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The Clinical phenotype and a novel COL7A1 mutation in a Chinese family with dystrophic epidermolysis bullosa pruriginosa.

Mu YZ, Du ZC, Zhang ZZ, Yang H, Chen X, Wang Y, Liu LL.

J Eur Acad Dermatol Venereol. 2018 Mar 6. doi: 10.1111/jdv.14917. [Epub ahead of print]


Acquired elastoma in a subungual location.

Wolner ZJ, Liebman TN, Lowenstein EJ.

Dermatol Online J. 2017 Sep 15;23(9). pii: 13030/qt7403m0g7.


Nail Biopsy: A User's Manual.

Grover C, Bansal S.

Indian Dermatol Online J. 2018 Jan-Feb;9(1):3-15. doi: 10.4103/idoj.IDOJ_268_17. Review.


Rare Variant of Ankyloblepharon-ectodermal Defect-cleft Lip/Cleft Palate Syndrome: Curly Hair-ankyloblepharon-nail Disease Syndrome.

Chopra A, Mitra D, Kandpal R, Agarwal R.

Int J Trichology. 2018 Jan-Feb;10(1):17-20. doi: 10.4103/ijt.ijt_55_17.


The keratin 16 null phenotype is modestly impacted by genetic strain background in mice.

Zieman A, Coulombe PA.

Exp Dermatol. 2018 Feb 6. doi: 10.1111/exd.13509. [Epub ahead of print]


Nail psoriasis: clinical features, pathogenesis, differential diagnoses, and management.

Haneke E.

Psoriasis (Auckl). 2017 Oct 16;7:51-63. doi: 10.2147/PTT.S126281. eCollection 2017. Review.


Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay.

Duverger O, Carlson JC, Karacz CM, Schwartz ME, Cross MA, Marazita ML, Shaffer JR, Morasso MI.

PLoS Genet. 2018 Jan 22;14(1):e1007168. doi: 10.1371/journal.pgen.1007168. eCollection 2018 Jan.


A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report.

Argyropoulou Z, Liu L, Ozoemena L, Branco CC, Senra R, Reis-Rego Â, Mota-Vieira L.

BMC Dermatol. 2018 Jan 20;18(1):1. doi: 10.1186/s12895-018-0069-x.


Hyperkeratotic nail dystrophy.

Sainz-Gaspar L, Rosón E, Suárez-Peñaranda JM, Vázquez-Veiga H.

Enferm Infecc Microbiol Clin. 2017 Dec 18. pii: S0213-005X(17)30371-3. doi: 10.1016/j.eimc.2017.11.010. [Epub ahead of print] English, Spanish. No abstract available.


Cutaneous Cysts with Nail Dystrophy in a Young Female: A Classical Association.

Ghosh R, Chatterjee K, Barua JK, Roy A.

Indian J Dermatol. 2017 Nov-Dec;62(6):661-664. doi: 10.4103/ijd.IJD_473_16.


Clinico-epidemiological Study of Congenital Ichthyosis in a Tertiary Care Center of Eastern India.

Ghosh A, Ahar R, Chatterjee G, Sharma N, Jadhav SA.

Indian J Dermatol. 2017 Nov-Dec;62(6):606-611. doi: 10.4103/ijd.IJD_411_17.


<i>CDH3</i> gene related hypotrichosis and juvenile macular dystrophy - A case with a novel mutation.

Karti O, Abali S, Ayhan Z, Gokmeydan E, Nalcaci S, Yaman A, Saatci AO.

Am J Ophthalmol Case Rep. 2017 Jun 26;7:129-133. doi: 10.1016/j.ajoc.2017.06.007. eCollection 2017 Sep.


Phenotypic Variation in Patients with Homozygous c.1678G>T Mutation in EVC Gene: Report of Two Mexican Families with Ellis-van Creveld Syndrome.

Ibarra-Ramirez M, Campos-Acevedo LD, Lugo-Trampe J, Martínez-Garza LE, Martinez-Glez V, Valencia-Benitez M, Lapunzina P, Ruiz-Peréz V.

Am J Case Rep. 2017 Dec 12;18:1325-1329.


Mutilating Keratoderma with Concomitant Alopecia and Keratoses Follicularis Spinulosa Decalvans: X-Linked Olmsted Syndrome and its Response to Isotretinoin.

Verma G, Sardana K, Gautam RK.

Indian Dermatol Online J. 2017 Nov-Dec;8(6):482-484. doi: 10.4103/idoj.IDOJ_422_16.


Do you know this syndrome? Clouston syndrome.

Sanches S, Rebellato PRO, Fabre AB, Campos GLM.

An Bras Dermatol. 2017 May-Jun;92(3):417-418. doi: 10.1590/abd1806-4841.20175716.


Pachyonychia Congenita.

Smith FJD, Hansen CD, Hull PR, Kaspar RL, McLean WHI, O’Toole E, Sprecher E.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2006 Jan 27 [updated 2017 Nov 30].


Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy.

Vahidnezhad H, Youssefian L, Saeidian AH, Mahmoudi H, Touati A, Abiri M, Kajbafzadeh AM, Aristodemou S, Liu L, McGrath JA, Ertel A, Londin E, Kariminejad A, Zeinali S, Fortina P, Uitto J.

Matrix Biol. 2018 Mar;66:22-33. doi: 10.1016/j.matbio.2017.11.003. Epub 2017 Nov 11.


The water-drop test for the diagnosis of koilonychia.

Chelidze K, Lipner SR.

J Am Acad Dermatol. 2017 Dec;77(6):e157-e158. doi: 10.1016/j.jaad.2017.06.034. No abstract available.


Clinicopathologic features of 28 cases of nail matrix nevi (NMNs) in Asians: Comparison between children and adults.

Lee JH, Lim Y, Park JH, Lee JH, Jang KT, Kwon EJ, Lee DY.

J Am Acad Dermatol. 2018 Mar;78(3):479-489. doi: 10.1016/j.jaad.2017.08.052. Epub 2017 Oct 26.


Ibrutinib-Associated Nail Plate Abnormalities: Case Reports and Review.

Heldt Manica LA, Cohen PR.

Drug Saf Case Rep. 2017 Nov 1;4(1):15. doi: 10.1007/s40800-017-0060-1.

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