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Items: 1 to 20 of 104

1.

Ulerythema ophryogenes and Noonan syndrome.

Guidry JA, Rees A, Chan AJ, Shuja F, Hsu S.

Dermatol Online J. 2013 Feb 15;19(2):14.

2.

Ulerythema ophryogenes, a rarely reported cutaneous manifestation of noonan syndrome: case report and review of the literature.

Li K, Ann Thomas M, Haber RM.

J Cutan Med Surg. 2013 May-Jun;17(3):212-8. Review.

PMID:
23673306
3.

Ulerythema ophryogenes: updates and insights.

Morton CM, Bhate C, Janniger CK, Schwartz RA.

Cutis. 2014 Feb;93(2):83-7.

PMID:
24605344
4.

Rubinstein--Taybi syndrome and ulerythema ophryogenes in a 9-year-old boy.

Gómez Centeno P, Rosón E, Peteiro C, Mercedes Pereiro M, Toribio J.

Pediatr Dermatol. 1999 Mar-Apr;16(2):134-6.

PMID:
10337678
5.

[Cutaneous signs of Noonan's syndrome. Apropos of a case with ulerythema ophyogenes, disseminated pilar and sudoral keratosis and progressive alopecia].

Grob JJ, Laure M, Berge G, Taramasco M, Bore P, Benderitter T, Andrac L, Collet AM, Bonerandi JJ.

Ann Dermatol Venereol. 1988;115(3):303-10. French.

PMID:
3408121
6.

Ulerythema ophryogenes in Noonan syndrome.

Snell JA, Mallory SB.

Pediatr Dermatol. 1990 Mar;7(1):77-8. No abstract available.

PMID:
2343011
7.
8.

Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome.

Liakou AI, Esteves de Carvalho AV, Nazarenko LP.

J Dermatol. 2014 May;41(5):371-6. doi: 10.1111/1346-8138.12442. Review.

PMID:
24801913
9.

Do you know this syndrome? Noonan syndrome.

Kondo RN, Martins LM, Lopes VC, Bittar RA, Araújo FM.

An Bras Dermatol. 2013 Jul-Aug;88(4):664-6. doi: 10.1590/abd1806-4841.20131934.

10.

Noonan syndrome: a case with recurrent keloid formation.

Güleç AT, Karaduman A, Seçkin D.

Cutis. 2001 Apr;67(4):315-6.

PMID:
11324394
11.

Keratosis pilaris and ulerythema ophryogenes in a woman with monosomy of the short arm of chromosome 18.

Carvalho CA, Carvalho AV, Kiss A, Paskulin G, Götze FM.

An Bras Dermatol. 2011 Jul-Aug;86(4 Suppl 1):S42-5. English, Portuguese.

13.

Neurofibromatosis with fully expressed Noonan syndrome.

Abuelo DN, Meryash DL.

Am J Med Genet. 1988 Apr;29(4):937-41.

PMID:
3135755
14.

Germline PTPN11 missense mutation in a case of Noonan syndrome associated with mediastinal and retroperitoneal neuroblastic tumors.

Mutesa L, Pierquin G, Janin N, Segers K, Thomée C, Provenzi M, Bours V.

Cancer Genet Cytogenet. 2008 Apr 1;182(1):40-2. doi: 10.1016/j.cancergencyto.2007.12.005.

PMID:
18328949
15.

Neurofibromatosis-Noonan syndrome or LEOPARD Syndrome? A clinical dilemma.

Tullu MS, Muranjan MN, Kantharia VC, Parmar RC, Sahu DR, Bavdekar SB, Bharucha BA.

J Postgrad Med. 2000 Apr-Jun;46(2):98-100.

16.

Ulerythema ophryogenes and keratosis pilaris in a child with monosomy 18p.

Zouboulis CC, Stratakis CA, Rinck G, Wegner RD, Gollnick H, Orfanos CE.

Pediatr Dermatol. 1994 Jun;11(2):172-5.

PMID:
8041661
17.

Bleeding diathesis in Noonan syndrome: a common association.

Witt DR, McGillivray BC, Allanson JE, Hughes HE, Hathaway WE, Zipursky A, Hall JG.

Am J Med Genet. 1988 Oct;31(2):305-17.

PMID:
3232698
18.

[CFC syndrome in mother and daughter: a syndrome distinct from Noonan syndrome].

Blanchet-Bardon C, Puppin D Jr, Fischer R, Dubertret L.

Ann Dermatol Venereol. 1991;118(11):778-80. French. No abstract available.

PMID:
1789629
19.

[Ulerythema ophryogenes and folliculitis ulerythematosa reticulata].

Azambuja R, Proença NG, Cardoso WV.

Hautarzt. 1987 Jul;38(7):411-3. German.

PMID:
3654209
20.

[Management of keratosis pilaris].

Gassia V, Restoueix C, Bonafé JL.

Ann Dermatol Venereol. 1991;118(1):69-75. French. No abstract available.

PMID:
2018310
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