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LRRK2 delays degradative receptor trafficking by impeding late endosomal budding through decreasing Rab7 activity

Human molecular genetics, 2014-12, Vol.23 (25), p.6779-6796

2014

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Dermic-derived fibroblasts for the study of amyotrophic lateral sclerosis

Neural regeneration research, 2020-11, Vol.15 (11), p.2043-2044

2020

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Genealogy of the neurodegenerative diseases based on a meta-analysis of age-stratified incidence data

Scientific reports, 2020-11, Vol.10 (1), p.18923-18923, Article 18923

2020

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Clinical and preclinical evidence of somatosensory involvement in amyotrophic lateral sclerosis

British journal of pharmacology, 2021-03, Vol.178 (6), p.1257-1268

2021

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RAB8, RAB10 and RILPL1 contribute to both LRRK2 kinase-mediated centrosomal cohesion and ciliogenesis deficits

Human molecular genetics, 2019-11, Vol.28 (21), p.3552-3568

2019

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Progranulin deficiency induces overactivation of WNT5A expression via TNF-α/NF-κB pathway in peripheral cells from frontotemporal dementia-linked granulin mutation carriers

Journal of psychiatry & neuroscience, 2016-07, Vol.41 (4), p.225-239

2016

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Amyotrophic lateral sclerosis: a complex syndrome that needs an integrated research approach

Neural regeneration research, 2019-02, Vol.14 (2), p.193-196

2019

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Association between total, processed, red and white meat consumption and all-cause, CVD and IHD mortality: a meta-analysis of cohort studies

British journal of nutrition, 2014-09, Vol.112 (5), p.762-775

2014

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ALS: A bucket of genes, environment, metabolism and unknown ingredients

Progress in neurobiology, 2016-07, Vol.142, p.104-129

2016

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Circulating microparticles reflect treatment effects and clinical status in multiple sclerosis

Biomarkers in medicine, 2014-06, Vol.8 (5), p.653-661

2014

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The increasing importance of environmental conditions in amyotrophic lateral sclerosis

International journal of biometeorology, 2018-08, Vol.62 (8), p.1361-1374

2018

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Amyotrophic lateral sclerosis (ALS), cancer, autoimmunity and metabolic disorders: An unsolved tantalizing challenge

British journal of pharmacology, 2021-03, Vol.178 (6), p.1269-1278

2021

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Impaired Mitophagy and Protein Acetylation Levels in Fibroblasts from Parkinson’s Disease Patients

Molecular neurobiology, 2019-04, Vol.56 (4), p.2466-2481

2019

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Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy

Nature communications, 2016-04, Vol.7 (1), p.11067-11067, Article 11067

2016

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Common Characteristics Between Frailty and Myotonic Dystrophy Type 1: A Narrative Review

Aging and disease, 2025-09

2025

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Neuropathology of Parkinson's disease with the R1441G mutation in LRRK2

Movement disorders, 2009-10, Vol.24 (13), p.1998-2001

2009

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Retinoids and Amyotrophic Lateral Sclerosis

JAMA neurology, 2018-09, Vol.75 (9), p.1153

2018

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Nonsense mutations in alpha-II spectrin in three families with juvenile onset hereditary motor neuropathy

Brain (London, England : 1878), 2019-09, Vol.142 (9), p.2605-2616

2019

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Assessing the role of TUBA4A gene in frontotemporal degeneration

Neurobiology of aging, 2016-02, Vol.38, p.215.e13-215.e14

2016

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Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia

Human genetics, 2012-03, Vol.131 (3), p.435-442

2012

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Oncogenicity of the Developmental Transcription Factor Sox9

Cancer research (Chicago, Ill.), 2012-03, Vol.72 (5), p.1301-1315

2012

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Genetic and epigenetic modifications of Sox2 contribute to the invasive phenotype of malignant gliomas

PloS one, 2011-11, Vol.6 (11), p.e26740

2011

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LRRK2 delays degradative receptor trafficking by impeding late endosomal budding through decreasing Rab7 activity

Dermic-derived fibroblasts for the study of amyotrophic lateral sclerosis

Genealogy of the neurodegenerative diseases based on a meta-analysis of age-stratified incidence data

Clinical and preclinical evidence of somatosensory involvement in amyotrophic lateral sclerosis

RAB8, RAB10 and RILPL1 contribute to both LRRK2 kinase-mediated centrosomal cohesion and ciliogenesis deficits

Progranulin deficiency induces overactivation of WNT5A expression via TNF-α/NF-κB pathway in peripheral cells from frontotemporal dementia-linked granulin mutation carriers

Amyotrophic lateral sclerosis: a complex syndrome that needs an integrated research approach

Association between total, processed, red and white meat consumption and all-cause, CVD and IHD mortality: a meta-analysis of cohort studies

ALS: A bucket of genes, environment, metabolism and unknown ingredients

Circulating microparticles reflect treatment effects and clinical status in multiple sclerosis

The increasing importance of environmental conditions in amyotrophic lateral sclerosis

Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism

Amyotrophic lateral sclerosis (ALS), cancer, autoimmunity and metabolic disorders: An unsolved tantalizing challenge

Clinical correlations with Lewy body pathology in LRRK2-related Parkinson disease

Impaired Mitophagy and Protein Acetylation Levels in Fibroblasts from Parkinson’s Disease Patients

Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy

Common Characteristics Between Frailty and Myotonic Dystrophy Type 1: A Narrative Review

Neuropathology of Parkinson's disease with the R1441G mutation in LRRK2

Retinoids and Amyotrophic Lateral Sclerosis

Nonsense mutations in alpha-II spectrin in three families with juvenile onset hereditary motor neuropathy

Assessing the role of TUBA4A gene in frontotemporal degeneration

Altered tubulin detyrosination due to SVBP malfunction induces cytokinesis failure and senescence, underlying a complex hereditary spastic paraplegia

Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia

Oncogenicity of the Developmental Transcription Factor Sox9

Genetic and epigenetic modifications of Sox2 contribute to the invasive phenotype of malignant gliomas

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