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Therapeutic applications of the cell-penetrating HIV-1 Tat peptide

Drug discovery today, 2015-01, Vol.20 (1), p.76-85

2015

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MicroRNA Metabolism and Dysregulation in Amyotrophic Lateral Sclerosis

Molecular neurobiology, 2018-03, Vol.55 (3), p.2617-2630

2018

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MicroRNA expression analysis identifies a subset of downregulated miRNAs in ALS motor neuron progenitors

Scientific reports, 2018-07, Vol.8 (1), p.10105-12, Article 10105

2018

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Mutations in DNA2 Link Progressive Myopathy to Mitochondrial DNA Instability

American journal of human genetics, 2013-02, Vol.92 (2), p.293-300

2013

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Investigation of New Morpholino Oligomers to Increase Survival Motor Neuron Protein Levels in Spinal Muscular Atrophy

International journal of molecular sciences, 2018-01, Vol.19 (1), p.167

2018

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Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G>A mitochondrial DNA mutation: a case report

BMC neurology, 2011-07, Vol.11 (1), p.85-85, Article 85

2011

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Charcot–Marie‐Tooth type 2A in vivo models: Current updates

Journal of cellular and molecular medicine, 2024-05, Vol.28 (9), p.e18293-n/a

2024

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SARS-CoV-2 infection and Spike protein exposure alter iPSC-derived human brain organoid homeostasis

The Journal of immunology (1950), 2023-05, Vol.210 (1_Supplement), p.236-236.16

2023

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Cell-penetrating peptide-conjugated Morpholino rescues SMA in a symptomatic preclinical model

Molecular therapy, 2022-03, Vol.30 (3), p.1288-1299

2022

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Insights into the identification of a molecular signature for amyotrophic lateral sclerosis exploiting integrated microRNA profiling of iPSC-derived motor neurons and exosomes

Cellular and molecular life sciences : CMLS, 2022-03, Vol.79 (3), p.189-189, Article 189

2022

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Shaping the Neurovascular Unit Exploiting Human Brain Organoids

Molecular neurobiology, 2024-09, Vol.61 (9), p.6642-6657

2024

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miR-129-5p: A key factor and therapeutic target in amyotrophic lateral sclerosis

Progress in neurobiology, 2020-07, Vol.190, p.101803-101803, Article 101803

2020

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Exploiting the role of CSF NfL, CHIT1, and miR-181b as potential diagnostic and prognostic biomarkers for ALS

Journal of neurology, 2024-09

2024

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Genomic and transcriptomic advances in amyotrophic lateral sclerosis

Ageing research reviews, 2023-12, Vol.92, p.102126, Article 102126

2023

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Human spinal cord-like organoids to model C9ORF72 ALS and test new therapies in vitro

Journal of the neurological sciences, 2021-10, Vol.429, p.117761, Article 117761

2021

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MicroRNAs as serum biomarkers in Becker muscular dystrophy

Journal of cellular and molecular medicine, 2022-09, Vol.26 (17), p.4678-4685

2022

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Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions

Brain (London, England : 1878), 2012-11, Vol.135 (Pt 11), p.3404-3415

2012

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Exploiting Integrated miRNAs Analysis of Patient-derived iPSCs-Motor Neurons to Develop a Molecular Therapy for ALS (P4.430)

Neurology, 2018-04, Vol.90 (15_supplement)

2018

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Lower motor neuron disease with respiratory failure caused by a novel MAPT mutation

Neurology, 2014-06, Vol.82 (22), p.1990-1998

2014

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Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T>C mutation

Biochemical and biophysical research communications, 2011-08, Vol.412 (2), p.245-248

2011

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Two novel mutations in PEO1 (Twinkle) gene associated with chronic external ophthalmoplegia

Journal of the neurological sciences, 2011-09, Vol.308 (1), p.173-176

2011

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The novel mitochondrial tRNA super(Asn) gene mutation m.5709T>C produces ophthalmoparesis and respiratory impairment

European journal of human genetics : EJHG, 2012-03, Vol.20 (3), p.357-360

2012

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The novel mitochondrial tRNAAsn gene mutation m.5709T > C produces ophthalmoparesis and respiratory impairment

European journal of human genetics : EJHG, 2012-03, Vol.20 (3), p.357-360

2012

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Therapeutic applications of the cell-penetrating HIV-1 Tat peptide

MicroRNA Metabolism and Dysregulation in Amyotrophic Lateral Sclerosis

MicroRNA expression analysis identifies a subset of downregulated miRNAs in ALS motor neuron progenitors

Mutations in DNA2 Link Progressive Myopathy to Mitochondrial DNA Instability

Investigation of New Morpholino Oligomers to Increase Survival Motor Neuron Protein Levels in Spinal Muscular Atrophy

Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G>A mitochondrial DNA mutation: a case report

Charcot–Marie‐Tooth type 2A in vivo models: Current updates

SARS-CoV-2 infection and Spike protein exposure alter iPSC-derived human brain organoid homeostasis

Cell-penetrating peptide-conjugated Morpholino rescues SMA in a symptomatic preclinical model

Insights into the identification of a molecular signature for amyotrophic lateral sclerosis exploiting integrated microRNA profiling of iPSC-derived motor neurons and exosomes

Shaping the Neurovascular Unit Exploiting Human Brain Organoids

miR-129-5p: A key factor and therapeutic target in amyotrophic lateral sclerosis

Exploiting the role of CSF NfL, CHIT1, and miR-181b as potential diagnostic and prognostic biomarkers for ALS

Genomic and transcriptomic advances in amyotrophic lateral sclerosis

Human spinal cord-like organoids to model C9ORF72 ALS and test new therapies in vitro

MicroRNAs as serum biomarkers in Becker muscular dystrophy

Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions

Exploiting Integrated miRNAs Analysis of Patient-derived iPSCs-Motor Neurons to Develop a Molecular Therapy for ALS (P4.430)

Lower motor neuron disease with respiratory failure caused by a novel MAPT mutation

Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T>C mutation

Two novel mutations in PEO1 (Twinkle) gene associated with chronic external ophthalmoplegia

The novel mitochondrial tRNA super(Asn) gene mutation m.5709T>C produces ophthalmoparesis and respiratory impairment

The novel mitochondrial tRNAAsn gene mutation m.5709T > C produces ophthalmoparesis and respiratory impairment

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