Results 101 to 110 of about 7,435 (127)

Total Joint Arthroplasty in Ochronotic Arthritis of Lower Extremities. [PDF]

Indian J Orthop
Basanagoudar PL, Inamdar DN, Thimmegowda B R, Tubaki V.   +3 more
europepmc   +1 more source

Routine histopathology in total joint arthroplasty: clinical utility and economic evaluation from a tertiary care center. [PDF]

Ir J Med Sci
Bhuyan AK, Acharya KKV, Kumar S.
europepmc   +1 more source

Treatment of Ochronotic Osteoarthropathy and the Evaluation of Selected Lower Limb Muscle Properties, Including the Patellar Tendon: A Case Report and Mini Literature Review. [PDF]

J Clin Med
Jarecki J, Tomczyk-Warunek A, Posturzyńska A, Warda E, Waśko M, Arciszewski K, Tomaszewska E, Muszyński S, Bieniaś J, Ostapiuk M, Skrzypek T, Gągała J.   +11 more
europepmc   +1 more source

Blackish Discoloration of Articular Cartilage during Total Knee Replacement; a Case Report. [PDF]

J Orthop Case Rep
Puthanveetil DE, Subhash VP, Kannu AN, Kavalakkatt K.   +3 more
europepmc   +1 more source

Combined alkaptonuria and osteoporosis contributing to chronic back pain. [PDF]

Endocrinol Diabetes Metab Case Rep
Riegler A, Anand G.
europepmc   +1 more source

Cardiac Manifestations of Alkaptonuria: Aortic Valve Stenosis and Coronary Artery Disease in a 63-Year-Old Patient. [PDF]

JACC Case Rep
Solís Chávez MB, Montero Cruces L, Romiti S, Saiz-Pardo Sanz M, Maroto Castellanos LC.   +4 more
europepmc   +1 more source

Alkaptonuria: Clinical Spectrum of a Diagnosed Case in Bahrain With a Literature Review. [PDF]

Cureus
Alsahlawi Z, Salman LI, Alaradi AM, Hamada F, Alsahlawi HS, Ali ZM.   +5 more
europepmc   +1 more source

Clinical and molecular characteristics of Chinese patients with alkaptonuria: 4-year follow-up of a pediatric patient and literature review. [PDF]

Mol Genet Metab Rep
Qiu X, Liu Y, Shao Y, Mao X, Zhang J, Chen X, Yin X, Sheng H, Li X, Lin Y.   +9 more
europepmc   +1 more source

Bilateral Hip Arthroplasty for Ochronotic Arthropathy

Clinical Rheumatology, 2000
Ochronosis is a musculoskeletal manifestation of alkaptonuria, a rare hereditary metabolic disorder characterised by the absence of the enzyme homogentisic acid oxidase and associated with various systemic abnormalities related to the deposition of ...
Aynaci, OSMAN, Turhan, AU, Onder, C
exaly   +2 more sources

OCHRONOTIC ARTHROPATHY

Bone and Joint Journal, 1970
1. Four cases of ochronotic arthropathy have been studied and the related literature has been reviewed. 2. Ochronotic arthropathy is a rare condition resulting from an inborn error of metabolism occurring as a Mendelian recessive characteristic.
F. H. Laskar, K. D. Sargison
exaly   +2 more sources