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Oncofetal H19 RNA promotes tumor metastasis

Biochimica et biophysica acta, 2014-07, Vol.1843 (7), p.1414-1426

2014

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A novel homozygous MSTO1 mutation in Ashkenazi Jewish siblings with ataxia and myopathy

Journal of human genetics, 2021-08, Vol.66 (8), p.835-840

2021

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The oncofetal H19 RNA connection: Hypoxia, p53 and cancer

Biochimica et biophysica acta, 2010-04, Vol.1803 (4), p.443-451

2010

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Complement-membrane regulatory proteins are absent from the nodes of Ranvier in the peripheral nervous system

Journal of neuroinflammation, 2023-10, Vol.20 (1), p.1-245, Article 245

2023

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Abundance of P‑glycoprotein and Breast Cancer Resistance Protein Measured by Targeted Proteomics in Human Epileptogenic Brain Tissue

Molecular pharmaceutics, 2021-06, Vol.18 (6), p.2263-2273

2021

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Liposomal Bupivacaine (Bupigel) Demonstrates Minimal Local Nerve Toxicity in a Rabbit Functional Model

Pharmaceutics, 2021-02, Vol.13 (2), p.185

2021

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Single Exon Skipping Can Address a Multi-Exon Duplication in the Dystrophin Gene

International journal of molecular sciences, 2020-06, Vol.21 (12), p.4511

2020

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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 myopathy is caused by mutation of HACD1

Human molecular genetics, 2013-12, Vol.22 (25), p.5229-5236

2013

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MicroRNAs as predictors for CNS relapse of systemic diffuse large B-cell lymphoma

Oncotarget, 2017-10, Vol.8 (49), p.86020-86030

2017

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Deep brain stimulation and bowstringing: Case report and pathological correlation

Interdisciplinary neurosurgery : Advanced techniques and case management, 2019-09, Vol.17, p.104-106

2019

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Congenital Hypotonia: Cracking a SAGA of consanguineous kindred harboring four genetic variants

Molecular genetics & genomic medicine, 2022-01, Vol.10 (1), p.e1849-n/a

2022

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Monitoring brain tumor vascular heamodynamic following anti-angiogenic therapy with advanced magnetic resonance imaging in mice

PloS one, 2014-12, Vol.9 (12), p.e115093

2014

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Olfactory Groove Schwannoma: A Case Report

Indian journal of neurosurgery, 2017-08, Vol.6 (2), p.153-154

2017

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NMO-IgG and AQP4 Peptide Can Induce Aggravation of EAMG and Immune-Mediated Muscle Weakness

Journal of Immunology Research, 2018-01, Vol.2018, p.5389282-10

2018

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Variable myopathic presentation in a single family with novel skeletal RYR1 mutation

PloS one, 2013-07, Vol.8 (7), p.e69296-e69296

2013

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Minocycline Effectively Protects the Rabbit’s Spinal Cord From Aortic Occlusion-Related Ischemia

Journal of cardiothoracic and vascular anesthesia, 2016-04, Vol.30 (2), p.282-290

2016

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Primary pleomorphic liposarcoma of the thoracic epidural space: case report

The spine journal, 2015-12, Vol.15 (12), p.e71-e75

2015

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Astrogliosis Induced by Brain Injury Is Regulated by Sema4B Phosphorylation

eNeuro, 2015-05, Vol.2 (3), p.ENEURO.0078-14.2015

2015

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Age-related changes in the morphology of the myenteric plexus of the human colon

Autonomic neuroscience, 2004-06, Vol.113 (1), p.71-78

2004

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Improvement of motor conduction velocity in hereditary neuropathy of LAMA2-CMD dy/dy mouse model by glatiramer acetate

Clinical neurophysiology, 2019-10, Vol.130 (10), p.1988-1994

2019

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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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Improvement of motor conduction velocity in hereditary neuropathy of LAMA2-CMD dy2J/dy2J mouse model by glatiramer acetate

Clinical neurophysiology, 2019-10, Vol.130 (10), p.1988-1994

2019

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CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathy

Blood, 2013-01, Vol.121 (1), p.129-135

2013

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Use of Colchicine for Pericardial Inflammation: Risks and Toxicities—A Cautionary Tale

JACC. Case reports, 2022-11, Vol.4 (21), p.1449-1452

2022

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Oncofetal H19 RNA promotes tumor metastasis

A novel homozygous MSTO1 mutation in Ashkenazi Jewish siblings with ataxia and myopathy

The oncofetal H19 RNA connection: Hypoxia, p53 and cancer

Complement-membrane regulatory proteins are absent from the nodes of Ranvier in the peripheral nervous system

Abundance of P‑glycoprotein and Breast Cancer Resistance Protein Measured by Targeted Proteomics in Human Epileptogenic Brain Tissue

Liposomal Bupivacaine (Bupigel) Demonstrates Minimal Local Nerve Toxicity in a Rabbit Functional Model

Single Exon Skipping Can Address a Multi-Exon Duplication in the Dystrophin Gene

Multi-system neurological disorder associated with a CRYAB variant

Congenital myopathy is caused by mutation of HACD1

MicroRNAs as predictors for CNS relapse of systemic diffuse large B-cell lymphoma

Deep brain stimulation and bowstringing: Case report and pathological correlation

Congenital Hypotonia: Cracking a SAGA of consanguineous kindred harboring four genetic variants

Monitoring brain tumor vascular heamodynamic following anti-angiogenic therapy with advanced magnetic resonance imaging in mice

Olfactory Groove Schwannoma: A Case Report

NMO-IgG and AQP4 Peptide Can Induce Aggravation of EAMG and Immune-Mediated Muscle Weakness

Variable myopathic presentation in a single family with novel skeletal RYR1 mutation

Minocycline Effectively Protects the Rabbit’s Spinal Cord From Aortic Occlusion-Related Ischemia

Primary pleomorphic liposarcoma of the thoracic epidural space: case report

Astrogliosis Induced by Brain Injury Is Regulated by Sema4B Phosphorylation

Age-related changes in the morphology of the myenteric plexus of the human colon

Improvement of motor conduction velocity in hereditary neuropathy of LAMA2-CMD dy/dy mouse model by glatiramer acetate

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

Improvement of motor conduction velocity in hereditary neuropathy of LAMA2-CMD dy2J/dy2J mouse model by glatiramer acetate

CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathy

Use of Colchicine for Pericardial Inflammation: Risks and Toxicities—A Cautionary Tale

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