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Items: 1 to 20 of 137

1.

Cutaneous features of Crouzon syndrome with acanthosis nigricans.

Mir A, Wu T, Orlow SJ.

JAMA Dermatol. 2013 Jun;149(6):737-41. doi: 10.1001/jamadermatol.2013.3019. Review.

PMID:
23571469
2.

[Acanthosis nigricans in children and Crouzon syndrome].

Lagaude M, Barreau M, Jokic M, Gerard M, DiRocco F, Hadj-Rabia S, Dompmartin A, Verneuil L.

Ann Dermatol Venereol. 2014 Nov;141(11):685-8. doi: 10.1016/j.annder.2014.06.020. Epub 2014 Aug 7. French.

PMID:
25442473
3.

Crouzon with acanthosis nigricans. Further delineation of the syndrome.

Arnaud-López L, Fragoso R, Mantilla-Capacho J, Barros-Núñez P.

Clin Genet. 2007 Nov;72(5):405-10.

PMID:
17935505
4.

Crouzon syndrome with acanthosis nigricans: a case-based update.

Di Rocco F, Collet C, Legeai-Mallet L, Arnaud E, Le Merrer M, Hadj-Rabia S, Renier D.

Childs Nerv Syst. 2011 Mar;27(3):349-54. doi: 10.1007/s00381-010-1347-z. Epub 2010 Dec 7.

PMID:
21136065
5.

A newborn with acanthosis nigricans: can it be Crouzon syndrome with acanthosis nigricans?

Sharda S, Panigrahi I, Gupta K, Singhi S, Kumar R.

Pediatr Dermatol. 2010 Jan-Feb;27(1):43-7. doi: 10.1111/j.1525-1470.2009.00871.x.

PMID:
20199409
6.

Familial acanthosis nigricans due to K650T FGFR3 mutation.

Berk DR, Spector EB, Bayliss SJ.

Arch Dermatol. 2007 Sep;143(9):1153-6.

PMID:
17875876
7.

An association of acanthosis nigricans and Crouzon syndrome.

Koizumi H, Tomoyori T, Sato KC, Ohkawara A.

J Dermatol. 1992 Feb;19(2):122-6. Review.

PMID:
1377724
8.

Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans.

Meyers GA, Orlow SJ, Munro IR, Przylepa KA, Jabs EW.

Nat Genet. 1995 Dec;11(4):462-4.

PMID:
7493034
9.

Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3.

Schweitzer DN, Graham JM Jr, Lachman RS, Jabs EW, Okajima K, Przylepa KA, Shanske A, Chen K, Neidich JA, Wilcox WR.

Am J Med Genet. 2001 Jan 1;98(1):75-91.

PMID:
11426459
10.

Multiple consequences of a single amino acid pathogenic RTK mutation: the A391E mutation in FGFR3.

Chen F, Sarabipour S, Hristova K.

PLoS One. 2013;8(2):e56521. doi: 10.1371/journal.pone.0056521. Epub 2013 Feb 20.

11.

A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans.

Wilkes D, Rutland P, Pulleyn LJ, Reardon W, Moss C, Ellis JP, Winter RM, Malcolm S.

J Med Genet. 1996 Sep;33(9):744-8.

12.

Crouzonodermoskeletal syndrome.

Jeftha A, Stephen L, Morkel JA, Beighton P.

J Clin Pediatr Dent. 2004 Winter;28(2):173-6.

PMID:
14969379
13.

FGFR3 mutations and the skin: report of a patient with a FGFR3 gene mutation, acanthosis nigricans, hypochondroplasia and hyperinsulinemia and review of the literature.

Blomberg M, Jeppesen EM, Skovby F, Benfeldt E.

Dermatology. 2010;220(4):297-305. doi: 10.1159/000297575. Epub 2010 May 4. Review.

PMID:
20453470
15.

Crouzon disease with acanthosis nigricans and melanocytic nevi.

Gines E, Rodriguez-Pichardo A, Jorquera E, Moreno JC, Camacho F.

Pediatr Dermatol. 1996 Jan-Feb;13(1):18-21. Review.

PMID:
8919518
16.

[Nevoid acanthosis nigricans or RAVEN (rounded and velvety epidermal nevus): three cases].

Petit A, Lemarchand-Venencie F, Pinquier L, Lebbe C, Bourrat E.

Ann Dermatol Venereol. 2012 Mar;139(3):183-8. doi: 10.1016/j.annder.2011.10.411. Epub 2011 Dec 16. French.

PMID:
22401682
17.

Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis.

Gürbüz F, Ceylaner S, Topaloğlu AK, Yüksel B.

J Clin Res Pediatr Endocrinol. 2016 Sep 1;8(3):373-4. doi: 10.4274/jcrpe.3343. Epub 2016 May 16. No abstract available.

18.

Extensive segmental acanthosis nigricans form of epidermal nevus.

de Waal AC, van Rossum MM, Bovenschen HJ.

Dermatol Online J. 2010 Jun 15;16(6):7.

PMID:
20579462
19.

Crouzon syndrome with acanthosis nigricans: case report and mutational analysis.

Nagase T, Nagase M, Hirose S, Ohmori K.

Cleft Palate Craniofac J. 2000 Jan;37(1):78-82.

PMID:
10670894
20.

Acanthosis nigricans and hypochondroplasia in a child with a K650Q mutation in FGFR3.

Berk DR, Boente Mdel C, Montanari D, Toloza MG, Primc NB, Prado MI, Bayliss SJ, Pique LM, Schrijver I.

Pediatr Dermatol. 2010 Nov-Dec;27(6):664-6.

PMID:
21510009

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