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Items: 1 to 20 of 3029

1.

Keratin 17 Mutations in Four Families from India with Pachyonychia Congenita.

Agarwala M, Salphale P, Peter D, Wilson NJ, Pulimood S, Schwartz ME, Smith FJD.

Indian J Dermatol. 2017 Jul-Aug;62(4):422-426. doi: 10.4103/ijd.IJD_321_16.

2.

Linear Palmoplantar Keratoderma.

Imbernón-Moya A, Aguilar-Martínez A, Vargas-Laguna E.

Actas Dermosifiliogr. 2017 Jun 30. pii: S0001-7310(17)30274-0. doi: 10.1016/j.ad.2017.02.023. [Epub ahead of print] English, Spanish. No abstract available.

PMID:
28673420
3.

[Molecular genetic study of a family affected with punctate palmoplantar keratoderma].

Jia Y, Wang S, Zhu Y, Luo D.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Jun 10;34(3):369-372. doi: 10.3760/cma.j.issn.1003-9406.2017.03.012. Chinese.

PMID:
28604957
4.

Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice.

Press E, Alaga KC, Barr K, Shao Q, Bosen F, Willecke K, Laird DW.

Cell Death Dis. 2017 Jun 1;8(6):e2845. doi: 10.1038/cddis.2017.234.

5.

PIGO deficiency: palmoplantar keratoderma and novel mutations.

Morren MA, Jaeken J, Visser G, Salles I, Van Geet C; NIHR BioResource, Simeoni I, Turro E, Freson K.

Orphanet J Rare Dis. 2017 May 25;12(1):101. doi: 10.1186/s13023-017-0654-9.

6.

Modeling the Structure of Keratin 1 and 10 Terminal Domains and their Misassembly in Keratoderma.

Badowski C, Sim AYL, Verma C, Szeverényi I, Natesavelalar C, Terron-Kwiatkowski A, Harper J, O'Toole EA, Lane EB.

J Invest Dermatol. 2017 May 16. pii: S0022-202X(17)31522-1. doi: 10.1016/j.jid.2017.03.038. [Epub ahead of print]

PMID:
28526297
7.

Erythema elevatum diutinum presenting with palmoplantar keratoderma.

Kamyab K, Balighi K, Azizpour A, Khani S, Safar F.

Clin Exp Dermatol. 2017 Jul;42(5):573-575. doi: 10.1111/ced.13103. Epub 2017 May 17. No abstract available.

PMID:
28512994
8.

Unilateral Linear Punctate Palmoplantar Keratoderma: A Case Report.

Kiatsurayanon C, Rojanamatin J, Sudtikoonaseth P, Kampirapap K, Wichaidit M, Niyonsaba F.

Case Rep Dermatol. 2017 Mar 29;9(1):86-89. doi: 10.1159/000468920. eCollection 2017 Jan-Apr.

9.

Electrical Storm or Naxos Syndrome in an Adult Causing Recurrent Syncope.

Maqbool MF, Sajid M, Noeman A.

J Coll Physicians Surg Pak. 2017 Apr;27(4):250-251. doi: 2599.

PMID:
28492156
10.

Exfoliative erythroderma and palmoplantar hyperkeratosis associated with Majocchi's granuloma by Trichophyton tonsurans in a patient with AIDS.

Lyra MR, Muniz Álvarez B, Lanziano AL, Imbeth MAA, Sá AM, Cuzzi T, Oliveira JC, Schubach AO.

Rev Iberoam Micol. 2017 Jul - Sep;34(3):185-188. doi: 10.1016/j.riam.2016.11.007. Epub 2017 Apr 25.

PMID:
28462859
11.

Duplicated Enhancer Region Increases Expression of CTSB and Segregates with Keratolytic Winter Erythema in South African and Norwegian Families.

Ngcungcu T, Oti M, Sitek JC, Haukanes BI, Linghu B, Bruccoleri R, Stokowy T, Oakeley EJ, Yang F, Zhu J, Sultan M, Schalkwijk J, van Vlijmen-Willems IMJJ, von der Lippe C, Brunner HG, Ersland KM, Grayson W, Buechmann-Moller S, Sundnes O, Nirmala N, Morgan TM, van Bokhoven H, Steen VM, Hull PR, Szustakowski J, Staedtler F, Zhou H, Fiskerstrand T, Ramsay M.

Am J Hum Genet. 2017 May 4;100(5):737-750. doi: 10.1016/j.ajhg.2017.03.012. Epub 2017 Apr 27.

PMID:
28457472
12.

Olmsted Syndrome in a Family.

Konathan R, Alur SK.

Int J Trichology. 2016 Oct-Dec;8(4):168-170. doi: 10.4103/0974-7753.203175.

13.

Keratoacanthoma, palmoplantar keratoderma developing in an advanced melanoma patient treated with vemurafenib regressed by blockade of mitogen-activated protein kinase kinase signaling.

Furudate S, Fujimura T, Kambayashi Y, Hidaka T, Sato Y, Tanita K, Hashimoto A, Aiba S.

J Dermatol. 2017 Apr 25. doi: 10.1111/1346-8138.13898. [Epub ahead of print] No abstract available.

PMID:
28439948
14.

A hypomorphic Egfr allele does not ameliorate the palmoplantar keratoderma caused by SLURP1 deficiency.

Allan CM, Tran D, Tu Y, Heizer PJ, Young LC, Fong LG, Beigneux AP, Young SG.

Exp Dermatol. 2017 Apr 18. doi: 10.1111/exd.13363. [Epub ahead of print]

PMID:
28418591
15.

A novel link between keratoderma and cardiomyopathy: Contiguous gene deletion involving the desmoglein gene cluster.

Brown S, Ahmed J, Zwolinski S, Brennan P, Rajan N.

Br J Dermatol. 2017 Apr 13. doi: 10.1111/bjd.15584. [Epub ahead of print]

PMID:
28407214
16.

Paraneoplastic palmoplantar keratoderma secondary to metastatic uterine adenocarcinoma.

Kallini JR, Sadeghani K, Khachemoune A.

Cutis. 2017 Mar;99(3):E32-E35.

PMID:
28398428
17.

Identification of a heterozygous p.Gly568Val missense mutation in the TRPV3 gene in a Japanese patient with Olmsted syndrome: In silico analysis of TRPV3.

Nagai H, Takaoka Y, Sugano A, Nakamachi Y, Kawano S, Nishigori C.

J Dermatol. 2017 Apr 9. doi: 10.1111/1346-8138.13844. [Epub ahead of print]

PMID:
28391651
18.

The Ca2+-Permeable Cation Transient Receptor Potential TRPV3 Channel: An Emerging Pivotal Target for Itch and Skin Diseases.

Wang G, Wang K.

Mol Pharmacol. 2017 Sep;92(3):193-200. doi: 10.1124/mol.116.107946. Epub 2017 Apr 4.

PMID:
28377424
19.

Whole Exome Sequencing Identified a Novel Frameshift Mutation in SDR9C7 underlying Autosomal Recessive Congenital Ichthyosis in a Pakistani Family.

Karim N, Murtaza G, Naeem M.

Br J Dermatol. 2017 Mar 31. doi: 10.1111/bjd.15535. [Epub ahead of print]

PMID:
28369735
20.

Disseminated punctate keratoderma: a rare case report and review of the literature.

Asemota E, Markova A, Ho J, Lichtman MK.

Dermatol Online J. 2017 Mar 15;23(3). pii: 13030/qt8jf1g7ff.

PMID:
28329514

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