Literature DB >> 14174045

[FAMILIAL FORM OF HYPERTELORISM ASSOCIATED WITH LISSENCEPHALIA WITH THE CLINICAL PICTURE OF A FORM OF MENTAL RETARDATION ASSOCIATED WITH EPILEPSY AND SPASTIC PARAPLEGIA].

M REZNIK, R ALBERCA-SERRANO.   

Abstract

Entities:  

Keywords:  ABNORMALITIES; CEREBRAL CORTEX; CRANIOFACIAL DYSOSTOSIS; DIAGNOSIS, DIFFERENTIAL; EPILEPSY; GENETICS, HUMAN; INFANT; MENTAL RETARDATION; PARAPLEGIA

Mesh：

Year:  1964        PMID： 14174045     DOI： 10.1016/0022-510x(64)90053-x

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN： 0022-510X            Impact factor:   3.181


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  4 in total

1.  Cerebral malformation associated with metabolic disorder. A report of 2 cases.

Authors:  M Erdohazi; N D Barnes; M J Robinson; B D Lake
Journal:  Acta Neuropathol       Date:  1976-12-21       Impact factor: 17.088

2.  [Familial microcephalies due to cerebral malformation. Anatomical and clinical study].

Authors:  O Robain; G Lyon
Journal:  Acta Neuropathol       Date:  1972       Impact factor: 17.088

3.  Lissencephaly and Pachygyria: an architectonic and topographical analysis.

Authors:  R M Stewart; D P Richman; V S Caviness
Journal:  Acta Neuropathol       Date:  1975       Impact factor: 17.088

4.  Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene.

Authors:  J M Pinard; J Motte; C Chiron; R Brian; E Andermann; O Dulac
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-08       Impact factor: 10.154
  4 in total

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