FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study
Suomalainen, Anu, Prof, Elo, Jenni M, MB, Pietiläinen, Kirsi H, MD, Hakonen, Anna H, MD, Sevastianova, Ksenia, MD, Korpela, Mari, MD, Isohanni, Pirjo, MD, Marjavaara, Sanna K, PhD, Tyni, Tiina, MD, Kiuru-Enari, Sari, MD, Pihko, Helena, Prof, Darin, Niklas, MD, Õunap, Katrin, MD, Kluijtmans, Leo AJ, MD, Paetau, Anders, MD, Buzkova, Jana, MSc, Bindoff, Laurence A, Prof, Annunen-Rasila, Johanna, MD, Uusimaa, Johanna, MD, Rissanen, Aila, Prof, Yki-Järvinen, Hannele, Prof, Hirano, Michio, MD, Tulinius, Mar, Prof, Smeitink, Jan, Prof, Tyynismaa, Henna, PhD
Published in Lancet neurology (01.09.2011)
Published in Lancet neurology (01.09.2011)
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A Novel Mutation in the SCO2 Gene in a Neonate With Early-Onset Cardioencephalomyopathy
Joost, Kairit, MD, Rodenburg, Richard, PhD, Piirsoo, Andres, PhD, van den Heuvel, Bert, PhD, Zordania, Riina, MD, PhD, Õunap, Katrin, MD, PhD
Published in Pediatric neurology (01.03.2010)
Published in Pediatric neurology (01.03.2010)
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Girl With Partial Turner Syndrome and Absence Epilepsy
Puusepp, Helen, MD, Zordania, Riina, MD, PhD, Paal, Mare, MD, Bartsch, Oliver, MD, PhD, Õunap, Katrin, MD, PhD
Published in Pediatric neurology (01.04.2008)
Published in Pediatric neurology (01.04.2008)
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