Arama Sonuçları - "Pitt–Hopkins syndrome"

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

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

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

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

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

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Broadening the <i>PHIP</i>-Associated Neurodevelopmental Phenotype Yazar: Giulia Pascolini, Giovanni Luca Scaglione, Balasubramanian Chandramouli, Daniele Castiglia, Giovanni Di Zenzo, Biagio Didona

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Transcription factor 4 expression in the developing non-human primate brain: a comparative analysis with the mouse brain Yazar: 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

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

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Expanding the clinical spectrum associated with defects in <it>CNTNAP2 </it>and <it>NRXN1</it> Yazar: 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

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