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Journal Abstract Search

129 related items for PubMed ID: 9504478

  • 1. Neuroradiologic findings in Marinesco-Sjögren syndrome.
    Georgy BA, Snow RD, Brogdon BG, Wertelecki W.
    AJNR Am J Neuroradiol; 1998 Feb; 19(2):281-3. PubMed ID: 9504478
    [Abstract] [Full Text] [Related]

  • 2. MR imaging features in Marinesco-Sjögren syndrome: severe cerebellar atrophy is not an obligatory finding.
    Reinhold A, Scheer I, Lehmann R, Neumann LM, Michael T, Varon R, Von Moers A.
    AJNR Am J Neuroradiol; 2003 May; 24(5):825-8. PubMed ID: 12748078
    [Abstract] [Full Text] [Related]

  • 3. Cerebellar dysplasia and unilateral cataract in Marinesco-Sjögren syndrome.
    Williams TE, Buchhalter JR, Sussman MD.
    Pediatr Neurol; 1996 Feb; 14(2):158-61. PubMed ID: 8703231
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  • 5. Autosomal recessive cerebellar hypoplasia and tapeto-retinal degeneration: a new syndrome.
    Dooley JM, LaRoche GR, Tremblay F, Riding M.
    Pediatr Neurol; 1992 Feb; 8(3):232-4. PubMed ID: 1622524
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  • 6. Mitochondrial myopathy in Marinesco-Sjögren syndrome.
    Torbergsen T, Aasly J, Borud O, Lindal S, Mellgren SI.
    J Ment Defic Res; 1991 Apr; 35 ( Pt 2)():154-9. PubMed ID: 2072394
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  • 7. A case of cranial meningocele associated with Joubert syndrome.
    Suzuki T, Hakozaki M, Kubo N, Kuroda K, Ogawa A.
    Childs Nerv Syst; 1996 May; 12(5):280-2. PubMed ID: 8737806
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  • 8. Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature.
    Pascual-Castroviejo I, Gutierrez M, Morales C, Gonzalez-Mediero I, Martínez-Bermejo A, Pascual-Pascual SI.
    Neuropediatrics; 1994 Aug; 25(4):183-90. PubMed ID: 7824090
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  • 9. Neuro-otological findings in a case of Marinesco-Sjögren syndrome with nystagmus.
    Yoshimoto Y.
    Auris Nasus Larynx; 1987 Aug; 14(3):171-6. PubMed ID: 3482781
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  • 10. Dominantly inherited hypoplasia of the vermis.
    Rivier F, Echenne B.
    Neuropediatrics; 1992 Aug; 23(4):206-8. PubMed ID: 1407388
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  • 13. Cerebellar cortical dysplasia: MR findings in a complex entity.
    Soto-Ares G, Delmaire C, Deries B, Vallee L, Pruvo JP.
    AJNR Am J Neuroradiol; 2000 Sep; 21(8):1511-9. PubMed ID: 11003288
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  • 14. The Marinesco-Sjögren syndrome examined by computed tomography, magnetic resonance, and 18F-2-fluoro-2-deoxy-D-glucose and positron emission tomography.
    Bromberg MB, Junck L, Gebarski SS, McLean MJ, Gilman S.
    Arch Neurol; 1990 Nov; 47(11):1239-42. PubMed ID: 2241622
    [Abstract] [Full Text] [Related]

  • 15. SIL1 mutations and clinical spectrum in patients with Marinesco-Sjogren syndrome.
    Krieger M, Roos A, Stendel C, Claeys KG, Sonmez FM, Baudis M, Bauer P, Bornemann A, de Goede C, Dufke A, Finkel RS, Goebel HH, Häussler M, Kingston H, Kirschner J, Medne L, Muschke P, Rivier F, Rudnik-Schöneborn S, Spengler S, Inzana F, Stanzial F, Benedicenti F, Synofzik M, Lia Taratuto A, Pirra L, Tay SK, Topaloglu H, Uyanik G, Wand D, Williams D, Zerres K, Weis J, Senderek J.
    Brain; 2013 Dec; 136(Pt 12):3634-44. PubMed ID: 24176978
    [Abstract] [Full Text] [Related]

  • 16. Marinesco-Sjögren syndrome: clinical and magnetic resonance imaging features in three children.
    McLaughlin JF, Pagon RA, Weinberger E, Haas JE.
    Dev Med Child Neurol; 1996 Apr; 38(4):363-70. PubMed ID: 8641542
    [Abstract] [Full Text] [Related]

  • 17. Noonan syndrome: Neuroimaging findings and morphometric analysis of the cranium base and posterior fossa in children.
    Ayaz E, Yıldırım R, Çelebi C, Ozalkak S.
    J Neuroimaging; 2023 Mar; 33(2):318-327. PubMed ID: 36480458
    [Abstract] [Full Text] [Related]

  • 18. Chiari III malformation: MRI.
    Aribal ME, Gürcan F, Aslan B.
    Neuroradiology; 1996 May; 38 Suppl 1():S184-6. PubMed ID: 8811711
    [No Abstract] [Full Text] [Related]

  • 19. Neuroepithelial cysts in a patient with Joubert syndrome plus renal cysts.
    Marsh SE, Grattan-Smith P, Pereira J, Barkovich AJ, Gleeson JG.
    J Child Neurol; 2004 Mar; 19(3):227-31. PubMed ID: 15119486
    [Abstract] [Full Text] [Related]

  • 20. [Marinesco-Sjögren syndrome with chronic progressive ophthalmoplegia caused by presumed defective oxidative phosphorylation].
    Berio A, Piazzi A.
    Pediatr Med Chir; 1996 Mar; 18(1):99-103. PubMed ID: 8685033
    [Abstract] [Full Text] [Related]

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