Cockayne-Touraine Disease

Known as: DDEB (dominant dystrophic epidermolysis bullosa), Epidermolysis Bullosa Dystrophica, Cockayne Touraine Type, Cockayne Touraine Disease 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1964-2017
012319642017

Papers overview

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2014
2014
Hypertrophic Osteoarthropathy secondary to various causes is not a common entity but primary hypertrophic osteoarthropathy (also… (More)
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2012
2012
The primary hypertrophic osteoarthropathy (HOA) (pachydermoperiostosis) is a rare hereditary disease characterized by skin… (More)
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2007
2007
Finger clubbing can be a single physical finding. In Touraine-Solente-Gole syndrome, the primary form of hypertrophic… (More)
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2004
2004
Ultrastructural examination was performed in 9 biopsy specimens from 4 patients with the Cockayne-Touraine type of epidermolysis… (More)
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2002
2002
BACKGROUND Dystrophic epidermolysis bullosa (DEB) is a genodermatosis resulting from mutations in COL7A1, the gene encoding type… (More)
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1993
1993
We have employed a successful therapy for epidermolysis bullosa with high-dose oral tocopherol acetate. Two siblings with… (More)
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1991
1991
Qualitative and quantitative comparisons of glycosaminoglycans e (GAG) production were made on fibroblast lines cultured from the… (More)
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1988
1988
In order to investigate the role of inflammatory cells in altering the collagenase production by epidermolysis bullosa (EB… (More)
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1987
1987
We report on a family with autosomal dominant dystrophic epidermolysis bullosa and congenital localized absence of skin… (More)
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1976
1976
Ultrastructural examination was performed in 9 biopsy specimens from 4 patients with the Cockayne-Touraine type of epidermolysis… (More)
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