Home News About Us Contact Contributors Disclaimer Privacy Policy Help FAQ

Home
Search
Quick Search
Advanced
Fulltext
Browse
Collections
Persons
My eDoc
Session History
Login
Name:
Password:
Documentation
Help
Support Wiki
Direct access to
document ID:


          Display Documents


Institute:
Collection:
Print in Citation style Print version     Display:
Sort by: Display records with Fulltext only
Entries: 1-4  
 Basket 
Altered cerebral glucose metabolism in a family with clinical features resembling mitochondrial neurogastrointestinal encephalomyopathy syndrome in association with multiple mitochondrial DNA deletions
Authors: Lehnhardt, Fritz-Georg; Horvath, Rita; Ullrich, Roland; Kracht, Lutz; Sobesky, Jan; Möller-Hartmann, Walter; Jacobs, Andreas H.; Haupt, Walter F.
Date of Publication (YYYY-MM-DD): 2008
Title of Journal: Archives of Neurology
Volume: 65
Issue / Number: 3
Start Page: 407
End Page: 411
Document Type: Article
ID: 376141.0
Altered cerebral glucose metabolism in a family with clinical features resembling mitochondrial neurogastrointestinal encephalomyopathy syndrome in association with multiple mitochondrial DNA deletions
Authors: Lehnhardt, Fritz-Georg; Horvath, Rita; Ullrich, Roland; Kracht, Lutz; Sobesky, Jan; Möller-Hartmann, Walter; Jacobs, Andreas H.; Haupt, Walter F.
Date of Publication (YYYY-MM-DD): 2008
Title of Journal: Archives of Neurology
Volume: 65
Issue / Number: 3
Start Page: 407
End Page: 411
Document Type: Article
ID: 379638.0
Altered cerebral glucose metabolism in a family with clinical features resembling mitochondrial neurogastrointestinal encephalomyopathy syndrome in association with multiple mitochondrial DNA deletions
Authors: Lehnhardt, Fritz-Georg; Horvath, Rita; Ullrich, Roland; Kracht, Lutz; Sobesky, Jan; Möller-Hartmann, Walter; Jacobs, Andreas H.; Haupt, Walter F.
Date of Publication (YYYY-MM-DD): 2008
Title of Journal: Archives of Neurology
Volume: 65
Issue / Number: 3
Start Page: 407
End Page: 411
Document Type: Article
ID: 572964.0
Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit
Authors: Hoffmann, Katrin; Müller, Juliane S.; Stricker, Sigmar; Megarbane, Andre; Rajab, Anna; Lindner, Tom H.; Cohen, Monika; Chouery, Eliane; Adaimy, Lynn; Ghanem, Ismat; Delague, Valerie; Boltshauser, Eugen; Talim, Beril; Horvath, Rita; Robinson, Peter N.; Lochmüller, Hanns; Hübner, Christoph; Mundlos, Stefan
Date of Publication (YYYY-MM-DD): 2006-08
Title of Journal: American Journal of Human Genetics (Chicago, IL)
Volume: 79
Issue / Number: 2
Start Page: 303
End Page: 312
Document Type: Article
ID: 313086.0
 
Full text / Content available
Entries: 1-4  
The scope and number of records on eDoc is subject to the collection policies defined by each institute - see "info" button in the collection browse view.