Results 121 to 130 of about 1,520,545 (236)
SIADH as an Underrecognized Manifestation of Porphyria-like Crises in Hereditary Tyrosinemia Type 1: Clinical and Pathophysiological Insights. [PDF]
Saraceno E +8 more
europepmc +1 more source
Different Clinic, Different Diagnosis: Tyrosinemia Type 3. [PDF]
Basan H +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 +4 more
core +1 more source
Mutation spectrum of fumarylacetoacetase gene and clinical aspects of tyrosinemia type I disease. [PDF]
Dursun A +10 more
europepmc +1 more source
Plantar keratoderma : A manifestation of tyrosinemia type II (Richner-Hanhart syndrome).
Al-Ratrout Jihad +3 more
doaj
Impaired cognitive functioning in patients with tyrosinemia type I receiving nitisinone.
F. Bendadi +8 more
semanticscholar +1 more source

