Mutations of mitochondrial DNA polymerase γA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia (Englisch)
- Neue Suche nach: Lamantea, Eleonora
- Neue Suche nach: Tiranti, Valeria
- Neue Suche nach: Bordoni, Andreina
- Neue Suche nach: Toscano, Antonio
- Neue Suche nach: Bono, Francesco
- Neue Suche nach: Servidei, Serena
- Neue Suche nach: Papadimitriou, Alex
- Neue Suche nach: Spelbrink, Hans
- Neue Suche nach: Silvestri, Laura
- Neue Suche nach: Casari, Giorgio
- Neue Suche nach: Comi, Giacomo P.
- Neue Suche nach: Zeviani, Massimo
- Neue Suche nach: Lamantea, Eleonora
- Neue Suche nach: Tiranti, Valeria
- Neue Suche nach: Bordoni, Andreina
- Neue Suche nach: Toscano, Antonio
- Neue Suche nach: Bono, Francesco
- Neue Suche nach: Servidei, Serena
- Neue Suche nach: Papadimitriou, Alex
- Neue Suche nach: Spelbrink, Hans
- Neue Suche nach: Silvestri, Laura
- Neue Suche nach: Casari, Giorgio
- Neue Suche nach: Comi, Giacomo P.
- Neue Suche nach: Zeviani, Massimo
In:
Annals of Neurology
;
52
, 2
;
211-219
;
2002
- Aufsatz (Zeitschrift) / Elektronische Ressource
-
Titel:Mutations of mitochondrial DNA polymerase γA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia
-
Beteiligte:Lamantea, Eleonora ( Autor:in ) / Tiranti, Valeria ( Autor:in ) / Bordoni, Andreina ( Autor:in ) / Toscano, Antonio ( Autor:in ) / Bono, Francesco ( Autor:in ) / Servidei, Serena ( Autor:in ) / Papadimitriou, Alex ( Autor:in ) / Spelbrink, Hans ( Autor:in ) / Silvestri, Laura ( Autor:in ) / Casari, Giorgio ( Autor:in )
-
Erschienen in:Annals of Neurology ; 52, 2 ; 211-219
-
Verlag:
- Neue Suche nach: Wiley Subscription Services, Inc., A Wiley Company
-
Erscheinungsdatum:01.08.2002
-
Format / Umfang:9 pages
-
ISSN:
-
DOI:
-
Medientyp:Aufsatz (Zeitschrift)
-
Format:Elektronische Ressource
-
Sprache:Englisch
-
Datenquelle:
Inhaltsverzeichnis – Band 52, Ausgabe 2
Zeige alle Jahrgänge und Ausgaben
Die Inhaltsverzeichnisse werden automatisch erzeugt und basieren auf den im Index des TIB-Portals verfügbaren Einzelnachweisen der enthaltenen Beiträge. Die Anzeige der Inhaltsverzeichnisse kann daher unvollständig oder lückenhaft sein.
- 133
-
New neurons for aging brainsMcKhann, Guy M. et al. | 2002
- 135
-
Neuroplasticity in old age: Sustained fivefold induction of hippocampal neurogenesis by long‐term environmental enrichmentKempermann, Gerd / Gast, Daniela / Gage, Fred H. et al. | 2002
- 144
-
Pallidal stimulation for Parkinsonism: Improved brain activation during sequence learningFukuda, Masafumi / Ghilardi, Maria Felice / Carbon, Maren / Dhawan, Vijay / Ma, Yilong / Feigin, Andrew / Mentis, Marc J. / Ghez, Claude / Eidelberg, David et al. | 2002
- 153
-
A nonischemic forearm exercise test for McArdle diseaseKazemi‐Esfarjani, Pedram / Skomorowska, Elwira / Dysgaard Jensen, Tina / Haller, Ronald G. / Vissing, John et al. | 2002
- 160
-
Gene transfer of HSP72 protects cornu ammonis 1 region of the hippocampus neurons from global ischemia: Influence of Bcl‐2Kelly, Stephen / Zhang, Zhijian J. / Zhao, Heng / Xu, Lijun / Giffard, Rona G. / Sapolsky, Robert M. / Yenari, Midori A. / Steinberg, Gary K. et al. | 2002
- 168
-
Early inflammation and dementia: A 25‐year follow‐up of the Honolulu‐Asia aging studySchmidt, Reinhold / Schmidt, Helena / Curb, J. David / Masaki, Kamal / White, Lon R. / Launer, Lenore J. et al. | 2002
- 175
-
Peripheral F2‐isoprostanes and F4‐neuroprostanes are not increased in Alzheimer's diseaseMontine, Thomas J. / Quinn, Joseph F. / Milatovic, Dejan / Silbert, Lisa C. / Dang, Theresa / Sanchez, Stephanie / Terry, Erin / Roberts, L. Jackson II / Kaye, Jeffrey A. / Morrow, Jason D. et al. | 2002
- 180
-
Differences in membrane properties of axonal and demyelinating Guillain‐Barré syndromesKuwabara, Satoshi / Ogawara, Kazue / Sung, Jia‐Ying / Mori, Masahiro / Kanai, Kazuaki / Hattori, Takamichi / Yuki, Nobuhiro / Lin, Cindy S.‐Y. / Burke, David / Bostock, Hugh et al. | 2002
- 188
-
Premotor cortex is involved in restoration of gait in strokeMiyai, Ichiro / Yagura, Hajime / Oda, Ichiro / Konishi, Ikuo / Eda, Hideo / Suzuki, Tsunehiko / Kubota, Kisou et al. | 2002
- 195
-
Cofactors of mitochondrial enzymes attenuate copper‐induced death in vitro and in vivoSheline, Christian T. / Choi, Eric H. / Kim‐Han, Jeong‐Sook / Dugan, Laura L. / Choi, Dennis W. et al. | 2002
- 205
-
Novel antibodies to synuclein show abundant striatal pathology in Lewy body diseasesDuda, John E. / Giasson, Benoit I. / Mabon, Meghann E. / Lee, Virginia M.‐Y. / Trojanowski, John Q. et al. | 2002
- 211
-
Mutations of mitochondrial DNA polymerase γA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegiaLamantea, Eleonora / Tiranti, Valeria / Bordoni, Andreina / Toscano, Antonio / Bono, Francesco / Servidei, Serena / Papadimitriou, Alex / Spelbrink, Hans / Silvestri, Laura / Casari, Giorgio et al. | 2002
- 220
-
Progressive loss of cardiac sympathetic innervation in Parkinson's diseaseLi, Sheng‐Ting / Dendi, Raghuveer / Holmes, Courtney / Goldstein, David S. et al. | 2002
- 224
-
No mutation in the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with hereditary sensory and autonomic neuropathy type VToscano, Ennio / Simonati, Alessandro / Indo, Yasuhiro / Andria, Generoso et al. | 2002
- 227
-
X‐linked creatine deficiency syndrome: A novel mutation in creatine transporter gene SLC6A8Bizzi, Alberto / Bugiani, Marianna / Salomons, Gajja S. / Hunneman, Donald H. / Moroni, Isabella / Estienne, Margherita / Danesi, Ugo / Jakobs, Cornelis / Uziel, Graziella et al. | 2002
- 231
-
Vertebrobasilar stroke as a late complication of a Blalock‐Taussig shuntGailloud, Philippe / Hillis, Argye / Perler, Bruce / Murphy, Kieran J. et al. | 2002
- 234
-
Cerebral X‐linked adrenoleukodystrophy in a girl with Xq27‐Ter deletionHershkovitz, Eli / Narkis, Ginat / Shorer, Zamir / Moser, Ann B. / Watkins, Paul A. / Moser, Hugo W. / Manor, Esther et al. | 2002
- 237
-
A novel mutation in the deoxyguanosine kinase gene causing depletion of mitochondrial DNATaanman, Jan‐Willem / Kateeb, Ihab / Muntau, Ania C. / Jaksch, Michaela / Cohen, Nadine / Mandel, Hanna et al. | 2002
- 240
-
Dyskinesias and grip control in Parkinson's disease are normalized by chronic stimulation of the subthalamic nucleusWenzelburger, Roland / Zhang, Bao‐Rong / Poepping, Meike / Schrader, Bettina / Müller, Dieter / Kopper, Florian / Fietzek, Urban / Mehdorn, Hubertus M. / Deuschl, Günther / Krack, Paul et al. | 2002
- 243
-
Demonstration of acute ischemic lesions in the fetal brain by diffusion magnetic resonance imagingBaldoli, Cristina / Righini, Andrea / Parazzini, Cecilia / Scotti, Giuseppe / Triulzi, Fabio et al. | 2002
- 247
-
Selective loss of cholinergic sudomotor fibers causes anhidrosis in Ross syndromeSommer, Claudia / Lindenlaub, Thies / Zillikens, Detlef / Toyka, Klaus V. / Naumann, Markus et al. | 2002
- 251
-
Normokalemic periodic paralysis revisited: Does it exist?Chinnery, Patrick F. / Walls, Timothy J. / Hanna, Michael G. / Bates, David / Fawcett, Peter R. W. et al. | 2002
- 253
-
Human antibodies against amyloid β peptide: A potential treatment for Alzheimer's diseaseDodel, Richard / Hampel, Harald / Depboylu, Candan / Lin, Suizhen / Gao, Feng / Schock, Sabine / Jäckel, Steffi / Wei, Xing / Buerger, Katharina / Höft, Christine et al. | 2002
- 257
-
Role of SCA2 mutations in early‐ and late‐onset dopa‐responsive parkinsonismKock, Norman / Müller, Birgitt / Vieregge, Peter / Pramstaller, Peter P. / Marder, Karen / Abbruzzese, Giovanni / Martinelli, Paolo / Lang, Anthony E. / Jacobs, Helfried / Hagenah, Johann et al. | 2002
- 258
-
ReplyShan, Din‐E / Soong, Bing‐Wen et al. | 2002
- 259
-
Book reviews| 2002
-
News and comment| 2002