Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy

M. Auranen; A. Paetau; P. Piirilä; A. Pohju; T. Salmi; A. Lamminen; M. Löfberg; S. Mosegaard; R. K. Olsen; T. Tyni

doi:10.1016/j.nmd.2017.03.003

Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy

M. Auranen, A. Paetau, P. Piirilä, A. Pohju, T. Salmi, A. Lamminen, M. Löfberg, S. Mosegaard, R. K. Olsen, T. Tyni

Forskningsoutput: Tidskriftsbidrag › Artikel › Vetenskaplig › Peer review

Originalspråk	engelska
Tidskrift	Neuromuscular Disorders
Volym	27
Nummer	6
Sidor (från-till)	581-584
Antal sidor	4
ISSN	0960-8966
DOI	https://doi.org/10.1016/j.nmd.2017.03.003
Status	Publicerad - juni 2017
MoE-publikationstyp	A1 Tidskriftsartikel-refererad

Vetenskapsgrenar

3112 Neurovetenskaper
3124 Neurologi och psykiatri

Åtkomst av dokument

10.1016/j.nmd.2017.03.003

PatientSlutlig publicerad version, 1,31 MB

Citera det här

@article{f95d6b4a8af1478e988922d04ff983a2,

title = "Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy",

keywords = "Genetics, Neuromuscular disease, Metabolic disease, Muscle disease, 3112 Neurosciences, 3124 Neurology and psychiatry",

author = "M. Auranen and A. Paetau and P. Piiril{\"a} and A. Pohju and T. Salmi and A. Lamminen and M. L{\"o}fberg and S. Mosegaard and Olsen, {R. K.} and T. Tyni",

year = "2017",

month = jun,

doi = "10.1016/j.nmd.2017.03.003",

language = "English",

volume = "27",

pages = "581--584",

journal = "Neuromuscular Disorders",

issn = "0960-8966",

publisher = "Elsevier Scientific Publ. Co",

number = "6",

}

TY - JOUR

T1 - Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy

AU - Auranen, M.

AU - Paetau, A.

AU - Piirilä, P.

AU - Pohju, A.

AU - Salmi, T.

AU - Lamminen, A.

AU - Löfberg, M.

AU - Mosegaard, S.

AU - Olsen, R. K.

AU - Tyni, T.

PY - 2017/6

Y1 - 2017/6

KW - Genetics

KW - Neuromuscular disease

KW - Metabolic disease

KW - Muscle disease

KW - 3112 Neurosciences

KW - 3124 Neurology and psychiatry

U2 - 10.1016/j.nmd.2017.03.003

DO - 10.1016/j.nmd.2017.03.003

M3 - Article

SN - 0960-8966

VL - 27

SP - 581

EP - 584

JO - Neuromuscular Disorders

JF - Neuromuscular Disorders

IS - 6

ER -