Results 101 to 110 of about 6,468 (222)

Case Report: Type II tyrosinemia caused by mutations at the c.843_844 inv p.(Trp282Gly) variant locus. [PDF]

Front Genet
Tong F, Peng M, Meng L, Shen J, Huang L, Huang W, Huang W, Song J.   +7 more
europepmc   +1 more source

Pediatric Hepatology: A three-year experience with pediatric liver transplantation with cyclosporine and steroids [PDF]

, 1986
Gartner, JC, Iwatsuki, S, Malatack, JJ, Shaw, BW, Starzl, TE, Urbach, AH, Zitelli, BH   +6 more
core  

Liver transplantation and portacaval shunt in genetic diseases [PDF]

, 1982
Starzl, TE
core  

Changing concepts: Liver replacement for hereditary tyrosinemia and hepatoma [PDF]

, 1985
Fox, IJ, Gartner, JC, Gordon, RD, Iwatsuki, S, Malatack, JJ, Shaw, BW, Starzl, TE, Urbach, AH, Van Thiel, DH, Zitelli, BJ   +9 more
core   +1 more source

In Vivo Confocal Microscopy and Anterior Segment Optical Coherence Tomography Features of Corneal Pseudodendritic Lesions in Hereditary Tyrosinemia Type 1. [PDF]

Am J Case Rep
Bruno R, Donatelli S, Mastropasqua L, Nubile M.   +3 more
europepmc   +1 more source

Pediatric liver transplantation with cyclosporine and steroids [PDF]

, 1984
Gartner, JC, Iwatsuki, S, Malatack, JJ, Shaw, BW, Starzl, TE, Urbach, AH, Zitelli, BJ   +6 more
core  

SIADH as an Underrecognized Manifestation of Porphyria-like Crises in Hereditary Tyrosinemia Type 1: Clinical and Pathophysiological Insights. [PDF]

Int J Mol Sci
Saraceno E, Serra I, Bracci B, Pagliardini V, Pinon M, Tuli G, Versace A, Bondone C, Spada M.   +8 more
europepmc   +1 more source

Different Clinic, Different Diagnosis: Tyrosinemia Type 3. [PDF]

Mol Syndromol
Basan H, Ceylaner S, Küçükcongar Yavaş A.   +2 more
europepmc   +1 more source

A minor alternative transcript of the fumarylacetoacetate hydrolase gene produces a protein despite being likely subjected to nonsense-mediated mRNA decay [PDF]

Natacha Dreumont, Antonella Maresca, Jean-François Boisclair-Lachance, Anne Bergeron, Robert M Tanguay   +4 more
core   +1 more source

Tyrosinemia [PDF]

, 2020
openaire   +1 more source