Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 10

1.

Ambras Syndrome with Gingival Hyperplasia: A Rare Entity.

Reddy Kundoor VK, Maloth KN, Kesidi S, Moni T.

Int J Trichology. 2016 Apr-Jun;8(2):81-3. doi: 10.4103/0974-7753.188036.

2.

Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes.

Pavone P, Pratic├▓ AD, Falsaperla R, Ruggieri M, Zollino M, Corsello G, Neri G.

Ital J Pediatr. 2015 Aug 5;41:55. doi: 10.1186/s13052-015-0161-3. Review.

3.

Congenital Generalized Hypertrichosis, Gingival Hyperplasia, a Coarse Facies with Constriction Bands: A Rare Association.

Bubna AK, Veeraraghavan M, Anandan S, Rangarajan S.

Int J Trichology. 2015 Apr-Jun;7(2):67-71. doi: 10.4103/0974-7753.160113.

4.

Hormonal profile and androgen receptor study in prepubertal girls with hypertrichosis.

Hernandez MI, Castro A, Bacallao K, Avila A, Espinoza A, Trejo L, I├▒iguez G, Codner E, Cassorla F.

Int J Pediatr Endocrinol. 2014;2014(1):6. doi: 10.1186/1687-9856-2014-6. Epub 2014 Apr 18.

5.

Trps1 and its target gene Sox9 regulate epithelial proliferation in the developing hair follicle and are associated with hypertrichosis.

Fantauzzo KA, Kurban M, Levy B, Christiano AM.

PLoS Genet. 2012;8(11):e1003002. doi: 10.1371/journal.pgen.1003002. Epub 2012 Nov 1.

6.

Sequence and structure based assessment of nonsynonymous SNPs in hypertrichosis universalis.

Waheed R, Khan MH, Bano R, Rashid H.

Bioinformation. 2012;8(7):316-8. doi: 10.6026/97320630008316. Epub 2012 Apr 13.

7.

Copy number variations on chromosome 4q26-27 are associated with Cantu syndrome.

Kurban M, Kim CA, Kiuru M, Fantauzzo K, Cabral R, Abbas O, Levy B, Christiano AM.

Dermatology. 2011;223(4):316-20. doi: 10.1159/000333800. Epub 2012 Feb 3.

8.

Epidermal patterning and induction of different hair types during mouse embryonic development.

Duverger O, Morasso MI.

Birth Defects Res C Embryo Today. 2009 Sep;87(3):263-72. doi: 10.1002/bdrc.20158. Review.

9.

A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice.

Fantauzzo KA, Tadin-Strapps M, You Y, Mentzer SE, Baumeister FA, Cianfarani S, Van Maldergem L, Warburton D, Sundberg JP, Christiano AM.

Hum Mol Genet. 2008 Nov 15;17(22):3539-51. doi: 10.1093/hmg/ddn247. Epub 2008 Aug 19.

10.

Childhood hypertrichosis: diagnosis and management.

Baumeister FA, Schwarz HP, Stengel-Rutkowski S.

Arch Dis Child. 1995 May;72(5):457-9. Review. No abstract available.

Supplemental Content

Support Center