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Pathogenesis of Acute Viral Disease Induced in Fish by Carp Interstitial Nephritis and Gill Necrosis Virus

Journal of Virology, 2004-09, Vol.78 (17), p.9544-9551

2004

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Vascular endothelial growth factor induced by hypoxia may mediate hypoxia-initiated angiogenesis

Nature (London), 1992-10, Vol.359 (6398), p.843-845

1992

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Longitudinal Assessment of Genetic and Epigenetic Markers in Oligodendrogliomas

Clinical cancer research, 2007-03, Vol.13 (5), p.1429-1437

2007

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Dural arachnoid granulations and “giant” arachnoid granulations

Surgical and radiologic anatomy (English ed.), 2008-07, Vol.30 (5), p.417-421

2008

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Severe Infantile Carnitine Palmitoyltransferase II Deficiency in 19-Week Fetal Sibs

Pediatric and developmental pathology, 2009-12, Vol.12 (6), p.481-486

2009

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Cerebral amyloid angiopathy--a disease or age-related condition

The Israel Medical Association journal, 2006-11, Vol.8 (11), p.803

Soffer, Dov

2006

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Mutations in the Fatty Acid 2-Hydroxylase Gene Are Associated with Leukodystrophy with Spastic Paraparesis and Dystonia

American journal of human genetics, 2008-11, Vol.83 (5), p.643-648

2008

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Germline SDHD mutation in paraganglioma of the spinal cord

Oncogene, 2001-08, Vol.20 (36), p.5084-5086

2001

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The impact of resecting radiation necrosis and pseudoprogression on survival of patients with glioblastoma

World neurosurgery, 2016-05, Vol.89, p.37-41

2016

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Clinical significance of diffuse dural enhancement detected by magnetic resonance imaging

Journal of neurosurgery, 1996-11, Vol.85 (5), p.777-783

1996

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Mast cells in experimental allergic encephalomyelitis: characterization, distribution in the CNS and in vitro activation by myelin basic protein and neuropeptides

Journal of the neurological sciences, 1994-04, Vol.122 (2), p.210-213

1994

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The neuropathology of cerebrotendinous xanthomatosis revisited : a case report and review of the literature

Acta neuropathologica, 1995-08, Vol.90 (2), p.213-220

1995

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Primary T-cell CNS lymphoma presenting with leptomeningeal spread and neurolymphomatosis

Journal of neuro-oncology, 2008-10, Vol.90 (1), p.77-83

2008

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A novel mutation in the GAN gene causes an intermediate form of giant axonal neuropathy in an Arab–Israeli family

European journal of paediatric neurology, 2013-05, Vol.17 (3), p.259-264

2013

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Multifocal Demyelinative Leukoencephalopathy Associated with 5-Fluorouracil and Levamisole

Acta oncologica, 2000, Vol.39 (1), p.117-120

2000

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Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329 Ser mutation in the glycogen-branching enzyme gene

Annals of neurology, 1998-12, Vol.44 (6), p.867-872

1998

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Early clinical heterogeneity in choreoacanthocytosis

Archives of neurology (Chicago), 2005-04, Vol.62 (4), p.611

2005

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Extraosseous aneurysmal bone cyst of cerebello-pontine angle with USP6 rearrangement

Acta neuropathologica, 2009-10, Vol.118 (4), p.579-581

2009

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Intracranial meningiomas following low-dose irradiation to the head

Journal of neurosurgery, 1983-12, Vol.59 (6), p.1048-1053

1983

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Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Clinical and genetic features

Brain (London, England : 1878), 2000-06, Vol.123 ( Pt 6), p.1229-1237

2000

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Intracranial meningiomas after high‐dose irradiation

Cancer, 1989-04, Vol.63 (8), p.1514-1519

1989

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Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family

Journal of neurology, 2003-06, Vol.250 (6), p.733-740

2003

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Leukoencephalopathy with neuroaxonal spheroids presenting as frontotemporal dementia

The Israel Medical Association journal, 2008-05, Vol.10 (5), p.386-387

2008

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A novel autosomal recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12

Brain (London, England : 1878), 2005-01, Vol.128 (1), p.42-51

2005

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Childhood macrophagic myofasciitis—consanguinity and clinicopathological features

Neuromuscular disorders : NMD, 2004-04, Vol.14 (4), p.246-252

2004

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Pathogenesis of Acute Viral Disease Induced in Fish by Carp Interstitial Nephritis and Gill Necrosis Virus

Vascular endothelial growth factor induced by hypoxia may mediate hypoxia-initiated angiogenesis

Longitudinal Assessment of Genetic and Epigenetic Markers in Oligodendrogliomas

Dural arachnoid granulations and “giant” arachnoid granulations

Severe Infantile Carnitine Palmitoyltransferase II Deficiency in 19-Week Fetal Sibs

Cerebral amyloid angiopathy--a disease or age-related condition

Mutations in the Fatty Acid 2-Hydroxylase Gene Are Associated with Leukodystrophy with Spastic Paraparesis and Dystonia

Germline SDHD mutation in paraganglioma of the spinal cord

The impact of resecting radiation necrosis and pseudoprogression on survival of patients with glioblastoma

Clinical significance of diffuse dural enhancement detected by magnetic resonance imaging

Mast cells in experimental allergic encephalomyelitis: characterization, distribution in the CNS and in vitro activation by myelin basic protein and neuropeptides

The neuropathology of cerebrotendinous xanthomatosis revisited : a case report and review of the literature

Primary T-cell CNS lymphoma presenting with leptomeningeal spread and neurolymphomatosis

A novel mutation in the GAN gene causes an intermediate form of giant axonal neuropathy in an Arab–Israeli family

Multifocal Demyelinative Leukoencephalopathy Associated with 5-Fluorouracil and Levamisole

Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329 Ser mutation in the glycogen-branching enzyme gene

Early clinical heterogeneity in choreoacanthocytosis

Extraosseous aneurysmal bone cyst of cerebello-pontine angle with USP6 rearrangement

Intracranial meningiomas following low-dose irradiation to the head

Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Clinical and genetic features

Intracranial meningiomas after high‐dose irradiation

Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family

Leukoencephalopathy with neuroaxonal spheroids presenting as frontotemporal dementia

A novel autosomal recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12

Childhood macrophagic myofasciitis—consanguinity and clinicopathological features

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