Treatment of Encephalotrigeminal Angiomatosis (Sturge-Weber Disease) by Hemispherectomy-Reference-Cited by-同舟云学术

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Treatment of Encephalotrigeminal Angiomatosis (Sturge-Weber Disease) by Hemispherectomy

Published:1960-10-01 Issue:183 Volume:35 Page:433-447
ISSN:0003-9888
Container-title:Archives of Disease in Childhood
language:en
Short-container-title:Archives of Disease in Childhood

Author:

Falconer M. A.,Rushworth R. G.

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference42 articles.

1. Gefassmissbildungen und Gefdssgeschwulste des Gehirns;Bergstrand, H.; Olivecrona, H.; Tonnis, W.,1936

2. An electroencephalographically localized focus in a case of Sturge-Weber syndrome, extirpated with good result;Broager, B.; Hertz, H.;Acta psvchiat. (Kbh.),1949

3. Fatal brain-stem shift after hemispherectomy;Cabieses, F.; Jeri, R.; Landa, R.;J. Neurosurg,1957

4. Hemispherectomy in the treatment of infantile hemiplegia;Cairns, H.; Davidson, M.A.;Lancet,1951

5. Cases of spontaneous intracranial hemorrhage associated with trigeminal nevi;Cushing, H.;J. Amer. med. Ass,1906

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1. Seizure outcomes in children with Sturge-Weber syndrome undergoing epilepsy surgery: An individual participant data meta-analysis;Seizure: European Journal of Epilepsy;2023-04

2. Neurosurgical Considerations of Neurocutaneous Syndromes;Neurosurgery Clinics of North America;2022-01

3. Sturge-Weber Syndrome;Textbook of Pediatric Neurosurgery;2020

4. Sturge-Weber Syndrome;Textbook of Pediatric Neurosurgery;2018

5. Sturge-Weber Syndrome;Textbook of Pediatric Neurosurgery;2018

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