Literature DB >> 3042663

Pathobiology of neuronal storage disease.

S U Walkley1.   

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Year:  1988        PMID： 3042663     DOI： 10.1016/s0074-7742(08)60087-2

Source DB:  PubMed          Journal:  Int Rev Neurobiol        ISSN： 0074-7742            Impact factor:   3.230


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  12 in total

1.  Feline sphingolipidosis resembling Niemann-Pick disease type C.

Authors:  A C Lowenthal; J F Cummings; D A Wenger; M A Thrall; P A Wood; A de Lahunta
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

Review 2.  Pathoarchitectonic pattern of iso- and allocortical lesions in juvenile and adult neuronal ceroid-lipofuscinosis.

Authors:  H Braak; E Braak
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

Review 3.  Biology of neuronal dysfunction in storage disorders.

Authors:  S U Walkley; P A March
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

4.  Lysosomal compromise and brain dysfunction: examining the role of neuroaxonal dystrophy.

Authors:  Steven U Walkley; Jakub Sikora; Matthew Micsenyi; Cristin Davidson; Kostantin Dobrenis
Journal:  Biochem Soc Trans       Date:  2010-12       Impact factor: 5.407

Review 5.  The role of sphingolipids in neuronal development: lessons from models of sphingolipid storage diseases.

Authors:  Rosaria Buccoliero; Jacques Bodennec; Anthony H Futerman
Journal:  Neurochem Res       Date:  2002-08       Impact factor: 3.996

Review 6.  The neuropsychiatry of inborn errors of metabolism.

Authors:  Mark Walterfang; Olivier Bonnot; Ramon Mocellin; Dennis Velakoulis
Journal:  J Inherit Metab Dis       Date:  2013-05-23       Impact factor: 4.982

7.  Adult onset lysosomal storage disease in a Tibetan terrier: clinical, morphological and biochemical studies.

Authors:  J Alroy; S H Schelling; J G Thalhammer; S S Raghavan; M R Natowicz; E M Prence; U Orgad
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

Review 8.  GM2 ganglioside and pyramidal neuron dendritogenesis.

Authors:  S U Walkley; D A Siegel; K Dobrenis
Journal:  Neurochem Res       Date:  1995-11       Impact factor: 3.996

9.  Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotype.

Authors:  J L Keulemans; A J Reuser; M A Kroos; R Willemsen; M M Hermans; A M van den Ouweland; J G de Jong; R A Wevers; W O Renier; D Schindler; M J Coll; A Chabas; H Sakuraba; Y Suzuki; O P van Diggelen
Journal:  J Med Genet       Date:  1996-06       Impact factor: 6.318

10.  Cerebellar degeneration in the Niemann-Pick type C mouse.

Authors:  Y Higashi; S Murayama; P G Pentchev; K Suzuki
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088
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