Rezultati pretrage - Anders Paetau

Detaljiziraj rezultate
  1. 1
    Recessive twinkle mutations cause severe epileptic encephalopathy

    Recessive twinkle mutations cause severe epileptic encephalopathy od Tuula Lönnqvist, Anders Paetau, Leena Valanne, Helena Pihko

    Izdano 2009
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  2. 2
    Leigh Syndrome

    Leigh Syndrome od Nicole J. Lake, Matthew Bird, Pirjo Isohanni, Anders Paetau

    Izdano 2015
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  3. 3
    Accuracy of the clinical diagnosis of vascular dementia: a prospective clinical and post-mortem neuropathological study.

    Accuracy of the clinical diagnosis of vascular dementia: a prospective clinical and post-mortem neuropathological study. od Timo Erkinjuntti, Matti Haltia, J. Palo, Raimo Sulkava, Anders Paetau

    Izdano 1988
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  4. 4
    Accuracy of clinical diagnosis in primary degenerative dementia: correlation with neuropathological findings.

    Accuracy of clinical diagnosis in primary degenerative dementia: correlation with neuropathological findings. od Raimo Sulkava, Matti Haltia, Anders Paetau, J. Wikström, J. Palo

    Izdano 1983
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  5. 5
    Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA

    Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA od Anu Suomalainen, L. Peltonen, Anders Paetau, Hannu Leinonen, Anna Majander, Hannu Somer

    Izdano 1992
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  6. 6
    Apoptosis dominant in the periinfarct area of human ischaemic stroke—a possible target of antiapoptotic treatments

    Apoptosis dominant in the periinfarct area of human ischaemic stroke—a possible target of antiapoptotic treatments od Tiina Sairanen, Marja‐Liisa Karjalainen‐Lindsberg, Anders Paetau, Petra Ijäs, Perttu J. Lindsberg

    Izdano 2005
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  7. 7
    Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion

    Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion od Anna H. Hakonen, Pirjo Isohanni, Anders Paetau, Riitta Herva, Anu Suomalainen, Tuula Lönnqvist

    Izdano 2007
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  8. 8
    Variant Alzheimer Disease With Spastic paraparesis: Neuropathological phenotype

    Variant Alzheimer Disease With Spastic paraparesis: Neuropathological phenotype od Auli Verkkoniemi, Hannu Kalimo, Anders Paetau, Mirja Somer, Takeshi Iwatsubo, John Hardy, Matti Haltia

    Izdano 2001
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  9. 9
    Remodeling of Saccular Cerebral Artery Aneurysm Wall Is Associated With Rupture

    Remodeling of Saccular Cerebral Artery Aneurysm Wall Is Associated With Rupture od Juhana Frösén, Anna Piippo, Anders Paetau, Marko Kangasniemi, Mika Niemelä, Juha Hernesniemi, Juha E. Jääskeläinen

    Izdano 2004
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  10. 10
    <i>CHCHD10</i> variant p.(Gly66Val) causes axonal Charcot-Marie-Tooth disease

    <i>CHCHD10</i> variant p.(Gly66Val) causes axonal Charcot-Marie-Tooth disease od Mari Auranen, Emil Ylikallio, Maria Shcherbii, Anders Paetau, Sari Kiuru‐Enari, Jussi Toppila, Henna Tyynismaa

    Izdano 2015
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  11. 11
    Consensus Recommendations on Pathologic Changes in the Hippocampus: A Postmortem Multicenter Inter-Rater Study

    Consensus Recommendations on Pathologic Changes in the Hippocampus: A Postmortem Multicenter Inter-Rater Study od Tuomas Rauramaa, Maria Pikkarainen, Elisabet Englund, Paul G. Ince, K. A. Jellinger, Anders Paetau, Irina Alafuzoff

    Izdano 2013
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  12. 12
    ERG Transcription Factor as an Immunohistochemical Marker for Vascular Endothelial Tumors and Prostatic Carcinoma

    ERG Transcription Factor as an Immunohistochemical Marker for Vascular Endothelial Tumors and Prostatic Carcinoma od Markku Miettinen, Zeng-Feng Wang, Anders Paetau, Shyh‐Han Tan, Albert Dobi, Shiv Srivastava, Isabell A. Sesterhenn

    Izdano 2011
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  13. 13
    Evolution of Cerebral Tumor Necrosis Factor-α Production During Human Ischemic Stroke

    Evolution of Cerebral Tumor Necrosis Factor-α Production During Human Ischemic Stroke od Tiina Sairanen, Olli Carpén, Marja‐Liisa Karjalainen‐Lindsberg, Anders Paetau, Ursula Turpeinen, Markku Kaste, Perttu J. Lindsberg

    Izdano 2001
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  14. 14
    Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome

    Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome od Sanna Matilainen, Christopher J. Carroll, Uwe Richter, Liliya Euro, Max Pohjanpelto, Anders Paetau, Pirjo Isohanni, Anu Suomalainen

    Izdano 2017
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  15. 15
    Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome

    Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome od Alexandra Götz, Pirjo Isohanni, Helena Pihko, Anders Paetau, Riitta Herva, Outi Saarenpää‐Heikkilä, Leena Valanne, Sanna Marjavaara, Anu Suomalainen

    Izdano 2008
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  16. 16
    Deficiency of the E3 ubiquitin ligase TRIM2 in early-onset axonal neuropathy

    Deficiency of the E3 ubiquitin ligase TRIM2 in early-onset axonal neuropathy od Emil Ylikallio, Rosanna Pöyhönen, M. Zimoń, Els De Vriendt, Taru Hilander, Anders Paetau, Albena Jordanova, Tuula Lönnqvist, Henna Tyynismaa

    Izdano 2013
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  17. 17
    Lewy-related pathology exhibits two anatomically and genetically distinct progression patterns: a population-based study of Finns aged 85+

    Lewy-related pathology exhibits two anatomically and genetically distinct progression patterns: a population-based study of Finns aged 85+ od Anna Raunio, Karri Kaivola, Jarno Tuimala, Mia Kero, Minna Oinas, Tuomo Polvikoski, Anders Paetau, Pentti J. Tienari, Liisa Myllykangas

    Izdano 2019
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  18. 18
    Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice

    Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice od Henna Tyynismaa, Katja Peltola Mjøsund, Sjoerd Wanrooij, Ilse Lappalainen, Emil Ylikallio, Anu Jalanko, Johannes N. Spelbrink, Anders Paetau, Anu Suomalainen

    Izdano 2005
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  19. 19
    Mice with Inactivation of Aryl Hydrocarbon Receptor-Interacting Protein (Aip) Display Complete Penetrance of Pituitary Adenomas with Aberrant ARNT Expression

    Mice with Inactivation of Aryl Hydrocarbon Receptor-Interacting Protein (Aip) Display Complete Penetrance of Pituitary Adenomas with Aberrant ARNT Expression od Anniina Raitila, Heli Lehtonen, Johanna Arola, Elina Heliövaara, Manuel Ahlsten, Marianthi Georgitsi, Anu Jalanko, Anders Paetau, Lauri A. Aaltonen, Auli Karhu

    Izdano 2010
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  20. 20
    Distal myopathy caused by homozygous missense mutations in the nebulin gene

    Distal myopathy caused by homozygous missense mutations in the nebulin gene od Carina Wallgren‐Pettersson, Vilma‐Lotta Lehtokari, Hannu Kalimo, Anders Paetau, E. Matti Nuutinen, Peter Hackman, Caroline A. Sewry, Katarina Pelin, Bjarne Udd

    Izdano 2007
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