127 related articles for article (PubMed ID: 11588991)
21. A CLN8 nonsense mutation in the whole genome sequence of a mixed breed dog with neuronal ceroid lipofuscinosis and Australian Shepherd ancestry.
Guo J; Johnson GS; Brown HA; Provencher ML; da Costa RC; Mhlanga-Mutangadura T; Taylor JF; Schnabel RD; O'Brien DP; Katz ML
Mol Genet Metab; 2014 Aug; 112(4):302-9. PubMed ID: 24953404
[TBL] [Abstract][Full Text] [Related]
22. MRI of neuronal ceroid lipofuscinosis. II. Postmortem MRI and histopathological study of the brain in 16 cases of neuronal ceroid lipofuscinosis of juvenile or late infantile type.
Autti T; Raininko R; Santavuori P; Vanhanen SL; Poutanen VP; Haltia M
Neuroradiology; 1997 May; 39(5):371-7. PubMed ID: 9189886
[TBL] [Abstract][Full Text] [Related]
23. Turkish variant late infantile neuronal ceroid lipofuscinosis (CLN7) may be allelic to CLN8.
Mitchell WA; Wheeler RB; Sharp JD; Bate SL; Gardiner RM; Ranta US; Lonka L; Williams RE; Lehesjoki AE; Mole SE
Eur J Paediatr Neurol; 2001; 5 Suppl A():21-7. PubMed ID: 11589000
[TBL] [Abstract][Full Text] [Related]
24. Phenotype-genotype correlation in eight patients with Finnish variant late infantile NCL (CLN5).
Holmberg V; Lauronen L; Autti T; Santavuori P; Savukoski M; Uvebrant P; Hofman I; Peltonen L; Järvelä I
Neurology; 2000 Aug; 55(4):579-81. PubMed ID: 10953198
[TBL] [Abstract][Full Text] [Related]
25. MRI of neuronal ceroid lipofuscinosis. I. Cranial MRI of 30 patients with juvenile neuronal ceroid lipofuscinosis.
Autti T; Raininko R; Vanhanen SL; Santavuori P
Neuroradiology; 1996 Jul; 38(5):476-82. PubMed ID: 8837098
[TBL] [Abstract][Full Text] [Related]
26. Glial cells are functionally impaired in juvenile neuronal ceroid lipofuscinosis and detrimental to neurons.
Parviainen L; Dihanich S; Anderson GW; Wong AM; Brooks HR; Abeti R; Rezaie P; Lalli G; Pope S; Heales SJ; Mitchison HM; Williams BP; Cooper JD
Acta Neuropathol Commun; 2017 Oct; 5(1):74. PubMed ID: 29041969
[TBL] [Abstract][Full Text] [Related]
27. High resolution MRI reveals global changes in brains of Cln3 mutant mice.
Greene ND; Lythgoe MF; Thomas DL; Nussbaum RL; Bernard DJ; Mitchison HM
Eur J Paediatr Neurol; 2001; 5 Suppl A():103-7. PubMed ID: 11588978
[TBL] [Abstract][Full Text] [Related]
28. Brain lysosomal hydrolases in neuronal ceroid-lipofuscinoses.
Prasad VV; Pullarkat RK
Mol Chem Neuropathol; 1996; 29(2-3):169-79. PubMed ID: 8971694
[TBL] [Abstract][Full Text] [Related]
29. Childhood neuronal ceroid-lipofuscinoses in Argentina.
Taratuto AL; Saccoliti M; Sevlever G; Ruggieri V; Arroyo H; Herrero M; Massaro M; Fejerman N
Am J Med Genet; 1995 Jun; 57(2):144-9. PubMed ID: 7668319
[TBL] [Abstract][Full Text] [Related]
30. MRI in neuronal ceroid lipofuscinosis.
D'Incerti L
Neurol Sci; 2000; 21(3 Suppl):S71-3. PubMed ID: 11073231
[TBL] [Abstract][Full Text] [Related]
31. Neuronal ceroid lipofuscinoses in childhood.
Santavuori P; Lauronen L; Kirveskari E; Aberg L; Sainio K; Autti T
Neurol Sci; 2000; 21(3 Suppl):S35-41. PubMed ID: 11073226
[TBL] [Abstract][Full Text] [Related]
32. Two novel CLN5 mutations in a Portuguese patient with vLINCL: insights into molecular mechanisms of CLN5 deficiency.
Bessa C; Teixeira CA; Mangas M; Dias A; Sá Miranda MC; Guimarães A; Ferreira JC; Canas N; Cabral P; Ribeiro MG
Mol Genet Metab; 2006 Nov; 89(3):245-53. PubMed ID: 16814585
[TBL] [Abstract][Full Text] [Related]
33. Neuronal ceroid lipofuscinoses and possible pathogenic mechanism.
Zhong N
Mol Genet Metab; 2000; 71(1-2):195-206. PubMed ID: 11001811
[TBL] [Abstract][Full Text] [Related]
34. Mass spectrometric analysis reveals changes in phospholipid, neutral sphingolipid and sulfatide molecular species in progressive epilepsy with mental retardation, EPMR, brain: a case study.
Hermansson M; Käkelä R; Berghäll M; Lehesjoki AE; Somerharju P; Lahtinen U
J Neurochem; 2005 Nov; 95(3):609-17. PubMed ID: 16086686
[TBL] [Abstract][Full Text] [Related]
35. The neuronal ceroid lipofuscinosis CLN8 membrane protein is a resident of the endoplasmic reticulum.
Lonka L; Kyttälä A; Ranta S; Jalanko A; Lehesjoki AE
Hum Mol Genet; 2000 Jul; 9(11):1691-7. PubMed ID: 10861296
[TBL] [Abstract][Full Text] [Related]
36. Late onset juvenile neuronal ceroid-lipofuscinosis with granular osmiophilic deposits (GROD).
Hofman IL; Taschner PE
Am J Med Genet; 1995 Jun; 57(2):165-7. PubMed ID: 7668323
[TBL] [Abstract][Full Text] [Related]
37. Neuronal ceroid lipofuscinoses: a clinical and morphological study of 17 patients from southern Brazil.
Puga AC; Jardim LB; Chimelli L; De Souza CF; Clivati M
Arq Neuropsiquiatr; 2000 Sep; 58(3A):597-606. PubMed ID: 10973097
[TBL] [Abstract][Full Text] [Related]
38. The neuronal ceroid-lipofuscinoses.
Goebel HH
Semin Pediatr Neurol; 1996 Dec; 3(4):270-8. PubMed ID: 8969009
[TBL] [Abstract][Full Text] [Related]
39. [Mechanisms of juvenile neuronal ceroid lipofuscinosis (JNCL)].
Wang SY; Jin WN; Wu D
Yi Chuan; 2009 Aug; 31(8):779-84. PubMed ID: 19689937
[TBL] [Abstract][Full Text] [Related]
40. Comparison of brain perfusion SPECT and MRI findings in children with neuronal ceroid-lipofuscinosis and in their families.
Sayit E; Yorulmaz I; Bekis R; Kaya G; Gumuser FG; Dirik E; Durak H
Ann Nucl Med; 2002 May; 16(3):201-6. PubMed ID: 12126045
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
