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Low-level laser therapy applied transcranially to rats after induction of stroke significantly reduces long-term neurological deficits

Stroke (1970), 2006-10, Vol.37 (10), p.2620-2624

2006

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Multi-system neurological disorder associated with a CRYAB variant

Neurogenetics, 2021-05, Vol.22 (2), p.117-125

2021

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Congenital myasthenic syndrome in Israel: Genetic and clinical characterization

Neuromuscular disorders : NMD, 2017-02, Vol.27 (2), p.136-140

2017

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The proteomic profile of hereditary inclusion body myopathy

PloS one, 2011-01, Vol.6 (1), p.e16334-e16334

2011

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The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

Nature genetics, 2001-09, Vol.29 (1), p.83-87

2001

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Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features

Annals of clinical and translational neurology, 2023-04, Vol.10 (4), p.553-567

2023

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Myotonia in DNM2-related centronuclear myopathy

Journal of Neural Transmission, 2014-05, Vol.121 (5), p.549-553

2014

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Chronic non-paroxysmal neuropathic pain — Novel phenotype of mutation in the sodium channel SCN9A gene

Journal of the neurological sciences, 2011-02, Vol.301 (1), p.90-92

2011

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A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B

Nature genetics, 1998-09, Vol.20 (1), p.37-42

1998

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Acute painful neuropathy induced by rapid correction of serum glucose levels in diabetic patients

Biomedicine & pharmacotherapy, 2009-12, Vol.63 (10), p.707-709

2009

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Riboflavin-responsive lipid-storage myopathy in elderly patients

Journal of the neurological sciences, 2024-01, Vol.456, p.122808-122808, Article 122808

2024

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Apparent C8-T1 radiculopathy with hand weakness due to mid-cervical spondylosis

Journal of clinical neuroscience, 2018-01, Vol.47, p.111-115

2018

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Neurodegeneration associated with genetic defects in phospholipase A2

Neurology, 2009-09, Vol.73 (10), p.819

Sadeh, Menachem

2009

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Acute steroid responsive small-fiber sensory neuropathy: a new entity?

Journal of the peripheral nervous system, 2006-03, Vol.11 (1), p.47-52

2006

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X-linked myopathy with excessive autophagy: First report of an Israeli family presenting with late onset lower limb girdle weakness

Neuromuscular disorders : NMD, 2021-09, Vol.31 (9), p.854-858

2021

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Early diagnosis of ATTR amyloidosis through targeted follow-up of identified carriers of TTR gene mutations

Amyloid, 2019-01, Vol.26 (1), p.3-9

2019

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Are post intracerebral hemorrhage seizures prevented by anti-epileptic treatment?

Epilepsy research, 2011-08, Vol.95 (3), p.227-231

2011

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Nitrous Oxide-induced Myeloneuropathy Due to Recreational Abuse

The Israel Medical Association journal, 2024-05, Vol.26 (5), p.294-298

2024

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Abdominal muscle weakness as a presenting symptom in GNE myopathy

Journal of clinical neuroscience, 2019-01, Vol.59, p.316-317

2019

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Auditory hallucinations in acute stroke

Behavioural neurology, 2005, Vol.16 (4), p.211-216

2005

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Intravenous administration of magnesium sulfate in acute stroke : A randomized double-blind study

Clinical neuropharmacology, 2001-01, Vol.24 (1), p.11-15

2001

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Clinical, epidemiological, genetic, and electrophysiological characteristics of transthyretin familial amyloid polyneuropathies in Israel

Orphanet journal of rare diseases, 2015-11, Vol.10 (S1), p.O5-O5, Article O5

2015

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Beneficial effect of albuterol in congenital myasthenic syndrome with epsilon‐subunit mutations

Muscle & nerve, 2011-08, Vol.44 (2), p.289-291

2011

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Cerebellar T2 hyperintensities in a patient with tremor

Neurology, 2008-02, Vol.70 (7), p.578

2008

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Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosis

Neurology, 2012-11, Vol.79 (22), p.2201

2012

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Low-level laser therapy applied transcranially to rats after induction of stroke significantly reduces long-term neurological deficits

Multi-system neurological disorder associated with a CRYAB variant

Congenital myasthenic syndrome in Israel: Genetic and clinical characterization

The proteomic profile of hereditary inclusion body myopathy

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features

Myotonia in DNM2-related centronuclear myopathy

Chronic non-paroxysmal neuropathic pain — Novel phenotype of mutation in the sodium channel SCN9A gene

A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B

Acute painful neuropathy induced by rapid correction of serum glucose levels in diabetic patients

Riboflavin-responsive lipid-storage myopathy in elderly patients

Apparent C8-T1 radiculopathy with hand weakness due to mid-cervical spondylosis

Neurodegeneration associated with genetic defects in phospholipase A2

Acute steroid responsive small-fiber sensory neuropathy: a new entity?

X-linked myopathy with excessive autophagy: First report of an Israeli family presenting with late onset lower limb girdle weakness

Early diagnosis of ATTR amyloidosis through targeted follow-up of identified carriers of TTR gene mutations

Are post intracerebral hemorrhage seizures prevented by anti-epileptic treatment?

Nitrous Oxide-induced Myeloneuropathy Due to Recreational Abuse

Abdominal muscle weakness as a presenting symptom in GNE myopathy

Auditory hallucinations in acute stroke

Intravenous administration of magnesium sulfate in acute stroke : A randomized double-blind study

Clinical, epidemiological, genetic, and electrophysiological characteristics of transthyretin familial amyloid polyneuropathies in Israel

Beneficial effect of albuterol in congenital myasthenic syndrome with epsilon‐subunit mutations

Cerebellar T2 hyperintensities in a patient with tremor

Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosis

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