Results 231 to 240 of about 4,803 (244)

[Renal involvement in type I tyrosinemia].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 1995
P, Cochat, P, Guibaud, G, Baverel
openaire   +1 more source

Spectrum of mutations in the fumarylacetoacetate hydrolase gene of tyrosinemia type 1 patients in northwestern Europe and Mediterranean countries

Human Mutation, 1998
R Berger
exaly  

Liver transplantation in type I tyrosinemia.

Transplantation proceedings, 1995
F J, Murcia, J, Vazquez, M, Gamez, M, Lopez Santamaria, A, de la Vega, M C, Diaz, P, Jara, J, Tovar   +7 more
openaire   +1 more source

HEREDITARY TYROSINEMIA

Acta Paediatrica, International Journal of Paediatrics, 1969
G Bodegard, Bengt Lindblad, Sven Lindstedt   +2 more
exaly  

[Hereditary tyrosinemia type III].

Ryoikibetsu shokogun shirizu, 1998
openaire   +3 more sources

Tissue-specific FAH deficiency alters sleep–wake patterns and results in chronic tyrosinemia in mice

Proceedings of the National Academy of Sciences of the United States of America, 2019
Sandra M Siepka, Kimberly H Cox, Vivek Kumar   +2 more
exaly  

Neurologic Crises in Hereditary Tyrosinemia

New England Journal of Medicine, 1990
Grant A Mitchell, Marie Lambert, J Michaud   +2 more
exaly  

Chromosomal Instability in Hereditary Tyrosinemia Type I

Pediatric Pathology, 1994
Kathleen S. Wilson, Charles F. Timmons, D. Sue Hilton, ArthurG Weinbug, Vijay Tonk   +4 more
openaire   +1 more source

Tyrosinemia type 1 and irreversible neurologic crisis after one month discontinuation of nitisone

Metabolic Brain Disease, 2016
Neslihan Onenli Mungan, Deniz Kor, Ozden Özgur Horoz   +2 more
exaly  

Renal proximal tubular cells acquire resistance to cell death stimuli in mice with hereditary tyrosinemia type 1

Kidney International, 2004
Markus Grompe, R Berger
exaly