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Journal Abstract Search

257 related items for PubMed ID: 2038425

  • 1. Magnetic resonance imaging in infantile encephalopathy with cerebral calcification and leukodystrophy.
    Boltshauser E, Steinlin M, Boesch C, Martin E, Schubiger G.
    Neuropediatrics; 1991 Feb; 22(1):33-5. PubMed ID: 2038425
    [Abstract] [Full Text] [Related]

  • 2. Infantile familial encephalopathy with cerebral calcifications and leukodystrophy.
    Razavi-Encha F, Larroche JC, Gaillard D.
    Neuropediatrics; 1988 May; 19(2):72-9. PubMed ID: 3287208
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  • 3. Diffuse white matter disease in three children: an encephalopathy with unique features on magnetic resonance imaging and proton magnetic resonance spectroscopy.
    Hanefeld F, Holzbach U, Kruse B, Wilichowski E, Christen HJ, Frahm J.
    Neuropediatrics; 1993 Oct; 24(5):244-8. PubMed ID: 8309512
    [Abstract] [Full Text] [Related]

  • 4. Autosomal recessive micrencephaly with simplified gyral pattern, abnormal myelination and arthrogryposis.
    Sztriha L, Al-Gazali LI, Várady E, Goebel HH, Nork M.
    Neuropediatrics; 1999 Jun; 30(3):141-5. PubMed ID: 10480209
    [Abstract] [Full Text] [Related]

  • 5. Leukodystrophy: diffuse cerebral sclerosis or Schilder's disease revisited.
    Norman MG.
    Perspect Pediatr Pathol; 1975 Jun; 2():61-100. PubMed ID: 48227
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  • 8. Ataxia, developmental delay and an extensive neuronal migration abnormality in 2 siblings.
    Harbord MG, Boyd S, Hall-Craggs MA, Kendall B, McShane MA, Baraitser M.
    Neuropediatrics; 1990 Nov; 21(4):218-21. PubMed ID: 2290486
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  • 10. Van der Knaap's vacuolating leukoencephalopathy: two additional cases.
    Thelle T, Balslev T, Christensen T.
    Eur J Paediatr Neurol; 1999 Nov; 3(2):83-6. PubMed ID: 10700544
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  • 11. Familial tremulous and myoclonic dystonia with white matter changes in brain magnetic resonance imaging.
    Bohlega S, Stigsby B, al-Kawi MZ, McLean DR, Ozand P, Omer S, Coates P.
    Mov Disord; 1995 Jul; 10(4):513-7. PubMed ID: 7565837
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  • 12. Autosomal recessive polymicrogyria with infantile spasms and limb deformities.
    Ciardo F, Zamponi N, Specchio N, Parmeggiani L, Guerrini R.
    Neuropediatrics; 2001 Dec; 32(6):325-9. PubMed ID: 11870589
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  • 13. Occidental type cerebromuscular dystrophy: a report of eleven cases.
    Topaloğlu H, Yalaz K, Renda Y, Cağlar M, Göğüs S, Kale G, Gücüyener K, Nurlu G.
    J Neurol Neurosurg Psychiatry; 1991 Mar; 54(3):226-9. PubMed ID: 2030350
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  • 14. Abnormal myelination in a patient with ring chromosome 18.
    Nakayama J, Hamano K, Shimakura Y, Iwasaki N, Nakahara C, Imoto N, Kobayashi K, Arinami T, Hamaguchi H.
    Neuropediatrics; 1997 Dec; 28(6):335-7. PubMed ID: 9453033
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  • 16. A new leukoencephalopathy with bilateral anterior temporal lobe cysts.
    Olivier M, Lenard HG, Aksu F, Gärtner J.
    Neuropediatrics; 1998 Oct; 29(5):225-8. PubMed ID: 9810556
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  • 17. [A case of leukodystrophy, suspected of Alexander's disease, and its magnetic resonance imaging].
    Yoshimura N, Nishizawa M, Hozumi I, Yuasa T, Miyatake T.
    Rinsho Shinkeigaku; 1987 Sep; 27(9):1141-4. PubMed ID: 3440358
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  • 18. Leber congenital amaurosis in siblings with diffuse dysmyelination.
    Curless RG, Flynn JT, Olsen KR, Post MJ.
    Pediatr Neurol; 1991 Sep; 7(3):223-5. PubMed ID: 1878105
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  • 19. Aicardi-Goutières syndrome: an expanding phenotype.
    McEntagart M, Kamel H, Lebon P, King MD.
    Neuropediatrics; 1998 Jun; 29(3):163-7. PubMed ID: 9706629
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