Search Results - "Normal family

Immunological profile in a family with nephrogenic diabetes insipidus with a novel 11 kb deletion in AVPR2 and ARHGAP4 genes by Arinami Tadao, Sasaki Sei, Kitazawa Katsuhiko, Morinishi Yoichi, Kashiwagi Reiichi, Hirata Kenji, Imai Kohsuke, Fujimoto Masaya, Nonoyama Shigeaki, Noguchi Emiko

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Inequalities in overweight and obesity among reproductive age group women in India: evidence from National Family Health Survey (2015-16) by Pradeep Kumar, Sherry Mangla, Sampurna Kundu

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Ethnopharmacological Approaches for Therapy of Jaundice: Part II. Highly Used Plant Species from Acanthaceae, Euphorbiaceae, Asteraceae, Combretaceae, and Fabaceae Families by Devesh Tewari, Andrei Mocan, Andrei Mocan, Emil D. Parvanov, Archana N. Sah, Seyed M. Nabavi, Lukasz Huminiecki, Zheng Feei Ma, Zheng Feei Ma, Yeong Yeh Lee, Jarosław O. Horbańczuk, Atanas G. Atanasov, Atanas G. Atanasov, Atanas G. Atanasov

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Influencing Factors Related to Female Sports Participation Under the Implementation of Chinese Government Interventions: An Analysis Based on the China Family Panel Studies by Ping Fang, Lei Sun, Shu Sheng Shi, Rizwan Ahmed Laar, Yan Lu

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Six-year follow-up of a child with familial chylomicronemia syndrome: disease course and effectiveness of gemfibrozil treatment --case report and literature review by Manal Mustafa, Mira Almheiri

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Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother by Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang

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A de novo KCNQ2 Gene Mutation Associated With Non-familial Early Onset Seizures: Case Report and Revision of Literature Data by Gianluigi Laccetta, Simona Fiori, Matteo Giampietri, Annarita Ferrari, Valentina Cetica, Manuela Bernardini, Francesca Chesi, Sara Mazzotti, Elena Parrini, Massimiliano Ciantelli, Andrea Guzzetta, Andrea Guzzetta, Paolo Ghirri

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Association between personality characteristics and sleep quality among Chinese middle-aged and older adults: evidence from China family panel studies by Zhen Wang, Zhi Zeng

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Protection Against Oxidative Stress-Induced Neurodegeneration by a Modulator for DJ-1, the Wild-Type of Familial Parkinson's Disease-Linked PARK7 by Takashi Yanagida, Yoshihisa Kitamura, Koichiro Yamane, Kazunori Takahashi, Kazuyuki Takata, Daijiro Yanagisawa, Hiroyuki Yasui, Takashi Taniguchi, Takahiro Taira, Toshio Honda, Hiroyoshi Ariga

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Occurrence of Esophageal Atresia With Tracheoesophageal Fistula in Siblings From Three-Generation Family Affected by Variable Expressivity MYCN Mutation: A Case Report by Magdalena Klaniewska, Krystian Toczewski, Anna Rozensztrauch, Michal Bloch, Agata Dzielendziak, Piotr Gasperowicz, Ryszard Slezak, Rafał Ploski, Małgorzata Rydzanicz, Robert Smigiel, Dariusz Patkowski

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Overexpression of Long Non-Coding RNA POU3F3 in Esophageal Squamous Cell Carcinoma is Associated with TNM Stage and Family History by Halime Rahimnia, Abdolvahab Moradi, Naemeh Javid, Yasaman Fateri, Shabbou Bahramian, Zahra Roohinejad, Hossein Sabouri, Eisa Jorjani

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Viewpoints from families for improving transition from NICU-to-home for infants with medical complexity at a safety net hospital: a qualitative study by Ashwini Lakshmanan, Katrina Kubicek, Roberta Williams, Marisela Robles, Douglas L. Vanderbilt, Christine B. Mirzaian, Philippe S. Friedlich, Michele Kipke

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Impact of a pharmacist-driven spirometry clinic service within a community family health center: A 5-year retrospective review by Michael J Cawley, William J Warning

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Presenting a structural model of analyzing the relationship between family communication patterns and achievement motivation with emphasis on the mediating role of students' academ... by Leila Talebi Khansari

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A Cross-sectional study to assess the Level of Utilization of Immediate Postpartum Family Planning among Postnatal women in Lira Regional Referral Hospital. by Benard Obua, Felex Okori

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Effect of family type on depression symptoms among high school students in Jiangsu province: a cross-sectional survey with propensity score matching analysis by Wenyi YANG, Yonglin ZHOU, Yan WANG, Yanjun CHEN, Xiyan ZHANG, Jingyang ZHANG, Yiliang XIN, Jie YANG

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A novel splicing mutation in the PKD1 gene causes autosomal dominant polycystic kidney disease in a Chinese family: a case report by Peiwen Xu, Sexing Huang, Jie Li, Yang Zou, Ming Gao, Ranran Kang, Junhao Yan, Xuan Gao, Yuan Gao

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Effects of common haplotypes of the ileal sodium dependent bile acid transporter gene on the development of sporadic and familial colorectal cancer: A case control study by Friedrichs Nicolaus, Plassmann Dominik, Schulte-Witte Hildegard, Becker Ursula, Keppeler Hildegard, Lamberti Christoph, Jungck Matthias, Grünhage Frank, Buettner Reinhard, Aretz Stefan, Sauerbruch Tilman, Lammert Frank

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De novo variation in EP300 gene cause Rubinstein-Taybi syndrome 2 in a Chinese family with severe early-onset high myopia by Xiaoyu Huang, Xue Rui, Shuang Zhang, Xiaolong Qi, Weining Rong, Xunlun Sheng

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Whole exome sequencing reveals a stop-gain mutation of PKD2 in an autosomal dominant polycystic kidney disease family complicated with aortic dissection by Wenwen Zhang, Qian Han, Zhao Liu, Wei Zhou, Qing Cao, Weimin Zhou

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