Canlyniadau Chwilio - Robyn A. Filipink
- Dangos 1 - 3 canlyniadau o 3
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Seizures in Fragile X Syndrome: Associations and Longitudinal Analysis of a Large Clinic-Based Cohort gan Elizabeth Berry‐Kravis, Robyn A. Filipink, Richard E. Frye, Sailaja Golla, Stephanie M. Morris, Howard Andrews, Tse‐Hwei Choo, Walter E. Kaufmann
Cyhoeddwyd 2021Artigo -
2
Assessment and Diagnosis of Down Syndrome Regression Disorder: International Expert Consensus gan Jonathan D. Santoro, Lina Patel, Ryan Kammeyer, Robyn A. Filipink, Grace Gombolay, Kathleen Cardinale, Diego Real de Asúa, Shahid Zaman, Stephanie L. Santoro, Sammer Marzouk, Mellad Khoshnood, Benjamin N. Vogel, Runi Tanna, Dania Pagarkar, Sofia Dhanani, M Ortega, Rebecca Partridge, Maria A. Stanley, Jessica Solomon Sanders, Alison Christy, Elise M. Sannar, Ruth C. Brown, Andrew McCormick, Heather Van Mater, Catherine Franklin, Gordon Worley, Eileen A. Quinn, George T. Capone, Brian Chicoine, Brian G. Skotko, Michael S. Rafii
Cyhoeddwyd 2022Artigo -
3
Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants gan Santhosh Girirajan, Jill A. Rosenfeld, Bradley P. Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A. Filipink, Juliann McConnell, Brad Angle, Wendy S. Meschino, Marjan M. Nezarati, Alexander Asamoah, Kelly E. Jackson, Gordon C. Gowans, Judith A. Martin, Erin P. Carmany, David W. Stockton, Rhonda E. Schnur, Lynette S. Penney, Donna M. Martin, Salmo Raskin, Kathleen A. Leppig, Heidi Thiese, Rosemarie Smith, Erika Aberg, Dmitriy M. Niyazov, Luis Escobar, Dima El‐Khechen, Kisha Johnson, Robert Roger Lebel, Kiana Siefkas, Susie Ball, Natasha Shur, Marianne McGuire, Campbell K. Brasington, J. Edward Spence, Laura Martin, Carol L. Clericuzio, Blake C. Ballif, Lisa G. Shaffer, Evan E. Eichler
Cyhoeddwyd 2012Artigo
Offerynnau Chwilio:
Pynciau Perthynol
Medicine
Cognition
Internal medicine
Psychiatry
Autism
Autism spectrum disorder
Biology
Carbamazepine
Cohort
Cohort study
Comparative genomic hybridization
Computer science
Copy number analysis
Copy-number variation
Delphi method
Epilepsy
Family medicine
Fragile X syndrome
Gene
Genetic heterogeneity
Genetics
Genome
Intellectual disability
Irritability
Lamotrigine
Levetiracetam
Mathematics
Medical physics
Neurocognitive
Odds ratio