246 related articles for article (PubMed ID: 12124689)
1. Prenatal diagnosis of Pierre-Robin sequence as part of Stickler syndrome.
Soulier M; Sigaudy S; Chau C; Philip N
Prenat Diagn; 2002 Jul; 22(7):567-8. PubMed ID: 12124689
[TBL] [Abstract][Full Text] [Related]
2. The prenatal diagnosis of Pierre-Robin sequence.
Hsieh YY; Chang CC; Tsai HD; Yang TC; Lee CC; Tsai CH
Prenat Diagn; 1999 Jun; 19(6):567-9. PubMed ID: 10416975
[TBL] [Abstract][Full Text] [Related]
3. Stickler syndrome in Pierre-Robin sequence prenatal ultrasonographic diagnosis and postnatal therapy: two cases report.
Pacella E; Malvasi A; Tinelli A; Laterza F; Dell'Edera D; Pacella F; Mazzeo F; Ferraresi A; Malarska KG; Cavallotti C
Eur Rev Med Pharmacol Sci; 2010 Dec; 14(12):1051-4. PubMed ID: 21375138
[TBL] [Abstract][Full Text] [Related]
4. Stickler syndrome: report of four cases.
Kulkarni ML; Sureshkumar C; George VG
Ann Dent; 1993; 52(2):23-7. PubMed ID: 8267375
[No Abstract] [Full Text] [Related]
5. The Stickler syndrome (hereditary arthro-ophthalmopathy).
Say B; Berry J; Barber N
Clin Genet; 1977 Sep; 12(3):179-82. PubMed ID: 409578
[TBL] [Abstract][Full Text] [Related]
6. Prenatal Identification of Pierre Robin Sequence: A Review of the Literature and Look towards the Future.
Kaufman MG; Cassady CI; Hyman CH; Lee W; Watcha MF; Hippard HK; Olutoye OA; Khechoyan DY; Monson LA; Buchanan EP
Fetal Diagn Ther; 2016; 39(2):81-9. PubMed ID: 25967128
[TBL] [Abstract][Full Text] [Related]
7. Fetal manifestation of the Fine-Lubinsky syndrome. Brachycephaly, deafness, cataract, microstomia and mental retardation syndrome complicated by Pierre-Robin anomaly and polyhydramnios.
Schoner K; Bald R; Fritz B; Rehder H
Fetal Diagn Ther; 2008; 23(3):228-32. PubMed ID: 18417983
[TBL] [Abstract][Full Text] [Related]
8. Marshall syndrome.
Stratton RF; Lee B; Ramirez F
Am J Med Genet; 1991 Oct; 41(1):35-8. PubMed ID: 1951461
[TBL] [Abstract][Full Text] [Related]
9. Feeding Difficulty in an Infant with Stickler's Syndrome.
Vijay P; Kumaran P; Xavier AM; Varma RB; Kumar JS
Contemp Clin Dent; 2019; 10(3):558-560. PubMed ID: 32308337
[TBL] [Abstract][Full Text] [Related]
10. Importance of early diagnosis of Stickler syndrome in newborns.
Antunes RB; Alonso N; Paula RG
J Plast Reconstr Aesthet Surg; 2012 Aug; 65(8):1029-34. PubMed ID: 22424767
[TBL] [Abstract][Full Text] [Related]
11. [Stickler's syndrome--an underdiagnosed condition?].
Klingenberg C; Fossen K; Tranebjaerg L
Tidsskr Nor Laegeforen; 2001 Nov; 121(27):3172-5. PubMed ID: 11876139
[TBL] [Abstract][Full Text] [Related]
12. Prenatal Diagnosis of Pierre Robin Sequence and Its Prognosis: A Retrospective Cohort Study.
Zhong C; Xie Z; Dong H; Chen T; Zhang X; Ran S
Am J Perinatol; 2024 May; 41(S 01):e1639-e1646. PubMed ID: 37068514
[TBL] [Abstract][Full Text] [Related]
13. Peripartum Management of Neonatal Pierre Robin Sequence.
Insalaco LF; Scott AR
Clin Perinatol; 2018 Dec; 45(4):717-735. PubMed ID: 30396414
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of Treacher Collins syndrome: A case report and literature review.
Wang Y; Wang Y; Yao M; Chen L; Wu S; Liu Y
Int J Gynaecol Obstet; 2023 Dec; 163(3):778-781. PubMed ID: 37231986
[TBL] [Abstract][Full Text] [Related]
15. Fast and early mandibular osteodistraction (FEMOD) in severe Pierre Robin Sequence.
Cascone P; Papoff P; Arangio P; Vellone V; Calafati V; Silvestri A
J Craniomaxillofac Surg; 2014 Oct; 42(7):1364-70. PubMed ID: 24787079
[TBL] [Abstract][Full Text] [Related]
16. [Genetic studies in Pierre Robin syndrome].
Jörgensen G; Freund HJ
ZWR; 1979 Nov; 88(21):958-60. PubMed ID: 294009
[No Abstract] [Full Text] [Related]
17. Visual complications of Stickler syndrome in paediatric patients with Robin sequence.
Huang F; Kuo HK; Hsieh CH; Lai JP; Chen PK
J Craniomaxillofac Surg; 2007 Mar; 35(2):76-80. PubMed ID: 17442580
[TBL] [Abstract][Full Text] [Related]
18. Stickler syndrome in a pedigree of Pierre Robin syndrome.
Schreiner RL; McAlister WH; Marshall RE; Shearer WT
Am J Dis Child; 1973 Jul; 126(1):86-90. PubMed ID: 4198747
[No Abstract] [Full Text] [Related]
19. First-trimester diagnosis of micrognathia as a presentation of Pierre Robin syndrome.
Teoh M; Meagher S
Ultrasound Obstet Gynecol; 2003 Jun; 21(6):616-8. PubMed ID: 12808682
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of Pierre Robin Sequence: accuracy and ability to predict phenotype and functional severity.
Lind K; Aubry MC; Belarbi N; Chalouhi C; Couly G; Benachi A; Lyonnet S; Abadie V
Prenat Diagn; 2015 Sep; 35(9):853-8. PubMed ID: 25982360
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]