98 related articles for article (PubMed ID: 9475589)
1. Favorable prognosis for children with Pfeiffer syndrome types 2 and 3: implications for classification.
Robin NH; Scott JA; Arnold JE; Goldstein JA; Shilling BB; Marion RW; Cohen MM
Am J Med Genet; 1998 Jan; 75(3):240-4. PubMed ID: 9475589
[TBL] [Abstract][Full Text] [Related]
2. Pfeiffer syndrome.
Vogels A; Fryns JP
Orphanet J Rare Dis; 2006 Jun; 1():19. PubMed ID: 16740155
[TBL] [Abstract][Full Text] [Related]
3. Further evidence of association between mutations in FGFR2 and syndromic craniosynostosis with sacrococcygeal eversion.
Oliveira NA; Alonso LG; Fanganiello RD; Passos-Bueno MR
Birth Defects Res A Clin Mol Teratol; 2006 Aug; 76(8):629-33. PubMed ID: 16955501
[TBL] [Abstract][Full Text] [Related]
4. FGFR1 and FGFR2 mutations in Pfeiffer syndrome.
Chokdeemboon C; Mahatumarat C; Rojvachiranonda N; Tongkobpetch S; Suphapeetiporn K; Shotelersuk V
J Craniofac Surg; 2013 Jan; 24(1):150-2. PubMed ID: 23348274
[TBL] [Abstract][Full Text] [Related]
5. Pfeiffer syndrome type 2: further delineation and review of the literature.
Plomp AS; Hamel BC; Cobben JM; Verloes A; Offermans JP; Lajeunie E; Fryns JP; de Die-Smulders CE
Am J Med Genet; 1998 Jan; 75(3):245-51. PubMed ID: 9475590
[TBL] [Abstract][Full Text] [Related]
6. Intestinal malrotation in a patient with Pfeiffer syndrome type 2.
Zarate YA; Putnam PE; Saal HM
Cleft Palate Craniofac J; 2010 Nov; 47(6):638-41. PubMed ID: 20509766
[TBL] [Abstract][Full Text] [Related]
7. [Type V acrocephalosyndactylia (Pfeiffer's syndrome). Apropos of 3 cases in the same family].
Manouvrier-Hanu S; Herbaux B; Pellerin P; Douchet P; Bouchez-Bonniere MC; Dubos JP; Farriaux JP
Arch Fr Pediatr; 1989; 46(6):433-7. PubMed ID: 2783004
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of type 2 Pfeiffer syndrome.
Bernstein PS; Gross SJ; Cohen DJ; Tiller GR; Shanske AL; Bombard AT; Marion RW
Ultrasound Obstet Gynecol; 1996 Dec; 8(6):425-8. PubMed ID: 9014285
[TBL] [Abstract][Full Text] [Related]
9. Prenatal ultrasound diagnosis of a case of Pfeiffer syndrome without cloverleaf skull and review of the literature.
Nazzaro A; Della Monica M; Lonardo F; Di Blasi A; Baffico M; Baldi M; Nazzaro G; De Placido G; Scarano G
Prenat Diagn; 2004 Nov; 24(11):918-22. PubMed ID: 15565658
[TBL] [Abstract][Full Text] [Related]
10. Tracheal anomalies in Pfeiffer syndrome.
Hockstein NG; McDonald-McGinn D; Zackai E; Bartlett S; Huff DS; Jacobs IN
Arch Otolaryngol Head Neck Surg; 2004 Nov; 130(11):1298-302. PubMed ID: 15545585
[TBL] [Abstract][Full Text] [Related]
11. Pfeiffer syndrome: analysis of a clinical series and development of a classification system.
Greig AV; Wagner J; Warren SM; Grayson B; McCarthy JG
J Craniofac Surg; 2013 Jan; 24(1):204-15. PubMed ID: 23348287
[TBL] [Abstract][Full Text] [Related]
12. Pfeiffer Syndrome type 2--case report.
Oyamada MK; Ferreira HS; Hoff M
Sao Paulo Med J; 2003 Jul; 121(4):176-9. PubMed ID: 14595512
[TBL] [Abstract][Full Text] [Related]
13. Pfeiffer syndrome: a clinical review.
Moore MH; Cantrell SB; Trott JA; David DJ
Cleft Palate Craniofac J; 1995 Jan; 32(1):62-70. PubMed ID: 7727489
[TBL] [Abstract][Full Text] [Related]
14. Pfeiffer Syndrome Type 3 and Prune Belly Anomaly in a Female: Case Report and Review.
Peña-Padilla C; Viramontes-Aguilar L; Tavares-Macías G; Bobadilla-Morales L; L Cunningham M; Park S; Zapata-Aldana E; Corona-Rivera JR
Fetal Pediatr Pathol; 2019 Oct; 38(5):412-417. PubMed ID: 31002276
[No Abstract] [Full Text] [Related]
15. [Syndromes 2. Pfeiffer syndrome].
Freihofer HP
Ned Tijdschr Tandheelkd; 1998 Jul; 105(7):245-6. PubMed ID: 11928428
[TBL] [Abstract][Full Text] [Related]
16. Pfeiffer syndrome: clinical and genetic findings in five Brazilian families.
Júnior HM; de Aquino SN; Machado RA; Leão LL; Coletta RD; Burle-Aguiar MJ
Med Oral Patol Oral Cir Bucal; 2015 Jan; 20(1):e52-8. PubMed ID: 25129254
[TBL] [Abstract][Full Text] [Related]
17. Pfeiffer syndrome: systemic and ocular implications.
Harb E; Kran B
Optometry; 2005 Jul; 76(7):352-62. PubMed ID: 16038862
[TBL] [Abstract][Full Text] [Related]
18. Clinical expression in Pfeiffer syndrome type 2 and 3: surveillance in Japan.
Koga H; Suga N; Nakamoto T; Tanaka K; Takahashi N
Am J Med Genet A; 2012 Oct; 158A(10):2506-10. PubMed ID: 22965899
[TBL] [Abstract][Full Text] [Related]
19. Familial arthropathy in Saudi Arabian children: demographic, clinical, and biochemical features.
Al-Mayouf SM
Semin Arthritis Rheum; 2007 Feb; 36(4):256-61. PubMed ID: 16996580
[TBL] [Abstract][Full Text] [Related]
20. Pfeiffer syndrome: an unusual type of acrocephalosyndactyl with broad thumbs and great toes.
Cracco J; Martzolf J; Carpenter GG; Jackson L; O'Hara AE
Neurology; 1970 Apr; 20(4):414. PubMed ID: 5535071
[No Abstract] [Full Text] [Related]
[Next] [New Search]