Literature DB >> 8411979

An animal model of the infantile type of neuronal ceroid-lipofuscinosis.

B Järplid1, M Haltia.   

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Year:  1993        PMID: 8411979     DOI: 10.1007/bf00710263

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


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  9 in total

1.  Infantile type of so-called neuronal ceroid-lipofuscinosis.

Authors:  P Santavuori; M Haltia; J Rapola
Journal:  Dev Med Child Neurol       Date:  1974-10       Impact factor: 5.449

2.  Infantile type of so-called neuronal ceroid-lipofuscinosis. 2. Morphological and biochemical studies.

Authors:  M Haltia; J Rapola; P Santavuori; A Keränen
Journal:  J Neurol Sci       Date:  1973-03       Impact factor: 3.181

3.  Infantile type of so-called neuronal ceroid-lipofuscinosis. 1. A clinical study of 15 patients.

Authors:  P Santavuori; M Haltia; J Rapola; C Raitta
Journal:  J Neurol Sci       Date:  1973-03       Impact factor: 3.181

4.  Infantile type of so-called neuronal ceroid-lipofuscinosis. Histological and electron microscopic studies.

Authors:  M Haltia; J Rapola; P Santavuori
Journal:  Acta Neuropathol       Date:  1973-10-11       Impact factor: 17.088

5.  Neuronal ceroid-lipofuscinosis (Batten's disease): relationship to amaurotic family idiocy?

Authors:  W Zeman; P Dyken
Journal:  Pediatrics       Date:  1969-10       Impact factor: 7.124

6.  Retina in various animal models of neuronal ceroid-lipofuscinosis.

Authors:  H H Goebel
Journal:  Am J Med Genet       Date:  1992-02-15

7.  English setter model and juvenile ceroid-lipofuscinosis in man.

Authors:  N Koppang
Journal:  Am J Med Genet       Date:  1992-02-15

Review 8.  Sheep and other animals with ceroid-lipofuscinoses: their relevance to Batten disease.

Authors:  R D Jolly; R D Martinus; D N Palmer
Journal:  Am J Med Genet       Date:  1992-02-15

9.  Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease).

Authors:  D N Palmer; I M Fearnley; J E Walker; N A Hall; B D Lake; L S Wolfe; M Haltia; R D Martinus; R D Jolly
Journal:  Am J Med Genet       Date:  1992-02-15
  9 in total
  4 in total

Review 1.  Cathepsin deficiency as a model for neuronal ceroid lipofuscinoses.

Authors:  John J Shacka; Kevin A Roth
Journal:  Am J Pathol       Date:  2005-12       Impact factor: 4.307

2.  Accumulation of sphingolipid activator proteins (SAPs) A and D in granular osmiophilic deposits in miniature Schnauzer dogs with ceroid-lipofuscinosis.

Authors:  D N Palmer; J Tyynelä; H C van Mil; V J Westlake; R D Jolly
Journal:  J Inherit Metab Dis       Date:  1997-03       Impact factor: 4.982

3.  A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration.

Authors:  J Tyynelä; I Sohar; D E Sleat; R M Gin; R J Donnelly; M Baumann; M Haltia; P Lobel
Journal:  EMBO J       Date:  2000-06-15       Impact factor: 11.598

4.  Manifestation of neuronal ceroid lipofuscinosis in Australian Merino sheep: observations on altered behaviour and growth.

Authors:  Greg M Cronin; Danai F Beganovic; Amanda L Sutton; DavidJ Palmer; Peter C Thomson; Imke Tammen
Journal:  Appl Anim Behav Sci       Date:  2016-02-01       Impact factor: 2.448

  4 in total

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