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Items: 1 to 20 of 173

1.

Upregulation of Melanogenesis and Tyrosinase Activity: Potential Agents for Vitiligo.

Niu C, Aisa HA.

Molecules. 2017 Aug 4;22(8). pii: E1303. doi: 10.3390/molecules22081303. Review.

2.

Whipple Disease.

Antunes C, Gossman W.

StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2017 Jun-.
2017 Jun 25.

3.

Pityriasis, Alba.

Givler D, Givler A.

StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2017 Jun-.
2017 May 14.

4.

McCune-Albright Syndrome.

Dean L.

In: Pratt V, McLeod H, Dean L, Malheiro A, Rubinstein W, editors. Medical Genetics Summaries [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2012-.
2012 Mar 8 [updated 2017 Mar 6].

5.

From chronic immune thrombocytopenia to severe aplastic anemia: recent insights into the evolution of eltrombopag.

Gill H, Wong RSM, Kwong YL.

Ther Adv Hematol. 2017 May;8(5):159-174. doi: 10.1177/2040620717693573. Epub 2017 Feb 1. Review.

6.

Waardenburg Syndrome Type I.

Milunsky JM.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2001 Jul 30 [updated 2017 May 4].

7.

Peutz-Jeghers syndrome with intermittent upper intestinal obstruction: A case report and review of the literature.

Duan SX, Wang GH, Zhong J, Ou WH, Fu MX, Wang FS, Ma SH, Li JH.

Medicine (Baltimore). 2017 Apr;96(17):e6538. doi: 10.1097/MD.0000000000006538. Review.

8.

[Piebaldism: a pigmentary anomaly to recognize: about a case and review of the literature].

El Kouarty H, Dakhama BS.

Pan Afr Med J. 2016 Nov 14;25:155. doi: 10.11604/pamj.2016.25.155.10499. eCollection 2016. Review. French.

9.

Fanconi Anemia.

Mehta PA, Tolar J.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2002 Feb 14 [updated 2017 Feb 23].

10.

Infantile tremor syndrome: A review and critical appraisal of its etiology.

Goraya JS, Kaur S.

J Pediatr Neurosci. 2016 Oct-Dec;11(4):298-304. doi: 10.4103/1817-1745.199475. Review.

11.

Association of protein tyrosine phosphatase, non-receptor type 22 +1858C→T polymorphism and susceptibility to vitiligo: Systematic review and meta-analysis.

Agarwal S, Changotra H.

Indian J Dermatol Venereol Leprol. 2017 Mar-Apr;83(2):183-189. doi: 10.4103/0378-6323.199422. Review.

12.

RNA Editing, ADAR1, and the Innate Immune Response.

Wang Q, Li X, Qi R, Billiar T.

Genes (Basel). 2017 Jan 18;8(1). pii: E41. doi: 10.3390/genes8010041. Review.

13.

Prospect of Human Pluripotent Stem Cell-Derived Neural Crest Stem Cells in Clinical Application.

Zhu Q, Lu Q, Gao R, Cao T.

Stem Cells Int. 2016;2016:7695836. doi: 10.1155/2016/7695836. Epub 2016 Dec 20. Review.

14.

Trends in Regenerative Medicine: Repigmentation in Vitiligo Through Melanocyte Stem Cell Mobilization.

Birlea SA, Costin GE, Roop DR, Norris DA.

Med Res Rev. 2017 Jul;37(4):907-935. doi: 10.1002/med.21426. Epub 2016 Dec 28. Review.

15.

Dysfunction of Autophagy: A Possible Mechanism Involved in the Pathogenesis of Vitiligo by Breaking the Redox Balance of Melanocytes.

Qiao Z, Wang X, Xiang L, Zhang C.

Oxid Med Cell Longev. 2016;2016:3401570. doi: 10.1155/2016/3401570. Epub 2016 Nov 29. Review.

16.

Coexistence of erythema dyschromicum perstans and vitiligo: a case report and review of the literature.

Tamer F.

Acta Dermatovenerol Alp Pannonica Adriat. 2016 Dec;25(4):77-78. Review.

18.

Molecular screening strategies for NF1-like syndromes with café-au-lait macules (Review).

Zhang J, Li M, Yao Z.

Mol Med Rep. 2016 Nov;14(5):4023-4029. doi: 10.3892/mmr.2016.5760. Epub 2016 Sep 22. Review.

19.

Epidemiological Assessments of Skin Outcomes in the Nurses' Health Studies.

Li WQ, Cho E, Weinstock MA, Mashfiq H, Qureshi AA.

Am J Public Health. 2016 Sep;106(9):1677-83. doi: 10.2105/AJPH.2016.303315. Epub 2016 Jul 26. Review.

20.

Peutz-Jeghers Syndrome.

McGarrity TJ, Amos CI, Baker MJ.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2001 Feb 23 [updated 2016 Jul 14].

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