Rett syndrome: clinical and molecular characterization of two Brazilian patients Síndrome de Rett: caracterização clínica e molecular de dois casos brasileiros by Andrea Stachon, Francisco Baptista Assumpção Jr, Salmo Raskin

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Rett Syndrome: From Bed to Bench by Shih-Ming Weng, Mark E.S. Bailey, Stuart R. Cobb

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Distribution of hand function by age in individuals with Rett syndrome by Jeffrey L. Neul, Tim A. Benke, Eric D. Marsh, Jane B. Lane, David N. Lieberman, Steven A. Skinner, Daniel G. Glaze, Bernhard Suter, Peter T. Heydemann, Arthur A. Beisang, Shannon M. Standridge, Robin C. C. Ryther, Richard H. Haas, Lloyd J. Edwards, Amitha Ananth, Alan K. Percy

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Huntingtin phosphorylation governs BDNF homeostasis and improves the phenotype of Mecp2 knockout mice by Yann Ehinger, Julie Bruyère, Nicolas Panayotis, Yah‐Se Abada, Emilie Borloz, Valérie Matagne, Chiara Scaramuzzino, Hélène Vitet, Benoit Delatour, Lydia Saidi, Laurent Villard, Frédéric Saudou, Jean‐Christophe Roux

Subjects: “…Mecp2…”
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Neural precursor cells rescue symptoms of Rett syndrome by activation of the Interferon γ pathway by Angelisa Frasca, Federica Miramondi, Erica Butti, Marzia Indrigo, Maria Balbontin Arenas, Francesca M Postogna, Arianna Piffer, Francesco Bedogni, Lara Pizzamiglio, Clara Cambria, Ugo Borello, Flavia Antonucci, Gianvito Martino, Nicoletta Landsberger

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Siblings with Rett Syndrome: A fatal male case and an asymptomatic female carrier by José M. Lazaro-Guevara, Karen M. Garrido-Lopez

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The enhancement of activity rescues the establishment of Mecp2 null neuronal phenotypes by Linda Scaramuzza, Giuseppina De Rocco, Genni Desiato, Clementina Cobolli Gigli, Martina Chiacchiaretta, Filippo Mirabella, Davide Pozzi, Marco De Simone, Paola Conforti, Massimiliano Pagani, Fabio Benfenati, Fabrizia Cesca, Francesco Bedogni, Nicoletta Landsberger

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Clinical and molecular evaluation of 16 patients with Rett syndrome by Pınar Zengin-Akkuş, Ekim Z Taşkıran, Serkan Kabaçam, Pelin Özlem Şimşek-Kiper, Göknur Haliloğlu, Koray Boduroğlu, Gülen Eda Utine

Subjects: “…MECP2…”
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The Evolving Landscape of Functional Models of Autism Spectrum Disorder by Jai Ranjan, Aniket Bhattacharya

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Hand Stereotypies in Rett Syndrome by Matheus G Ferreira, Helio A. G. Teive

Subjects: “…motor stereotypies, rett syndrome, movement disorders, mecp2, child neurolgy…”
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Early neural dysfunction reflected in degraded auditory cortex responses in pre-regression heterozygous Mecp2 rats by Yuko Tamaoki, Samantha L. Kroon, Brendan M. Williams, Jonathan R. Riley, Crystal T. Engineer

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Neuronal Plasticity-Dependent Paradigm and Young Plasma Treatment Prevent Synaptic and Motor Deficit in a Rett Syndrome Mouse Model by Sofía Espinoza, Camila Navia, Rodrigo F. Torres, Nuria Llontop, Verónica Valladares, Cristina Silva, Ariel Vivero, Exequiel Novoa-Padilla, Jessica Soto-Covasich, Jessica Mella, Ricardo Kouro, Sharin Valdivia, Marco Pérez-Bustamante, Patricia Ojeda-Provoste, Nancy Pineda, Sonja Buvinic, Dasfne Lee-Liu, Juan Pablo Henríquez, Bredford Kerr

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Interpreting the rich dialogue between astrocytes and neurons: An overview in Rett syndrome by Francesca M. Postogna, Ottavia M. Roggero, Fabio Biella, Angelisa Frasca

Subjects: “…MECP2…”
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Structural variant allelic heterogeneity in MECP2 duplication syndrome provides insight into clinical severity and variability of disease expression by Davut Pehlivan, Jesse D. Bengtsson, Sameer S. Bajikar, Christopher M. Grochowski, Ming Yin Lun, Mira Gandhi, Angad Jolly, Alexander J. Trostle, Holly K. Harris, Bernhard Suter, Sukru Aras, Melissa B. Ramocki, Haowei Du, Michele G. Mehaffey, KyungHee Park, Ellen Wilkey, Cemal Karakas, Jesper J. Eisfeldt, Maria Pettersson, Lynn Liu, Marwan S. Shinawi, Virginia E. Kimonis, Wojciech Wiszniewski, Kyle Mckenzie, Timo Roser, Angela M. Vianna-Morgante, Alberto S. Cornier, Ahmed Abdelmoity, James P. Hwang, Shalini N. Jhangiani, Donna M. Muzny, Tadahiro Mitani, Kazuhiro Muramatsu, Shin Nabatame, Daniel G. Glaze, Jawid M. Fatih, Richard A. Gibbs, Zhandong Liu, Anna Lindstrand, Fritz J. Sedlazeck, James R. Lupski, Huda Y. Zoghbi, Claudia M. B. Carvalho

Subjects: “…MECP2 duplication syndrome…”
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Pharmacological reversal of synaptic and network pathology in human MECP2‐KO neurons and cortical organoids by Cleber A Trujillo, Jason W Adams, Priscilla D Negraes, Cassiano Carromeu, Leon Tejwani, Allan Acab, Ben Tsuda, Charles A Thomas, Neha Sodhi, Katherine M Fichter, Sarah Romero, Fabian Zanella, Terrence J Sejnowski, Henning Ulrich, Alysson R Muotri

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Broadening the Phenotype Spectrum of MECP2 Variants in Men by Johannes Lötjönen, Venla Kurra, Hannele Laivuori, Nina Bjelogrlić

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<i>MECP2</i> mRNA Profile in Brain Tissues from a Rett Syndrome Patient and Three Human Controls: Mutated Allele Preferential Transcription and In Situ RNA Mapping by Martina Mietto, Silvia Montanari, Maria Sofia Falzarano, Elisa Manzati, Paola Rimessi, Marina Fabris, Rita Selvatici, Francesca Gualandi, Marcella Neri, Fernanda Fortunato, Miryam Rosa Stella Foti, Stefania Bigoni, Marco Gessi, Marcella Vacca, Silvia Torelli, Joussef Hayek, Alessandra Ferlini

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Altered dendritic morphology of MEC II pyramidal and stellate cells in Rett syndrome mice by Manigandan Krishnan, Ayishal B. Mydeen, Mohammed M. Nakhal, Marwa F. Ibrahim, Richard L. Jayaraj, Milos R. Ljubisavljevic, Mohammad I. K. Hamad, Fatima Y. Ismail, Fatima Y. Ismail

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Clinical and genetic characteristics associated with dual-positive gene variations by Li Wang, Jinghe Shi, Xiaojing Yin, Pingyun Qiao, Fuwei Li, Weixing Feng

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Multi-gene duplication removal in an engineered human cellular MECP2 duplication syndrome model with an IRAK1-MECP2 duplication by Samar Z. Rizvi, Wing Suen Chan, Eleonora Maino, Sydney Steiman, Georgiana Forguson, Maya Klepfish, Ronald D. Cohn, Evgueni A. Ivakine

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