McKiernan, P. J.

Recommendations for the management of tyrosinaemia type 1

de Laet, C., Dionisi-Vici, C., Leonard, J. V., McKiernan, P., Mitchell, G., Monti, L., de Baulny, H. O., Pintos-Morell, G., & Spiekerkötter, U. (2013) · Orphanet Journal of Rare Diseases

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 227

Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice

Mayorandan, S., Meyer, U., Gokcay, G., Segarra, N. G., de Baulny, H. O., van Spronsen, F., Zeman, J., de Laet, C., Spiekerkoetter, U., Thimm, E., et al. (2014) · Orphanet Journal of Rare Diseases

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 131

Indications and outcome of liver transplantation in tyrosinaemia type 1

Mohan, N., McKiernan, P., Kelly, D. A., Preece, M. A., Green, A., Buckels, J., & Mayer, A. D. (1999) · European Journal of Pediatrics

Metabolism and Genetic DisordersOrgan Transplantation Techniques and Outcomes

Cited by 111

Hyperinsulinism in tyrosinaemia type I

Baumann, U., Preece, M. A., Green, A., Kelly, D. A., & McKiernan, P. J. (2005) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 54

Ophthalmic follow‐up of patients with tyrosinaemia type I on NTBC

Gissen, P., Preece, M. A., Willshaw, H. A., & McKiernan, P. J. (2003) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 49

Cardiomyopathy in tyrosinaemia type I is common but usually benign

Arora, N., Stumper, O., Wright, J., Kelly, D. A., & McKiernan, P. J. (2006) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 48

Renal tubular function in children with tyrosinaemia type I treated with nitisinone

Santra, S., Preece, M. A., Hulton, S. ‐., & McKiernan, P. J. (2008) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 43

Lectin‐reactive α‐Fetoprotein in Patients with Tyrosinemia Type I and Hepatocellular Carcinoma

Baumann, U., Duhme, V., Auth, M. K. H., McKiernan, P. J., & Holme, E. (2006) · Journal of Pediatric Gastroenterology and Nutrition

Hepatocellular Carcinoma Treatment and PrognosisMetabolism and Genetic Disorders

Cited by 25

Plasma succinylacetone is persistently raised after liver transplantation in tyrosinaemia type 1

Bartlett, D. C., Preece, M. A., Holme, E., Lloyd, C., Newsome, P. N., & McKiernan, P. J. (2013) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersPorphyrin Metabolism and Disorders

Cited by 21

Disorders of Tyrosine Metabolism

Chakrapani, A., Gissen, P., & McKiernan, P. (2012) · Inborn Metabolic Diseases

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 17