Artikkelit - Selaus tekijän mukaan "Paetau A"
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A distinct phenotype of distal myopathy in a large Finnish family.
Mahjneh I; Haravuori H; Paetau A; Anderson LVB; Saarinen A; Udd B; Somer H
Neurology : 1 (2003) -
Aikuisiässä alkavan ataksian uusia perinnöllisiä syitä
Rantamäki M; Wartiovaara A; Luoma P; Hakonen A; Majamaa K; Soini H; Finnilä S; Hietaharju A; Paetau A; Kääriäinen H; Udd B
Duodecim (2007) -
Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease
Suomalainen A; Majander A; Wallin M; Setala K; Kontula K; Leinonen H; Salmi T; Paetau A; Haltia M; Valanne L; Lönnqvist J
Neurology : 5 (1997) -
Expression of KIT Receptor Tyrosine Kinase in Endothelial Cells of Juvenile Brain Tumors
Puputti M; Tynninen O; Pernilä P; Salmi M; Jalkanen S; Paetau A; Sihto H; Joensuu H
BRAIN PATHOL (2010) -
Hydrolethalus syndrome: neuropathology of 21 cases confirmed by HYLS1 gene mutation analysis
Paetau A; Honkala H; Salonen R; Ignatius J; Kestilä M; Herva R
J NEUROPATHOL EXP NEUROL (2008) -
Mice with Inactivation of Aryl Hydrocarbon Receptor Interacting Protein (Aip) Display Complete Penetrance of Pituitary Adenomas with aberrant ARNT Expression
Raitila A; Lehtonen HJ; Arola J; Heliövaara E; Ahlsten M; Georgitsi M; Jalanko A; Paetau A; Aaltonen LA; Karhu A
AM J PATHOL (2010) -
Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin
Hakonen AH; Heiskanen S; Juvonen V; Lappalainen I; Luoma PT; Rantamaki M; Goethem GV; Lofgren A; Hackman P; Paetau A; Kaakkola S; Majamaa K; Varilo T; Udd B; Kääriäinen H; Bindoff LA; Suomalainen A
Am J Hum Genet : 3 (2005) -
Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice
Tyynismaa H; Mjosund K P; Wanrooij S; Lappalainen I; Ylikallio E; Jalanko A; Spelbrink J N; Paetau A; Suomalainen A
Proc Natl Acad Sci U S A : 49 (2005) -
The gene disrupted in Marinesco-Sjogren syndrome encodes SIL1, an HSPA5 cochaperone
Anttonen A K; Mahjned I; Hämäläinen R H; Lagier-Tourenne C; Kopra O; Waris L; Anttonen M; Joensuu T; Kalimo H; Paetau A; Tranebjaerg L; Chaigne D; Koenig M; Eeg-Olofsson O; Udd B; Somer M; Somer H; Lehesjoki A E
Nat Genet : 12 (2005)