Search Results - "Normal family

Parents' experiences of family and daily life after their child's stay in the pediatric intensive care unit: a qualitative descriptive study by Sandra Stalder, Daniela Händler-Schuster, Franzisca Domeisen Benedetti

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Empowering Young People Living With Juvenile Idiopathic Arthritis to Better Communicate With Families and Care Teams: Content Analysis of Semistructured Interviews by Grande, Stuart W, Longacre, Meghan R, Palmblad, Karin, Montan, Meera V, Berquist, Rikard P, Hager, Andreas, Kotzbauer, Greg

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The impact of online interprofessional learning on family health education to prepare collaborative-ready health professionals: A mixed-method study by Bulan K. Hermasari, Atik Maftuhah, Dian Nugroho, Veronika I. Budiastuti, Eti P. Pamungkasari

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Estimarea unor markeri ai disfuncției endoteliale la copiii hipertensivi supraponderali și obezi cu istoric familial agravat. by Liliana Bichir-Thoreac, Nelea Mătrăgună, Svetlana Cojocari

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Familienleitbilder in Deutschland Kulturelle Vorstellungen zu Partnerschaft, Elternschaft und Familienleben

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Familienleitbilder in Deutschland Kulturelle Vorstellungen zu Partnerschaft, Elternschaft und Familienleben

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OAPEN Library: description of the publication

NAA10 dysfunction with normal NatA-complex activity in a girl with non-syndromic ID and a de novo NAA10 p.(V111G) variant - a case report by Nina McTiernan, Svein Isungset Støve, Ingvild Aukrust, Marita Torrisen Mårli, Line M. Myklebust, Gunnar Houge, Thomas Arnesen

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Clinical Relevance of CYP2D6 Polymorphisms in Patients of an Austrian Medical Practice: A Family Practice-Based Observational Study by Gustav Kamenski, Seda Ayazseven, Anne Berndt, Waltraud Fink, Lukas Kamenski, Sonja Zehetmayer, Helene Pühringer

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Epigenetic role of the nuclear factor NF-Y on ID gene family in endometrial tissues of women with endometriosis: a case control study by Shirin Amirteimouri, Manan Ashini, Fariba Ramazanali, Reza Aflatoonian, Parvaneh Afsharian, Maryam Shahhoseini

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Prenatal diagnosis of a familial Y long-arm and chromosome 15 short-arm translocation inherited from a mother carrier by Chih-Ping Chen, Pu-Tsui Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Chen-Chi Lee, Dai-Dyi Town, Wayseen Wang

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Identification of a novel RPGR mutation associated with retinitis pigmentosa and primary ciliary dyskinesia in a Slovak family: a case report by Zuzana Kolkova, Peter Durdik, Peter Durdik, Veronika Holubekova, Anna Durdikova, Anna Durdikova, Milos Jesenak, Milos Jesenak, Milos Jesenak, Milos Jesenak, Peter Banovcin, Peter Banovcin

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Identification and in silico characterization of p.G380R substitution in FGFR3, associated with achondroplasia in a non-consanguineous Pakistani family by Muhammad Ajmal, Asif Mir, Muhammad Shoaib, Salman Akbar Malik, Muhammad Nasir

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A deep intronic splice variant of the COL4A5 gene in a Chinese family with X-linked Alport syndrome by Pei Qian, Ying Bao, Hui-mei Huang, Lei Suo, Yan Han, Zhi-juan Li, Min Zhang

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Bardet-Biedl syndrome caused by compound heterozygosity in BBS12 gene: a case report of one family with three affected members by Ana Simičić Majce, Darija Tudor, Marko Simunovic, Marko Simunovic, Marko Todorovic, Mladenka Parlov, Bernarda Lozic, Bernarda Lozic, Mirna Saraga-Babić, Marijan Saraga, Marijan Saraga, Adela Arapović

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Exploring the problems faced by menopausal women and the impact of family support during menopausal transition in Pinarayi Panchayat, Kerala: A qualitative study by Sabitha Nayak, Meena K., Nalini M., Swapna Jose, Seethalakshmi

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A female patient carrying a novel DMD mutation with non-random X-chromosome inactivation from a DMD family by Ming-Xia Sun, Miao Jing, Ying Hua, Jian-Biao Wang, Sheng-Quan Wang, Li-Lan Chen, Liang Ju, Yan-Shan Liu

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A novel SALL1 C757T mutation in a Chinese family causes a rare disease --Townes-Brocks syndrome by Yunqian Chi, Yi Yao, Futao Sun, Wenhong Zhang, Zihan Zhang, Yunhe Wang, Wei Hao

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Profound downregulation of neural transcription factor Npas4 and Nr4a family in fetal mice neurons infected with Zika virus. by Sergio P Alpuche-Lazcano, James Saliba, Vivian V Costa, Gabriel H Campolina-Silva, Fernanda M Marim, Lucas S Ribeiro, Volker Blank, Andrew J Mouland, Mauro M Teixeira, Anne Gatignol

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Case Report: Liver Transplantation in Homozygous Familial Hypercholesterolemia (HoFH)-Long-Term Follow-Up of a Patient and Literature Review by Matej Mlinaric, Nevenka Bratanic, Vlasta Dragos, Ajda Skarlovnik, Matija Cevc, Tadej Battelino, Tadej Battelino, Urh Groselj, Urh Groselj

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Clinical and Functional Characterization of a Novel Mutation in AVPR2 Causing Nephrogenic Diabetes Insipidus in a Four-Generation Chinese Family by Shusen Guo, Shimin Wu, Zhuxi Li, Lianjing Huang, Di Zhan, Cai Zhang, Xiaoping Luo

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