Features of Menstruation and Menstruation Management in Individuals with Rett Syndrome.
Humphrey, KN; Horn, PS; Olshavsky, L; Reebals, L; Standridge, SM.
Journal of Pediatric and Adolescent Gynecology.
2021;
34:144-153.
Multisite Study of Evoked Potentials in Rett Syndrome.
Saby, JN; Benke, TA; Peters, SU; Standridge, SM; Matsuzaki, J; Cutri-French, C; Swanson, LC; Lieberman, DN; Key, AP; Percy, AK; et al.
Annals of Neurology.
2021;
89:790-802.
Rett Syndrome: A Timely Review From Recognition to Current Clinical Approaches and Clinical Study Updates.
Ivy, AS; Standridge, SM.
Seminars in Pediatric Neurology.
2021;
37.
Well-woman care and HPV vaccination rates in women with Rett syndrome.
Humphrey, KN; Horn, PS; Olshavsky, L; Reebals, L; Standridge, SM.
Disability and Health Journal.
2021;
14.
A Psychometric Evaluation of the Motor-Behavioral Assessment Scale for Use as an Outcome Measure in Rett Syndrome Clinical Trials.
Raspa, M; Bann, CM; Gwaltney, A; Benke, TA; Fu, C; Glaze, DG; Haas, R; Heydemann, P; Jones, M; Kaufmann, WE; et al.
American Journal on Intellectual and Developmental Disabilities.
2020;
125:493-509.
Multisystem comorbidities in classic Rett syndrome: a scoping review.
Fu, C; Armstrong, D; Marsh, E; Lieberman, D; Motil, K; Witt, R; Standridge, S; Lane, J; Dinkel, T; Jones, M; et al.
BMJ Paediatrics Open.
2020;
4.
Consensus guidelines on managing Rett syndrome across the lifespan.
Fu, C; Armstrong, D; Marsh, E; Lieberman, D; Motil, K; Witt, R; Standridge, S; Nues, P; Lane, J; Dinkel, T; et al.
BMJ Paediatrics Open.
2020;
4.
Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome.
Peters, SU; Fu, C; Suter, B; Marsh, E; Benke, TA; Skinner, SA; Lieberman, DN; Standridge, S; Jones, M; Beisang, A; et al.
Clinical Genetics.
2019;
95:575-581.
Double-blind, randomized, placebo-controlled study of trofinetide in pediatric Rett syndrome.
Glaze, DG; Neul, JL; Kaufmann, WE; Berry-Kravis, E; Condon, S; Stoms, G; Oosterholt, S; Della Pasqua, O; Glass, L; Jones, NE; et al.
Neurology.
2019;
92:e1912-e1925.
The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2.
Neul, JL; Benke, TA; Marsh, ED; Skinner, SA; Merritt, J; Lieberman, DN; Standridge, S; Feyma, T; Heydemann, P; Peters, S; et al.
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics.
2019;
180:55-67.