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Journal Abstract Search

69 related items for PubMed ID: 21977511

  • 1. Spastic paraplegia in a 4-year-old boy.
    Sharma S, Juneja M, Kochhar AM, Prakash A.
    J Clin Neurosci; 2011 Oct; 18(10):1382, 1427. PubMed ID: 21977511
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  • 2. [Optical coherence tomography in Sjögren-Larsson Syndrome diagnosis].
    Loukil I, Naija O, Hachicha F.
    Bull Soc Belge Ophtalmol; 2012 Oct; (320):11-5. PubMed ID: 22978179
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  • 3. Sjogren-Larsson syndrome.
    Phanthumchinda K, Srimanuthipol K, Yodnophaklao P.
    J Med Assoc Thai; 1996 Aug; 79(8):541-4. PubMed ID: 8855639
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  • 6. Sjögren-Larsson syndrome: report of monozygote twins and a case with a novel mutation.
    Yiş U, Terrinoni A.
    Turk J Pediatr; 2012 Aug; 54(1):64-6. PubMed ID: 22397046
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  • 7. [A 2-year-old girl with a generalized scaling of the skin and developmental delay].
    Watanabe T.
    No To Hattatsu; 2007 May; 39(3):167-8. PubMed ID: 17515126
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  • 8. A Moroccan patient with Sjögren-Larsson syndrome.
    Haruna K, Suga Y, Mizuno Y, Kourou K, Muramatsu S, Hasegawa T, Inoue A, Ogawa H, Ikeda S, Lakhmiri M, Seto A.
    J Dermatol; 2007 Feb; 34(2):153-5. PubMed ID: 17239159
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  • 9. [MRI study of three siblings of suspicious Sjögren-Larsson syndrome].
    Morishita S, Konagaya M, Konagaya Y, Takayanagi T.
    Rinsho Shinkeigaku; 1990 Oct; 30(10):1118-22. PubMed ID: 2279363
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  • 13. Sjögren-Larsson syndrome: Indian and Central European similarities.
    Möhrenschlager M, Braun-Falco M, Ring J.
    Pediatr Dermatol; 2005 Oct; 22(6):574-5. PubMed ID: 16354271
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  • 14. A very rare neurocutaneous disorder in 2 siblings: Sjögren-Larsson syndrome.
    Caglayan AO, Gumus H.
    J Child Neurol; 2010 Aug; 25(8):1003-5. PubMed ID: 20142464
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  • 16. Ocular features of Sjogren-Larsson syndrome.
    Aslam SA, Sheth HG.
    Clin Exp Ophthalmol; 2007 Aug; 35(1):98-9. PubMed ID: 17300584
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  • 19. Persistent, aberrant Mongolian spots in Sjögren-Larsson syndrome.
    Inamadar AC, Palit A.
    Pediatr Dermatol; 2007 Aug; 24(1):98-9. PubMed ID: 17300667
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  • 20. Sjögren-Larsson syndrome due to a novel mutation in the FALDH gene.
    Botelho Gomes JM, Vieira AP, Navarro J, Maré R, Tavares P, Brito C.
    Eur J Dermatol; 2011 Aug; 21(3):412-3. PubMed ID: 21524986
    [No Abstract] [Full Text] [Related]

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