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Poikiloderma of Kindler

Known as: POIKILODERMA, HEREDITARY ACROKERATOTIC, Poikiloderma, congenital, with bullae, weary type, KNDLRS 
National Institutes of Health

Papers overview

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2016
2016
Epidermolysis bullosa (EB) comprises a clinically heterogeneousgroupofdisorderscharacterizedbyfragilityof skin, leading to… 
2014
2014
Kindler syndrome (KS) in humans is a severe skin blistering disease associated with inflammation and increased risk of epidermal… 
2011
2011
Poikiloderma vasculare atrophicans (PVA) is a rare variant of mycosis fungoides, and is characterized by generalized… 
2008
2008
Background  Kindler syndrome (KS) is a rare genodermatosis characterized by four major features (acral blisters, photosensitivity… 
2007
2007
9-formyljulolidine was oxidized via a microwave-assisted Willgerodt-Kindler reaction to the N-piperidine or N-morpholine… 
2006
2006
Kindler syndrome is a rare autosomal recessive disorder characterized by acral blisters in infancy and early childhood, followed… 
2002
2002
ZusammenfassungEs wird über eine 18-jährige Patientin berichtet, die wegen Synechien der Labien zur weiteren Abklärung überwiesen… 
1998
1998
  • M. HoL. Chong
  • 1998
  • Corpus ID: 26083262
Primary cutaneous amyloidosis is the deposition of amyloid in the skin without involvement of internal organs. It is easily… 
1994
1994
Kindler syndrome is a rare, blistering skin disease characterized by acral bullae, poikiloderma, and diffuse cutaneous atrophy…