|1.||Velinovic, Milos: 1 article (11/2014)|
|2.||Kovacevic-Kostic, Natasa: 1 article (11/2014)|
|3.||Mikic, Aleksandar: 1 article (11/2014)|
|4.||Vranes, Mile: 1 article (11/2014)|
|5.||Nikolic, Dejan: 1 article (11/2014)|
|6.||Karan, Radmila: 1 article (11/2014)|
|7.||Bilbija, Ilija: 1 article (11/2014)|
|8.||Obrenovic-Kircanski, Biljana: 1 article (11/2014)|
|9.||Tagarelli, Giuseppe: 1 article (08/2010)|
|10.||Tagarelli, Antonio: 1 article (08/2010)|
01/01/1978 - "[Metabolic studies in brothers affected by alcaptonuria (ochronosis)]."
10/01/1952 - "Alcaptonuria and ochronosis; with a report of three patients and metabolic studies in two."
11/01/2014 - "Alcaptonuria, Aortic valve, Cardiac ochronosis, Surgery. "
11/01/2014 - "This case suggests that although alcaptonuria is a slow progressive disease with cardiac ochronosis as a predictable late complication, it can nevertheless be a first sign. "
06/01/1981 - "[The clinical and Radiological Pictures of Alcaptonuria and Ochronosis (author's transl)]."
02/01/1991 - "Alcaptonuria and ochronotic arthritis."
04/01/1989 - "Cartilage damage termed ochronotic arthritis is the major pathology occurring in adult patients with alcaptonuria. "
05/01/1958 - "Alcaptonuria and ochronotic arthritis."
11/01/1994 - "We present a 57 year old female patient in whom we diagnosed alcaptonuria by the appearance of the typical symptom trias homogentisic acid excretion in the urine, ochronosis and arthritis. "
01/01/1993 - "Diseases of the connective tissues discussed include those of nutritional origin (scurvy, lathyrism, starvation, and protein deficiency), the genetic diseases (dermatosparaxis, Ehlers-Danlos syndrome, osteogenesis imperfecta, Marfan syndrome, homocystinuria, alcaptonuria, epidermolysis bullosa, rheumatoid arthritis in humans, polyarthritis in swine, Aleutian disease of mink, and the several types of systemic lupus erythematosus) and the acquired diseases of connective tissues (abnormal calcification, systemic sclerosis, interstitial lung disease, hepatic fibrosis, and carcinomas of the connective tissues). "
|3.||Inborn Genetic Diseases (Disease, Hereditary)
07/01/2007 - "Alcaptonuria is a hereditary disease, also known as black hip, where there is an accumulation of homogentisic acid pigmentation in joint cartilages. "
08/01/2000 - "Alcaptonuria is a rare hereditary disease, characterized by an abnormal blackish coloration of the urine and dark pigmentation of the conjunctive tissue which is due to a deficiency in homogentisate 1,2-dioxygenase (HGO), a phenylalanine catabolizing enzyme. "
10/01/1984 - "Ochronotic alcaptonuria is a rare hereditary disease in which the metabolism of phenylalanine and tyrosine is disturbed, leading to accumulation and urinary excretion of homogentisic acid. "
07/01/1978 - "Alcaptonuria with diabetes mellitus (a case report with review of literature)."
04/01/1975 - "The method has detected 5 infants with phenylketonuria, 4 with histidinaemia, 5 with cystinuria, 5 with diabetes mellitus, and one with alcaptonuria. "
01/01/1969 - "Alcaptonuria and ochronosis with diabetes mellitus and mycosis fungoides. "
|3.||Homogentisate 1,2-Dioxygenase (Homogentisate 1,2 Dioxygenase)
|5.||Pyrrolidonecarboxylic Acid (Pyroglutamic Acid)
|8.||Glutathione (Reduced Glutathione)
|9.||gamma-Glutamyltransferase (gamma-Glutamyl Transpeptidase)