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1

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

出版事項 2009

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Artigo

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2

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

出版事項 2015

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Revisão

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3

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

出版事項 1988

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Artigo

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4

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

出版事項 1983

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Artigo

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5

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

出版事項 1992

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Artigo

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6

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

出版事項 2005

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Artigo

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7

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

出版事項 2007

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Artigo

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8

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

出版事項 2001

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Artigo

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9

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

出版事項 2004

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Artigo

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10

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

出版事項 2015

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Artigo

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11

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

出版事項 2013

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Artigo

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12

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

出版事項 2011

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Artigo

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13

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

出版事項 2001

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Artigo

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14

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

出版事項 2017

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Artigo

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15

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

出版事項 2008

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Artigo

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16

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

出版事項 2013

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Artigo

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17

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

出版事項 2019

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Artigo

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18

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

出版事項 2005

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Artigo

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19

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

出版事項 2010

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Artigo

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20

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

出版事項 2007

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Artigo

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検索結果 - Anders Paetau

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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