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Anesthetic management of a pediatric patient with arginase-1 deficiency undergoing strabismus operation: a case report

Abstract Background Urea cycle disorders are rare; arginase-1 deficiency is one of those extremely rare autosomal recessive metabolic disorders. Arginase-1 is one among the enzymes involved in the production of urea from ammonia in the liver, and its deficiency produces the characteristic feature, h...

Бүрэн тодорхойлолт

-д хадгалсан:
Номзүйн дэлгэрэнгүй
Үндсэн зохиолчид: Hideya Kato, Ken Kawaguchi, Teiji Sawa
Формат: Artigo
Хэл сонгох:Inglês
Хэвлэсэн: SpringerOpen 2019-08-01
Цуврал:JA Clinical Reports
Нөхцлүүд:
Онлайн хандалт:http://link.springer.com/article/10.1186/s40981-019-0274-6
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