Literature DB >> 5471924

Histochemical, ultrastructural and biochemical studies of a case with leukodystrophy due to congenital deficiency of myelin.

M Adachi, L Schneck, J Torii, B W Volk.   

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Year:  1970        PMID： 5471924     DOI： 10.1097/00005072-197010000-00006

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN： 0022-3069            Impact factor:   3.685


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  5 in total

1.  Seitelberger's connatal form of Pelizaeus-Merzbacher Disease. Case report, clinical, pathological and biochemical findings.

Authors:  J Ulrich; N Herschkowitz
Journal:  Acta Neuropathol       Date:  1977-10-10       Impact factor: 17.088

2.  Modeling the natural history of Pelizaeus-Merzbacher disease.

Authors:  Joshua A Mayer; Ian R Griffiths; James E Goldman; Chelsey M Smith; Elizabeth Cooksey; Abigail B Radcliff; Ian D Duncan
Journal:  Neurobiol Dis       Date:  2015-01-03       Impact factor: 5.996

3.  Myelin deficiency (md): a neurologic mutant in the Wistar rat.

Authors:  C K Csiza; A de Lahunta
Journal:  Am J Pathol       Date:  1979-04       Impact factor: 4.307

4.  Postnatal sudanophilic leukodystrophy in two siblings.

Authors:  S Yokoi; N Amano; H Hanawa; K Isoyama; A Ishikawa; T Ogino
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

5.  Connatal Pelizaeus-Merzbacher disease with congenital stridor in two maternal cousins.

Authors:  W O Renier; F J Gabreëls; T W Hustinx; H H Jaspar; J A Geelen; U J Van Haelst; E J Lommen; B G Ter Haar
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088
  5 in total

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