Similar articles for PMID: 21447811

Year	Number of Results
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1

Neuronal ceroid lipofuscinosis in Qatar: report of a novel mutation in ceroid-lipofuscinosis, neuronal 5 in the Arab population.

Al-Kowari MK, Hassan S, El-Said MF, Ben-Omran T, Hedin L, Mole SE, Badii R. Al-Kowari MK, et al. J Child Neurol. 2011 May;26(5):625-9. doi: 10.1177/0883073810387298. Epub 2011 Mar 29. J Child Neurol. 2011. PMID: 21447811

2

Variant late infantile neuronal ceroid lipofuscinosis (CLN6 gene) in Saudi Arabia.

Al-Muhaizea MA, Al-Hassnan ZN, Chedrawi A. Al-Muhaizea MA, et al. Pediatr Neurol. 2009 Jul;41(1):74-6. doi: 10.1016/j.pediatrneurol.2009.01.012. Pediatr Neurol. 2009. PMID: 19520283 Review.

3

A CLN5 mutation causing an atypical neuronal ceroid lipofuscinosis of juvenile onset.

Pineda-Trujillo N, Cornejo W, Carrizosa J, Wheeler RB, Múnera S, Valencia A, Agudelo-Arango J, Cogollo A, Anderson G, Bedoya G, Mole SE, Ruíz-Linares A. Pineda-Trujillo N, et al. Neurology. 2005 Feb 22;64(4):740-2. doi: 10.1212/01.WNL.0000151974.44980.F1. Neurology. 2005. PMID: 15728307

4

Late infantile neuronal ceroid lipofuscinosis: a new mutation in Arabs.

Goldberg-Stern H, Halevi A, Marom D, Straussberg R, Mimouni-Bloch A. Goldberg-Stern H, et al. Pediatr Neurol. 2009 Oct;41(4):297-300. doi: 10.1016/j.pediatrneurol.2009.04.022. Pediatr Neurol. 2009. PMID: 19748052

5

CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis.

Savukoski M, Klockars T, Holmberg V, Santavuori P, Lander ES, Peltonen L. Savukoski M, et al. Nat Genet. 1998 Jul;19(3):286-8. doi: 10.1038/975. Nat Genet. 1998. PMID: 9662406

6

Late-infantile neuronal ceroid lipofuscinosis (CLN2/Jansky-Bielschowsky type) in Oman.

Koul R, Al-Futaisi A, Ganesh A, Rangnath Bushnarmuth S. Koul R, et al. J Child Neurol. 2007 May;22(5):555-9. doi: 10.1177/0883073807302613. J Child Neurol. 2007. PMID: 17690061

7

Novel mutations in the CLN6 gene causing a variant late infantile neuronal ceroid lipofuscinosis.

Teixeira CA, Espinola J, Huo L, Kohlschütter J, Persaud Sawin DA, Minassian B, Bessa CJ, Guimarães A, Stephan DA, Sá Miranda MC, MacDonald ME, Ribeiro MG, Boustany RM. Teixeira CA, et al. Hum Mutat. 2003 May;21(5):502-8. doi: 10.1002/humu.10207. Hum Mutat. 2003. PMID: 12673792

8

Detection of eight novel palmitoyl protein thioesterase (PPT) mutations underlying infantile neuronal ceroid lipofuscinosis (INCL;CLN1).

Salonen T, Järvelä I, Peltonen L, Jalanko A. Salonen T, et al. Hum Mutat. 2000;15(3):273-9. doi: 10.1002/(SICI)1098-1004(200003)15:3<273::AID-HUMU8>3.0.CO;2-L. Hum Mutat. 2000. PMID: 10679943

9

Spectrum of CLN6 mutations in variant late infantile neuronal ceroid lipofuscinosis.

Sharp JD, Wheeler RB, Parker KA, Gardiner RM, Williams RE, Mole SE. Sharp JD, et al. Hum Mutat. 2003 Jul;22(1):35-42. doi: 10.1002/humu.10227. Hum Mutat. 2003. PMID: 12815591

10

Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosis.

Cannelli N, Nardocci N, Cassandrini D, Morbin M, Aiello C, Bugiani M, Criscuolo L, Zara F, Striano P, Granata T, Bertini E, Simonati A, Santorelli FM. Cannelli N, et al. Neuropediatrics. 2007 Feb;38(1):46-9. doi: 10.1055/s-2007-981449. Neuropediatrics. 2007. PMID: 17607606

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