Literature DB >> 13123591

Sturge-Weber-Dimitri syndrome, cephalic form of neurocutaneous hemangiomatosis.

B W LICHTENSTEIN.   

Abstract

Entities:  

Keywords:  ANGIOMATOSIS; BRAIN/pathology

Mesh：

Year:  1954        PMID： 13123591     DOI： 10.1001/archneurpsyc.1954.02320390021002

Source DB:  PubMed          Journal:  AMA Arch Neurol Psychiatry        ISSN： 0096-6886


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  4 in total

1.  Treatment of encephalotrigeminal angiomatosis (Sturge-Weber disease) by hemispherectomy.

Authors:  M A FALCONER; R G RUSHWORTH
Journal:  Arch Dis Child       Date:  1960-10       Impact factor: 3.791

2.  EEG evolution in Sturge-Weber syndrome.

Authors:  Eric H Kossoff; Catherine D Bachur; Angela M Quain; Joshua B Ewen; Anne M Comi
Journal:  Epilepsy Res       Date:  2014-02-03       Impact factor: 3.045

3.  Meningocerebral hemangiomatosis resembling Sturge-Weber disease in a horse.

Authors:  M McEntee; B A Summers; A de Lahunta; J Cummings
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

4.  Focal venous hypertension as a pathophysiologic mechanism for tissue hypertrophy, port-wine stains, the Sturge-Weber syndrome, and related disorders: proof of concept with novel hypothesis for underlying etiological cause (an American Ophthalmological Society thesis).

Authors:  Cameron F Parsa
Journal:  Trans Am Ophthalmol Soc       Date:  2013-09
  4 in total

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