نتایج جستجو برای: homogentisic acid

تعداد نتایج: 747448  

Journal: :the archives of bone and joint surgery 0
babak mirzashahi joint research center, imam khomeini hospital, tehran university of medical sciences, tehran, iran abbas tafakhori tehran university of medical sciences, tehran, iran arvin najafi joint research center, imam khomeini hospital, tehran university of medical sciences, tehran, iran mahmoud farzan joint research center, imam khomeini hospital, tehran university of medical sciences, tehran, iran

even though intervertebral disc degeneration can be found in the natural course of alkaptonuria, detection of the disease by black disc color change in a patient without any other presentation of alkaptonuria is an exceptionally rare condition. we have reported a very rare case of alkaptonuria presented with low back pain and steppage gait in a 51-year-old male with a complaint of chronic low-b...

2016
Mozhdeh Zabihiyeganeh Haleh Chehrehgosha Alireza Mirzaei

Introduction: Ochronosis is a rare autosomal recessive disorder of tyrosine metabolism, leading to deposition of elevated levels of homogentisic acid in different parts of the body, especially in fibrous and cartilaginous tissues. The current study presents a case with delayed diagnosis and osteoporotic fracture in addition to severe osteoarthritis and calcification. Case Presentation: A 56-yea...

2015
Adam Mullan Derek Cocker Gordon Taylor Colin Millar Lakshminarayan Ranganath

Alkaptonuria (AKU) is a rare inherited disorder of tyrosine metabolism, which leads to an accumulation of homogentisic acid (HGA) and is associated with a progressive arthropathy. Fatal complications are unusual and usually result from cardiac disease or progressive renal impairment; rapidly fatal haematological complications are exceptionally rare and described in only a handful of case report...

2016
Farooq A. Rathore Saeed B. Ayaz Sahibzada N. Mansoor

Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is due to the lack of an enzyme homogentisate 1,2-dioxygenase, which results in an accumulation of homogentisic acid in different areas of the body, including sclera, skin, cardiac valves, articular cartilage of the large joints and intervertebral disks. We present two cases of alkaptonuria resulting...

2014
Shuai Le Xinyue Yao Shuguang Lu Yinling Tan Xiancai Rao Ming Li Xiaolin Jin Jing Wang Yan Zhao Nicholas C. Wu Renate Lux Xuesong He Wenyuan Shi Fuquan Hu

Bacteria develop a broad range of phage resistance mechanisms, such as prevention of phage adsorption and CRISPR/Cas system, to survive phage predation. In this study, Pseudomonas aeruginosa PA1 strain was infected with lytic phage PaP1, and phage-resistant mutants were selected. A high percentage (~30%) of these mutants displayed red pigmentation phenotype (Red mutant). Through comparative gen...

Journal: :Zeitschrift fur Naturforschung. C, Journal of biosciences 2013
Dominik Szwajgier

The ability of 36 phenolic acids and their derivatives to inhibit acetyl- and butyrylcholinesterase was studied. The most efficient acetylcholine inhibitors were: carnosic acid = gentisic acid > 3-hydroxy-4-methoxycinnamic acid = ethyl ferulate = ethyl vanillate = nordihydroguaiaretic acid > ethyl 4-hydroxybenzoate = methyl ferulate. The order of effectiveness towards butyrylcholinesterase was:...

Journal: :Talanta 2006
Nadia Spano Lucia Casula Angelo Panzanelli Maria I Pilo Paola C Piu Roberta Scanu Andrea Tapparo Gavino Sanna

The use of the RP-HPLC official method of the International Honey Commission (IHC) for the determination of 5-hydroxymethylfurfural (HMF) in strawberry tree honey (Arbutus unedo, a typical Sardinian honey) has brought to light a specific and heavy chromatographic interference that prevents accurate quantification. The interference has been identified as homogentisic acid (HA), i.e. the marker o...

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