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Journal Abstract Search

311 related items for PubMed ID: 19380073

  • 1. Early-onset neurodegenerative disease of the cerebellum and motor axons.
    Salman MS, Marles SL, Booth FA, Del Bigio MR.
    Pediatr Neurol; 2009 May; 40(5):365-70. PubMed ID: 19380073
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  • 2. Infantile onset progressive cerebellar atrophy and anterior horn cell degeneration--a late onset variant of PCH-1?
    Lev D, Michelson-Kerman M, Vinkler C, Blumkin L, Shalev SA, Lerman-Sagie T.
    Eur J Paediatr Neurol; 2008 Mar; 12(2):97-101. PubMed ID: 17681808
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  • 3. A mild variant of pontocerebellar hypoplasia type 1 in a 12-year-old Indian boy.
    Kalpana D, Parvathy L, Ahamed SM, Iype M, Kunju MP.
    Pediatr Neurol; 2009 Apr; 40(4):302-5. PubMed ID: 19302945
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  • 4. 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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  • 6. Crossed cerebellar atrophy in children: a neurologic sequela of extreme prematurity.
    Rollins NK, Wen TS, Dominguez R.
    Pediatr Radiol; 1995 Nov; 25 Suppl 1():S20-5. PubMed ID: 8577528
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  • 7. Progressive cavitating leukoencephalopathy: a novel childhood disease.
    Naidu S, Bibat G, Lin D, Burger P, Barker P, Rosemberg S, Braverman N, Arroyo H, Dowling M, Hamosh A, Kimonis V, Blank C, Fiumara A, Facchini S, Singhal B, Moser H, Kelley R, DiMauro S.
    Ann Neurol; 2005 Dec; 58(6):929-38. PubMed ID: 16315274
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  • 8. Familial pontocerebellar hypoplasia type I with anterior horn cell disease.
    Görgen-Pauly U, Sperner J, Reiss I, Gehl HB, Reusche E.
    Eur J Paediatr Neurol; 1999 Dec; 3(1):33-8. PubMed ID: 10727190
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  • 9. Hypomyelination neuropathy in a female newborn presenting as arthrogryposis multiplex congenita.
    Seitz RJ, Wechsler W, Mosny DS, Lenard HG.
    Neuropediatrics; 1986 Aug; 17(3):132-6. PubMed ID: 3762869
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  • 11. Olivopontocerebellar atrophy in children: a report of seven cases in two families.
    Colan RV, Snead OC, Ceballos R.
    Ann Neurol; 1981 Oct; 10(4):355-63. PubMed ID: 7316488
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  • 13. Neuroacanthocytosis. A clinical, haematological and pathological study of 19 cases.
    Hardie RJ, Pullon HW, Harding AE, Owen JS, Pires M, Daniels GL, Imai Y, Misra VP, King RH, Jacobs JM.
    Brain; 1991 Feb; 114 ( Pt 1A)():13-49. PubMed ID: 1998879
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  • 14. Congenital cervical spinal atrophy: an intrauterine hypoxic insult.
    Kaiboriboon K, Hayat GR.
    Neuropediatrics; 2001 Dec; 32(6):330-4. PubMed ID: 11870590
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  • 15. "Vanishing white matter" and ovarian dysgenesis in an infant with cerebro-oculo-facio-skeletal phenotype.
    Boltshauser E, Barth PG, Troost D, Martin E, Stallmach T.
    Neuropediatrics; 2002 Apr; 33(2):57-62. PubMed ID: 12075484
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