Results 101 to 110 of about 2,511,484 (202)

Ochronosis ,The Rare Cause of Chronic Low Back Pain: Report of A Case

Iranian Journal of Neurosurgery, 2019
Background and Importance: Alkaptonuria is a rare genetic disorder due to deficiency of the enzyme homogentisic acid Oxidase which results in the accumulation of homogentisic acid in various body tissues; it produces a multisystemic disorder with a ...
Ali Baradaran Bagheri, Farsad Biglari, Somayeh Soroureddin, Salman Azarsina, Mohammad Kamangar   +4 more
doaj  

Determination of homogentisic acid in urine for diagnosis of alcaptonuria: Capillary electrophoretic method optimization using experimental design

, 2018
Homogentisic acid (HGA) is a diagnostic metabolite that accumulates in the urine and tissues of patients with alkaptonuria which is a rare autosomal recessive disease.
Balta, Gulfem S., Gülfem S. Balta, Öztekin, Nevin, M. Şerif Cansever, Cansever, M. Serif, Nevin Öztekin   +5 more
core   +1 more source

A Previously Undiagnosed Case of Alkaptonuria: A Case Report

The Turkish Journal of Gastroenterology, 2013
Alkaptonuria is a rare metabolic disorder in the phenylalanine and tyrosine catabolic pathway which is characterized by the excessive excretion of homogentisic acid in the urine, ochronosis, and debilitating arthritis of the spine and large joints ...
Mohammed ALSBOU, Nesrin MWAFI
doaj  

HOMOGENTISIC ACID OXIDASE

Journal of Biological Chemistry, 1954
Dana I. Crandall, Demetreos N. Halikis
openaire   +1 more source

Reaction of quinone of homogentisic acid with biological amines [PDF]

Arthritis & Rheumatism, 1967
R, Stoner, B B, Blivaiss
openaire   +2 more sources

THE ENZYMATIC CONVERSION OF HOMOGENTISIC ACID TO 4-FUMARYLACETOACETIC ACID

Journal of Biological Chemistry, 1951
R G, RAVDIN, D I, CRANDALL
openaire   +2 more sources

The uniformity of the homogentisic acid excretion in alkaptonuria

The Journal of Physiology, 1905
A E, Garrod, T S, Hele
openaire   +3 more sources

Secondary osteoarthritis due to alkaptonuria: a case report [PDF]

Journal of Research in Applied and Basic Medical Sciences
Background & Aims: Alkaptonuria is a rare autosomal recessive genetic disorder caused by a deficiency of homogentisate 1,2-dioxygenase, leading to the accumulation of homogentisic acid.
Sabina Lois, Aruna Veeruswamy, Kamalanathan Kulandaivelu, Mohan Prasad Muthusamy, Yee Tun Oo   +4 more
doaj  

Absorbance measurements of oxidation of homogentisic acid accelerated by the addition of alkaline solution with sodium hypochlorite pentahydrate. [PDF]

Sci Rep, 2018
Tokuhara Y, Shukuya K, Tanaka M, Sogabe K, Ejima Y, Hosokawa S, Ohsaki H, Morinishi T, Hirakawa E, Yatomi Y, Shimosawa T.   +10 more
europepmc   +1 more source

Shikimate crosstalk enables record-level homogentisic acid production in <i>Yarrowia lipolytica</i>. [PDF]

Synth Syst Biotechnol
Xu C, Zhang W, Zhao Q, Lin X, Wang K, Wang M, Tan T.   +6 more
europepmc   +1 more source