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Items: 1 to 20 of 151

1.

Use of Epidermal Grafting for Treatment of Depigmented Skin in Piebaldism.

Maderal AD, Kirsner RS.

Dermatol Surg. 2017 Jan;43(1):159-160. doi: 10.1097/DSS.0000000000000833. No abstract available.

PMID:
27399941
2.

Optimising size and depth of punch grafts in autologous transplantation of vitiligo and piebaldism: a randomised controlled trial.

Komen L, Vrijman C, Prinsen CA, van der Veen JP, Luiten RM, Wolkerstorfer A.

J Dermatolog Treat. 2017 Feb;28(1):86-91. doi: 10.1080/09546634.2016.1179251. Epub 2016 Jun 16.

PMID:
27309418
3.

A case of piebaldism in a two-year-old female infant.

Tammaro A, Parisella FR, Colapietra D, Romano I, Persechino S.

G Ital Dermatol Venereol. 2016 Apr;151(2):208-9. No abstract available.

PMID:
27068599
4.

Piebaldism in children.

Grob A, Grekin S.

Cutis. 2016 Feb;97(2):90-2. Review.

PMID:
26919497
5.

Autologous cell suspension transplantation using a cell extraction device in segmental vitiligo and piebaldism patients: A randomized controlled pilot study.

Komen L, Vrijman C, Tjin EP, Krebbers G, de Rie MA, Luiten RM, van der Veen JP, Wolkerstorfer A.

J Am Acad Dermatol. 2015 Jul;73(1):170-2. doi: 10.1016/j.jaad.2015.03.036. No abstract available.

PMID:
26089056
6.

Piebaldism.

Bassi A, Berti S, Galeone M.

QJM. 2015 Nov;108(11):915. doi: 10.1093/qjmed/hcv101. Epub 2015 May 18. No abstract available.

PMID:
25991872
7.

Molecular characterization of piebaldism in a Tunisian family.

Kerkeni E, Boubaker S, Sfar S, Bizid M, Besbes H, Bouaziz S, Ghedira N, Amara A, Manoubi W, Gribaa M, Monastiri K.

Pathol Biol (Paris). 2015 Jun;63(3):113-6. doi: 10.1016/j.patbio.2015.03.004. Epub 2015 Apr 21.

PMID:
25910686
8.

Systemic conditions in children associated with pigmentary changes.

Treadwell PA.

Clin Dermatol. 2015 May-Jun;33(3):362-7. doi: 10.1016/j.clindermatol.2014.12.014. Epub 2014 Dec 8.

PMID:
25889139
9.

Spontaneous repigmentation in an infant with piebaldism.

Frances L, Betlloch I, Leiva-Salinas M, Silvestre JF.

Int J Dermatol. 2015 Jun;54(6):e244-6. doi: 10.1111/ijd.12776. Epub 2015 Mar 13. No abstract available.

PMID:
25773601
10.

4q12-4q21.21 deletion genotype-phenotype correlation and the absence of piebaldism in presence of KIT haploinsufficiency.

Hemati P, du Souich C, Boerkoel CF.

Am J Med Genet A. 2015 Jan;167A(1):231-7. doi: 10.1002/ajmg.a.36821. Epub 2014 Oct 29.

PMID:
25355368
11.

A novel mutation of KIT gene results in piebaldism in a Chinese family.

Xu XH, Ma L, Weng L, Xing H.

J Eur Acad Dermatol Venereol. 2016 Feb;30(2):336-8. doi: 10.1111/jdv.12738. Epub 2014 Sep 8. No abstract available.

PMID:
25199540
12.

Novel mutations of KIT gene in two Korean patients: variegated shades of phenotypes in tyrosine kinase 1 domain.

Lee H, Oh SH, Koo KY, Suzuki T, Lee JS.

J Dermatol Sci. 2014 Oct;76(1):74-6. doi: 10.1016/j.jdermsci.2014.07.009. Epub 2014 Aug 7. No abstract available.

PMID:
25176472
13.

Piebaldism in a 3-month-old infant--case report.

Milankov O, Savić R, Radulović A.

Med Pregl. 2014 Mar-Apr;67(3-4):109-10.

PMID:
24961053
14.

Piebaldism with non-intertriginous freckles: what does it mean?

Sarma N, Chakraborty S, Bhanja DC, Bhattachraya SR.

Indian J Dermatol Venereol Leprol. 2014 Mar-Apr;80(2):163-5. doi: 10.4103/0378-6323.129404. No abstract available.

15.

SNAI2 mutation causes human piebaldism.

Yang YJ, Zhao R, He XY, Li LP, Chen W, Wang KW, Zhao L, Tu M, Tang JS, Xie ZG, Zhu YM.

Am J Med Genet A. 2014 Mar;164A(3):855-7. doi: 10.1002/ajmg.a.36332. Epub 2014 Jan 17. No abstract available.

PMID:
24443330
16.

Biology and genetics of oculocutaneous albinism and vitiligo - common pigmentation disorders in southern Africa.

Manga P, Kerr R, Ramsay M, Kromberg JG.

S Afr Med J. 2013 Jul 29;103(12 Suppl 1):984-8. doi: 10.7196/samj.7046.

PMID:
24300644
17.

A novel splicing mutation of KIT results in piebaldism and auburn hair color in a Chinese family.

Yang YJ, Zhao R, He XY, Li LP, Wang KW, Zhao L, Tu M, Tang JS, Xie ZG, Zhu YM.

Biomed Res Int. 2013;2013:689756. doi: 10.1155/2013/689756. Epub 2013 Aug 13.

18.

Poliosis circumscripta: overview and underlying causes.

Sleiman R, Kurban M, Succaria F, Abbas O.

J Am Acad Dermatol. 2013 Oct;69(4):625-33. doi: 10.1016/j.jaad.2013.05.022. Epub 2013 Jul 12. Review.

PMID:
23850259
19.

A novel mutation of the KIT gene in a Chinese family with piebaldism.

Wen GD, Zhou C, Yu C, DU J, Xu QX, Liu ZY, Zhang JZ.

Chin Med J (Engl). 2013 Jun;126(12):2325-8.

PMID:
23786947
20.

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