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Oral manifestations in the epidermolysis bullosa spectrum.

Oral manifestations in the epidermolysis bullosa spectrum.

http://www.wikidata.org/entity/Q37454829

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Target gene analyses of 39 amelogenesis imperfecta kindreds Inherited epidermolysis bullosa: clinical and therapeutic aspects.Diagnosis of Lingual Atrophic Conditions: Associations with Local and Systemic Factors. A Descriptive Review Factors affecting quality of life in epidermolysis bullosa.Developmental defects of enamel and dentine: challenges for basic science research and clinical management.Epidermolysis bullosa in animals: a review."Pitted" lesions in dermatology.Type VII collagen is enriched in the enamel organic matrix associated with the dentin-enamel junction of mature human teeth.Evaluation of internal consistency of the epidermolysis bullosa oropharyngeal severity score (EBOS).Pain in Patients with Dystrophic Epidermolysis Bullosa: Association with Anxiety and Depression.General anesthesia for dental care management of a patient with epidermolysis bullosa: 24-month follow-up.Inpatient management of children with recessive dystrophic epidermolysis bullosa: A review.

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Oral manifestations in the epidermolysis bullosa spectrum.

http://www.wikidata.org/entity/Q37454829

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on January 2010

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Oral manifestations in the epidermolysis bullosa spectrum.

@en

Oral manifestations in the epidermolysis bullosa spectrum.

@nl

type

label

Oral manifestations in the epidermolysis bullosa spectrum.

@en

Oral manifestations in the epidermolysis bullosa spectrum.

@nl

prefLabel

Oral manifestations in the epidermolysis bullosa spectrum.

@en

Oral manifestations in the epidermolysis bullosa spectrum.

@nl

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J.DET.2009.10.022

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Dermatologic Clinics

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Oral manifestations in the epidermolysis bullosa spectrum.

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J Timothy Wright

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Mutations in the 180-kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa

Epidermolysis bullosa. II. Type VII collagen mutations and phenotype-genotype correlations in the dystrophic subtypes

Regulation of human skeletal stem cells differentiation by Dlk1/Pref-1

A missense mutation in type VII collagen in two affected siblings with recessive dystrophic epidermolysis bullosa

The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB

Hereditary epidermolysis bullosa: oral manifestations and dental therapy.

Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome.

Oro-dental manifestations in Hallopeau-Siemens-type recessive dystrophic epidermolysis bullosa.

Epidermolysis bullosa. I. Molecular genetics of the junctional and hemidesmosomal variants.

Kindler syndrome: a focal adhesion genodermatosis.

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