These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 4042822)

  • 21. Electrophysiology in some animal and human hereditary diseases involving the retinal pigment epithelium.
    Nilsson SE; Wrigstad A
    Eye (Lond); 1997; 11 ( Pt 5)():698-706. PubMed ID: 9474321
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Multifocal retinopathy in Dachshunds with CLN2 neuronal ceroid lipofuscinosis.
    Whiting RE; Pearce JW; Castaner LJ; Jensen CA; Katz RJ; Gilliam DH; Katz ML
    Exp Eye Res; 2015 May; 134():123-32. PubMed ID: 25697710
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Juvenile neuronal ceroid lipofuscinosis (Batten-Mayou) disease. Ophthalmologic diagnosis and findings].
    Seeliger M; Rüther K; Apfelstedt-Sylla E; Schlote W; Wohlrab M; Zrenner E
    Ophthalmologe; 1997 Aug; 94(8):557-62. PubMed ID: 9376693
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Amacrine and horizontal cell dysfunction in adult ceroid-lipofuscinosis (Kufs disease) and anatomical correlates in the ovine model.
    Armstrong D; Benedetto M; Samuelson D
    Int Ophthalmol; 1985 Apr; 8(1):37-42. PubMed ID: 4019036
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Ultrastructural and electrophysiological correlation of the genotypes of NCL.
    Williams RE; Boyd S; Lake BD
    Mol Genet Metab; 1999 Apr; 66(4):398-400. PubMed ID: 10191136
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Long-term follow-up of two siblings with adult-onset neuronal ceroid lipofuscinosis, Kufs type A.
    Özkara Ç; Gündüz A; Coşkun T; Alpaslan BG; Zeydan B; Delil Ş; Muona M; Lehesjoki AE; Kızıltan ME
    Epileptic Disord; 2017 Jun; 19(2):147-151. PubMed ID: 28587997
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Electrophysiologic findings in neuronal ceroid-lipofuscinosis (Batten-Spielmayer-Vogt)].
    Heilig P; Thaler AR; Lessel MR; Fourtis N
    Fortschr Ophthalmol; 1982; 79(4):364-6. PubMed ID: 6985253
    [No Abstract]   [Full Text] [Related]  

  • 28. Familial retinoschisis in female patients.
    Shimazaki J; Matsuhashi M
    Doc Ophthalmol; 1987 Mar; 65(3):393-400. PubMed ID: 3678011
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Retinal Degeneration In A Mouse Model Of CLN5 Disease Is Associated With Compromised Autophagy.
    Leinonen H; Keksa-Goldsteine V; Ragauskas S; Kohlmann P; Singh Y; Savchenko E; Puranen J; Malm T; Kalesnykas G; Koistinaho J; Tanila H; Kanninen KM
    Sci Rep; 2017 May; 7(1):1597. PubMed ID: 28487519
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Ocular phenotype in a mouse gene knockout model for infantile neuronal ceroid lipofuscinosis.
    Lei B; Tullis GE; Kirk MD; Zhang K; Katz ML
    J Neurosci Res; 2006 Oct; 84(5):1139-49. PubMed ID: 16881055
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Profound infantile neuroretinal dysfunction in a heterozygote for the CLN3 genetic defect.
    de los Reyes E; Dyken PR; Phillips P; Brodsky M; Bates S; Glasier C; Mrak RE
    J Child Neurol; 2004 Jan; 19(1):42-6. PubMed ID: 15032383
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Neuronal ceroid lipofuscinosis: a clinicopathological study.
    Sinha S; Satishchandra P; Santosh V; Gayatri N; Shankar SK
    Seizure; 2004 Jun; 13(4):235-40. PubMed ID: 15121131
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Further Characterization of the Predominant Inner Retinal Degeneration of Aging Cln3
    Volz C; Mirza M; Langmann T; Jägle H
    Adv Exp Med Biol; 2018; 1074():403-411. PubMed ID: 29721970
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Retinal degeneration in mice and humans with neuronal ceroid lipofuscinosis type 8.
    Salpeter EM; Leonard BC; Lopez AJ; Murphy CJ; Thomasy S; Imai DM; Grimsrud K; Lloyd KCK; Yan J; Sanchez Russo R; Shankar SP; Moshiri A
    Ann Transl Med; 2021 Aug; 9(15):1274. PubMed ID: 34532411
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Classic late infantile neuronal ceroid lipofuscinosis in a Chinese patient.
    Ko CH; Kong CK; Chow TC; Lee KC
    Hong Kong Med J; 2001 Mar; 7(1):93-6. PubMed ID: 11406682
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Electroencephalographic findings in Kufs disease.
    Vadlamudi L; Westmoreland BF; Klass DW; Parisi JE
    Clin Neurophysiol; 2003 Sep; 114(9):1738-43. PubMed ID: 12948804
    [TBL] [Abstract][Full Text] [Related]  

  • 37. EEG and evoked potentials in infantile neuronal ceroid-lipofuscinosis.
    Vanhanen SL; Sainio K; Lappi M; Santavuori P
    Dev Med Child Neurol; 1997 Jul; 39(7):456-63. PubMed ID: 9285436
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Batten disease--deteriorating course of ocular findings.
    Horiguchi M; Miyake Y
    Jpn J Ophthalmol; 1992; 36(1):91-6. PubMed ID: 1635301
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Dementia and psychiatric disorders in Kufs disease].
    Charles N; Vighetto A; Pialat J; Confavreux C; Aimard G
    Rev Neurol (Paris); 1990; 146(12):752-6. PubMed ID: 2291038
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Ceroid-lipofuscinosis (Batten's disease). Sequential electrophysiologic and pathologic changes in the retina of the ovine model.
    Graydon RJ; Jolly RD
    Invest Ophthalmol Vis Sci; 1984 Mar; 25(3):294-301. PubMed ID: 6538190
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.