Search Results - "Pitt–Hopkins syndrome"

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  1. 1
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    Osteopathic Manipulative Treatment Limits Chronic Constipation in a Child with Pitt-Hopkins Syndrome by Alessandro Aquino, Mattia Perini, Silvia Cosmai, Silvia Zanon, Viviana Pisa, Carmine Castagna, Stefano Uberti

    Published 2017
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  2. 2
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    Pitt-Hopkins syndrome: report of a case with a TCF4 gene mutation by Orsini Alessandro, Mantellassi Ilaria, Bonuccelli Alice, Taddeucci Grazia, Tarantino Enrico

    Published 2010
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  3. 3
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    Expanding the phenotype in Pitt-Hopkins syndrome; description of new oral finding and dental management considerations by Yazan Hassona, Dua'a Alqaisi, Asma Alkilani, Iyas AbuHijleh

    Published 2024
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  4. 4
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    Daughterless, the Drosophila orthologue of TCF4, is required for associative learning and maintenance of the synaptic proteome by Laura Tamberg, Mariliis Jaago, Kristi Säälik, Alex Sirp, Jürgen Tuvikene, Anastassia Shubina, Carl Sander Kiir, Kaja Nurm, Mari Sepp, Tõnis Timmusk, Mari Palgi

    Published 2020
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  5. 5
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    Region and Cell Type Distribution of TCF4 in the Postnatal Mouse Brain by Hyojin Kim, Hyojin Kim, Noah C. Berens, Nicole E. Ochandarena, Benjamin D. Philpot, Benjamin D. Philpot, Benjamin D. Philpot

    Published 2020
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  6. 6
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    Broadening the <i>PHIP</i>-Associated Neurodevelopmental Phenotype by Giulia Pascolini, Giovanni Luca Scaglione, Balasubramanian Chandramouli, Daniele Castiglia, Giovanni Di Zenzo, Biagio Didona

    Published 2024
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  7. 7
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    Transcription factor 4 expression in the developing non-human primate brain: a comparative analysis with the mouse brain by Alain C. Burette, Alain C. Burette, Hanna Vihma, Hanna Vihma, Audrey L. Smith, Audrey L. Smith, Siddhi S. Ozarkar, Siddhi S. Ozarkar, Jeff Bennett, Jeff Bennett, David G. Amaral, David G. Amaral, Benjamin D. Philpot, Benjamin D. Philpot, Benjamin D. Philpot

    Published 2024
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  8. 8
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    Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures by Raffaele Falsaperla, Xena Giada Pappalardo, Xena Giada Pappalardo, Catia Romano, Simona Domenica Marino, Giovanni Corsello, Martino Ruggieri, Enrico Parano, Piero Pavone

    Published 2020
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  9. 9
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    Expanding the clinical spectrum associated with defects in <it>CNTNAP2 </it>and <it>NRXN1</it> by Ullmann Reinhard, Tinschert Sigrid, Prott Eva, Nagl Sandra, Maystadt Isabelle, Kohlhase Jürgen, Klapecki Jakub, Hoyer Juliane, Horn Denise, Hackmann Karl, Engels Hartmut, Ekici Arif B, Bijlsma Emilia K, Bader Ingrid, Albrecht Beate, Gregor Anne, Wohlleber Eva, Woods Geoffrey, Reis André, Rauch Anita, Zweier Christiane

    Published 2011
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