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Items: 1 to 20 of 349

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.

Schöpf-Schulz-Passarge syndrome with an unusual pattern of inheritance.

Craigen WJ, Levy ML, Lewis RA.

Am J Med Genet. 1997 Aug 8;71(2):186-8.

PMID:
9217219
3.

A case of Schöpf-Schulz-Passarge syndrome.

Hampton PJ, Angus B, Carmichael AJ.

Clin Exp Dermatol. 2005 Sep;30(5):528-30.

PMID:
16045686
4.

[Schopf-Schulz-Passarge syndrome: 2 cases].

Gkolfinopoulos T, Ingen-Housz-Oro S, Cavelier-Balloy B, Blanchet-Bardon C.

Ann Dermatol Venereol. 2001 Dec;128(12):1330-3. French.

PMID:
11908136
5.

The Schöpf-Schulz-Passarge syndrome.

Verplancke P, Driessen L, Wynants P, Naeyaert JM.

Dermatology. 1998;196(4):463-6.

PMID:
9669133
6.

[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.

7.

JAAD Grand Rounds quiz. Palmoplantar keratoderma, hypodontia, hypotrichosis, nail dystrophy, and multiple eyelid cysts.

DiGiorgio CM, Bohlke AK, Oswald BJ, Wang AR, Boh EE.

J Am Acad Dermatol. 2011 Nov;65(5):1066-9. doi: 10.1016/j.jaad.2010.09.771. No abstract available.

PMID:
22000878
8.

Syndrome of cystic eyelids, palmo-plantar keratosis, hypodontia and hypotrichosis as a possible autosomal recessive trait.

Schöpf E, Schulz HJ, Passarge E.

Birth Defects Orig Artic Ser. 1971 Jun;7(8):219-21.

PMID:
4281327
9.

Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.

Tziotzios C, Petrof G, Liu L, Verma A, Wedgeworth EK, Mellerio JE, McGrath JA.

Br J Dermatol. 2014 Nov;171(5):1211-4. doi: 10.1111/bjd.13158. Epub 2014 Oct 15.

PMID:
24902757
10.

[Schöpf syndrome. Clinical, genetic and lipid biochemical studies].

Küster W, Hammerstein W.

Hautarzt. 1992 Dec;43(12):763-6. German.

PMID:
1473970
11.

Genetic study in a suspected case of Schöpf-Schulz-Passarge syndrome.

Vilas-Sueiro A, Monteagudo B, González-Vilas D, Varela-Veiga A, De las Heras C.

Indian J Dermatol Venereol Leprol. 2015 Jul-Aug;81(4):408-10. doi: 10.4103/0378-6323.158657. No abstract available.

12.

Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A.

Petrof G, Fong K, Lai-Cheong JE, Cockayne SE, McGrath JA.

Australas J Dermatol. 2011 Aug;52(3):224-6. doi: 10.1111/j.1440-0960.2011.00788.x. Epub 2011 Jun 29.

PMID:
21834823
13.

Schöpf-Schulz-Passarge syndrome with pili torti: A new association?

SZEPETIUK G, VANHOOTEGHEM O, MULLER G, STENE JJ, NIKKELS AF.

Eur J Dermatol. 2009 Sep-Oct;19(5):517-8. doi: 10.1684/ejd.2009.0743. Epub 2009 Jun 15. No abstract available.

PMID:
19527991
14.

Multiple apocrine hidrocystomas of the eyelids.

Alessi E, Gianotti R, Coggi A.

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

PMID:
9390347
15.
16.

Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A.

Nagy N, Wedgeworth E, Hamada T, White JM, Hashimoto T, McGrath JA.

J Dermatol Sci. 2010 Jun;58(3):220-2. doi: 10.1016/j.jdermsci.2010.03.012. Epub 2010 Mar 23. No abstract available.

PMID:
20418069
17.

Late diagnosis of ectodermal dysplasia syndrome.

Granger RH, Marshman G, Liu L, McGrath JA.

Australas J Dermatol. 2013 Feb;54(1):46-8. doi: 10.1111/j.1440-0960.2012.00895.x. Epub 2012 Jun 4.

PMID:
22670871
18.

Variability in dentofacial phenotypes in four families with WNT10A mutations.

Vink CP, Ockeloen CW, ten Kate S, Koolen DA, Ploos van Amstel JK, Kuijpers-Jagtman AM, van Heumen CC, Kleefstra T, Carels CE.

Eur J Hum Genet. 2014 Sep;22(9):1063-70. doi: 10.1038/ejhg.2013.300. Epub 2014 Jan 8.

20.

Schöpf-Schulz-Passarge syndrome.

Monk BE, Pieris S, Soni V.

Br J Dermatol. 1992 Jul;127(1):33-5.

PMID:
1637691

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