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Date 2018 ISSN 0885-3185

1. 123I‐FP‐CIT SPECT [(123) I‐2β‐carbomethoxy‐3β‐(4‐iodophenyl)‐N‐(3‐fluoropropyl) nortropane single photon emission computed tomography] Imaging in a p.A53T α‐synuclein Parkinson's disease cohort versus Parkinson's disease. Issue 11 (4th October 2018)

Authors:
Koros, Christos; Simitsi, Athina; Prentakis, Andreas; Beratis, Ion; Papadimitriou, Dimitra; Kontaxopoulou, Dionysia; Fragkiadaki, Stella; Papagiannakis, Nikolaos; Seibyl, John; Marek, Kenneth; Papageorgiou, Sokratis G.; Trapali, Xenia Geronicola; Stamelou, Maria; Stefanis, Leonidas
Journal:
Movement disorders
Issue:
Volume 33:Issue 11(2018)
Page Start:
1734
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

8. A homozygous loss‐of‐function mutation in PDE2A associated to early‐onset hereditary chorea. Issue 3 (2nd February 2018)

Authors:
Salpietro, Vincenzo; Perez‐Dueñas, Belen; Nakashima, Kosuke; San Antonio‐Arce, Victoria; Manole, Andreea; Efthymiou, Stephanie; Vandrovcova, Jana; Bettencourt, Conceicao; Mencacci, Niccolò E.; Klein, Christine; Kelly, Michy P.; Davies, Ceri H.; Kimura, Haruhide; Macaya, Alfons; Houlden, Henry
Journal:
Movement disorders
Issue:
Volume 33:Issue 3(2018)
Page Start:
482
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

10. A novel missense mutation in GRIN2A causes a nonepileptic neurodevelopmental disorder. Issue 6 (11th April 2018)

Authors:
Fernández‐Marmiesse, Ana; Kusumoto, Hirofumi; Rekarte, Saray; Roca, Iria; Zhang, Jin; Myers, Scott J.; Traynelis, Stephen F.; Couce, Mª Luz; Gutierrez‐Solana, Luis; Yuan, Hongjie
Journal:
Movement disorders
Issue:
Volume 33:Issue 6(2018)
Page Start:
992
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗