Arama Sonuçları - Sanna Marjavaara
- Gösterilen 1 - 5 sonuçlar arası kayıtlar. 5
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1
Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome Yazar: Alexandra Götz, Pirjo Isohanni, Helena Pihko, Anders Paetau, Riitta Herva, Outi Saarenpää‐Heikkilä, Leena Valanne, Sanna Marjavaara, Anu Suomalainen
Baskı/Yayın Bilgisi 2008Artigo -
2
Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion Yazar: Anna H. Hakonen, Steffi Goffart, Sanna Marjavaara, Anders Paetau, Helen Cooper, Keijo Mattila, Milla Lampinen, Antti Sajantila, Tuula Lönnqvist, Johannes N. Spelbrink, Anu Suomalainen
Baskı/Yayın Bilgisi 2008Artigo -
3
Deficiency of the INCL protein Ppt1 results in changes in ectopic F1-ATP synthase and altered cholesterol metabolism Yazar: Annina Lyly, Sanna Marjavaara, Aija Kyttälä, Kristiina Uusi-Rauva, Kaisu Luiro, Outi Kopra, Laurent O. Martinez, Kimmo Tanhuanpää, Nisse Kalkkinen, Anu Suomalainen, Matti Jauhiainen, Anu Jalanko
Baskı/Yayın Bilgisi 2008Artigo -
4
DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosis Yazar: Pirjo Isohanni, Tarja Linnankivi, Jana Buzková, Tuula Lönnqvist, Helena Pihko, Leena Valanne, Pentti J. Tienari, Irina Elovaara, Tuula Pirttilä, Mauri Reunanen, Keijo Koivisto, Sanna Marjavaara, Anu Suomalainen
Baskı/Yayın Bilgisi 2009Artigo -
5
FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study Yazar: Anu Suomalainen, Jenni M. Elo, Kirsi H. Pietiläinen, Anna H. Hakonen, Ksenia Sevastianova, Mari Korpela, Pirjo Isohanni, Sanna Marjavaara, Tiina Tyni, Sari Kiuru‐Enari, Helena Pihko, Niklas Darín, Katrin Õunap, Leo A. J. Kluijtmans, Anders Paetau, Jana Buzková, Laurence A. Bindoff, Johanna Annunen‐Rasila, Johanna Uusimaa, Aila Rissanen, Hannele Yki‐Järvinen, Michio Hirano, M. Tulinius, Jan Smeitink, Henna Tyynismaa
Baskı/Yayın Bilgisi 2011Artigo
Arama Araçları:
İlgili Konular
Biology
Genetics
Medicine
Mitochondrion
Gene
Internal medicine
Mutation
Ataxia
Mitochondrial DNA
Mitochondrial myopathy
Neuroscience
Pathology
Respiratory chain
ATP synthase
Biochemistry
Bioinformatics
Biomarker
Cell biology
Compound heterozygosity
Disease
Enzyme
Genotype
Haplotype
Immunology
Mitochondrial encephalomyopathy
Mitochondrial respiratory chain
Multiple sclerosis
Myopathy
Neurodegeneration
Physical therapy