1 to 10 of 24 literature results

• Mutations in the fatty acid 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia.

  Myelination is a complex, developmentally regulated process whereby myelin proteins and lipids are coordinately expressed by myelinating glial cells. …

  Authors: Simon Edvardson, Hiroko Hama, Avraham Shaag, John Moshe Gomori, Itai Berger, Dov Soffer, Stanley H Korman, Ilana Taustein, Ann Saada, Orly Elpeleg

  Source: American journal of human genetics. 2008 Nov

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• Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia.

  Homozygosity mapping was performed in a consanguineous Sephardic Jewish family with three patients who presented with severe infantile encephalopathy …

  Authors: Simon Edvardson, Avraham Shaag, Olga Kolesnikova, John Moshe Gomori, Ivan Tarassov, Tom Einbinder, Ann Saada, Orly Elpeleg

  Source: American journal of human genetics. 2007 Oct

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• Chemotherapy as initial treatment in gliomatosis cerebri: results with temozolomide.

  The optimal therapy for gliomatosis cerebri is unclear, and the rate of response to chemotherapy is not known. Eleven radiotherapy-naive patients rece…

  Authors: Netta Levin, John Moshe Gomori, Tali Siegal

  Source: Neurology. 2004 Jul 27

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• CT of the ear in Pendred syndrome.

  PURPOSE: To prospectively determine the structural anomalies of the inner ear by using thin-section computed tomography (CT) in an extended family wit…

  Authors: Moshe Goldfeld, Benjamin Glaser, Elias Nassir, John Moshe Gomori, Elitsur Hazani, Nassir Bishara

  Source: Radiology. 2005 May

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• Hemipseudoathetosis due to a hemorrhage at the cervicomedullary junction.

  Authors: Marc Gotkine, John Moshe Gomori

  Source: Neurology. 2007 Oct 9

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• Complete and persistent occlusion of arteriovenous malformations of the mandible after endovascular embolization.

  OBJECTIVE: Arteriovenous malformation (AVM) of the mandible is a rare but potentially life-threatening entity. Traditional treatment involved complex …

  Authors: José E Cohen, John Moshe Gomori, Savvas Grigoriadis, Zion Sibly, Gustavo Rajz

  Source: Neurological research. 2009 Jun

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• The unique neuroradiology of complex I deficiency due to NDUFA12L defect.

  In two patients who presented at late infancy with hypotonia, nystagmus and ataxia, interspersed with acute episodes of encephalopathy, we identified …

  Authors: Flora Barghuti, Khaled Elian, John Moshe Gomori, Avraham Shaag, Simon Edvardson, Ann Saada, Orly Elpeleg

  Source: Molecular genetics and metabolism. 2008 May

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• Spontaneous thrombosis of cerebral aneurysms presenting with ischemic stroke.

  Complete spontaneous thrombosis of an unruptured cerebral aneurysm is a rare event that can be discovered incidentally on advanced neuroradiologic stu…

  Authors: José E Cohen, Eyal Itshayek, Eyal Yitshayek, John Moshe Gomori, Savvas Grigoriadis, Guy Raphaeli, Sergei Spektor, Gustavo Rajz

  Source: Journal of the neurological sciences. 2007 Mar 15

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• Prenatal thrombosis of torcular Herophili with spontaneous resolution and normal outcome.

  BACKGROUND: Prenatal thrombosis of torcular Herophili is a rare condition. It may be suspected during the routine ultrasonographic follow-up of the fe…

  Authors: Savvas Grigoriadis, Jose E Cohen, John Moshe Gomori

  Source: Journal of neuroimaging : official journal of the American Society of Neuroimaging. 2008 Apr

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• Automatic segmentation and classification of multiple sclerosis in multichannel MRI.

  We introduce a multiscale approach that combines segmentation with classification to detect abnormal brain structures in medical imagery, and demonstr…

  Authors: Ayelet Akselrod-Ballin, Meirav Galun, John Moshe Gomori, Massimo Filippi, Paola Valsasina, Ronen Basri, Achi Brandt

  Source: IEEE transactions on bio-medical engineering. 2009 Oct

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