130 related articles for article (PubMed ID: 15841618)
1. Prenatal diagnosis of hemifacial microsomia by magnetic resonance imaging.
Hattori Y; Tanaka M; Matsumoto T; Uehara K; Ueno K; Miwegishi K; Ishimoto H; Miyakoshi K; Yoshimura Y
J Perinat Med; 2005; 33(1):69-71. PubMed ID: 15841618
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of hemifacial microsomia and ipsilateral cerebellar hypoplasia in a fetus with oculoauriculovertebral spectrum.
Martinelli P; Maruotti GM; Agangi A; Mazzarelli LL; Bifulco G; Paladini D
Ultrasound Obstet Gynecol; 2004 Aug; 24(2):199-201. PubMed ID: 15287060
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of Goldenhar syndrome with unusual features by 3D ultrasonography.
Guzelmansur I; Ceylaner G; Ceylaner S; Ceylan N; Daplan T
Genet Couns; 2013; 24(3):319-25. PubMed ID: 24341148
[TBL] [Abstract][Full Text] [Related]
4. Hemifacial Microsomia : Clinicoradiological Insight and Report of a Case.
Chhabra N; Chhabra A
Ethiop J Health Sci; 2017 Jan; 27(1):91-94. PubMed ID: 28458495
[TBL] [Abstract][Full Text] [Related]
5. Hemifacial microsomia with spinal and rib anomalies: prenatal diagnosis and postmortem confirmation using 3-D computed tomography reconstruction.
Haratz K; Vinkler C; Lev D; Schreiber L; Malinger G
Fetal Diagn Ther; 2011; 30(4):309-13. PubMed ID: 21997517
[TBL] [Abstract][Full Text] [Related]
6. Facial Paralysis in Patients With Hemifacial Microsomia: Frequency, Distribution, and Association With Other OMENS Abnormalities.
Li Q; Zhou X; Wang Y; Qian J; Zhang Q
J Craniofac Surg; 2018 Sep; 29(6):1633-1637. PubMed ID: 29771843
[TBL] [Abstract][Full Text] [Related]
7. Antenatal presentation of the oculo-auriculo-vertebral spectrum (OAVS).
Castori M; Brancati F; Rinaldi R; Adami L; Mingarelli R; Grammatico P; Dallapiccola B
Am J Med Genet A; 2006 Jul; 140(14):1573-9. PubMed ID: 16761296
[TBL] [Abstract][Full Text] [Related]
8. Goldenhar syndrome: a rare diagnosis with possible prenatal findings.
Ribeiro B; Igreja J; Gonçalves-Rocha M; Cadilhe A
BMJ Case Rep; 2016 Jun; 2016():. PubMed ID: 27329096
[TBL] [Abstract][Full Text] [Related]
9. Hemifacial microsomia and hypodontia: a case report.
Alkumru HN; Cölok G
J Oral Rehabil; 1992 Nov; 19(6):671-5. PubMed ID: 1469503
[TBL] [Abstract][Full Text] [Related]
10. Prenatal sonographic diagnosis of hemifacial microsomia (Goldenhar-Gorlin syndrome).
Tamas DE; Mahony BS; Bowie JD; Woodruff WW; Kay HH
J Ultrasound Med; 1986 Aug; 5(8):461-3. PubMed ID: 3528526
[No Abstract] [Full Text] [Related]
11. Unusual presentation of hemifacial microsomia.
Handler MZ; Alabi O; Miller J
J Plast Reconstr Aesthet Surg; 2011 Dec; 64(12):e306-8. PubMed ID: 21624853
[TBL] [Abstract][Full Text] [Related]
12. Early prenatal diagnosis of oculoauriculovertebral dysplasia or the Goldenhar syndrome.
De Catte L; Laubach M; Legein J; Goossens A
Ultrasound Obstet Gynecol; 1996 Dec; 8(6):422-4. PubMed ID: 9014284
[TBL] [Abstract][Full Text] [Related]
13. Ultrafast MR imaging of the fetus.
Kubik-Huch RA; Huisman TA; Wisser J; Gottstein-Aalame N; Debatin JF; Seifert B; Ladd ME; Stallmach T; Marincek B
AJR Am J Roentgenol; 2000 Jun; 174(6):1599-606. PubMed ID: 10845491
[TBL] [Abstract][Full Text] [Related]
14. Preterm diagnosis of choristoma and choroidal coloboma in Goldenhar's syndrome.
Herwig MC; Gembruch U; Born M; Gevensleben H; Loeffler KU; Müller AM
Pediatr Dev Pathol; 2011; 14(4):322-6. PubMed ID: 21345085
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of intestinal nonrotation using magnetic resonance imaging: Is it possible?
Blask AR; Fagen KE; Rubio EI; Badillo AT; Bulas DI
Pediatr Radiol; 2021 Jul; 51(8):1332-1338. PubMed ID: 33608743
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of midgut volvulus by sonography and magnetic resonance imaging.
Miyakoshi K; Ishimoto H; Tanigaki S; Minegishi K; Tanaka M; Miyazaki T; Yoshimura Y
Am J Perinatol; 2001 Dec; 18(8):447-50. PubMed ID: 11733860
[TBL] [Abstract][Full Text] [Related]
17. Thrombophilia gene mutations in oculoauriculovertebral spectrum.
Tug E; Atasoy HI; Koybasi Sanal S
Genet Couns; 2012; 23(1):65-72. PubMed ID: 22611644
[TBL] [Abstract][Full Text] [Related]
18. A case of Goldenhar-Gorlin syndrome with unusual association of hypoplastic thumb.
Das A; Ray B; Das D; Das S
Indian J Ophthalmol; 2008; 56(2):150-2. PubMed ID: 18292629
[TBL] [Abstract][Full Text] [Related]
19. Ipsilateral hemifacial microsomia with dextrocardia and pulmonary hypoplasia: A case report.
Guo R; Chang SH; Wang BQ; Zhang QG
World J Clin Cases; 2022 Mar; 10(9):2948-2953. PubMed ID: 35434090
[TBL] [Abstract][Full Text] [Related]
20. Goldenhar syndrome (oculoauriculovertebral dysplasia): report of one case.
Ng YY; Hu JM; Su PH; Chen JY; Yang MS; Chen SJ
Acta Paediatr Taiwan; 2006; 47(3):142-5. PubMed ID: 17078468
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]