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Journal Abstract Search

134 related items for PubMed ID: 7167408

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  • 2. Lectin histochemical study of lipopigments with special regard to neuronal ceroid-lipofuscinosis. Results with concanavalin A.
    Elleder M.
    Histochemistry; 1989; 93(2):197-205. PubMed ID: 2482280
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  • 13. Human pathology in NCL.
    Anderson GW, Goebel HH, Simonati A.
    Biochim Biophys Acta; 2013 Nov; 1832(11):1807-26. PubMed ID: 23200925
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  • 14. Morphologic diagnosis in neuronal ceroid lipofuscinosis.
    Goebel HH.
    Neuropediatrics; 1997 Feb; 28(1):67-9. PubMed ID: 9151327
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  • 15. Morphologic studies on adult neuronal-ceroid lipofuscinosis (NCL).
    Goebel HH, Braak H, Seidel D, Doshi R, Marsden CD, Gullotta F.
    Clin Neuropathol; 1982 Feb; 1(4):151-62. PubMed ID: 7168921
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  • 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
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  • 17. Pigment variant of neuronal ceroid-lipofuscinosis.
    Goebel HH, Gullotta F, Bajanowski T, Hansen FJ, Braak H.
    Am J Med Genet; 1995 Jun 05; 57(2):155-9. PubMed ID: 7668321
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  • 19. [An autopsy case of juvenile neuronal ceroid-lipofuscinosis with dilated cardiomyopathy].
    Tomiyasu H, Takahashi W, Ohta T, Yoshii F, Shibuya M, Shinohara Y.
    Rinsho Shinkeigaku; 2000 Apr 05; 40(4):350-7. PubMed ID: 10967652
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