Cause-specific risks of childhood death in inherited epidermolysis bullosa.
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Inherited epidermolysis bullosaInterventions for preventing keratinocyte cancer in high-risk groups not receiving immunosuppressive therapyPain care for patients with epidermolysis bullosa: best care practice guidelines.Dystrophic epidermolysis bullosa in pregnancy: a case report of the autosomal dominant subtype and review of the literature.A mouse model of generalized non-Herlitz junctional epidermolysis bullosa.A consensus approach to wound care in epidermolysis bullosa.An unusual case of epidermolysis bullosa complicated by persistent oligoarticular juvenile idiopathic arthritis; lessons to be learnedEpidermolysis bullosaeHereditary nonmelanoma skin cancerNutritional outcomes in children with epidermolysis bullosa: the experiences of two centers in Korea.Factors affecting quality of life in epidermolysis bullosa.Immunological mapping in hereditary epidermolysis bullosa.Diagnosing epidermolysis bullosa type and subtype in infancy using immunofluorescence microscopy: the Stanford experience.Age and etiology of childhood epidermolysis bullosa mortality.Neonatal junctional epidermolysis bullosa: treatment conundrums and ethical decision making.Rescue of the mucocutaneous manifestations by human cord blood derived nonhematopoietic stem cells in a mouse model of recessive dystrophic epidermolysis bullosa.Feasibility, efficacy, and safety of ultrasound-guided axillary plexus blockade in pediatric patients with epidermolysis bullosa dystrophica.Effectiveness of saltwater baths in the treatment of epidermolysis bullosa.Induced pluripotent stem cells from human revertant keratinocytes for the treatment of epidermolysis bullosa.Long-term follow-up of patients with Herlitz-type junctional epidermolysis bullosa.A practical approach to the evaluation and treatment of an infant with aplasia cutis congenita.Molecular epidemiology of junctional epidermolysis bullosa: discovery of novel and frequent LAMB3 mutations in Chilean patients with diagnostic significance.Hallopeau-Siemens dystrophic epidermolysis bullosa due to homozygous 5818delC mutation in theCOL7AgeneLiving with Keratinocytes
P2860
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P2860
Cause-specific risks of childhood death in inherited epidermolysis bullosa.
description
2007 nî lūn-bûn
@nan
2007 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Cause-specific risks of childhood death in inherited epidermolysis bullosa.
@ast
Cause-specific risks of childhood death in inherited epidermolysis bullosa.
@en
Cause-specific risks of childhood death in inherited epidermolysis bullosa.
@nl
type
label
Cause-specific risks of childhood death in inherited epidermolysis bullosa.
@ast
Cause-specific risks of childhood death in inherited epidermolysis bullosa.
@en
Cause-specific risks of childhood death in inherited epidermolysis bullosa.
@nl
prefLabel
Cause-specific risks of childhood death in inherited epidermolysis bullosa.
@ast
Cause-specific risks of childhood death in inherited epidermolysis bullosa.
@en
Cause-specific risks of childhood death in inherited epidermolysis bullosa.
@nl
P2093
P1476
Cause-specific risks of childhood death in inherited epidermolysis bullosa.
@en
P2093
Chirayath Suchindran
Jo-David Fine
Lorraine B Johnson
Madeline Weiner
P304
P356
10.1016/J.JPEDS.2007.06.039
P407
P577
2007-10-22T00:00:00Z