Heterogeneity in phenotype of usher-congenital hyperinsulinism syndrome: hearing loss, retinitis pigmentosa, and hyperinsulinemic hypoglycemia ranging from severe to mild with conversion to diabetes.
about
Congenital hyperinsulinism: current status and future perspectives.Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome.Late presentation of necrotizing enterocolitis associated with rotavirus infection in a term infant with hyperinsulinism on octreotide therapy: A case report.Congenital hyperinsulinism: global and Japanese perspectives.
P2860
Heterogeneity in phenotype of usher-congenital hyperinsulinism syndrome: hearing loss, retinitis pigmentosa, and hyperinsulinemic hypoglycemia ranging from severe to mild with conversion to diabetes.
description
2012 nî lūn-bûn
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2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
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2012年论文
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name
Heterogeneity in phenotype of ...... d with conversion to diabetes.
@ast
Heterogeneity in phenotype of ...... d with conversion to diabetes.
@en
type
label
Heterogeneity in phenotype of ...... d with conversion to diabetes.
@ast
Heterogeneity in phenotype of ...... d with conversion to diabetes.
@en
prefLabel
Heterogeneity in phenotype of ...... d with conversion to diabetes.
@ast
Heterogeneity in phenotype of ...... d with conversion to diabetes.
@en
P2093
P2860
P356
P1433
P1476
Heterogeneity in phenotype of ...... d with conversion to diabetes.
@en
P2093
Adnan Al Shaikh
Angham N Al Mutair
Bassam Bin-Abbas
Khalid Hussain
Naila Felimban
P2860
P304
P356
10.2337/DC12-1174
P407
P577
2012-11-12T00:00:00Z