Arama Sonuçları - "craniosynostosis"

Neurological and Neurosurgical Aspects of Hypophosphatasia Yazar: Vadim P. Ivanov, Leonid A. Satanin, Alexander V. Kim, Ludmila M. Kuzenkova, Tea V. Margieva, Sofia G. Popovich

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Analysis of phenotypic characteristics and mutation patterns in syndromic craniofacial anomalies: Insights from a tertiary care medical genetics unit in South India Yazar: Rekha Aaron, Roopa Kunthavai Chellappa, Sumita Danda

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Chromosome 15q overgrowth syndrome: Prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3) Yazar: Chih-Ping Chen, Yi-Hui Lin, Heng-Kien Au, Yi-Ning Su, Chin-Yuan Hsu, Yu-Peng Liu, Pei-Chen Wu, Schu-Rern Chern, Yu-Ting Chen, Li-Feng Chen, Adam Hwa-Ming Hsieh, Wayseen Wang

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Adeno-Associated Virus-Mediated RNAi against Mutant Alleles Attenuates Abnormal Calvarial Phenotypes in an Apert Syndrome Mouse Model Yazar: Fengtao Luo, Yangli Xie, Zuqiang Wang, Junlan Huang, Qiaoyan Tan, Xianding Sun, Fangfang Li, Can Li, Mi Liu, Dali Zhang, Meng Xu, Nan Su, Zhenhong Ni, Wanling Jiang, Jinhong Chang, Hangang Chen, Shuai Chen, Xiaoling Xu, Chuxia Deng, Zhugang Wang, Xiaolan Du, Lin Chen

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Apert's syndrome: A rare case Yazar: Tarun Kumar, Neha Arora, Gagan Puri, Aravinda Konidena

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The significance or insignificance of prematurely fused bilateral squamosal sutures Yazar: Vybhav Deraje, Anisha Sawkar Tandon

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Fronto-orbito-nasal advancement a surgical approach based on skull development in treatment of craniofacial deformities Yazar: U. Joos

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Microcephaly: Significance and how to approach during the zika era Yazar: Tharangrut Hanprasertpong

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Leczenie chirurgiczne pacjentki z zespołem Aperta - opis przypadku = Surgical treatment of patient with Apert syndrome - case report Yazar: Aleksandra Szczepkowska, Piotr Osica, Anna Janas-Naze

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Leczenie chirurgiczne pacjentki z zespołem Aperta - opis przypadku = Surgical treatment of patient with Apert syndrome - case report Yazar: Aleksandra Szczepkowska, Piotr Osica, Anna Janas-Naze

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First person - Susan M. Motch Perrine and Meng Wu

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Female infant with apert syndrome and high imperforate anus without fistula Yazar: Setya Mithra Hariastuti, Risa Etika, Martono Tri Utomo, Quri Meihaerani Savitri

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Crouzon syndrome: Genetic and intervention review Yazar: N.M. Al-Namnam, F. Hariri, M.K. Thong, Z.A. Rahman

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Co-occurrence of Carpenter syndrome and double outlet right ventricle Yazar: Osman Güvenç, Derya Çimen, Derya Arslan, İbrahim Güler

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Cephalometric analysis of hard and soft tissues in a 12-year-old syndromic child: A case report and update on dentofacial features of Crouzon syndrome Yazar: K Nagaraju, E Ranadheer, P Suresh, S P Tarun

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Surgical Technique in Pediatric Craniofacial Surgery Yazar: Leopoldo Mandic Ferreira Furtado, José Aloysio da Costa Val Filho, Aieska Kellen Dantas Dantas dos Santos, Rayane Toledo Simas, João Paulo Uvera Ferreira

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CROUZON SYNDROME - CLINICAL-EVOLUTIVE PARTICULARITIES. CASE REPORT Yazar: Aniko Maria Manea, Nicoleta Kiritescu, Dobre Mihaela, Mariana Boia

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Case Report: Pansynostosis, Chiari I Malformation and Syringomyelia in a Child With Frontometaphyseal Dysplasia 1 Yazar: Jaewon Kim, Dong-Woo Lee, Dae-Hyun Jang

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Crouzon syndrome with acanthosis nigricans: A case report and literature review Yazar: Quan Duy Nguyen, Tu Nguyen Anh Tran, Hao Trong Nguyen

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Oral and systemic manifestations of congenital hypothyroidism in children. A case report. Yazar: Carmen Ayala, Obed Lemus, Maribel Frías

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