J. Gallagher

发表

Asymptomatic Corneal Keratopathy Secondary to Hypertyrosinaemia Following Low Dose Nitisinone and a Literature Review of Tyrosine Keratopathy in Alkaptonuria.

E. Lock, L. Ranganath, A. Milan, 2018, JIMD reports.

Homogentisic acid is not only eliminated by glomerular filtration and tubular secretion but also produced in the kidney in alkaptonuria

J. Jarvis, A. Zatkova, L. Ranganath, 2020, Journal of inherited metabolic disease.

Acute fatal metabolic complications in alkaptonuria

L. Ranganath, A. Milan, A. Davison, 2016, Journal of Inherited Metabolic Disease.

Ochronotic pigmentation is caused by homogentisic acid and is the key event in alkaptonuria leading to the destructive consequences of the disease—A review

L. Ranganath, B. Norman, J. Gallagher, 2019, Journal of inherited metabolic disease.

ANNALS EXPRESS: Alkaptonuria - many questions answered, further challenges beckon.

A. Milan, A. Davison, J. Gallagher, 2019, Annals of clinical biochemistry.

Investigating the Robustness and Diagnostic Potential of Extracellular Matrix Remodelling Biomarkers in Alkaptonuria.

M. Karsdal, L. Ranganath, A. Milan, 2015, JIMD reports.

A. Santucci, O. Spiga, W. Introne, 2024, Nature reviews. Disease primers.

Raman Spectroscopy identifies differences in ochronotic and non-ochronotic cartilage; a potential novel technique for monitoring ochronosis.

J. Kerns, A. Taylor, D.D. Jenks, 2019, Osteoarthritis and cartilage.

Ochronosis and calcification in the mediastinal mass of a patient with alkaptonuria

L. Ranganath, A. M. Taylor, V. L. Adams, 2011, Journal of Clinical Pathology.