Search Results - "Normal family

Ovarian dysfunction and <it>FMR1 </it>alleles in a large Italian family with POF and FRAXA disorders: case report by D'Urso Michele, Chiurazzi Pietro, Laperuta Carmela, Miano Maria, Ursini Matilde

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A novel pathogenic variant in OSBPL2 linked to hereditary late-onset deafness in a Mongolian family by Ningjin Wu, Husile Husile, Liqing Yang, Yaning Cao, Xing Li, Wenyan Huo, Haihua Bai, Yangjian Liu, Qizhu Wu

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Fully penetrant genetic mutation results in wide familial variability: a cardiac magnetic resonance focused report by Maria Livia Iovanescu, Andreea Sorina Marcu, Cristian Militaru, Octavian Istratoaie, Ioana Gheonea, Sebastian Militaru

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Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa by Huang Yukan, Zhang Jing, Li Chang, Yang Guohua, Liu Mugen, Wang Qing K, Tang Zhaohui

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"The real pandemic's been there forever": qualitative perspectives of domestic and family violence workforce in Australia during COVID-19 by Rachel Baffsky, Kristen Beek, Sarah Wayland, Janani Shanthosh, Amanda Henry, Patricia Cullen

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Evaluation of Growth Hormone Therapy in Seven Chinese Children With Familial Short Stature Caused by Novel ACAN Variants by Jie Sun, Lihong Jiang, Geli Liu, Chen Ma, Jiaqi Zheng, Lele Niu

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Mitigating Social Isolation Among Peritoneal Dialysis Patients: The Impact of Educational Level, Physical Activity, and Familial Support by Cai H, Wu Z, Xu J, Wang T, Li Y, Jiang Y, Xu M

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A novel frameshift mutation in FRMD7 causes X-linked infantile nystagmus in a Chinese family by Junjue Chen, Yan Wei, Linlu Tian, Xiaoli Kang

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The spatiotemporal expression pattern of the bone morphogenetic protein family in rat ovary cell types during the estrous cycle by Shimasaki Shunichi, Erickson Gregory F

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Novel PRKAG2 variant presenting as liver cirrhosis: report of a family with 2 cases and review of literature by Zahra Beyzaei, Fatih Ezgu, Bita Geramizadeh, Alireza Alborzi, Alireza Shojazadeh

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Sustaining the well-being of family with working spouse: income sharing dimension / Fadhilah Adibah Ismail ... [et al.] by Ismail, Fadhilah Adibah, Ab Manan, Siti Khadijah, Saidon, Rafeah, Sahari, Noorul Huda, Abd Aziz, Azhar, Jaapar, Nurzahidah

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Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation by Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Mohammad Keramatipour, Saeid Morovvati

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A case report of a boy suffering from type 1 diabetes mellitus and familial Mediterranean fever by Maria Francesca Gicchino, Dario Iafusco, Angela Zanfardino, Emanuele Miraglia del Giudice, Alma Nunzia Olivieri

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Community based maternal and child health nutrition project, Uttar Pradesh: An innovative strategy focusing on "At risk" families by Sheila C Vir

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A Missense Mutation of the α-Galactosidase A Gene in a Chinese Family of Fabry Disease with Renal Failure by Chunli Wang, Yang Wang, Feng Zhu, Jing Xiong

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The Relationship of Family Communication Level With The Sexual Behavior of Adolescent With Disability In The Umbrella Disability Project (UDP) Bukittinggi City by Liza Andriani, Chyka Febria, Resi Oktavia

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The Role of Epidermal Growth Factor Receptor Family of Receptor Tyrosine Kinases in Mediating Diabetes-Induced Cardiovascular Complications by Bara A. Shraim, Bara A. Shraim, Moaz O. Moursi, Moaz O. Moursi, Ibrahim F. Benter, Abdella M. Habib, Abdella M. Habib, Saghir Akhtar, Saghir Akhtar

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A Subgroup of First-Degree Relatives of Crohn's Disease Patients Shows a Profile of Inflammatory Markers in the Blood Which is More Typical of Crohn's Disease Patients Than of Norm...

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A Subgroup of First-Degree Relatives of Crohn's Disease Patients Shows a Profile of Inflammatory Markers in the Blood Which Is More Typical of Crohn's Disease Patients Than of Norm... by Broide Efrat, Goren Iris, Hongbin Wang, Scapa Eitan, Keisari Yona

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Feasibility of enhancing well‐child visits with family nutrition and physical activity risk assessment on body mass index by L. Bailey‐Davis, S. M. R. Kling, G. C. Wood, W. J. Cochran, J. W. Mowery, J. S. Savage, R. A. Stametz, G. J. Welk

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