Sage Journals: Discover world-class research

Free access

Case report

First published 1992-12

Richner-Hanhart Syndrome (Oculo-Cutaneous Tyrosinaemia,Tyrosinaemia Type II)

D G Paige, P Clayton, A Bowron [...]

Journal of the Royal Society of Medicine

Open access

Research article

First published 2017

The Incidence of Transient Neonatal Tyrosinemia Within a Mexican Population

Alexandra V. Zea-Rey, Héctor Cruz-Camino, Diana L. Vazquez-Cantu [...]

Journal of Inborn Errors of Metabolism and Screening

Open access

Research article

First published 2024

Clinical Spectrum of Hereditary Tyrosinemia Type 1 in a Cohort of Pakistani Children

Sabeen Abid Khan, Misbah Fakih, Nida Taufiq [...]

Clinical Medicine Insights: Pediatrics

Free access

Research article

First published 2012-10

Sleeping Beauty Transposon System is a Reliable Gene Delivery Tool for Hereditary Tyrosinaemia Type 1 Disease Gene Therapy: Size of the Foreign Gene Decides the Timing of Stable Integration into the Host Chromosomes

X-J Pan, Z-Z Ma, Q-J Zhang [...]

Journal of International Medical Research

Free access

Research article

First published 2020-11

Clinical utilization of dried blood spot nitisinone (NTBC) and succinylacetone (SA) concentrations in hereditary tyrosinaemia type 1 – A UK centre experience

Mildrid Yeo, Charles Turner, Neil R Dalton [...]

Annals of Clinical Biochemistry: International Journal of Laboratory Medicine

Retricted access

Other

First published 2001-5

Tyrosinemia: A Review

Pierre A. Russo, Grant A. Mitchell, Robert M. Tanguay

Pediatric and Developmental Pathology

Retricted access

Case report

First published 2005-10

Brain magnetic resonance imaging in tyrosinemia

R. N. Sener

Acta Radiologica

Free access

Research article

First published 2007-09

A rapid ultra performance liquid chromatography tandem mass spectrometric method for measuring amino acids associated with maple syrup urine disease,tyrosinaemia and phenylketonuria

Annals of Clinical Biochemistry: International Journal of Laboratory Medicine

Retricted access

Other

First published 2005-11

Diagnosis: Hereditary Type I Tyrosinema (hepatorenal tyrosinemia)

Stuart Rowe, John F. Pohl

Clinical Pediatrics

Retricted access

Other

First published 2001-09

Carnitine-Deficient Myopathy as a Presentation of Tyrosinemia Type I

Andrea Nissenkom, Stanley H. Korman, Orna Vardi [...]

Journal of Child Neurology

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