Works matching DE "EPIDERMOLYTIC hyperkeratosis"

Results: 26

Novel mutation in NIPAL4 in a Romanian family with autosomal recessive congenital ichthyosis.

Published in:

Clinical & Experimental Dermatology, 2016, v. 41, n. 3, p. 279, doi. 10.1111/ced.12740

By:

Maier, D.;
Mazereeuw‐Hautier, J.;
Tilinca, M.;
Cosgarea, R.;
Jonca, N.

Publication type:

Article

Epidermolytic Acanthoma on Fingers, Mimicking Flat Warts.

Published in:

Case Reports in Dermatology, 2017, v. 9, n. 2, p. 98, doi. 10.1159/000478890

By:

Rojhirunsakool, Salinee;
Jirasuthat, Suthep;
Chanprapaph, Kumutnart

Publication type:

Article

Reticulate pigmentation in non-bullous ichthyosiform erythroderma.

Published in:

2016

By:

Khullar, Geeti;
De, Dipankar;
Handa, Sanjeev

Publication type:

journal article

Superficial epidermolytic ichthyosis.

Published in:

2015

By:

Das, Anirban;
Das, Anupam;
Bhattacharya, Sabari;
Ghosh, Anupama;
Shome, Kaushik

Publication type:

Case Study

Annular epidermolytic ichthyosis: A rare phenotypic variant of bullous congenital ichthyosiform erythroderma.

Published in:

2015

By:

Jha, Aditi;
Taneja, Jitender;
Ramesh, V.;
Singh, Avninder

Publication type:

Letter to the Editor

Coxsackie Eruption Arising in Areas of Epidermolytic Ichthyosis.

Published in:

Pediatric Dermatology, 2015, v. 32, n. 3, p. e132, doi. 10.1111/pde.12562

By:

Lewis, Suzanna;
Rico, Tace

Publication type:

Article

Mutation p.R156H of KRT10 responsible for severe phenotype of epidermolytic ichthyosis in a Chinese family.

Published in:

2014

By:

Zhiliang Li;
Qiao Liu;
Aimin Wang;
Hongsheng Wang;
Chengrang Li

Publication type:

Case Study

A novel keratin 10 gene mutation causing epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma) in a term neonate.

Published in:

Case Reports in Perinatal Medicine, 2017, v. 6, n. 1, p. 1, doi. 10.1515/crpm-2016-0050

By:

Pegu, Satyaranjan;
Bodani, Jaya. P.;
Lemire, Edmond G.;
Holfeld, Karen I.

Publication type:

Article

Nevoid Psoriasis Coexisting with Verrucous Epidermal Nevus.

Published in:

2017

By:

Masatkar, Vaishali;
Gupta, Lalit K.;
Mehta, Sharad;
Khare, Ashok K.;
Mittal, Asit

Publication type:

Case Study

PREVALENCE OF TINEA CAPITIS IN A TERTIARY CARE HOSPITAL, NORTH INDIA.

Published in:

Era's Journal of Medical Research, 2016, v. 3, n. 2, p. 7

By:

Shukla, Priyanka;
Haider, Fareya;
Yaqoob, Shadma;
Khare, Vineeta;
Singh, Mastan

Publication type:

Article

Case report of harlequin ichthyosis who had similar history in two earlier siblings.

Published in:

2014

By:

Rasul, Shazia;
Gul, Asma;
Tahir, Shabnum;
Hameed, Abdul

Publication type:

Case Study

Mutations Affecting Keratin 10 Surface-Exposed Residues Highlight the Structural Basis of Phenotypic Variation in Epidermolytic Ichthyosis.

Published in:

Journal of Investigative Dermatology, 2015, v. 135, n. 12, p. 3041, doi. 10.1038/jid.2015.284

By:

Mirza, Haris;
Kumar, Anil;
Craiglow, Brittany G;
Zhou, Jing;
Saraceni, Corey;
Torbeck, Richard;
Ragsdale, Bruce;
Rehder, Paul;
Ranki, Annamari;
Choate, Keith A

Publication type:

Article

Epidermolytic Hyperkeratosis - A rare case report.

Published in:

2015

By:

Kataria, Usha;
Chhillar, Dinesh;
Dhattarwal, S. K.

Publication type:

Case Study

Congenital unilateral reticulate keratotic papules on the lower extremity.

Published in:

2018

By:

Bains, Anupama;
Singh, Saurabh

Publication type:

Case Study

Multiple epidermolytic acanthomas mimicking condyloma: a retrospective study of 8 cases.

Published in:

International Journal of Dermatology, 2018, v. 57, n. 1, p. 28, doi. 10.1111/ijd.13818

By:

Lee, Tsung‐Ju;
Wu, Yu‐Hung

Publication type:

Article

Solitary and multiple epidermolytic acanthoma: A demographic and clinical study of 131 cases.

Published in:

Journal of Cutaneous Pathology, 2019, v. 46, n. 5, p. 305, doi. 10.1111/cup.13422

By:

Roy, Simon F.;
Ghazawi, Feras M.;
Choate, Keith A.;
McNiff, Jennifer M.

Publication type:

Article

Use of the frozen section 'jelly-roll' technique to aid in the diagnosis of bullous congenital ichthyosiform erythroderma (epidermolytic hyperkeratosis).

Published in:

Journal of Cutaneous Pathology, 2016, v. 43, n. 5, p. 434, doi. 10.1111/cup.12680

By:

Galler, Blake;
Bowen, Casey;
Arnold, Jason;
Kobayashi, Todd;
Dalton, Scott R.

Publication type:

Article

Vörner syndrome. Different stages of clinical manifestation in an Indian family.

Published in:

European Journal of Pediatric Dermatology, 2015, v. 25, n. 3, p. 138

By:

Biswal S. G.;
Mehta R. D.

Publication type:

Article

A p.478I>T KRT1 mutation in a case of annular epidermolytic ichthyosis.

Published in:

2018

By:

Zaki, Theodore D.;
Yoo, Ki‐Young;
Kassardjian, Michael;
Choate, Keith A.

Publication type:

Case Study

An unusual guest in the panel of differentials!

Published in:

2016

By:

Chandrashekar, B. S.;
Mukherjee, Samipa Samir

Publication type:

Case Study

Loricrin keratoderma presenting as nonbullous ichthyosiform erythroderma: A rare case report.

Published in:

2015

By:

Brar, B. K.;
Kaur, Sandeep;
Singh, Ravinder

Publication type:

Case Study

Epidermolytic hyperkeratosis: clinical update.

Published in:

Clinical, Cosmetic & Investigational Dermatology, 2019, v. 12, p. 333, doi. 10.2147/CCID.S166849

By:

Rout, Denice Peter;
Nair, Anushka;
Gupta, Anand;
Kumar, Piyush

Publication type:

Article

Extensive lentigo simplex, linear epidermolytic naevus and epidermolytic naevus comedonicus caused by a somatic mutation in KRT10.

Published in:

British Journal of Dermatology, 2015, v. 173, n. 1, p. 293, doi. 10.1111/bjd.13616

By:

Samuelov, L.;
Sarig, O.;
Gat, A.;
Halachmi, S.;
Shalev, S.;
Sprecher, E.

Publication type:

Article

Novel <italic>PNPLA1</italic> mutations in two Italian siblings with autosomal recessive congenital ichthyosis.

Published in:

Journal of the European Academy of Dermatology & Venereology, 2018, v. 32, n. 3, p. e110, doi. 10.1111/jdv.14618

By:

Diociaiuti, A.;
Pisaneschi, E.;
Zambruno, G.;
Angioni, A.;
Novelli, A.;
Boldrini, R.;
El Hachem, M.

Publication type:

Article

S159P mutation of keratin 10 gene causes severe form of epidermolytic hyperkeratosis.

Published in:

Journal of the European Academy of Dermatology & Venereology, 2016, v. 30, n. 10, p. e102, doi. 10.1111/jdv.13345

By:

Chen, P. ‐ J.;
Li, C. ‐ X.;
Wen, J.;
Peng, Y. ‐ S.;
Zeng, K.;
Zhang, S. ‐ Q.;
Tian, X.;
Zhang, X. ‐ B.

Publication type:

Article

Epidermolytic hyperkeratosis of the vulva.

Published in:

Dermatology Online Journal, 2021, v. 27, n. 1, p. 1, doi. 10.5070/d3271052038

By:

Dai, Christina;
Sokumbi, Olayemi;
Bruce, Alison;
Thielen, Jacqueline M.;
Sluzevich, Jason C.

Publication type:

Article