Literature DB >> 8897047

Central nervous system abnormalities in oculodentodigital dysplasia.

C T Schrander-Stumpel, C L Franke.   

Abstract

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Mesh：

Year:  1996        PMID： 8897047

Source DB:  PubMed          Journal:  Genet Couns        ISSN： 1015-8146


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  4 in total

Review 1.  Gap junctions in inherited human disease.

Authors:  Georg Zoidl; Rolf Dermietzel
Journal:  Pflugers Arch       Date:  2010-02-07       Impact factor: 3.657

Review 2.  Gap junctions in inherited human disorders of the central nervous system.

Authors:  Charles K Abrams; Steven S Scherer
Journal:  Biochim Biophys Acta       Date:  2011-08-16

3.  Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement.

Authors:  I Harting; S Karch; U Moog; A Seitz; P J W Pouwels; N I Wolf
Journal:  AJNR Am J Neuroradiol       Date:  2019-05-02       Impact factor: 3.825

4.  Epilepsy as a rare neurologic manifestation of oculodentodigitalis dysplasia.

Authors:  Mohammad Barzegar; Mohammad Sayadnasiri; Aidin Tabrizi
Journal:  Iran J Child Neurol       Date:  2012
  4 in total

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