Development defects of enamel in humans with hereditary epidermolysis bullosa.
about
Inherited epidermolysis bullosaIntegrating the genotype and phenotype in hominid paleontologyPathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutationsMouse genetic background influences the dental phenotype.Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta.Oral health care for patients with epidermolysis bullosa--best clinical practice guidelines.A mouse model of generalized non-Herlitz junctional epidermolysis bullosa.The molecular basis of hereditary enamel defects in humans.Clinical management for epidermolysis bullosa dystrophica.Targeted disruption of the LAMA3 gene in mice reveals abnormalities in survival and late stage differentiation of epithelial cells.Periodontal manifestation of epidermolysis bullosa: Looking through the lens.Oral manifestations in the epidermolysis bullosa spectrum.Dental and Anaesthetic Challenges in a Patient with Dystrophic Epidermolysis Bullosa.Dystrophic epidermolysis bullosa: report of a case with electron microscopic study.DENTAL ENAMEL FORMATION AND IMPLICATIONS FOR ORAL HEALTH AND DISEASE.Amelogenesis Imperfecta; Genes, Proteins, and Pathways.Expression of Sox genes in tooth development.Laminin gamma2 expression is developmentally regulated during murine tooth morphogenesis and is intense in ameloblasts.Equine epitheliogenesis imperfecta in two american saddlebred foals is a lamina lucida defect.Epidermolysis bullosa acquisita: clinical manifestations, microscopic findings, and surgical periodontal therapy. A case report.Sucralfate: a help during oral management in patients with epidermolysis bullosa.Epidermolysis bullosa and dental developmental age.Dystrophic epidermolysis bullosa: oral findings and problems.The chemical composition of tooth enamel in recessive dystrophic epidermolysis bullosa: significance with respect to dental caries.[Mucosal manifestations of epidermolysis bullosa : Clinical presentation and management].
P2860
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P2860
Development defects of enamel in humans with hereditary epidermolysis bullosa.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh-hant
name
Development defects of enamel in humans with hereditary epidermolysis bullosa.
@en
Development defects of enamel in humans with hereditary epidermolysis bullosa.
@nl
type
label
Development defects of enamel in humans with hereditary epidermolysis bullosa.
@en
Development defects of enamel in humans with hereditary epidermolysis bullosa.
@nl
prefLabel
Development defects of enamel in humans with hereditary epidermolysis bullosa.
@en
Development defects of enamel in humans with hereditary epidermolysis bullosa.
@nl
P2093
P1476
Development defects of enamel in humans with hereditary epidermolysis bullosa.
@en
P2093
P304
P356
10.1016/0003-9969(93)90107-W
P577
1993-11-01T00:00:00Z