Search Results - "Williams Syndrome"

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  1. 21
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    A method for determining haploid and triploid genotypes and their association with vascular phenotypes in Williams syndrome and 7q11.23 duplication syndrome by Michael D. Gregory, Bhaskar Kolachana, Yin Yao, Tiffany Nash, Dwight Dickinson, Daniel P. Eisenberg, Carolyn B. Mervis, Karen F. Berman

    Published 2018
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  2. 22
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    ['Dental anomalies in a patient with Williams syndrome. Case report', 'Anomalías dentarias en un paciente con síndrome de Williams.... by Daniela Paulina Carreño Cancino, Tannia Andrea Urrea Zaldívar, Andrea Del Pilar Ormeño Quintana

    Published 2021
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  3. 23
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    ['Dental anomalies in a patient with Williams syndrome. Case report', 'Anomalías dentarias en un paciente con síndrome de Williams.... by Daniela Paulina Carreño Cancino, Tannia Andrea Urrea Zaldívar, Andrea Del Pilar Ormeño Quintana

    Published 2021
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  4. 24
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    The Multi-Dimensional Contributions of Prefrontal Circuits to Emotion Regulation during Adulthood and Critical Stages of Development by Roberts, Angela

    Published 2019
    Subjects: “…Williams Syndrome…”
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  5. 25
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    Williams-Beuren Syndrome: A Case Report by Seren Kaya, Kaan Orhan, Firdevs Tulga Öz

    Published 2019
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  6. 26
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    Williams and Down Syndromes: Brain Anatomy by J Gordon Millichap

    Published 1993
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  7. 27
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    Diagnosis and Management of Genetic Causes of Middle Aortic Syndrome in Children: A Comprehensive Literature Review by Lazea C, Al-Khzouz C, Sufana C, Miclea D, Asavoaie C, Filimon I, Fufezan O

    Published 2022
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  8. 28
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    Valsalva Sinus Aneurysm of the Non-Coronary Cuspid Presenting as Cyclops Sign on Multi-Detector Computed Tomography by Wei-Yi Ting, Chui-Mei Tiu, Jen-Dar Chen, Yi-Hong Chou, Cheng-Yen Chang

    Published 2012
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  9. 29
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    Williams-Beuren Syndrome treated with orthognathic surgery and combined partial glossectomy: case report by Ilaria Zollino, Vittoria Perrotti, Francesco Carinci

    Published 2011
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  10. 30
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    Radio-Tartaglia Syndrome: A Rare Cause of Delay in Neurodevelopment - A Case Report by Maria Arteaga Pichardo, Felipe Bernate, Juan Trujillo Angel, Maria Santana Alba, Maria Lubo, Natalia Avellaneda Perdigon, Lev Bladimir Ramirez, Daniel Jimenez, Sofia Atuesta Escobar, Isabel Fernandez Gonzalez, Luis Celis Regalado

    Published 2024
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  11. 31
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    Fluorescence in situ hybridization (FISH) as an irreplaceable diagnostic tool for Williams-Beuren syndrome in developing countries: a literature review by Bianca Soares Carlotto, Desirée Deconte, Bruna Lixinski Diniz, Priscila Ramires da Silva, Paulo Ricardo Gazzola Zen, André Anjos da Silva

    Published 2023
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  12. 32
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    Heterogeneidade nos deficits de percepção do movimento em perturbações do desenvolvimento: o caso do Autismo e da Síndrome de Williams by Ana Maria Abreu, Scania de Schonen

    Published 2009
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  13. 33
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    Avaliação da motricidade ampla e fina na Síndrome de Williams: relato de caso Findings of the gross and fine motor in the Syndrome William Case: case Report by Marcela Melo Almeida, Cibelle Kayenne Martins Roberto Formiga

    Published 2010
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  14. 34
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    Williams and Down Syndromes by J Gordon Millichap

    Published 1989
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  15. 35
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    Fissured and geographic tongue in Williams-Beuren syndrome by Neeta Sharma, Reet Kamal

    Published 2014
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  16. 36
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    Implications of Visuospatial Skills and Executive Functions for Learning Mathematics by Helyn Kim, Claire E. Cameron

    Published 2016
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  17. 37
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    Brazilian growth charts for Williams-Beuren Syndrome at ages 2 to 18 years by Amanda de Sousa Lima Strafacci, Fabio Bertapelli, Chong Ae Kim, Maria José Rivadeneira, Rachel Sayuri Honjo, Leslie Domenici Kulikowski, Danilo Moretti Ferreira, Letícia Cassimiro Batista, Vera Lúcia Gil da Silva Lopes, Gil Guerra Junior

    Published 2024
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  18. 38
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    The Impact of Oxidative Stress on Pediatrics Syndromes by Ginevra Micangeli, Michela Menghi, Giovanni Profeta, Francesca Tarani, Alessandro Mariani, Carla Petrella, Christian Barbato, Giampiero Ferraguti, Mauro Ceccanti, Luigi Tarani, Marco Fiore

    Published 2022
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  19. 39
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    The Clinical Spectrum of Inflammatory Bowel Disease Associated With Specific Genetic Syndromes: Two Novel Pediatric Cases and a Systematic Review by Simona Gatti, Giulia Gelzoni, Giulia N. Catassi, Carlo Catassi

    Published 2021
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  20. 40
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    Overview of Social Cognitive Dysfunctions in Rare Developmental Syndromes With Psychiatric Phenotype by Aurore Morel, Elodie Peyroux, Arnaud Leleu, Emilie Favre, Nicolas Franck, Caroline Demily

    Published 2018
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