Transient Visual Loss in Ornithine Transcarbamoylase Deficiency

Author:

Snebold Neal G.,Rizzo Joseph F.,Lessell Simmons,Pruett Ronald C.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference32 articles.

1. Urea cycle disorders and other hyperammonemic syndromes;Walser,1982

2. Hereditary urea-cycle disorders;Shih,1976

3. Ornithine transcarbamylase deficiency. A cause of bizarre behavior in man;DiMagno;N. Engl. J. Med.,1986

4. A new instance of an inborn enzymatic defect of the biosynthesis of urea;Russell;Lancet,1962

5. Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea cycle enzymopathies;Msall;N. Engl. J. Med.,1984

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1. Neuroophthalmologic Disease of the Retina;Albert and Jakobiec's Principles and Practice of Ophthalmology;2022

2. Transient Cortical Blindness in a Toddler With Heterozygous Ornithine Transcarbamylase Deficiency;Cureus;2021-11-30

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4. Multimodal imaging in urea cycle-related neurological disease – What can imaging after hyperammonemia teach us?;Translational Science of Rare Diseases;2020-08-03

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