about
Drug treatment of inborn errors of metabolism: a systematic reviewNovel mutation causing partial biotinidase deficiency in a Syrian boy with infantile spasms and retardationClinical review of genetic epileptic encephalopathiesBiotinidase deficiency: Genotype-biochemical phenotype association in Brazilian patients.Biotinidase deficiency: clinical and genetic studies of 38 Brazilian patients.Biotinidase deficiency mimicking primary immune deficiencies.A biotinidase Km variant causing late onset bilateral optic neuropathy.Biotinidase deficiency: a reversible neurometabolic disorder (an Iranian pediatric case series).Comparison of Spectrophotometric and Fluorimetric Methods in Evaluation of Biotinidase Deficiency.Biotinidase deficiency: "if you have to have an inherited metabolic disease, this is the one to have".Biotinidase deficiency--clinching the diagnosis rapidly can make all the difference!Nutritional therapy for selected inborn errors of metabolism.Biotinidase deficiency.Biotinidase deficiency: A treatable cause of infantile seizures.Biotin-deficient diet induces chromosome misalignment and spindle defects in mouse oocytes.
P2860
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P2860
description
1988 nî lūn-bûn
@nan
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
1988年论文
@zh
1988年论文
@zh-cn
name
Biotinidase deficiency: a survey of 10 cases
@ast
Biotinidase deficiency: a survey of 10 cases
@en
type
label
Biotinidase deficiency: a survey of 10 cases
@ast
Biotinidase deficiency: a survey of 10 cases
@en
prefLabel
Biotinidase deficiency: a survey of 10 cases
@ast
Biotinidase deficiency: a survey of 10 cases
@en
P2093
P2860
P356
P1476
Biotinidase deficiency: a survey of 10 cases
@en
P2093
P2860
P304
P356
10.1136/ADC.63.10.1244
P407
P577
1988-10-01T00:00:00Z