143 related articles for article (PubMed ID: 23953647)
1. Goldenhar syndrome and medulloblastoma: a coincidental association? The first case report.
Aizenbud D; Shoham NV; Constantini S; Nevo N; Ben Arush M; Raz M; Rachmiel A; Goldsher D
J Craniomaxillofac Surg; 2014 Jul; 42(5):e91-6. PubMed ID: 23953647
[TBL] [Abstract][Full Text] [Related]
2. Cytogenetic evaluation of isochromosome 17q in posterior fossa tumors of children and correlation with clinical outcome in medulloblastoma. Detection of a novel chromosomal abnormality.
DeChiara C; Borghese A; Fiorillo A; Genesio R; Conti A; D'Amore R; Pettinato G; Varone A; Maggi G
Childs Nerv Syst; 2002 Aug; 18(8):380-4. PubMed ID: 12192498
[TBL] [Abstract][Full Text] [Related]
3. Primitive neuroectodermal tumor in the cerebellopontine angle with isochromosome 17q presenting as meningioma in a woman 26 years of age.
Izycka-Swieszewska E; Debiec-Rychter M; Kloc W
Clin Neuropathol; 2003; 22(2):66-70. PubMed ID: 12670052
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 7q21.11 Microdeletion in a Neonate With Goldenhar Syndrome: Case Report and a Literature Review.
Puvabanditsin S; February M; Francois L; Garrow E; Bruno C; Mehta R
Cleft Palate Craniofac J; 2016 Mar; 53(2):249-52. PubMed ID: 26068384
[TBL] [Abstract][Full Text] [Related]
6. Medulloblastoma in the nevoid basal-cell carcinoma syndrome: case reports and review of the literature.
Lacombe D; Chateil JF; Fontan D; Battin J
Genet Couns; 1990; 1(3-4):273-7. PubMed ID: 2098052
[TBL] [Abstract][Full Text] [Related]
7. Goldenhar syndrome with rare associations.
Kumar R; Balani B; Patwari AK; Anand VK; Ahuja B
Indian J Pediatr; 2000 Mar; 67(3):231-3. PubMed ID: 10838727
[TBL] [Abstract][Full Text] [Related]
8. Atypical adult medulloblastoma.
Behbahani M; St George EJ; Dunn LT; Hadley DM; Stewart W
Acta Neurochir (Wien); 2011 Jul; 153(7):1511-7; discussion 1517. PubMed ID: 21553317
[TBL] [Abstract][Full Text] [Related]
9. Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q).
Herman GE; Greenberg F; Ledbetter DH
Am J Med Genet; 1988 Apr; 29(4):909-15. PubMed ID: 3400736
[TBL] [Abstract][Full Text] [Related]
10. Distraction osteogenesis in Goldenhar Syndrome: case report and 8-year follow-up.
Lima Mde D; Marques YM; Alves Sde M; Ortega KL; Soares MM; Magalhães MH
Med Oral Patol Oral Cir Bucal; 2007 Nov; 12(7):E528-31. PubMed ID: 17978778
[TBL] [Abstract][Full Text] [Related]
11. Basal cell nevus syndrome and medulloblastoma: a case report.
Romero Pérez JA; Lleras Santana I
Bol Asoc Med P R; 1993; 85(1-3):24-6. PubMed ID: 8060441
[TBL] [Abstract][Full Text] [Related]
12. Infectious keratitis in a newborn with goldenhar syndrome.
Mittal S; Mittal A; Meenakshi R; Bharathi JM; Rengappa R
J Pediatr Ophthalmol Strabismus; 2010; 47(1):43-5. PubMed ID: 20128554
[TBL] [Abstract][Full Text] [Related]
13. Correlation of chromosome 17p loss with clinical outcome in medulloblastoma.
Emadian SM; McDonald JD; Gerken SC; Fults D
Clin Cancer Res; 1996 Sep; 2(9):1559-64. PubMed ID: 9816333
[TBL] [Abstract][Full Text] [Related]
14. Goldenhar sequence and mosaic trisomy 22.
Pridjian G; Gill WL; Shapira E
Am J Med Genet; 1995 Dec; 59(4):411-3. PubMed ID: 8585556
[TBL] [Abstract][Full Text] [Related]
15. Trisomy 9 mosaicism: another etiology for the manifestations of Goldenhar syndrome.
Wilson GN; Barr M
J Craniofac Genet Dev Biol; 1983; 3(4):313-6. PubMed ID: 6662905
[TBL] [Abstract][Full Text] [Related]
16. Isochromosome breakpoints on 17p in medulloblastoma are flanked by different classes of DNA sequence repeats.
Mendrzyk F; Korshunov A; Toedt G; Schwarz F; Korn B; Joos S; Hochhaus A; Schoch C; Lichter P; Radlwimmer B
Genes Chromosomes Cancer; 2006 Apr; 45(4):401-10. PubMed ID: 16419060
[TBL] [Abstract][Full Text] [Related]
17. Branchial cleft anomaly, congenital heart disease, and biliary atresia: Goldenhar complex or Lambert syndrome?
Cohen J; Schanen NC
Genet Couns; 2000; 11(2):153-6. PubMed ID: 10893666
[TBL] [Abstract][Full Text] [Related]
18. Primary Burkitt lymphoma of the fourth ventricle mimicking a medulloblastoma in a child.
Liu H; Hou H; Cheng J
J Neurooncol; 2016 Mar; 127(1):205-7. PubMed ID: 26703786
[No Abstract] [Full Text] [Related]
19. Goldenhar syndrome and autistic behaviour.
Landgren M; Gillberg C; Strömland K
Dev Med Child Neurol; 1992 Nov; 34(11):999-1005. PubMed ID: 1426690
[TBL] [Abstract][Full Text] [Related]
20. Medulloblastoma in two brothers.
Yamashita Y; Handa H; Toyama M
Surg Neurol; 1975 Aug; 4(2):225-7. PubMed ID: 1162594
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
