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Results: 1 to 20 of 115

Similar articles for PubMed (Select 20001484)

1.

Pontobulbar palsy and sensorineural deafness (Brown-Vialetto-van Laere syndrome): the first case from Libya.

Dakhil FO, Bensreiti SM, Zew MH.

Amyotroph Lateral Scler. 2010 Aug;11(4):397-8. doi: 10.3109/17482960903440775.

PMID:
20001484
2.

Brown-Vialetto-Van Laere syndrome: a rare syndrome in otology.

Prabhu HV, Brown MJ.

J Laryngol Otol. 2005 Jun;119(6):470-2. Review.

PMID:
15992475
3.

Brown-Vialetto-Van Laere syndrome: case report and literature review.

Sathasivam S, O'Sullivan S, Nicolson A, Tilley PJ, Shaw PJ.

Amyotroph Lateral Scler Other Motor Neuron Disord. 2000 Sep;1(4):277-81. Review.

PMID:
11465021
4.

[A case of Brown-Vialetto-van Laere (BVVL) syndrome in Japan].

Nemoto H, Konno S, Nomoto N, Wakata N, Kurihara T.

Rinsho Shinkeigaku. 2005 May;45(5):357-61. Japanese.

PMID:
15960172
6.

Brown-Vialetto-Van Laere syndrome; variability in age at onset and disease progression highlighting the phenotypic overlap with Fazio-Londe disease.

Dipti S, Childs AM, Livingston JH, Aggarwal AK, Miller M, Williams C, Crow YJ.

Brain Dev. 2005 Sep;27(6):443-6. Epub 2004 Dec 15.

PMID:
16122634
7.

Brown-Vialetto-Van Laere syndrome: a riboflavin-unresponsive patient with a novel mutation in the C20orf54 gene.

Koy A, Pillekamp F, Hoehn T, Waterham H, Klee D, Mayatepek E, Assmann B.

Pediatr Neurol. 2012 Jun;46(6):407-9. doi: 10.1016/j.pediatrneurol.2012.03.008.

PMID:
22633641
8.

Vialetto-Van Laere syndrome in two sisters born to consanguineous parents.

RamachandranNair R, Parameswaran M, Girija AS.

Pediatr Neurol. 2004 May;30(5):354-5.

PMID:
15165639
9.
10.

Brown-Vialetto-van Laere syndrome; the first Turkish case.

Aydin OF, Ozçelikel D, Senbil N, Gürer YK.

Acta Neurol Belg. 2004 Sep;104(3):111-3.

PMID:
15508264
11.

Brown-Vialetto-Van Laere syndrome.

Sathasivam S.

Orphanet J Rare Dis. 2008 Apr 17;3:9. doi: 10.1186/1750-1172-3-9. Review.

12.

Ponto-bulbar palsy with deafness (Brown-Vialetto-Van Laere syndrome).

Gallai V, Hockaday JM, Hughes JT, Lane DJ, Oppenheimer DR, Rushworth G.

J Neurol Sci. 1981 May;50(2):259-75.

PMID:
7229669
13.

Four cases of brown-vialetto-van laere syndrome from Iran: Clinical and electrophysiologic findings.

Yadegari S, Ghorbani A, Dezfouli MA, Nafissi S.

Iran J Neurol. 2011;10(3-4):54-7.

14.

A Brazilian family with Brown-Vialetto-van Laere syndrome with autosomal recessive inheritance.

Malheiros JA, Camargos ST, Oliveira JT, Cardoso FE.

Arq Neuropsiquiatr. 2007 Mar;65(1):32-5. Review.

15.

Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: confirmation of autosomal recessive inheritance?

Mégarbané A, Desguerres I, Rizkallah E, Delague V, Nabbout R, Barois A, Urtizberea A.

Am J Med Genet. 2000 May 15;92(2):117-21. Review.

PMID:
10797435
16.

Infantile progressive bulbar palsy with deafness.

Voudris KA, Skardoutsou A, Vagiakou EA.

Brain Dev. 2002 Oct;24(7):732-5.

PMID:
12427524
17.

Pontobulbar palsy and sensorineural deafness (Brown-Vialetto-van Laere syndrome): A case from Northwest Iran.

Toopchizadeh V, Akbari MG, Habibzadeh A.

J Pediatr Neurosci. 2013 Sep;8(3):257-9. doi: 10.4103/1817-1745.123709. No abstract available.

18.

Protracted disease course after deafness in a man with Brown-Vialetto-Van Laere syndrome.

Yadegari S, Razmjoo K, Nafissi S.

Neurosciences (Riyadh). 2012 Jul;17(3):253-5.

PMID:
22772932
19.

[Brown-Vialetto-Van Laere syndrome: a case with anti-ganglioside GM1 antibodies and literature review].

Sztajzel R, Kohler A, Reichart M, Djientcheu VP, Chofflon M, Magistris MR.

Rev Neurol (Paris). 1998 Jan;154(1):51-4. Review. French.

PMID:
9773026
20.

[Case report Brown-Vialetto-Van laere syndrome].

Introini S, Sasso GM, Moioli G, Morandini WL.

Minerva Anestesiol. 2003 Jan-Feb;69(1-2):75-9. Italian.

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