نتایج جستجو برای: hypotonia

تعداد نتایج: 1818  

Journal: :Turkish Journal of Pediatric Disease 2013

Journal: :International journal of pediatric research 2022

A protein kinase domain, a Rhodanase-like and the Tre-2/Bub2/Cdc16 (TBC) domain are all encoded by TBCK gene. By modulating mammalian target of rapamycin (mTOR) signaling pathway, is hypothesized to play role in actin organization, cell growth, proliferation. Has organization cytoskeleton.

2014
Jihua Zhang Caiyun Ma Guanghui Liu Qing Shang Jingjie Li Chao Xu

To analyze the relationship between arginine and blood ammonia, nutritional status, immunity, and to explore the regulating function of arginine in cerebral palsy infants with muscle hypotonia. We chose 96 cases with muscle hypotonia cerebral palsy from January 2009 to January 2012 in rehabilitation center of Zhengzhou children hospital as the research object, using the questionnaire survey to ...

Journal: :iranian journal of child neurology 0
shadab salehpour assistant professor of pediatric endocrinology and fellowship of bone and inherited metabolic disorders,shahid beheshti university of medical sciences, tehan ,iran farzaneh rohani assistant professor of pediatric endocrinology, tehran university of medical sciences, tehran, iran omid aryani senior researcher, molecular genetics, department of medical genetics, special medical center, tehran, iran massoud houshmand assistant professor of human genetics, department of medical genetics, national institute of genetic engineering and biotechnology (nigeb), tehran, iran farhad hasheminezhad pulmonologist, tehran, iran morteza rezvani kashani pediatric neurologist, tehran, iran

objective prader-willi syndrome (pws) is a genetic syndrome presenting with severe hypotonia and decreased agility. growth hormone (gh), which is often used in these patients to treat short stature and obesity, seems improve hypotonia, physical strength, activity, and locomotor developmental ability. the aim of this study was to find the effects of growth hormone on agility and strength of thes...

Journal: :Arquivos De Neuro-psiquiatria 2023

Case presentation: 5-year-old girl, born from a consanguineous couple, is referred to our service due weakness and hypotonia. It was necessary hospitalization, after birth, respiratory insufficiency severe motor delay already evident in the first months of life. At 6 she did not have head control at 12 able sit without support. She developed problems with apneas hypercapnia, 3 years age, that t...

2016
Pragashnie Govender Robin W E Joubert

BACKGROUND Clinical assessment of hypotonia is challenging due to the subjective nature of the initial clinical evaluation. This poses dilemmas for practitioners in gaining accuracy, given that the presentation of hypotonia can be either a non-threatening or malevolent sign. The research question posed was how clinical assessment can be improved, given the current contentions expressed in the s...

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