Sudden unexpected fatal encephalopathy in adults with OTC gene mutations-Clues for early diagnosis and timely treatment
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Genotype-Phenotype Correlations in Ornithine Transcarbamylase Deficiency: A Mutation UpdateSevere hyperammonemia in late-onset ornithine transcarbamylase deficiency triggered by steroid administration.Long-term outcomes in Ornithine Transcarbamylase deficiency: a series of 90 patientsFatal coma in a young adult due to late-onset urea cycle deficiency presenting with a prolonged seizure: a case report.The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype.Late-Onset N-Acetylglutamate Synthase Deficiency: Report of a Paradigmatic Adult Case Presenting with Headaches and Review of the Literature.
P2860
Sudden unexpected fatal encephalopathy in adults with OTC gene mutations-Clues for early diagnosis and timely treatment
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2014 nî lūn-bûn
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2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2014年の論文
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2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Sudden unexpected fatal enceph ...... diagnosis and timely treatment
@ast
Sudden unexpected fatal enceph ...... diagnosis and timely treatment
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type
label
Sudden unexpected fatal enceph ...... diagnosis and timely treatment
@ast
Sudden unexpected fatal enceph ...... diagnosis and timely treatment
@en
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Sudden unexpected fatal enceph ...... diagnosis and timely treatment
@ast
Sudden unexpected fatal enceph ...... diagnosis and timely treatment
@en
P2093
P2860
P50
P1476
Sudden unexpected fatal enceph ...... diagnosis and timely treatment
@en
P2093
Aniello Colasante
Catia Cavicchi
Elisabetta Pasquini
Francesca Orfei
Maria Donati
Mauro Bernardi
Miriam Rigoldi
Nicolò Gentiloni Silveri
Renzo Guerrini
Sean Mooney
P2860
P2888
P356
10.1186/S13023-014-0105-9
P577
2014-07-16T00:00:00Z
P5875
P6179
1004063060