List of works - Marina Scarlato

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

scientific article published on 30 April 2011

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

scientific article published on 16 December 2014

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

scientific article published in December 2015

Absence of angiogenic genes modification in Italian ALS patients

scientific article published in February 2008

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

CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis

scientific article published on 8 January 2015

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

scientific article published on 31 January 2011

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

scientific article published on 11 September 2013

Diffuse intraneural leiomyoma in a case of sensorimotor neuropathy

scientific article published on 17 March 2009

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

scientific article published on 27 July 2017

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

scientific article published on 22 January 2015

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

scientific article published on 24 September 2015

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

scientific article published in October 2003

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

scientific article

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

scientific article

Is erythropoietin gene a modifier factor in amyotrophic lateral sclerosis?

scientific article published in May 2009

Motor nerve biopsy: Clinical usefulness and histopathological criteria

scientific article published on 12 November 2010

Muscle MRI findings in facioscapulohumeral muscular dystrophy

scientific article published on 27 June 2015

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

scientific article

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

scientific article published on 25 January 2009

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

scientific article published on 05 October 2014

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

scientific article published on 23 June 2005

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

scientific article

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

article

Spontaneous intracerebral hemorrhage in Urbach-Wiethe disease

scientific article published on 3 October 2012

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

scientific article published on 24 June 2010

The extracellular matrix affects axonal regeneration in peripheral neuropathies.

scientific article published in July 2008

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

scientific article

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

scientific article published in March 2006

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

scientific article published in March 2005

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

scientific article published on 16 November 2010

List of works by 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