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Items: 1 to 20 of 221

1.

Hay-wells syndrome of ectodermal dysplasia.

Kulkarni ML, Deshmukh S, Matani D, Gayatri K.

Indian J Pediatr. 2006 Jan;73(1):101. No abstract available.

PMID:
16444073
2.

Hay-Wells syndrome in a child with mutation in the TP73L gene.

Garcia Bartels N, Neumann LM, Mleczko A, Rubach K, Peters H, Rossi R, Sterry W, Blume-Peytavi U.

J Dtsch Dermatol Ges. 2007 Oct;5(10):919-23. English, German.

PMID:
17910675
3.

Aplasia cutis associated with coarctation of the aorta: could this be an incomplete form of Adams-Oliver syndrome?

Heras Mulero C, Bartralot Soler R, Rodríguez-Cano L, Mollet Sánchez J, Palacio Aller L, Aparicio Español G, Bodet Castillo D, Bassas Freixas P, García-Patos V.

Br J Dermatol. 2007 Oct;157(4):836-7. Epub 2007 Aug 17. No abstract available.

PMID:
17711517
4.

Hay-Wells syndrome: a case report.

Rosa DJ, Machado RF, Martins Neto MP, Sá AA, Gamonal A.

An Bras Dermatol. 2010 Mar-Apr;85(2):232-5.

5.

A new syndrome?

Cambiaghi S, Tadini G.

Pediatr Dermatol. 1993 Sep;10(3):298. No abstract available.

PMID:
8415315
6.

[Aplasia cutis congenita, epidermolysis bullosa and ungual dystrophy].

Vázquez López ME, Fernandez Díaz ML, Somoza Rubio C, Morales Redondo R.

An Esp Pediatr. 1998 Sep;49(3):294-6. Review. Spanish. No abstract available.

PMID:
9803555
7.

[Case of anhidrotic ectodermal dysplasia].

Rujner J, Mielczarska K, Wojtanowska H.

Wiad Lek. 1981 Aug 1;34(15):1299-303. Polish. No abstract available.

PMID:
6277087
8.

Hay-Wells syndrome (AEC): a case report.

Macias E, de Carlos F, Cobo J.

Oral Dis. 2006 Sep;12(5):506-8.

PMID:
16910923
9.
10.

Ectodermal dysplasia with hypodontia in a set of Nigerian twins--a case report.

Denloye OO, Dosunmu OO, Aderinokun GA, Onadeko MO.

Afr J Med Med Sci. 1996 Sep;25(3):299-301.

PMID:
10457810
11.

Ectrodactyly, ectodermal dysplasia and clefting (EEC) syndrome.

Glorio R, Haas R, Jaimovich L.

J Eur Acad Dermatol Venereol. 2003 May;17(3):356-8. No abstract available.

PMID:
12702090
12.

Ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC): report of a case with perioral papillomatosis.

Fernandes B, Ruas E, Machado A, Figueiredo A.

Pediatr Dermatol. 2002 Jul-Aug;19(4):330-2.

PMID:
12220279
13.

[Pigmentosum retinis and tubulo-interstitial nephronophtisis in Sensenbrenner syndrome: a case report].

Costet C, Betis F, Bérard E, Tsimaratos M, Sigaudy S, Antignac C, Gastaud P.

J Fr Ophtalmol. 2000 Feb;23(2):158-60. French.

14.

[Epilepsy and psychomotor retardation in a child with aplasia cutis and brachydactyly (Adams-Oliver syndrome)].

Verdú Pérez A, Pantoja Bajo A, Alonso García LA, Garde Morales T.

An Esp Pediatr. 1996 Mar;44(3):289-91. Review. Spanish. No abstract available.

PMID:
8830611
15.

Familial epidermolysis bullosa with aplasia cutis congenita: Bart's syndrome?

Benvenuto C, Kraemer CK, Kruse RL, Cestari TF.

Skinmed. 2003 Sep-Oct;2(5):319-21. No abstract available.

PMID:
14673268
16.

Truncal aplasia cutis congenita associated with ileal atresia and mesenteric defect.

Al-Sawan RM, Soni AL, Al-Kobrosly AM, Shawkat MM, Al-Saleh Q, Al-Sabah HY, Tahmiscija DV.

Pediatr Dermatol. 1999 Sep-Oct;16(5):408-9. No abstract available.

PMID:
10627221
17.

The ectodermal dysplasias. Problems of classification and some newer syndromes.

Solomon LM, Keuer EJ.

Arch Dermatol. 1980 Nov;116(11):1295-9. Review.

PMID:
7002047
18.

Stomatologic aspects of cutaneous diseases. Incontinentia pigmenti.

Gorlin RJ, Sedano HO.

J Dermatol Surg Oncol. 1978 May;4(5):374. No abstract available.

PMID:
641254
19.

Absent meibomian glands: a marker for EEC syndrome.

Bonnar E, Logan P, Eustace P.

Eye (Lond). 1996;10 ( Pt 3):355-61. Review.

PMID:
8796162
20.

[Isochromosome long arm 18].

Rodiere M, Donadio D, Emberger JM, Astruc J, Brunel D.

Ann Pediatr (Paris). 1977 Sep;24(8-9):611-6. French. No abstract available.

PMID:
16211915

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