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Keratosis Follicularis

Known as: DD, WHITE-DARIER DISEASE, Follicular keratosis 
An autosomal dominantly inherited skin disorder characterized by warty malodorous papules that coalesce into plaques. It is caused by mutations in… Expand
National Institutes of Health

Related topics

Related topics

29 relations
ATP2A2 geneAcantholytic Dyskeratotic Epidermal NevusAcrokeratosis Verruciformis of HopfAutosomal dominant inheritance
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Narrower (5)

Burnett Schwartz Berberian syndromeKERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (disorder)Keratosis follicularis dwarfism cerebral atrophyKyrle disease
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Broader (4)

Hereditary DiseasesKeratinization, functionKeratosisTyloma

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2018
Review
2018
Production of Bioactive Peptides by Lactobacillus Species: From Gene to Application
To compensate for their amino acid auxotrophy, lactobacilli have developed the ability to hydrolyze proteins present in their… Expand
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Review
2018
Review
2018
Organic Acids and Potential for Modifying the Avian Gastrointestinal Tract and Reducing Pathogens and Disease
Recently, antibiotics have been withdrawn from some poultry diets; leaving the birds at risk for increased incidence of… Expand
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Review
2018
Review
2018
Parenting Stress through the Lens of Different Clinical Groups: a Systematic Review & Meta-Analysis
Research has demonstrated an association between parenting stress and child behavior problems, and suggested levels of parenting… Expand
Is this relevant?
Review
2018
Review
2018
Effects of balneotherapy and spa therapy on quality of life of patients with knee osteoarthritis: a systematic review and meta-analysis
Knee osteoarthritis (OA) is a degenerative disease which is expected to become one of the leading causes of disability by the… Expand
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Highly Cited
2011
Highly Cited
2011
Elevated plasma cytokines in autism spectrum disorders provide evidence of immune dysfunction and are associated with impaired behavioral outcome
Autism spectrum disorders (ASD) are characterized by impairment in social interactions, communication deficits, and restricted… Expand
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Highly Cited
2006
Highly Cited
2006
Sensory Experiences Questionnaire: discriminating sensory features in young children with autism, developmental delays, and typical development.
BACKGROUND This study describes a new caregiver-report assessment, the Sensory Experiences Questionnaire (SEQ), and explicates… Expand
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Highly Cited
2000
Highly Cited
2000
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
Hailey-Hailey disease (HHD, MIM 16960) is inherited in an autosomal dominant manner and characterized by persistent blisters and… Expand
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Highly Cited
1999
Highly Cited
1999
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease
Darier disease (DD) is an autosomal-dominant skin disorder characterized by loss of adhesion between epidermal cells… Expand
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Highly Cited
1996
Highly Cited
1996
A meta-analysis of the association of the deletion allele of the angiotensin-converting enzyme gene with myocardial infarction.
BACKGROUND The ACE gene is characterized by a polymorphism based on the presence (insertion [I]) or absence (deletion [D]) within… Expand
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Highly Cited
1993
Highly Cited
1993
Mistyping ACE heterozygotes.
Depar tment of Pathology, Emory University School of Medicine, Atlanta, Georgia 30322 Human angiotensin I-converting enzyme (ACE… Expand
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