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 *

106 related articles for article (PubMed ID: 3017114)

  • 1. Ocular features of the Hagberg-Santavuori syndrome.
    Bateman JB; Philippart M
    Am J Ophthalmol; 1986 Aug; 102(2):262-71. PubMed ID: 3017114
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An ultramicroscopic study of the skin in the diagnosis of the infantile and late infantile types of ceroid-lipofuscinosis.
    Arsénio-Nunes ML; Goutières F
    J Neurol Neurosurg Psychiatry; 1975 Oct; 38(10):994-9. PubMed ID: 172610
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Olivopontocerebellar atrophy with retinal degeneration. A clinical and ocular histopathologic study.
    Traboulsi EI; Maumenee IH; Green WR; Freimer ML; Moser H
    Arch Ophthalmol; 1988 Jun; 106(6):801-6. PubMed ID: 3163477
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Retinal and optic nerve degeneration in α-mannosidosis.
    Matlach J; Zindel T; Amraoui Y; Arash-Kaps L; Hennermann JB; Pitz S
    Orphanet J Rare Dis; 2018 Jun; 13(1):88. PubMed ID: 29859105
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ocular involvement in acute intermittent porphyria.
    Wolter JR; Clark RL; Kallet HA
    Am J Ophthalmol; 1972 Oct; 74(4):666-74. PubMed ID: 5075136
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. Adult type of neuronal ceroid-lipofuscinosis with retinal involvement.
    Ikeda K; Kosaka K; Oyanagi S; Yamada K
    Clin Neuropathol; 1984; 3(6):237-9. PubMed ID: 6518685
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Late infantile neuronal ceroid lipofuscinosis: an ultrastructural investigation.
    Buhl L; Muirhead D; Litthander J; Raj G
    Pediatr Pathol; 1994; 14(3):397-404. PubMed ID: 8065998
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Retinal pigment epithelial dysfunction in early ovine ceroid lipofuscinosis: electrophysiologic and pathologic correlates.
    Samuelson D; Dawson WW; Webb AI; Dowson J; Jolly R; Armstrong D
    Ophthalmologica; 1985; 190(3):150-7. PubMed ID: 4039810
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Frequent causes of blindness].
    Makabe R
    Med Klin; 1973 Mar; 68(9):279-82. PubMed ID: 4693705
    [No Abstract]   [Full Text] [Related]  

  • 11. Electron microscopy of skin and peripheral blood lymphocytes in infantile (Santavuori) neuronal ceroid lipofuscinosis.
    Haynes ME; Manson JI; Carter RF; Robertson E
    Neuropadiatrie; 1979 Aug; 10(3):245-63. PubMed ID: 228218
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Results of study of the organ of vision in the dynamics of students of schools for blind and poor-sighted children in the L'vov region].
    Kalenik NI; Samchenko IM
    Oftalmol Zh; 1975; 30(7):531-3. PubMed ID: 1208012
    [No Abstract]   [Full Text] [Related]  

  • 13. Ocular manifestations of the mucopolysaccharidoses.
    François J
    Ophthalmologica; 1974; 169(5):345-61. PubMed ID: 4370235
    [No Abstract]   [Full Text] [Related]  

  • 14. The dystrophic retina in multisystem disorders: the electroretinogram in neuronal ceroid lipofuscinoses.
    Weleber RG
    Eye (Lond); 1998; 12 ( Pt 3b)():580-90. PubMed ID: 9775220
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical, electrophysiological, imaging, and ultrastructural description in 68 patients with neuronal ceroid lipofuscinoses and its subtypes.
    Jadav RH; Sinha S; Yasha TC; Aravinda H; Gayathri N; Rao S; Bindu PS; Satishchandra P
    Pediatr Neurol; 2014 Jan; 50(1):85-95. PubMed ID: 24120650
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Juvenile-onset neuronal ceroid-lipofuscinosis in Rambouillet sheep.
    Edwards JF; Storts RW; Joyce JR; Shelton JM; Menzies CS
    Vet Pathol; 1994 Jan; 31(1):48-54. PubMed ID: 8140725
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Muscular biopsy in ceroid lipofuscinosis: 3 case reports of juvenile form].
    Pego R; Amigo MC; Escriche D; Romero J; Navarro C
    Rev Neurol; 1995; 23(121):627-31. PubMed ID: 8597983
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Juvenile neuronal ceroid-lipofusoinosis (Batten's disease). A new case with ultrastructural examination of the skin and lymphocytes].
    Beauvais P; Arsenio-Nunes ML; Boccon-Gibod L; Brissaud HE
    Ann Pediatr (Paris); 1978 Dec; 25(10):543-53. PubMed ID: 16114142
    [No Abstract]   [Full Text] [Related]  

  • 20. Electroretinographic and clinicopathologic correlations of retinal dysfunction in infantile neuronal ceroid lipofuscinosis (infantile Batten disease).
    Weleber RG; Gupta N; Trzupek KM; Wepner MS; Kurz DE; Milam AH
    Mol Genet Metab; 2004; 83(1-2):128-37. PubMed ID: 15464427
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.