Results 111 to 120 of about 1,374 (165)
Thiamidol in Melasma in Patients of Skin of Color: A Preliminary Report of Efficacy and Safety. [PDF]
Indian Dermatol Online JSarkar R +3 more
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Cardiac Manifestations of Alkaptonuria: Aortic Valve Stenosis and Coronary Artery Disease in a 63-Year-Old Patient. [PDF]
JACC Case RepSolís Chávez MB +4 more
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Exogenous Ochronosis With Vitiligo: A Therapeutic Challenge. [PDF]
Skin Res TechnolLi ZZ, Zhang C.
europepmc +1 more source
An anatomical investigation of alkaptonuria: Novel insights into ochronosis of cartilage and bone. [PDF]
J AnatHughes JH +8 more
europepmc +1 more source
Black tendon-identifying a rare autosomal recessive disorder: Intraoperative diagnosis of alkaptonuria: A case report. [PDF]
SAGE Open Med Case RepPushpan P +3 more
europepmc +1 more source
From Chronic Use of Minocycline to Pigmented Unicuspid Aortic Valve: A Unique Single Case. [PDF]
Methodist Debakey Cardiovasc JOdeh NB +4 more
europepmc +1 more source
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Cardiovascular Pathology, 2020
In this review, we summarize previously reported case reports (n=66) in which the presence of ochronotic pigment was found in one or more cardiovascular structures either at necropsy or after operative excision of a cardiac valve or portions of arteries or both.
William Roberts
exaly +3 more sources
In this review, we summarize previously reported case reports (n=66) in which the presence of ochronotic pigment was found in one or more cardiovascular structures either at necropsy or after operative excision of a cardiac valve or portions of arteries or both.
William Roberts
exaly +3 more sources
Clinical and Experimental Dermatology, 2009
Endogenous ochronosis or alkaptonuria is a rare, autosomal recessive disease of tyrosine metabolism that is caused by a deficiency of the enzyme homogentisic acid oxidase. The disease results in the accumulation and deposition of homogentisic acid in the cartilage, eyelids, forehead, cheeks, axillae, genital region, buccal mucosa, larynx, tympanic ...
Turgay, E. +5 more
openaire +2 more sources
Endogenous ochronosis or alkaptonuria is a rare, autosomal recessive disease of tyrosine metabolism that is caused by a deficiency of the enzyme homogentisic acid oxidase. The disease results in the accumulation and deposition of homogentisic acid in the cartilage, eyelids, forehead, cheeks, axillae, genital region, buccal mucosa, larynx, tympanic ...
Turgay, E. +5 more
openaire +2 more sources