Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 47

1.

Schöpf-Schulz-Passarge syndrome: further delineation of the phenotype and genetic considerations.

Castori M, Ruggieri S, Giannetti L, Annessi G, Zambruno G.

Acta Derm Venereol. 2008;88(6):607-12. doi: 10.2340/00015555-0547. Review.

2.

[Multiple eccrine hydrocystomas of the eyelids in the framework of Schöpf syndrome. A case report].

Dot C, Dordain M, Boucher E, Metge F, Millet P, Maille M, Maurin J.

J Fr Ophtalmol. 2000 Oct;23(8):809-16. Review. French.

3.

Multiple apocrine hidrocystomas of the eyelids.

Alessi E, Gianotti R, Coggi A.

Br J Dermatol. 1997 Oct;137(4):642-5. Review.

PMID:
9390347
5.

Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas.

Stevens HP, Kelsell DP, Bryant SP, Bishop DT, Spurr NK, Weissenbach J, Marger D, Marger RS, Leigh IM.

Arch Dermatol. 1996 Jun;132(6):640-51. Review.

PMID:
8651714
6.

GAPO syndrome: a report of two siblings and a review of literature.

Nanda A, Al-Ateeqi WA, Al-Khawari MA, Alsaleh QA, Anim JT.

Pediatr Dermatol. 2010 Mar-Apr;27(2):156-61. doi: 10.1111/j.1525-1470.2010.01100.x. Review.

PMID:
20537066
7.

[Syndromes 17. Hypohidrotic ectodermal dysplasia].

Baart JA, van Hagen JM.

Ned Tijdschr Tandheelkd. 2000 Jan;107(1):12-4. Review. Dutch.

PMID:
12621820
8.

Finlay-Marks syndrome: report of two siblings and review of literature.

Naik P, Kini P, Chopra D, Gupta Y.

Am J Med Genet A. 2012 Jul;158A(7):1696-701. doi: 10.1002/ajmg.a.35389. Epub 2012 May 25. Review.

PMID:
22639454
9.

[Ectodermal dysplasia syndrome].

Mortier K, Wackens G.

Ned Tijdschr Tandheelkd. 2003 May;110(5):190-2. Review. Dutch.

PMID:
12784514
10.

[Pachyonychia congenita. Keratin gene mutations with pleiotropic effect].

Swensson O.

Hautarzt. 1999 Jul;50(7):483-90. Review. German.

PMID:
10464680
11.

Congenital atrichia, palmoplantar hyperkeratosis, mental retardation, and early loss of teeth in four siblings: a new syndrome?

Steijlen PM, Neumann HA, der Kinderen DJ, Smeets DF, van der Kerkhof PC, Happle R.

J Am Acad Dermatol. 1994 May;30(5 Pt 2):893-8. Review.

PMID:
8169270
12.

Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome).

Steiner CE, Cintra ML, Marques-de-Faria AP.

Am J Med Genet. 2002 Dec 15;113(4):381-4. Review.

PMID:
12457412
13.
14.

Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) in siblings.

Senecky Y, Halpern GJ, Inbar D, Attias J, Shohat M.

Am J Med Genet. 2001 Jul 1;101(3):195-7. Review.

PMID:
11424132
15.

Heterogeneity in genetic disorders that affect the orofacies.

Shapiro SD, Jorgenson RJ.

Birth Defects Orig Artic Ser. 1983;19(1):155-66. Review.

PMID:
6419792
16.

Yunis-Varon syndrome: further delineation of the phenotype.

Basel-Vanagaite L, Kornreich L, Schiller O, Yacobovich J, Merlob P.

Am J Med Genet A. 2008 Feb 15;146A(4):532-7. doi: 10.1002/ajmg.a.32135. Review.

PMID:
18203163
17.

Papillon-Lefèvre syndrome and malignant melanoma. A high incidence of melanoma development in Japanese palmoplantar keratoderma patients.

Nakajima K, Nakano H, Takiyoshi N, Rokunohe A, Ikenaga S, Aizu T, Kaneko T, Mitsuhashi Y, Sawamura D.

Dermatology. 2008;217(1):58-62. doi: 10.1159/000124340. Epub 2008 Apr 9. Review.

PMID:
18401176
18.

Palmoplantar keratoderma with sclerodactyly (Huriez syndrome).

Patrizi A, Di Lernia V, Patrone P.

J Am Acad Dermatol. 1992 May;26(5 Pt 2):855-7. Review.

PMID:
1613149
19.

Towards characterization of palmoplantar keratoderma caused by gain-of-function mutation in loricrin: analysis of a family and review of the literature.

Gedicke MM, Traupe H, Fischer B, Tinschert S, Hennies HC.

Br J Dermatol. 2006 Jan;154(1):167-71. Review.

PMID:
16403113
20.

Connexin disorders of the skin.

Richard G.

Adv Dermatol. 2001;17:243-77. Review. No abstract available.

PMID:
11758118

Supplemental Content

Support Center