243 related articles for article (PubMed ID: 26914936)
1. Ultrasound and MR imaging findings in prenatal diagnosis of craniosynostosis syndromes.
Rubio EI; Blask A; Bulas DI
Pediatr Radiol; 2016 May; 46(5):709-18. PubMed ID: 26914936
[TBL] [Abstract][Full Text] [Related]
2. Perinatal imaging findings of a fetus with Pfeiffer syndrome and a heterozygous c.1019A>G, p.Tyr340Cys (Y340C) mutation in FGFR2 presenting a cloverleaf skull, craniosynostosis and short limbs on prenatal ultrasound mimicking thanatophoric dysplasia type II.
Chen CP; Huang JP; Huang KS; Chen YY; Wu FT; Pan YT; Chiu CL; Wang W
Taiwan J Obstet Gynecol; 2024 May; 63(3):387-390. PubMed ID: 38802203
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of Apert syndrome using ultrasound, magnetic resonance imaging, and three-dimensional virtual/physical models: three case series and literature review.
Werner H; Castro P; Daltro P; Lopes J; Ribeiro G; Araujo Júnior E
Childs Nerv Syst; 2018 Aug; 34(8):1563-1571. PubMed ID: 29441430
[TBL] [Abstract][Full Text] [Related]
4. Ultrasound diagnosis of craniosynostosis.
Miller C; Losken HW; Towbin R; Bowen A; Mooney MP; Towbin A; Faix RS
Cleft Palate Craniofac J; 2002 Jan; 39(1):73-80. PubMed ID: 11772173
[TBL] [Abstract][Full Text] [Related]
5. Progressive development of sonographic features in prenatal diagnosis of Apert syndrome--case report and literature review.
Respondek-Liberska M; Smigiel R; Zielinski A; Sasiadek MM
Ginekol Pol; 2010 Dec; 81(12):935-9. PubMed ID: 21391441
[TBL] [Abstract][Full Text] [Related]
6. Prenatal sonographic findings and prognosis of craniosynostosis diagnosed during the fetal and neonatal periods.
Harada A; Miyashita S; Nagai R; Makino S; Murotsuki J
Congenit Anom (Kyoto); 2019 Jul; 59(4):132-141. PubMed ID: 30132994
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of craniosynostosis: value of MR imaging.
Fjørtoft MI; Sevely A; Boetto S; Kessler S; Sarramon MF; Rolland M
Neuroradiology; 2007 Jun; 49(6):515-21. PubMed ID: 17310357
[TBL] [Abstract][Full Text] [Related]
8. Diagnostic accuracy of ultrasonography and magnetic resonance imaging for the detection of fetal anomalies: a blinded case-control study.
Gonçalves LF; Lee W; Mody S; Shetty A; Sangi-Haghpeykar H; Romero R
Ultrasound Obstet Gynecol; 2016 Aug; 48(2):185-92. PubMed ID: 26444861
[TBL] [Abstract][Full Text] [Related]
9. Severe nasomaxillary hypoplasia (Binder phenotype) on prenatal US/MRI: an important marker for the prenatal diagnosis of chondrodysplasia punctata.
Blask AR; Rubio EI; Chapman KA; Lawrence AK; Bulas DI
Pediatr Radiol; 2018 Jul; 48(7):979-991. PubMed ID: 29572747
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of Apert syndrome: report of two cases.
Skidmore DL; Pai AP; Toi A; Steele L; Chitayat D
Prenat Diagn; 2003 Dec; 23(12):1009-13. PubMed ID: 14663839
[TBL] [Abstract][Full Text] [Related]
11. Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following suspicious ultrasound findings.
Ferreira JC; Carter SM; Bernstein PS; Jabs EW; Glickstein JS; Marion RW; Baergen RN; Gross SJ
Ultrasound Obstet Gynecol; 1999 Dec; 14(6):426-30. PubMed ID: 10658283
[TBL] [Abstract][Full Text] [Related]
12. Differential diagnosis of syndromic craniosynostosis: a case series.
Casteleyn T; Horn D; Henrich W; Verlohren S
Arch Gynecol Obstet; 2022 Jul; 306(1):49-57. PubMed ID: 34633507
[TBL] [Abstract][Full Text] [Related]
13. Prenatal ultrasound diagnosis of fetal craniosynostosis.
Delahaye S; Bernard JP; Rénier D; Ville Y
Ultrasound Obstet Gynecol; 2003 Apr; 21(4):347-53. PubMed ID: 12704742
[TBL] [Abstract][Full Text] [Related]
14. Isolated craniosynostosis: prenatal ultrasound of scaphocephaly with polyhydramnios.
Huang HW; Lin H; Chang SY; Hsu YH; Hsu TY
Chang Gung Med J; 2001 Dec; 24(12):816-9. PubMed ID: 11858399
[TBL] [Abstract][Full Text] [Related]
15. Diagnosis of Apert syndrome in the second-trimester using 2D and 3D ultrasound.
David AL; Turnbull C; Scott R; Freeman J; Bilardo CM; van Maarle M; Chitty LS
Prenat Diagn; 2007 Jul; 27(7):629-32. PubMed ID: 17497749
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Prenatal magnetic resonance and ultrasonographic findings in small-bowel obstruction: imaging clues and postnatal outcomes.
Rubio EI; Blask AR; Badillo AT; Bulas DI
Pediatr Radiol; 2017 Apr; 47(4):411-421. PubMed ID: 28116474
[TBL] [Abstract][Full Text] [Related]
18. Twin pregnancies in the second trimester in women in an alpha-fetoprotein screening program: sonographic evaluation and outcome.
Pretorius DH; Budorick NE; Scioscia AL; Krabbe JK; Ko S; Myhre CM
AJR Am J Roentgenol; 1993 Nov; 161(5):1007-13. PubMed ID: 7506005
[TBL] [Abstract][Full Text] [Related]
19. Craniosynostosis: prenatal diagnosis by 2D/3D ultrasound, magnetic resonance imaging and computed tomography.
Helfer TM; Peixoto AB; Tonni G; Araujo Júnior E
Med Ultrason; 2016 Sep; 18(3):378-85. PubMed ID: 27622416
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of Pfeiffer syndrome and role of three-dimensional ultrasound: case report and review of literature.
Vimercati A; Olivieri C; Dellino M; Gentile M; Tinelli R; Cicinelli E
J Matern Fetal Neonatal Med; 2022 Dec; 35(25):7840-7843. PubMed ID: 34182859
[No Abstract] [Full Text] [Related]
[Next] [New Search]