Latest Articles
- ArticleDysfunctional ADAM22 implicated in progressive encephalopathy with cortical atrophy and epilepsyMikko Muona, Yuko Fukata, Anna-Kaisa Anttonen, et al.January 21, 2016
- Clinical/Scientific NotesCo-occurrence of 16p13.11 microdeletion and ring chromosome 20 syndromeLance H. Rodan, Maria Zak, James Stavropoulos, et al.January 14, 2016
- ArticleOverlap between Parkinson disease and Alzheimer disease in ABCA7 functional variantsKaren Nuytemans, Lizmarie Maldonado, Aleena Ali, et al.January 14, 2016
- ArticleSegregation of a rare TTC3 variant in an extended family with late-onset Alzheimer diseaseMartin A. Kohli, Holly N. Cukier, Kara L. Hamilton-Nelson, et al.January 14, 2016
- ArticleIn silico prioritization based on coexpression can aid epileptic encephalopathy gene discoveryKaren L. Oliver, Vesna Lukic, Saskia Freytag, et al.January 14, 2016
- ArticleAtypical parkinsonism caused by Pro105Leu mutation of prion proteinA broad clinical spectrumKagari Koshi Mano, Takashi Matsukawa, Jun Mitsui, et al.January 07, 2016
- Clinical/Scientific NotesPolyneuropathy in a young Belgian patient: A novel heterozygous mutation in the WNK1/HSN2 geneJeroen de Filette, Danielle Hasaerts, Sara Seneca, et al.January 07, 2016
- The HelixWhole-exome sequencing in neurologic practiceReducing the diagnostic odysseyNicholas E. JohnsonDecember 24, 2015
- Clinical/Scientific NotesLate diagnosis of cerebral folate deficiency: Fewer seizures with folinic acid in adult siblingsPatrick Ferreira, Stephanie M. Luco, Sarah L. Sawyer, et al.December 23, 2015
- Clinical/Scientific NotesBenign hereditary chorea related to NKX2-1 with ataxia and dystoniaClaudio M. de Gusmao, Fernando Kok, Erasmo Barbante Casella, et al.December 23, 2015
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Dr. Daniel Friedman and Dr. Sharon Chiang