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Author/Creator Paciorkowski, Alexander R.

1. Autosomal dominant mitochondrial membrane protein‐associated neurodegeneration (MPAN). Issue 7 (13th May 2019)

Authors:
Gregory, Allison; Lotia, Mitesh; Jeong, Suh Young; Fox, Rachel; Zhen, Dolly; Sanford, Lynn; Hamada, Jeff; Jahic, Amir; Beetz, Christian; Freed, Alison; Kurian, Manju A.; Cullup, Thomas; van der Weijden, Marlous C. M.; Nguyen, Vy; Setthavongsack, Naly; Garcia, Daphne; Krajbich, Victoria; Pham, Tha...
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 7(2019)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Delineation of the movement disorders associated with FOXG1 mutations. (10th May 2016)

Authors:
Papandreou, Apostolos; Schneider, Ruth B.; Augustine, Erika F.; Ng, Joanne; Mankad, Kshitij; Meyer, Esther; McTague, Amy; Ngoh, Adeline; Hemingway, Cheryl; Robinson, Robert; Varadkar, Sophia M.; Kinali, Maria; Salpietro, Vincenzo; O'Driscoll, Margaret C.; Basheer, S. Nigel; Webster, Richard I.; M...
Journal:
Neurology
Issue:
Volume 86:Number 19(2016)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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