The accumulation of homogentisic acid (HGA) in patients with alkaptonuria is associated with the concomitant deposition of pigments contain significant amounts of polymerised HGA (polyHGA) in the bodily tissues of the patients. The polymerisation of HGA under various different conditions in vitro was investigated to attempt to understand if there is a correlation between the conditions and rate of pigment deposition in vivo. In this study, we applied a selection of different analytical chemistry techniques including: nuclear magnetic resonance spectroscopy (NMR), high-performance liquid chromatography (HPLC), gel permeation chromatography (GPC), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and energy di...
The urine of patients with alkaptonuria turns dark brown due to the oxidation of homogentisic acid (...
OBJECTIVES: Alkaptonuria (AKU) is a genetic disorder caused by lack of the enzyme responsible for br...
Ochronosis is the process in alkaptonuria (AKU) that causes all the debilitating morbidity. The proc...
The accumulation of homogentisic acid (HGA) in patients with alkaptonuria is associated with the con...
Alkaptonuria (AKU), a rare genetic disorder, is characterized by the accumulation of homogentisic ac...
Melanins are a class of biopolymers that are widespread in nature, with diverse origins, composition...
Alkaptonuria is an iconic disease used by Archibald Garrod to demonstrate the theory of “inborn erro...
Alkaptonuria is a medical condition where patients have elevated levels of homogentisic acid (HGA) a...
International audiencePyomelanin is a brown-black phenolic polymer and results from the oxidation of...
Alkaptonuria (AKU) is a rare metabolic disease due to a deficient activity of the enzyme homogentisa...
Objectives. Alkaptonuria (AKU) is a genetic disorder caused by lack of the enzyme responsible for br...
SIR, we report a female with known alkaptonuria (AKU) undergoing routine hip replacement surgery due...
Pyomelanin mimics from homogentisic acid (HGA) and gentisic acid (GA) were biosynthesized by the oxi...
Alkaptonuria (AKU) is a rare inborn error of metabolism associated with a deficient activity of homo...
The urine of patients with alkaptonuria turns dark brown due to the oxidation of homogentisic acid (...
OBJECTIVES: Alkaptonuria (AKU) is a genetic disorder caused by lack of the enzyme responsible for br...
Ochronosis is the process in alkaptonuria (AKU) that causes all the debilitating morbidity. The proc...
The accumulation of homogentisic acid (HGA) in patients with alkaptonuria is associated with the con...
Alkaptonuria (AKU), a rare genetic disorder, is characterized by the accumulation of homogentisic ac...
Melanins are a class of biopolymers that are widespread in nature, with diverse origins, composition...
Alkaptonuria is an iconic disease used by Archibald Garrod to demonstrate the theory of “inborn erro...
Alkaptonuria is a medical condition where patients have elevated levels of homogentisic acid (HGA) a...
International audiencePyomelanin is a brown-black phenolic polymer and results from the oxidation of...
Alkaptonuria (AKU) is a rare metabolic disease due to a deficient activity of the enzyme homogentisa...
Objectives. Alkaptonuria (AKU) is a genetic disorder caused by lack of the enzyme responsible for br...
SIR, we report a female with known alkaptonuria (AKU) undergoing routine hip replacement surgery due...
Pyomelanin mimics from homogentisic acid (HGA) and gentisic acid (GA) were biosynthesized by the oxi...
Alkaptonuria (AKU) is a rare inborn error of metabolism associated with a deficient activity of homo...
The urine of patients with alkaptonuria turns dark brown due to the oxidation of homogentisic acid (...
OBJECTIVES: Alkaptonuria (AKU) is a genetic disorder caused by lack of the enzyme responsible for br...
Ochronosis is the process in alkaptonuria (AKU) that causes all the debilitating morbidity. The proc...