نتایج جستجو برای: familial hypophosphatemic rickets

تعداد نتایج: 58833  

2009
Eri Suzuki Makoto Yamada Daisuke Ariyasu Masako Izawa Junko Miyamoto Shinobu Koto Yukihiro Hasegawa

The treatment for hypophosphatemic rickets in children includes phosphate and vitamin D preparations. In children, this regimen significantly improves symptoms, while a treatment for adult patients has not been established. We therefore investigated the clinical courses of 15 adult patients who discontinued therapy when final height was achieved in order to assess the necessity of treatment in ...

Journal: :Sudanese journal of paediatrics 2017
Stepan Kutilek

Burosumab (KRN23) is a fully human monoclonal IgG1 antibody that binds excess fibroblast growth factor 23 (FGF23) and has been successfully tested in clinical trials in children with X-linked hypophosphatemic rickets. A report enclosed in this letter gives a brief review of current knowledge on burosumab therapy.

Journal: :Infection control and hospital epidemiology 1999
S Fishbane B A Cunha S K Mittal J Ruggian K Shea P E Schoch

2016
Salman KHAZAEI Hamid SALEHINIYA Shahin SOLTANI Abdollah MOHAMMADIAN-HAFSHEJANI

1. Dept. of Epidemiology & Biostatistics, School of Public Health, Hamadan University of Medical Sciences, Hamadan, Iran 2. Minimally Invasive Surgery Research Center, Iran University of Medical Sciences, Tehran, Iran 3. Dept. of Health Management and Economics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran 4. Dept. of Epidemiology & Biostatistics, School of Publi...

Journal: :Korean Journal of Electrolyte Metabolism 2004

Journal: :Seminars in nephrology 2004
Lori A Brame Kenneth E White Michael J Econs

Rickets and osteomalacia are associated with hypophosphatemia in several disease states, including X-linked hypophosphatemic rickets, autosomal-dominant hypophosphatemic rickets, and tumor-induced osteomalacia. Recent advances in the understanding of these diseases include discovery of mutations in the genes encoding human phosphate-regulating gene with homologies to endopeptidases on the X chr...

Journal: :international journal of pediatrics 0
peyman eshraghi department of pediatric endocrinology, imam reza hospital, mashhad university of medical sciences, mashhad, iran. foad faroughi student research committee, faculty of medicine, mashhad university of medical sciences, mashhad, iran. mohammad karim alizadeh student research committee, faculty of paramedicine, mashhad university of medical sciences, mashhad, iran.

background: tyrosinemia type 1 is an autosomal recessive metabolic disorder, which typically affects liver and kidneys. it is caused by a defect in fumarylacetoacetate hydrolase or fumarylacetoacetase (fah) enzyme, the final enzyme in the tyrosine degradation pathway. the disease typically manifests as early onset type in early infancy with acute hepatic crisis with hepatomegaly and bleeding te...

Journal: :international journal of pediatrics 0
fereshteh ghaljaei ph.d, assistance professor of science, school of nursing and midwifery, community nursing research center, zahedan university of medical sciences, zahedan, ir iran hamideh goli msc. in nursing, school of nursing and midwifery, community nursing research center, zahedan university of medical sciences, zahedan, ir iran alia jalalodini msc. in nursing, school of nursing and midwifery, community nursing research center, zahedan university of medical sciences, zahedan, ir iran nasrin mahmoodi msc. in nursing, school of nursing and midwifery, community nursing research center, zahedan university of medical sciences, zahedan, ir iran

backgroundrickets is a disorder due to impaired metabolism of bone mineralization which caused by low concentrations of extra-cellular calcium or phosphate. in children, hypophosphatemic rickets (hr) happen malabsorption of phosphate and increasing of renal tubular loss.case presentation we present the case of a 4-year-old girl who had medical history of hr with failure to thrive (ftt). child h...

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