Lista de obras - Marina Scarlato - Dominio Público Uruguay

A fatal case of Churg–Strauss syndrome presenting with acute polyneuropathy mimicking Guillain–Barré syndrome

artículo científico publicado en 2011

A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutation

artículo científico publicado en 2014

A novel heat shock protein 27 homozygous mutation: widening of the continuum between MND/dHMN/CMT2.

artículo científico publicado en 2015

Absence of angiogenic genes modification in Italian ALS patients

artículo científico publicado en 2008

Analyzing Histopathological Features of Rare Charcot-Marie-Tooth Neuropathies to Unravel Their Pathogenesis

CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis

artículo científico publicado en 2015

Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations.

artículo científico publicado en 2011

Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15

artículo científico publicado en 2013

Diffuse intraneural leiomyoma in a case of sensorimotor neuropathy

artículo científico publicado en 2009

Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21.

artículo científico publicado en 2017

Hereditary Spastic Paraplegia: Beyond Clinical Phenotypes toward a Unified Pattern of Central Nervous System Damage

artículo científico publicado en 2015

ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases

artículo científico publicado en 2015

Induction of neuropilins-1 and -2 and their ligands, Sema3A, Sema3F, and VEGF, during Wallerian degeneration in the peripheral nervous system.

artículo científico publicado en 2003

Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy

artículo científico publicado en 2015

Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysis

artículo científico publicado en 2005

Is erythropoietin gene a modifier factor in amyotrophic lateral sclerosis?

artículo científico publicado en 2009

Motor nerve biopsy: Clinical usefulness and histopathological criteria

artículo científico publicado en 2010

Muscle MRI findings in facioscapulohumeral muscular dystrophy

artículo científico publicado en 2015

Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2.

artículo científico publicado en 2011

Neurolupus is associated with anti-ribosomal P protein antibodies: An inception cohort study

artículo científico publicado en 2009

Pentraxin-3 and VEGF in POEMS syndrome: a 2-year longitudinal study

artículo científico publicado en 2014

Polyneuropathy in POEMS syndrome: role of angiogenic factors in the pathogenesis

artículo científico publicado en 2005

Quantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measures

artículo científico publicado en 2012

Role of VEGF gene variability in longevity: A lesson from the Italian population

article

Spontaneous intracerebral hemorrhage in Urbach-Wiethe disease

artículo científico publicado en 2012

Subcutaneous immunoglobulin therapy for the treatment of multifocal motor neuropathy: a case report

artículo científico publicado en 2010

The extracellular matrix affects axonal regeneration in peripheral neuropathies.

artículo científico publicado en 2008

Urokinase plasminogen receptor and the fibrinolytic complex play a role in nerve repair after nerve crush in mice, and in human neuropathies

artículo científico publicado en 2012

VEGF gene variability and type 1 diabetes: evidence for a protective role

artículo científico publicado en 2006

Vascular endothelial growth factor gene variability is associated with increased risk for AD.

artículo científico publicado en 2005

Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias

artículo científico publicado en 2010

Lista de obras de Marina Scarlato

A fatal case of Churg–Strauss syndrome presenting with acute polyneuropathy mimicking Guillain–Barré syndrome

A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutation

A novel heat shock protein 27 homozygous mutation: widening of the continuum between MND/dHMN/CMT2.

Absence of angiogenic genes modification in Italian ALS patients

Analyzing Histopathological Features of Rare Charcot-Marie-Tooth Neuropathies to Unravel Their Pathogenesis

CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis

Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations.

Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15

Diffuse intraneural leiomyoma in a case of sensorimotor neuropathy

Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21.

Hereditary Spastic Paraplegia: Beyond Clinical Phenotypes toward a Unified Pattern of Central Nervous System Damage

ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases

Induction of neuropilins-1 and -2 and their ligands, Sema3A, Sema3F, and VEGF, during Wallerian degeneration in the peripheral nervous system.

Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy

Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysis

Is erythropoietin gene a modifier factor in amyotrophic lateral sclerosis?

Motor nerve biopsy: Clinical usefulness and histopathological criteria

Muscle MRI findings in facioscapulohumeral muscular dystrophy

Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2.

Neurolupus is associated with anti-ribosomal P protein antibodies: An inception cohort study

Pentraxin-3 and VEGF in POEMS syndrome: a 2-year longitudinal study

Polyneuropathy in POEMS syndrome: role of angiogenic factors in the pathogenesis

Quantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measures

Role of VEGF gene variability in longevity: A lesson from the Italian population

Spontaneous intracerebral hemorrhage in Urbach-Wiethe disease

Subcutaneous immunoglobulin therapy for the treatment of multifocal motor neuropathy: a case report

The extracellular matrix affects axonal regeneration in peripheral neuropathies.

Urokinase plasminogen receptor and the fibrinolytic complex play a role in nerve repair after nerve crush in mice, and in human neuropathies

VEGF gene variability and type 1 diabetes: evidence for a protective role

Vascular endothelial growth factor gene variability is associated with increased risk for AD.

Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias