TY  - JOUR
AU  - Dominguez-Gonzalez, Cristina
AU  - Fernandez-Torron, Roberto
AU  - Moore, Ursula
AU  - de-Fuenmayor-Fernandez-de-la-Hoz, Carlos Pablo
AU  - Velez-Gomez, Beatriz
AU  - Cabezas, Juan Antonio
AU  - Alonso-Perez, Jorge
AU  - Gonzalez-Mera, Laura
AU  - Olive, Montse
AU  - Garcia-Garcia, Jorge
AU  - Moris, German
AU  - Leon-Hernandez, Juan Carlos
AU  - Muelas, Nuria
AU  - Servian-Morilla, Emilia
AU  - Martin, Miguel A
AU  - Diaz-Manera, Jordi
AU  - Paradas, Carmen
PY  - 2022
DO  - 10.1007/s00415-021-10957-0
UR  - http://hdl.handle.net/10668/20008
T2  - Journal of neurology
AB  - TK2 deficiency (TK2d) is a rare mitochondrial disorder that manifests predominantly as a progressive myopathy with a broad spectrum of severity and age of onset. The rate of progression is variable, and the prognosis is poor due to early and severe...
LA  - en
PB  - Springer Medizin
KW  - MRI
KW  - Mitochondrial myopathy
KW  - TK2
KW  - Adult
KW  - DNA, Mitochondrial
KW  - Humans
KW  - Magnetic Resonance Imaging
KW  - Mitochondrial Myopathies
KW  - Muscle, Skeletal
KW  - Muscular Diseases
TI  - Muscle MRI characteristic pattern for late-onset TK2 deficiency diagnosis.
TY  - research article
VL  - 269
ER  -