MICE, DISEASE, DEFICIENCY, ACTIVATION, MUTATIONS, DELETIONS, MYOPATHY, TWINKLE, OBESITY, 3124 Neurology and psychiatry, 3111 Biomedicine",
author = "Lehtonen, {Jenni M.} and Saara Forsstrom and Emanuela Bottani and Carlo Viscomi and Baris, {Olivier R.} and Helena Isoniemi and Krister Hockerstedt and Pia Osterlund and Mikko Hurme and Juulia Jylhava and Sirpa Leppa and Ritva Markkula and Tiina Helio and Giuliana Mombelli and Johanna Uusimaa and Reijo Laaksonen and Hannu Laaksovirta and Mari Auranen and Massimo Zeviani and Jan Smeitink and Wiesner, {Rudolf J.} and Kazuto Nakada and Pirjo Isohanni and Anu Suomalainen",
year = "2016",
month = "11",
day = "29",
doi = "10.1212/WNL.0000000000003374",
language = "English",
volume = "87",
pages = "2290--2299",
journal = "Neurology",
issn = "0028-3878",
publisher = "Lippincott williams & wilkins",
number = "22",

}

Lehtonen, JM, Forsstrom, S, Bottani, E, Viscomi, C, Baris, OR, Isoniemi, H, Hockerstedt, K, Osterlund, P, Hurme, M, Jylhava, J, Leppa, S, Markkula, R, Helio, T, Mombelli, G, Uusimaa, J, Laaksonen, R, Laaksovirta, H, Auranen, M, Zeviani, M, Smeitink, J, Wiesner, RJ, Nakada, K, Isohanni, P & Suomalainen, A 2016, 'FGF21 is a biomarker for mitochondrial translation and mtDNA maintenance disorders', Neurology, vol. 87, nr. 22, s. 2290-2299. https://doi.org/10.1212/WNL.0000000000003374

FGF21 is a biomarker for mitochondrial translation and mtDNA maintenance disorders. / Lehtonen, Jenni M.; Forsstrom, Saara; Bottani, Emanuela; Viscomi, Carlo; Baris, Olivier R.; Isoniemi, Helena; Hockerstedt, Krister; Osterlund, Pia; Hurme, Mikko; Jylhava, Juulia; Leppa, Sirpa; Markkula, Ritva; Helio, Tiina; Mombelli, Giuliana; Uusimaa, Johanna; Laaksonen, Reijo; Laaksovirta, Hannu; Auranen, Mari; Zeviani, Massimo; Smeitink, Jan; Wiesner, Rudolf J.; Nakada, Kazuto; Isohanni, Pirjo; Suomalainen, Anu.

I: Neurology, Vol. 87, Nr. 22, 29.11.2016, s. 2290-2299.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

TY - JOUR

T1 - FGF21 is a biomarker for mitochondrial translation and mtDNA maintenance disorders

AU - Lehtonen, Jenni M.

AU - Forsstrom, Saara

AU - Bottani, Emanuela

AU - Viscomi, Carlo

AU - Baris, Olivier R.

AU - Isoniemi, Helena

AU - Hockerstedt, Krister

AU - Osterlund, Pia

AU - Hurme, Mikko

AU - Jylhava, Juulia

AU - Leppa, Sirpa

AU - Markkula, Ritva

AU - Helio, Tiina

AU - Mombelli, Giuliana

AU - Uusimaa, Johanna

AU - Laaksonen, Reijo

AU - Laaksovirta, Hannu

AU - Auranen, Mari

AU - Zeviani, Massimo

AU - Smeitink, Jan

AU - Wiesner, Rudolf J.

AU - Nakada, Kazuto

AU - Isohanni, Pirjo

AU - Suomalainen, Anu

PY - 2016/11/29

Y1 - 2016/11/29

KW - GROWTH

KW - MICE

KW - DISEASE

KW - DEFICIENCY

KW - ACTIVATION

KW - MUTATIONS

KW - DELETIONS

KW - MYOPATHY

KW - TWINKLE

KW - OBESITY

KW - 3124 Neurology and psychiatry

KW - 3111 Biomedicine

U2 - 10.1212/WNL.0000000000003374

DO - 10.1212/WNL.0000000000003374

M3 - Article

VL - 87

SP - 2290

EP - 2299

JO - Neurology

JF - Neurology

SN - 0028-3878

IS - 22

ER -