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KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (disorder)

Known as: KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT, KFSD 
 
National Institutes of Health

Related topics

Related topics

14 relations

Broader (2)

AlopeciaKeratosis Follicularis
Autosomal dominant inheritanceBlepharitisConjunctivitisDental Enamel Hypoplasia
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Papers overview

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2014
2014
Spatial depth-based classification for functional data
We enlarge the number of available functional depths by introducing the kernelized functional spatial depth (KFSD). KFSD is a… Expand
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2012
2012
MBTPS2 mutation in a British pedigree with keratosis follicularis spinulosa decalvans.
Keratosis follicularis spinulosa decalvans (KFSD; OMIM 308800) is an X-linked disorder characterized by widespread hyperkeratotic… Expand
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2011
2011
Keratosis follicularis spinulosa decalvans in a female.
Keratosis follicularis spinulosa decalvans (KFSD), is a rare follicular syndrome associated with widespread keratosis pilaris and… Expand
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2010
2010
Keratosis Follicularis Spinulosa Decalvans is caused by mutations in MBTPS2.
Keratosis Follicularis Spinulosa Decalvans (KFSD) is a rare genetic disorder characterized by development of hyperkeratotic… Expand
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Highly Cited
2009
Highly Cited
2009
Complete chloroplast genome sequence of a tree fern Alsophila spinulosa: insights into evolutionary changes in fern chloroplast genomes
BackgroundFerns have generally been neglected in studies of chloroplast genomics. Before this study, only one polypod and two… Expand
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2008
2008
Keratosis follicularis spinulosa decalvans in a family.
Keratosis follicularis spinulosa decalvans (KFSD) is a rare condition characterized by diffuse keratosis pilaris with a scarring… Expand
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2007
2007
Familial keratosis follicularis spinulosa decalvans associated with woolly hair.
Keratosis follicularis spinulosa decalvans (KFSD) is a rare inherited disorder of keratinization clinically characterized by… Expand
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2002
2002
Gene dosage of the spermidine/spermine N1-acetyltransferase (SSAT) gene with putrescine accumulation in a patient with a Xp21.1p22.12 duplication and keratosis follicularis spinulosa decalvans (KFSD)
Abstract. Keratosis follicularis spinulosa decalvans (KFSD) or Siemens-1 syndrome is a rare X-linked disease of unknown etiology… Expand
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Highly Cited
1997
Highly Cited
1997
The nitrogen supply from soils and insects during growth of the pitcher plants Nepenthes mirabilis, Cephalotus follicularis and Darlingtonia californica
Abstract This study investigated the nitrogen (N) acquisition from soil and insect capture during the growth of three species of… Expand
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1992
1992
Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
Keratosis follicularis spinulosa decalvans (KFSD) is a rare X linked disease which is characterised by follicular hyperkeratosis… Expand
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