Rett Syndrome: Exploring the Autism Link

Por Percy, Alan K.
Publicado em 2011

Progress in Rett Syndrome: from discovery to clinical trials

Por Percy, Alan K.
Publicado no Wien Med Wochenschr (2016)

ON EXPERIMENTAL MODELS OF RETT SYNDROME BASED ON Mecp2 DYSFUNCTION

Por Calfa, Gaston, Percy, Alan K., Pozzo-Miller, Lucas
Publicado em 2011

Rett Syndrome: Reaching for Clinical Trials

Por Pozzo-Miller, Lucas, Pati, Sandipan, Percy, Alan K.
Publicado no Neurotherapeutics (2015)

Evaluation of Current Pharmacological Treatment Options in the Management of Rett Syndrome: From the Present to Future Therapeutic Alternatives

Por Chapleau, Christopher A., Lane, Jane, Pozzo-Miller, Lucas, Percy, Alan K.
Publicado em 2013

Variable phenotypic expression of a MECP2 mutation in a family

Por Augenstein, Kimberly, Lane, Jane B., Horton, Antony, Schanen, Carolyn, Percy, Alan K.
Publicado em 2009

Recent Progress in Rett Syndrome and MeCP2 Dysfunction: Assessment of Potential Treatment Options

Por Chapleau, Christopher A., Lane, Jane, Larimore, Jennifer, Li, Wei, Pozzo-Miller, Lucas, Percy, Alan K.
Publicado em 2013

Bdnf Overexpression in Hippocampal Neurons Prevents Dendritic Atrophy Caused by Rett-Associated MECP2 Mutations

Por Larimore, Jennifer L., Chapleau, Christopher A., Kudo, Shinichi, Theibert, Anne, Percy, Alan K., Pozzo-Miller, Lucas
Publicado em 2009

Hippocampal CA1 Pyramidal Neurons of Mecp2 Mutant Mice Show a Dendritic Spine Phenotype Only in the Presymptomatic Stage

Por Chapleau, Christopher A., Boggio, Elena Maria, Calfa, Gaston, Percy, Alan K., Giustetto, Maurizio, Pozzo-Miller, Lucas
Publicado em 2012

FXYD1, a modulator of Na(+),K(+)-ATPase activity, facilitates female sexual development by maintaining GnRH neuronal excitability

Por Garcia-Rudaz, Cecilia, Deng, Vivianne, Matagne, Valerie, Ronnekleiv, Oline, Bosch, Martha, Han, Victor, Percy, Alan K., Ojeda, Sergio R.
Publicado em 2009

Detection of Rarely Identified Multiple Mutations in MECP2 Gene Do Not Contribute to Enhanced Severity in Rett Syndrome

Por Chapleau, Christopher A., Lane, Jane, Kirwin, Susan M., Schanen, Carolyn, Vinette, Kathy M. B., Stubbolo, Danielle, MacLeod, Patrick, Percy, Alan K.
Publicado em 2013

Longevity in Rett Syndrome: Analysis of the North American Database

Por Kirby, Russell S., Lane, Jane B, Childers, Jerry, Skinner, Steve A., Annese, Fran, Barrish, Judy O., Glaze, Daniel G., MacLeod, Patrick, Percy, Alan K.
Publicado em 2010

From Function to Phenotype: Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2

Por Sheikh, Taimoor I., Ausió, Juan, Faghfoury, Hannah, Silver, Josh, Lane, Jane B., Eubanks, James H., MacLeod, Patrick, Percy, Alan K., Vincent, John B.
Publicado no Sci Rep (2016)

Treatment of cardiac arrhythmias in a mouse model of Rett syndrome with Na(+)-channel-blocking antiepileptic drugs

Por Herrera, José A., Ward, Christopher S., Pitcher, Meagan R., Percy, Alan K., Skinner, Steven, Kaufmann, Walter E., Glaze, Daniel G., Wehrens, Xander H. T., Neul, Jeffrey L.
Publicado no Dis Model Mech (2015)

DENDRITIC SPINE PATHOLOGIES IN HIPPOCAMPAL PYRAMIDAL NEURONS FROM RETT SYNDROME BRAIN AND AFTER EXPRESSION OF RETT-ASSOCIATED MECP2 MUTATIONS

Por Chapleau, Christopher A., Calfa, Gaston D., Lane, Meredith C., Albertson, Asher J., Larimore, Jennifer L., Kudo, Shinichi, Armstrong, Dawna L., Percy, Alan K., Pozzo-Miller, Lucas
Publicado em 2009

The changing face of survival in Rett syndrome and MECP2-related disorders

Por Tarquinio, Daniel C., Hou, Wei, Neul, Jeffrey L., Kaufmann, Walter E., Glaze, Daniel G., Motil, Kathleen J., Skinner, Steven A., Lee, Hye-Seung, Percy, Alan K.
Publicado no Pediatr Neurol (2015)

Vitamin D Deficiency is Prevalent in Females with Rett Syndrome

Por Motil, Kathleen J., Barrish, Judy O., Lane, Jane, Geerts, Suzanne P., Annese, Fran, McNair, Lauren, Percy, Alan K., Skinner, Steven A, Neul, Jeffrey L., Glaze, Daniel G.
Publicado em 2011

Longitudinal course of epilepsy in Rett syndrome and related disorders

Por Tarquinio, Daniel C, Hou, Wei, Berg, Anne, Kaufmann, Walter E, Lane, Jane B, Skinner, Steven A, Motil, Kathleen J, Neul, Jeffrey L, Percy, Alan K, Glaze, Daniel G
Publicado no Brain (2017)

Assessment of Caregiver Inventory for Rett Syndrome

Por Lane, Jane B., Salter, Amber R., Jones, Nancy E., Cutter, Gary, Horrigan, Joseph, Skinner, Steve A., Kaufmann, Walter E., Glaze, Daniel G., Neul, Jeffrey L., Percy, Alan K.
Publicado no J Autism Dev Disord (2017)

Pubertal Development in Rett Syndrome Deviates from Typical Females

Por Killian, John T., Lane, Jane B., Cutter, Gary R., Skinner, Steven A., Kaufmann, Walter E., Tarquinio, Daniel C., Glaze, Daniel G., Motil, Kathleen J., Neul, Jeffrey L., Percy, Alan K.
Publicado no Pediatr Neurol (2014)