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Acral keratosis

Known as: Acral keratoses 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Cowden syndrome (CS) is an uncommon autosomal dominant multiorgan/system genodermatosis. It is characterized by the development… 
2016
2016
  • B. WorleyS. J. Glassman
  • Clincal and Experimental Dermatology
  • 2016
  • Corpus ID: 32741533
Hydroxyurea is used in essential thrombocythaemia to lower thromboembolic risk. Cutaneous adverse effects from hydroxyurea are… 
2015
2015
Here, we report a case of Cowden syndrome with an unusual clinical course of late-onset oral papillomatosis and a novel germline… 
2008
2008
TO THE EDITOR: In the article by Lu et al, 1 the investigators conducted a prospective assessment of the prevalence of Lynch… 
2007
2007
Cowden disease (CD) is a rare autosomal dominant disease with variable expression, affecting a number of systems in the form of… 
Review
2004
Review
2004
  • J. Reifenberger
  • Der Hautarzt; Zeitschrift fur Dermatologie…
  • 2004
  • Corpus ID: 6948519
Several hereditary tumor syndromes are associated with characteristic skin lesions which may facilitate an early diagnosis. We… 
2004
2004
ZusammenfassungEine Reihe von hereditären Tumorsyndromen zeichnet sich durch charakteristische Veränderungen der Haut aus, die… 
Review
1989
Review
1989
Abstract: We evaluated two patients Mrith hereditary bullous polkiloderma. Both had acral buliae, generalized poiidloderma with… 
1987
1987
REPORT OF A CASE A 62-year-old man had thyroid goiter (Fig 1) of approximately ten years' duration. There were no signs or…