Search Results - "Normal family

Orthodontic Treatment of a Patient with Dentin Dysplasia Type I and Bilateral Maxillary Canine Impaction: Case Presentation and a Family-Based Genetic Analysis by Alexandros Papagiannis, Galinos Fanourakis, Anastasia Mitsea, Kety Karayianni, Heleni Vastardis, Iosif Sifakakis

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The influence of vitamin D administration on the clinical presentation, body mass index, and osteoprotegerin (OPG) level in a sample of Egyptian children with familial Mediterranea... by Hanaa Reyad Abdallah, Manal Micheal Thomas, Walaa Alsharany Abuelhamd, Adel Mohamed Ashour, Eman Refaat Youness, Hazem Mohamed El-Hariri, Hala Tabie El-Bassyouni

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In silico analysis of the solute carrier (SLC) family in cancer indicates a link among DNA methylation, metabolic adaptation, drug response, and immune reactivity by Alessandro Lavoro, Luca Falzone, Barbara Tomasello, Giuseppe Nicolò Conti, Massimo Libra, Massimo Libra, Saverio Candido, Saverio Candido

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Identification of a novel compound heterozygous SMG9 variants in a Chinese family with heart and brain malformation syndrome using whole exome sequencing by Qi Yang, Zailong Qin, Qinle Zhang, Shang Yi, Sheng Yi, Jingsi Luo

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Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound by Chih-Ping Chen, Shu-Yuan Chang, Yen-Ni Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Li-Feng Chen, Wayseen Wang

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Analysis of deviant behaviors and family functions in the population at risk of internet addiction among primary and secondary school students in Chengdu city, Sichuan province of... by Xiujuan Zhang, Xiujuan Zhang, Xi Huang, Xi Huang, Qiong Chen, Qiong Chen, Yan Song, Yan Song, Xixi Jiang, Junxia Zhou, Junxia Zhou, Xiufang Zhao, Xiufang Zhao, Li Zhao, Li Zhao

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A newly identified mutation (c.2029 C > T) in SLC26A4 gene is associated with enlarged vestibular aqueducts in a Chinese family by Ting Wu, Limei Cui, Yakui Mou, Wentao Guo, Dawei Liu, Jingjing Qiu, Cong Xu, Jiamin Zhou, Fengchan Han, Yan Sun

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The conserved p.Arg108 residue in S1PR2 (DFNB68) is fundamental for proper hearing: evidence from a consanguineous Iranian family by Michaela A. H. Hofrichter, Majid Mojarad, Julia Doll, Clemens Grimm, Atiye Eslahi, Neda Sadat Hosseini, Mohsen Rajati, Tobias Müller, Marcus Dittrich, Reza Maroofian, Thomas Haaf, Barbara Vona

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High-intensity activity is more strongly associated with metabolic health in children compared to sedentary time: a cross-sectional study of the I.Family cohort by Jonatan Fridolfsson, Christoph Buck, Monica Hunsberger, Joanna Baran, Fabio Lauria, Denes Molnar, Luis A. Moreno, Mats Börjesson, Lauren Lissner, Daniel Arvidsson, on behalf of the I.Family consortium

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Apoyo familiar en el apego al tratamiento de la hipertensión arterial esencial Family support and drug therapy compliance in essential hypertension by Florentina Marín-Reyes, Martha Rodríguez-Morán

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Lebensgeschichten alter Eltern kognitiv beeinträchtigter Menschen Über die biografische Bedeutung des Zusammenlebens mit einem erwachsenen kognitiv beeinträchtigten Kind aus der... by Oermann, Lisa

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Lebensgeschichten alter Eltern kognitiv beeinträchtigter Menschen Über die biografische Bedeutung des Zusammenlebens mit einem erwachsenen kognitiv beeinträchtigten Kind aus der Pe... by Oermann, Lisa

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Gene expression meta-analysis supports existence of molecular apocrine breast cancer with a role for androgen receptor and implies interactions with ErbB family by Cristini Vittorio, Broom Bradley M, Sanga Sandeep, Edgerton Mary E

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Instructions to authors of the Brazilian Journal of Family and Community Medicine Instrução aos autores da Revista Brasileira de Medicina de Família e Comunidade by Sociedade Brasileira de Medicina de Família e Comunidade SBMFC

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Family Environment and Its Effect on Self Esteem and Adjustment Behaviour among School Children: A Cross Sectional Study from Hubli Taluka, Dharwad, Karnataka by Rana Sarvar, Anjana Joshi, Dattatraya D Bant

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Prenatal diagnosis of familial 2p15 microduplication associated with pulmonary artery stenosis, single umbilical artery and left foot postaxial polydactyly on fetal ultrasound by Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang

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Identification of a novel <it>KCNQ1 </it>mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family by Liu Jing, Yang Junguo, Cheng Lingling, Zhang Shirong, Wang Pengyun, Ren Xiang, Yin Ke, Zhang Su, Liu Mugen, Wang Qing

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Family Members' Perceptions of Their Psychological Responses One Year Following Pediatric Intensive Care Unit (PICU) Hospitalization: Qualitative Findings From the Caring Intensive... by Janet E. Rennick, Janet E. Rennick, Janet E. Rennick, Janet E. Rennick, Alyssa M. Knox, Stephanie C. Treherne, Karen Dryden-Palmer, Karen Dryden-Palmer, Robyn Stremler, Robyn Stremler, Christine T. Chambers, Lyndsey McRae, Michelle Ho, Michelle Ho, Dale M. Stack, Geoffrey Dougherty, Geoffrey Dougherty, Geoffrey Dougherty, Hailey Fudge, Marsha Campbell-Yeo, Marsha Campbell-Yeo

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De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia by Xiaoyu Huang, Huiping Li, Shangying Yang, Meijiao Ma, Yuanyuan Lian, Xueli Wu, Xiaolong Qi, Xuhui Wang, Weining Rong, Xunlun Sheng

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Silencing of circRNA.2837 Plays a Protective Role in Sciatic Nerve Injury by Sponging the miR-34 Family via Regulating Neuronal Autophagy by Zhi-bin Zhou, Yu-long Niu, Gao-xiang Huang, Jia-jia Lu, Aimin Chen, Lei Zhu

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