Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

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
Expand

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
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
  • figure 1
  • figure 2
  • table 2
  • table 3
  • table 5
2013
2013
Targeted sequence capture and high-throughput sequencing in the molecular diagnosis of ichthyosis and other skin diseases.
cated that MBTPS2 is mainly expressed in the upper granular layer in normal skin, as previously shown (Aten et al., 2010… Expand
  • table 1
  • table 2
Highly Cited
2010
Highly Cited
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
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
  • table 1
  • table 2
  • table 3
  • table 4
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
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
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
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
  • figure 1
  • table 1
  • table 2
  • figure 3
  • figure 2
1996
1996
An Xp22.1–p22.2 YAC Contig Encompassing the Disease Loci for RS, KFSD, CLS, HYP and RP15: Refined Localization of RS
To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans… Expand
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
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License
ACCEPT & CONTINUE