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Donato Di Pierro, Chiara Ciaccio, Diego Sbardella, Grazia Raffaella Tundo, Roberta Bernardini, Paolo Curatolo, Cinzia Galasso, Virginia Pironi, Massimiliano Coletta, Stefano Marini

Molecular and cellular biochemistry 2020;463(1-2):101-113

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The Management of Bone Defects in Rett Syndrome.

Stefano Gonnelli, Carla Caffarelli

Calcified tissue international 2025;116(1):11

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Genetic effects of methylation diets.

Ignatia B Van den Veyver

Annual review of nutrition 2002;22():255-82

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Investigating the impact of probiotic on neurological outcomes in Rett syndrome: A randomized, double-blind, and placebo-controlled pilot study.

Hsin-Pei Wang, Wen-Che Tsai, Su-Ching Hu, Hsu-Feng Chu, Lee Chin Wong, Ying-Chieh Tsai, Yen-Tzu Wu, Jui-Hsiang Lin, Wang-Tso Lee, Chia-Jui Hsu

Autism : the international journal of research and practice 2024;28(9):2267-2281

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S-adenosylmethionine and S-adenosylhomocysteine in plasma and cerebrospinal fluid in Rett syndrome and the effect of folinic acid supplementation.

Eveline E O Hagebeuk, Marinus Duran, Nico G G M Abeling, Arno Vyth, Bwee Tien Poll-The

Journal of inherited metabolic disease 2014;36(6):967-72

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Clinical Guidelines for Management of Bone Health in Rett Syndrome Based on Expert Consensus and Available Evidence.

Jenny Downs, Ingegerd Witt Engerström, Helen Woodhead, Carolyn Ellaway, Giangennaro Coppola, Anne-Marie Bisgaard, Bruria Ben-Zeev, Batia Weiss, Jay R Shapiro, Daniel Tarquinio, Kathleen Motil, Craig Munns, Leanne M Ward, Sue Fyfe, Torkel Brismar, Aris Siafarikas, Helen Leonard, Amanda Jefferson, Sue Thompson, Gunilla Larsson, Jane Lane, Mary Jones, Peter Humphreys, Suzanne Geerts, Michael Freilinger, Meir Lotan, Alan Percy, Mercedes Pineda, Steven Skinner, Birgit Syhler

PloS one 2016;11(2):e0146824

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Tyr120Asp mutation alters domain flexibility and dynamics of MeCP2 DNA binding domain leading to impaired DNA interaction: Atomistic characterization of a Rett syndrome causing mutation.

Daniele Di Marino, Nicoletta Landsberger, Angelisa Frasca, Gilda Stefanelli, Anna Gandaglia, Ilda D'Annessa, Elena Brivio

Biochimica et biophysica acta. General subjects 2018;1862(5):1180-1189

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Results for ""Rett Syndrome""[mesh_terms]

Treatment guidelines for rare, early-onset conditions associated with epileptic seizures: a literature review on Rett syndrome and tuberous sclerosis complex.

The psychopharmacology of autism spectrum disorder and Rett syndrome.

Recommendations for the management of gastrointestinal comorbidities with or without trofinetide use in Rett syndrome.

Proton MR spectroscopy in Rett syndrome.

Rett syndrome: model of neurodevelopmental disorders.

Multiscale Computational Study of the Conformation of the Full-Length Intrinsically Disordered Protein MeCP2.

Emerging therapies for childhood-onset movement disorders.

Rett syndrome and epilepsy: an update for child neurologists.

Effects of oral administration of common antioxidant supplements on the energy metabolism of red blood cells. Attenuation of oxidative stress-induced changes in Rett syndrome erythrocytes by CoQ10.

The Management of Bone Defects in Rett Syndrome.

Genetic effects of methylation diets.

Investigating the impact of probiotic on neurological outcomes in Rett syndrome: A randomized, double-blind, and placebo-controlled pilot study.

S-adenosylmethionine and S-adenosylhomocysteine in plasma and cerebrospinal fluid in Rett syndrome and the effect of folinic acid supplementation.

Clinical Guidelines for Management of Bone Health in Rett Syndrome Based on Expert Consensus and Available Evidence.

Tyr120Asp mutation alters domain flexibility and dynamics of MeCP2 DNA binding domain leading to impaired DNA interaction: Atomistic characterization of a Rett syndrome causing mutation.

Results for
""Rett Syndrome""[mesh_terms]