214 related articles for article (PubMed ID: 11927079)
1. [Crouzon's syndrome with acanthosis nigricans].
Lapunzina P; Fernández MC; Varela Junquera JM; Arberas C; Tello AM; Gracia Bouthelier R
An Esp Pediatr; 2002 Apr; 56(4):342-6. PubMed ID: 11927079
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 17935505
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 7493034
[TBL] [Abstract][Full Text] [Related]
4. Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3.
Schweitzer DN; Graham JM; Lachman RS; Jabs EW; Okajima K; Przylepa KA; Shanske A; Chen K; Neidich JA; Wilcox WR
Am J Med Genet; 2001 Jan; 98(1):75-91. PubMed ID: 11426459
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 8880573
[TBL] [Abstract][Full Text] [Related]
6. The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans.
Vajo Z; Francomano CA; Wilkin DJ
Endocr Rev; 2000 Feb; 21(1):23-39. PubMed ID: 10696568
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 10670894
[TBL] [Abstract][Full Text] [Related]
8. An unusual association of acanthosis nigricans and Crouzon's disease--a case report.
Reddy BS; Garg BR; Padiyar NV; Krishnaram AS
J Dermatol; 1985 Feb; 12(1):85-90. PubMed ID: 3894462
[No Abstract] [Full Text] [Related]
9. 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; 27(1):43-7. PubMed ID: 20199409
[TBL] [Abstract][Full Text] [Related]
10. Crouzon's syndrome associated with acanthosis nigricans: ramifications for the craniofacial surgeon.
Breitbart AS; Eaton C; McCarthy JG
Ann Plast Surg; 1989 Apr; 22(4):310-5. PubMed ID: 2650599
[TBL] [Abstract][Full Text] [Related]
11. Crouzon with Acanthosis Nigricans and Odontogenic Tumors: A Rare Form of Syndromic Craniosynostosis.
Xu W; McDonald-McGinn DM; Melchiorre AJ; Zackai EH; Bartlett SP; Taylor JA
Cleft Palate Craniofac J; 2018 Feb; 55(2):296-300. PubMed ID: 29351036
[TBL] [Abstract][Full Text] [Related]
12. [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. PubMed ID: 25442473
[TBL] [Abstract][Full Text] [Related]
13. Crouzon's disease correlates with low fibroblastic growth factor receptor activity in stenosed cranial sutures.
Bresnick S; Schendel S
J Craniofac Surg; 1995 May; 6(3):245-8. PubMed ID: 9020696
[TBL] [Abstract][Full Text] [Related]
14. An association of acanthosis nigricans and Crouzon syndrome.
Koizumi H; Tomoyori T; Sato KC; Ohkawara A
J Dermatol; 1992 Feb; 19(2):122-6. PubMed ID: 1377724
[TBL] [Abstract][Full Text] [Related]
15. Acanthosis nigricans in a boy with achondroplasia due to the classical Gly380Arg mutation in FGFR3.
Van Esch H; Fryns JE
Genet Couns; 2004; 15(3):375-7. PubMed ID: 15517832
[No Abstract] [Full Text] [Related]
16. [On the effect of mutations of the fibroblast growth factor receptors as exemplified by three cases of craniosynostoses].
Preising MN; Schindler S; Friedrich M; Wagener H; Golan I; Lorenz B
Klin Monbl Augenheilkd; 2003 Oct; 220(10):669-81. PubMed ID: 14577033
[TBL] [Abstract][Full Text] [Related]
17. A rare association of acanthosis nigricans with Crouzon syndrome.
Gupta AK; Koley S; Choudhary S; Bhake A; Saoji V; Salodkar A
Indian J Dermatol Venereol Leprol; 2010; 76(1):65-7. PubMed ID: 20061739
[No Abstract] [Full Text] [Related]
18. Clinical signs, interventions, and treatment course of three different treatment protocols in patients with Crouzon syndrome with acanthosis nigricans.
de Planque CA; Wall SA; Dalton L; Paternoster G; Arnaud É; van Veelen MC; Versnel SL; Johnson D; Jayamohan J; Mathijssen IMJ
J Neurosurg Pediatr; 2021 Aug; 28(4):425-431. PubMed ID: 34388723
[TBL] [Abstract][Full Text] [Related]
19. [ENT changes in Crouzon's syndrome].
Campos Del Alamo MA; Pérez Obón J; Gil Paraíso P; Marín García J; Damborenea Tajada J; Llorente Arenas E; Alfaro García J; Martínez-Berganza y Asensio R; Asensio
An Otorrinolaringol Ibero Am; 1999; 26(2):117-23. PubMed ID: 10230084
[TBL] [Abstract][Full Text] [Related]
20. Clinical features of Crouzon's syndrome patients with and without a positive family history of Crouzon's syndrome.
al-Qattan MM; Phillips JH
J Craniofac Surg; 1997 Jan; 8(1):11-3. PubMed ID: 10332291
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
