ALKAPTONURIA SYNDROME-A REVIEW [PDF]
Alkaptonuria, also called endogenous ochronosis, and also called as Black Urine Disease, is a rare metabolic autosomal recessive disorder. It occurs by complete inhibition of homogentisic acid oxidase enzyme having its deposition in various tissues ...
AMURUTHAVALLI, B. +4 more
core +1 more source
A case of argyria as consequence of alternative medical treatment
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 7, Page 871-873, July 2025.
Murat Cavdar +5 more
wiley +1 more source
Rancangan Pusat Informasi dan Konsultasi Obat, Kosmetika, dan Makanan di Unisba [PDF]
Among other things, health quality is an important indicator to judge life quality in Indonesia. But, despite juggling efforts conducted by many institutions, a serious lack of health quality still become one of the greatest problems in Indonesia ...
Priani, S. E. (Sani)
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Jens Martin, Rohrbach, Daniel, Röck
openaire +2 more sources
Alcaptonúria (ocronose): relato de dois casos Alkaptonuria (ochronosis): report of two cases
A alcaptonúria (ocronose) é um erro inato do metabolismo da fenilalanina e tirosina, transmitido de forma autossômica recessiva. Resulta da deficiência completa da enzima ácido homogentísico oxidase (HGO), causada por mutação no gene 3q (3q21 - q23 ...
Letícia R. Brandão +5 more
doaj +1 more source
Ein Fall von Argyrie als Folge einer alternativmedizinischen Selbstbehandlung
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 7, Page 871-873, July 2025.
Murat Cavdar +5 more
wiley +1 more source
Age related deviation of gait from normality in alkaptonuria. [PDF]
Alkaptonuria is a rare metabolic disease leading to systemic changes including early and severe arthropathy which affects mobility. Due to unknown reasons, the onset of degenerative changes is delayed to around 30 years of age when both objective and ...
Barton, GJ +4 more
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The dark side of cartilage: ochronosis unmasked during femoral neck fracture surgery [PDF]
Alkaptonuria is a rare autosomal recessive disorder caused by a deficiency in homogentisic acid oxidase, leading to the accumulation of homogentisic acid in connective tissues.
Bava, Surendar S. +5 more
core +2 more sources
Alcaptonuria and Ochronosis with Diabetes Mellitus and Mycosis Fungoides: A Case Report [PDF]
A Negro woman with alcaptonuria, ochronosis, ochronotic arthropathy, diabetes mellitus and mycosis fungoides died of acute renal failure due to diabetic glomerulonephropathy and ochronotic nephrosis.
Haq, Jamshed U., Patton, Roy B.
core +1 more source
Determination of hydroquinone in food and pharmaceutical samples using a voltammetric based sensor employing NiO nanoparticle and ionic liquids [PDF]
A sensitive modified carbon paste electrode (MCPE) employing NiO nanoparticle (NiO/NPs) and 1-butyl-3- methylimidazolium tetrafluoroborate (BMITFB) ionic liquid was used for trace level analysis of hydroquinone (HQ) in aqueous solution.
Ahmadzadeh, Saeid +2 more
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