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Palmoplantar Keratosis
Known as:
Palmoplantar keratoderma
, Hyperkeratosis of palms and soles
, Keratosis Palmaris et Plantaris
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Group of mostly hereditary disorders characterized by thickening of the palms and soles as a result of excessive keratin formation leading to…
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National Institutes of Health
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Related topics
Related topics
45 relations
Narrower (15)
Basaran Yilmaz syndrome
Corneodermatoosseous syndrome
Fitzsimmons-McLachlan-Gilbert syndrome
Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome
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CATARACT-ALOPECIA-SCLERODACTYLY SYNDROME
Cardiomyopathy dilated with Woolly hair and keratoderma
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome
Dermatologic disorders
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Broader (2)
Keratinization, function
Tyloma
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2015
Highly Cited
2015
Epidemiology of psoriasis and palmoplantar pustulosis: a nationwide study using the Japanese national claims database
K. Kubota
,
Y. Kamijima
,
+4 authors
H. Nakagawa
BMJ Open
2015
Corpus ID: 6728319
Objective The primary objective was to estimate the national prevalence of psoriasis and palmoplantar pustulosis (PPP) in Japan…
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Highly Cited
2012
Highly Cited
2012
Mode-division multiplexed transmission with inline few-mode fiber amplifier.
N. Bai
,
E. Ip
,
+18 authors
Ting Wang
Optics Express
2012
Corpus ID: 1888549
We demonstrate mode-division multiplexed WDM transmission over 50-km of few-mode fiber using the fiber's LP01 and two degenerate…
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Highly Cited
2012
Highly Cited
2012
Design of a Compact Two-Mode Multi/Demultiplexer Consisting of Multimode Interference Waveguides and a Wavelength-Insensitive Phase Shifter for Mode-Division Multiplexing Transmission
T. Uematsu
,
Y. Ishizaka
,
Y. Kawaguchi
,
K. Saitoh
,
M. Koshiba
Journal of Lightwave Technology
2012
Corpus ID: 1299001
A compact two-mode (de)multiplexer (TM-MUX) based on Si nanowire for mode-division multiplexing is designed. The TM-MUX is…
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Highly Cited
2008
Highly Cited
2008
Efficient HIV-1 transmission from macrophages to T cells across transient virological synapses.
F. Groot
,
Sonja Welsch
,
Q. Sattentau
Blood
2008
Corpus ID: 595191
Macrophages are reservoirs of HIV-1 infection, proposed to transmit virus to CD4(+) T cells, the primary target of the virus…
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Highly Cited
2003
Highly Cited
2003
Genetic analysis of PSORS1 distinguishes guttate psoriasis and palmoplantar pustulosis.
Kati Asumalahti
,
M. Ameen
,
+15 authors
J. Barker
Journal of Investigative Dermatology
2003
Corpus ID: 43465277
The PSORS1 locus in the major histocompatibility complex region is the major genetic determinant for psoriasis vulgaris. Within…
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Highly Cited
2002
Highly Cited
2002
Psoriasis of early and late onset: a clinical and epidemiologic study from Spain.
C. Ferrándiz
,
R. Pujol
,
V. García-Patos
,
X. Bordas
,
J. A. Smandia
Journal of American Academy of Dermatology
2002
Corpus ID: 4865098
BACKGROUND The existence of 2 distinct forms of psoriasis related to age at onset has been postulated. However, precise data…
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Highly Cited
1999
Highly Cited
1999
Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome
T. Hart
,
Suzanne Hart
,
+7 authors
Michalec S A Callison
Journal of Medical Genetics
1999
Corpus ID: 23891572
Papillon-Lefèvre syndrome (PLS) is an autosomal recessive disorder characterised by palmoplantar hyperkeratosis and severe early…
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Highly Cited
1999
Highly Cited
1999
Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratoderma.
D. Armstrong
,
K. Mckenna
,
+4 authors
A. Hughes
Human Molecular Genetics
1999
Corpus ID: 2640456
Desmosomes are highly organized intercellular adhesive junctions that are particularly prominent in epidermis and other tissues…
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Highly Cited
1999
Highly Cited
1999
Natural evolution of skin test sensitivity in patients allergic to β-lactam antibiotics
M. Blanca
,
Marta E. Torres
,
+6 authors
C. Juarez
1999
Corpus ID: 19735702
Highly Cited
1998
Highly Cited
1998
Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma
G. Richard
,
T. W. White
,
+4 authors
S. Bale
Human Genetics
1998
Corpus ID: 9365497
Mutations in GJB2 encoding the gap junction protein connexin-26 (Cx26) have been established as the basis of autosomal recessive…
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