AliyaFrederickMD

PubMed

• 1 citations
  Expanding the phenotypic and molecular spectrum of NFS1-related disorders that cause functional deficiencies in mitochondrial and cytosolic iron-sulfur cluster contain...
  Jennifer H Yang, Marisa W Friederich, Katarzyna A Ellsworth, Aliya Frederick, Emily Foreman, Denise Malicki, David Dimmock, Jerica Lenberg, Chitra Prasad, Andrea C Yu,...> ;Human Mutation. 2022 Mar 1
• 2 citations
  To Be or No B2: A Rare Cause of Stridor and Weakness in a Toddler:
  Aliya Frederick, Jennifer H. Yang, Sarah Schneider, Alexis Quade, Lucia Guidugli, Kristen Wigby, Melissa Cameron> ;Child Neurology Open. 2021 Aug 5
• 6 citations
  Triacetyluridine treats epileptic encephalopathy from CAD mutations: a case report and review.
  Aliya Frederick, Kimberly Sherer, Linda Nguyen, Shawn Ali, Anupam Garg, Richard H. Haas, Michelle Sahagian, Jonathan D. Bui> ;Annals of Clinical and Translational Neurology. 2021 Jan 1
• 80 citations
  Evidence against dopamine D1/D2 receptor heteromers.
  Aliya L. Frederick, Hideaki Yano, Pierre Trifilieff, Harshad D. Vishwasrao, Dominik Biezonski, Jozsef Meszaros, Eneko Urizar, Christoph Kellendonk, Kai C. Sonntag, Dev...> ;Molecular Psychiatry. 2015 Jan 6
• 23 citations
  Neurobehavioral phenotyping of G(αq) knockout mice reveals impairments in motor functions and spatial working memory without changes in anxiety or behavioral despair.
  Aliya L. Frederick, Tommy P. Saborido, Gregg D. Stanwood> ;Frontiers in Behavioral Neuroscience. 2012 Jun 19
• 54 citations
  Drugs, biogenic amine targets and the developing brain
  Aliya L. Frederick, Gregg D. Stanwood> ;Developmental Neuroscience. 2009 Apr 17
• Join now to see all