نتایج جستجو برای: hypophosphatasia

تعداد نتایج: 591  

Journal: :Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2013
Haiou Yang Lili Wang Juan Geng Tingting Yu Ru-En Yao Yongnian Shen Lei Yin Daming Ying Rongkui Huang Yunfang Zhou Huijin Chen Lanbo Liu Xi Mo Yiping Shen Qihua Fu Yongguo Yu

AIMS Hypophosphatasia, a rare inherited disease characterized by defective mineralization of bone and teeth, is caused by various mutations in the tissue-nonspecific isoenzyme of alkaline phosphatase (TNSALP) gene. Our aim was to determine the mutations on TNSALP gene in three Chinese children diagnosed as having hypophosphatasia. METHODS Genomic DNA was extracted from whole blood samples of ...

Journal: :Archives of Disease in Childhood 1990

Journal: :Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases 2009
Krupa B Doshi Amir H Hamrahian Angelo A Licata

We describe the case of a woman with hypophosphatasia previously exposed to bisphosphonate and subsequently treated with teriparatide (recombinant human PTH 1-34).A Caucasian woman sustained bilateral femur stress fractures when she was fifty years old, which widened despite use of calcium, vitamin D and risedronate for 2.5 years and required intramedullary rods for stabilization. Hypophosphata...

Journal: :Clinical chemistry 1988
J D Macfarlane B J Poorthuis J J van de Kamp R G Russell A M Caswell

Hypophosphatasia is an inherited disease in which a deficiency of the bone/liver/kidney or tissue nonspecific isoenzyme of alkaline phosphatase (AP; EC 3.1.3.1) occurs. All forms of the disease are characterized clinically by defective mineralization. Several biochemical abnormalities are associated with the deficiency of AP activity, e.g., increased urinary excretion of inorganic pyrophosphate...

Journal: :Journal of Research and Practice on the Musculoskeletal System 2018

Journal: :Pediatric dentistry 1996
C C Hu D L King H F Thomas J P Simmer

H ypophosphatasia is a rare inherited disorder characterized by a wide spectrum of defects in mineralized tissues. The disease is usually inherited as an autosomal recessive trait with a prevalence of approximately 1/100,000 live births. 1 The clinical manifestations are highly variable, ranging from an almost total lack of skeletal formation to the premature loss of the permanent anterior teet...

2016
Nick Bishop Craig F Munns Keiichi Ozono

Hypophosphatasia (HPP) is a rare, potentially life-threatening disease characterised by hypomineralisation of bones and teeth. The fundamental defect is reduced functional activity of the enzyme tissue-nonspecific alkaline phosphatase (usually just termed alkaline phosphatase [ALP] in clinical practice). Homozygous or compound heterozygous mutations in the ALPL gene result in the most severe ph...

Journal: :The Journal of clinical investigation 1985
M P Whyte J D Mahuren L A Vrabel S P Coburn

Markedly increased circulating concentrations of pyridoxal-5'-phosphate (PLP) were found in each of 14 patients representing all clinical forms of hypophosphatasia, an inborn error characterized by deficient activity of the tissue nonspecific (bone/liver/kidney) isoenzyme of alkaline phosphatase (AP). The mean PLP concentration in plasma was 1174 nM (range, 214-3839 nM) in the patients and 57 +...

2013
WILLIAM H. FISHMAN

phatase may reflect enzyme contributions from bone, liver, and intestine. We have investigated serum alkaline phosphatases in two siblings with hypophosphatasia. After administration of long-chain triglycerides, the major alkaline phosphatase component of their sera was shown to be of intestinal origin on the basis of inhibition by l-phenylalanine. Starch block electrophoresis suggested that th...

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