Search Results - "recession"

Beta-thalassemia mutation types and the relationship with the demographic factors in Sanliurfa, Turkey by Ebru Tuncez, Özlem Öz, Burcu Akıncı, Fatma Demir

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The polymorphic locus rs1799945 of the <i>HFE</i> gene determines the risk of severe preeclampsia by Maria Yu. Abramova, Irina V. Ponomarenko, Valentina S. Orlova, Irina V. Batlutskaya, Olga A. Efremova, Mikhail I. Churnosov

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Neonatal Polycystic Kidney Disease in a One-Day-Old Baby: A Case Report by Mchaile D, Mrindoko P, Mselle M, Meleki E, Kimambo E, Likiliwike A, Lodhia J

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Precision Medicine Based on CFTR Genotype for People with Cystic Fibrosis by Haq I, Almulhem M, Soars S, Poulton D, Brodlie M

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School-based intervention that integrates nutrition education and supportive healthy school food environment among Malaysian primary school children: a study protocol by Choon Huey Teo, Yit Siew Chin, Poh Ying Lim, Shahril Azian Haji Masrom, Zalilah Mohd Shariff

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Enzymatic testing for mucopolysaccharidosis type I in Kuwaiti newborns: a preliminary study toward newborn screening by Hind Alsharhan, Hind Alsharhan, Hind Alsharhan, Mohammad Z. Haider, Bann Qadoura, Mariam Ayed, Gursev S. Dhaunsi, Hessa Alkandari

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Identification of Two Novel Variants of the DMD Gene in Chinese Families with Duchenne Muscular Dystrophy by Wu J, Ren L, Huang X, Hu L, Zhang L, Xie D, Li Z, Han N, Huang S

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Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center by Jingjing Zhang, Dingyuan Ma, Gang Liu, Yuguo Wang, An Liu, Li Li, Chunyu Luo, Ping Hu, Zhengfeng Xu

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Modeling Niemann-Pick disease type C1 in zebrafish: a robust platform for in vivo screening of candidate therapeutic compounds by Wei-Chia Tseng, Hannah E. Loeb, Wuhong Pei, Chon-Hw, Lisha Xu, Celine V. Cluzeau, Christopher A. Wassif, Benjamin Feldman, Shawn M. Burgess, William J. Pavan, Forbes D. Porter

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Genetic and Clinical Features of Shwachman-Diamond Syndrome in Russian Population: Prospective Study by Maria G. Ipatova, Ekaterina A. Deordieva, Oksana A. Shvets, Anna A. Mukhina, Anna A. Moiseeva, Yulya A. Rodina, Petr V. Shumilov, Anna V. Pavlova, Elena V. Raikina, Aliy Yu. Asanov, Maria M. Litvinova, Anna Y. Shcherbina

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Function of Ltbp-4L and fibulin-4 in survival and elastogenesis in mice by Insa Bultmann-Mellin, Jeroen Essers, Paula M. van Heijingen, Harald von Melchner, Gerhard Sengle, Anja Sterner-Kock

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Effects of Mobile Health Including Wearable Activity Trackers to Increase Physical Activity Outcomes Among Healthy Children and Adolescents: Systematic Review by Böhm, Birgit, Karwiese, Svenja D, Böhm, Harald, Oberhoffer, Renate

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Are gene polymorphisms related to adverse events of methotrexate in patients with rheumatoid arthritis? A retrospective cohort study based on an updated meta-analysis by Jing Huang, Huizhen Fan, Qi Qiu, Kunpeng Liu, Shuang Lv, Jiang Li, Hui Yang, Xiaoming Shu, Yuan Xu, Xiangchen Lu, Cheng Lu, Yunnan Zhang, Cheng Xiao

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Two Novel HSD17B4 Heterozygous Mutations in Association With D-Bifunctional Protein Deficiency: A Case Report and Literature Review by Si Chen, Linrun Du, Yihui Lei, Yuanyuan Lin, Shangqin Chen, Yanli Liu

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Molecular and neurological characterizations of three Saudi families with lipoid proteinosis by Al-Fakey Yasser H, Van Maldergem Lionel, McGrath John A, Liu Lu, Alorainy Ibrahim A, Alrasheed Saleh, Abu-Amero Khaled K, Salih Mustafa A, AlSuhaibani Adel H, Oystreck Darren T, Bosley Thomas M

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Mechanisms of Congenital Myasthenia Caused by Three Mutations in the COLQ Gene by Xiaona Luo, Chunmei Wang, Longlong Lin, Fang Yuan, Simei Wang, Yilin Wang, Anqi Wang, Chao Wang, Shengnan Wu, Xiaoping Lan, Quanmei Xu, Rongrong Yin, Hongyi Cheng, Yuanfeng Zhang, Jiaming Xi, Jie Zhang, Xiaomin Sun, Jingbin Yan, Fanyi Zeng, Yucai Chen, Yucai Chen

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The Magnitude of Hereditary Spherocytosis Among Human Immunodeficiency Virus-Infected Adults Attending University of Gondar Comprehensive Specialized Hospital Northwest Ethiopia 20... by Sahile Kebede S, Yalew A, Yesuf T, Mesfin Bambo G, Duguma T, Woldu B

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DOCK8 mutation diagnosed using whole-exome sequencing of the dried blood spot-derived DNA: a case report of an Iraqi girl diagnosed in Japan by Lika'a Fasih Y. Al-Kzayer, Hanadi Munaf H. Al-Aradi, Tomonari Shigemura, Kenji Sano, Miyuki Tanaka, Motoharu Hamada, Kenan Hussien Ali, Osamah Mohammed Aldaghir, Yozo Nakazawa, Yusuke Okuno

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Digenetic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome by Yuanmei Kong, Ke Xu, Ke Yuan, Jianfang Zhu, Weiyue Gu, Li Liang, Chunlin Wang

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Molecular characterization of CTNS mutations in Tunisian patients with ocular cystinosis by Latifa Chkioua, Yessine Amri, Chaima Saheli, Wassila Mili, Sameh Mabrouk, Imen Chabchoub, Hela Boudabous, Wissem Ben Azzouz, Hadhami Ben Turkia, Salima Ferchichi, Neji Tebib, Taieb Massoud, Mohamed Ghorbel, Sandrine Laradi

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