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Best matches for keratoderma, palmoplantar:

[Hereditary palmoplantar keratoderma - a focus on clinical and molecular genetic aspects]. Kamaleswaran S et al. Ugeskr Laeger. (2014)

Palmoplantar keratoderma (PPK): acquired and genetic causes of a not so rare disease. Schiller S et al. J Dtsch Dermatol Ges. (2014)

[Palmoplantar keratoderma: molecular identification of two new subtypes]. Dereure O et al. Ann Dermatol Venereol. (2014)

Search results

Items: 1 to 20 of 2751

1.

Tatami Mats: A Source of Pitted Keratolysis in a Martial Arts Athlete?

Balić A, Bukvić Mokos Z, Marinović B, Ledić Drvar D.

Acta Dermatovenerol Croat. 2018 Apr;26(1):68-70.

PMID:
29782305
2.

A novel heterozygous missense mutation of the desmoglein 1 gene in a Chinese family with diffuse nonepidermolytic palmoplantar keratoderma.

Wang D, He Y, Wang S.

Indian J Dermatol Venereol Leprol. 2018 May 17. doi: 10.4103/ijdvl.IJDVL_431_17. [Epub ahead of print] No abstract available.

PMID:
29770786
3.

A Rare Syndrome Resembling Scleroderma: Huriez Syndrome.

Çelik NS, Yaşar Ş, Aytekin S, Güneş P.

Skin Appendage Disord. 2018 Apr;4(2):82-85. doi: 10.1159/000479036. Epub 2017 Aug 12.

PMID:
29765964
4.

Aberrant expression of aquaporin-3 in hereditary papulotranslucent acrokeratoderma and aquagenic palmoplantar keratoderma.

Gironi LC, Colombo E, Zottarelli F, Guala A, Arduino C, Leutner M, Camillo L, Valente G, Boldorini RL, Savoia P.

Eur J Dermatol. 2018 Apr 1;28(2):262-263. doi: 10.1684/ejd.2018.3235. No abstract available.

PMID:
29724688
5.

Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar Keratoderma.

Xiao H, Guo Y, Yi J, Xia H, Xu H, Yuan L, Hu P, Yang Z, He Z, Lu H, Deng H.

Cell Physiol Biochem. 2018;46(5):1919-1929. doi: 10.1159/000489381. Epub 2018 Apr 26.

6.

Role of the keratin 1 and keratin 10 tails in the pathogenesis of ichthyosis hystrix of Curth Macklin.

Terrinoni A, Didona B, Caporali S, Chillemi G, Lo Surdo A, Paradisi M, Annichiarico-Petruzzelli M, Candi E, Bernardini S, Melino G.

PLoS One. 2018 Apr 24;13(4):e0195792. doi: 10.1371/journal.pone.0195792. eCollection 2018.

7.

[Epidermolytic palmoplantar keratoderma of Vörner].

Varela-Veiga A, Monteagudo B, León-Muiños E, Durana C.

An Pediatr (Barc). 2018 Apr 13. pii: S1695-4033(18)30125-5. doi: 10.1016/j.anpedi.2018.02.018. [Epub ahead of print] Spanish. No abstract available.

8.

Olmsted Syndrome with Lateral Supraciliary Madarosis and Clubbing: A Rare Case Report.

Zeeshan M, Jha AK, Chaudhary RKP.

Indian Dermatol Online J. 2018 Mar-Apr;9(2):114-116. doi: 10.4103/idoj.IDOJ_95_17.

9.

Compound heterozygous mutations in desmoplakin associated with skin fragility, follicular hyperkeratosis, alopecia, and nail dystrophy.

Bari O, Skillman S, Lah MD, Haggstrom AN.

Pediatr Dermatol. 2018 Apr 6. doi: 10.1111/pde.13498. [Epub ahead of print]

PMID:
29633331
10.

A novel heterozygous missense mutation of DSP in a Chinese Han pedigree with palmoplantar keratoderma.

Xue K, Zheng Y, Cui Y.

J Cosmet Dermatol. 2018 Apr 1. doi: 10.1111/jocd.12533. [Epub ahead of print]

PMID:
29607617
11.

SAM syndrome is characterized by extensive phenotypic heterogeneity.

Taiber S, Samuelov L, Mohamad J, Cohen Barak E, Sarig O, Shalev SA, Lestringant G, Sprecher E.

Exp Dermatol. 2018 Mar 31. doi: 10.1111/exd.13551. [Epub ahead of print]

PMID:
29604126
12.

Three novel GJB2 (connexin 26) variants associated with autosomal dominant syndromic and nonsyndromic hearing loss.

DeMille D, Carlston CM, Tam OH, Palumbos JC, Stalker HJ, Mao R, Zori RT, Viskochil DH, Park AH, Carey JC.

Am J Med Genet A. 2018 Apr;176(4):945-950. doi: 10.1002/ajmg.a.38648.

PMID:
29575629
13.

Novel RSPO1 mutation causing 46,XX testicular disorder of sex development with palmoplantar keratoderma: A review of literature and expansion of clinical phenotype.

Tallapaka K, Venugopal V, Dalal A, Aggarwal S.

Am J Med Genet A. 2018 Apr;176(4):1006-1010. doi: 10.1002/ajmg.a.38646.

PMID:
29575617
14.

p63 is a key regulator of iRHOM2 signalling in the keratinocyte stress response.

Arcidiacono P, Webb CM, Brooke MA, Zhou H, Delaney PJ, Ng KE, Blaydon DC, Tinker A, Kelsell DP, Chikh A.

Nat Commun. 2018 Mar 9;9(1):1021. doi: 10.1038/s41467-018-03470-y.

15.

Case of punctate palmoplantar keratoderma type I treated with combination of low-dose oral acitretin and topical salicylic acid and steroid.

Jo JW, Jeong DS, Kim CY.

J Dermatol. 2018 May;45(5):609-612. doi: 10.1111/1346-8138.14255. Epub 2018 Mar 3.

PMID:
29500825
16.

Punctate palmoplantar keratoderma: an unusual mutation causing an unusual phenotype.

Vodo D, Sarig O, Jeddah D, Malchin N, Eskin-Schwarz M, Mohamad J, Rabinowitz T, Goldberg I, Shomron N, Khamaysi Z, Bergman R, Sprecher E.

Br J Dermatol. 2018 Mar 1. doi: 10.1111/bjd.16502. [Epub ahead of print] No abstract available.

PMID:
29494755
17.

Hereditary palmoplantar keratodermas. Part I. Non-syndromic palmoplantar keratodermas: classification, clinical and genetic features.

Guerra L, Castori M, Didona B, Castiglia D, Zambruno G.

J Eur Acad Dermatol Venereol. 2018 May;32(5):704-719. doi: 10.1111/jdv.14902. Epub 2018 Mar 24. Review.

PMID:
29489036
18.

Photophobia accompanied by painful plantar punctate hyperkeratotic patches: Tyrosinemia type 2.

Mohite AA, Abbott J.

Indian J Ophthalmol. 2018 Mar;66(3):449. doi: 10.4103/ijo.IJO_820_17. No abstract available.

19.

NEK3-mediated SNAP29 phosphorylation modulates its membrane association and SNARE fusion dependent processes.

Rapaport D, Fichtman B, Weidberg H, Sprecher E, Horowitz M.

Biochem Biophys Res Commun. 2018 Mar 4;497(2):605-611. doi: 10.1016/j.bbrc.2018.02.116. Epub 2018 Feb 15.

PMID:
29454964
20.

Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in TRPV3 Gene.

Choi JY, Kim SE, Lee SE, Kim SC.

Yonsei Med J. 2018 Mar;59(2):341-344. doi: 10.3349/ymj.2018.59.2.341.

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