Lista de obras - Martina Minnerop - Dominio Público Uruguay

A randomized pilot study of stochastic vibration therapy in spinocerebellar ataxia

artículo científico publicado en 2014

Accuracy and repeatability of two methods of gait analysis - GaitRite™ und Mobility Lab™ - in subjects with cerebellar ataxia

artículo científico publicado en 2016

Alexithymia in healthy young men: a voxel-based morphometric study

artículo científico publicado en 2011

Ataxia with oculomotor apraxia type 2: novel mutations in six patients with juvenile age of onset and elevated serum alpha-fetoprotein.

artículo científico publicado en 2008

Autosomal recessive cerebellar ataxia 3 due to homozygote c.132dupA mutation within the ANO10 gene

artículo científico publicado en 2015

Bell's palsy: combined treatment of famciclovir and prednisone is superior to prednisone alone

artículo científico publicado en 2008

Brain morphometry shows effects of long-term musical practice in middle-aged keyboard players.

artículo científico publicado en 2013

CNS infection with Chlamydia pneumoniae complicated by multiple strokes

artículo científico publicado en 2002

Callosal tissue loss in multiple system atrophy--a one-year follow-up study

artículo científico publicado en 2010

Cerebellar Involvement in DYT-THAP1 Dystonia

artículo científico publicado en 2019

Cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency

artículo científico publicado en 2015

Cerebellar pathology in Friedreich's ataxia: atrophied dentate nuclei with normal iron content.

artículo científico publicado en 2014

Clinical and neurophysiological profile of four German families with spinocerebellar ataxia type 14

artículo científico publicado en 2014

Current Progress in CNS Imaging of Myotonic Dystrophy

Cytoarchitectonic mapping of the human brain cerebellar nuclei in stereotaxic space and delineation of their co-activation patterns

artículo científico publicado en 2015

Derivation of Fiber Orientations From Oblique Views Through Human Brain Sections in 3D-Polarized Light Imaging

Dopamine transporter positron emission tomography in spinocerebellar ataxias type 1, 2, 3, and 6.

artículo científico publicado en 2005

Dual task effect on postural control in patients with degenerative cerebellar disorders

artículo científico publicado en 2015

Early signs of VCP-related frontotemporal dementia: a neuropsychological, FDG-PET and fMRI study

scholarly article by Elke Kalbe et al published 12 October 2010 in Journal of Neurology

Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2.

artículo científico publicado en 2009

Expanded phenotype and hippocampal involvement in a novel compound heterozygosity of adult PLA2G6 associated neurodegeneration (PARK14).

artículo científico publicado en 2017

Experience in a short-term trial with 4-aminopyridine in cerebellar ataxia.

artículo científico publicado en 2013

Feasibility of 2-deoxy-2-[18F]fluoro-D-glucose- A85380-PET for imaging of human cardiac nicotinic acetylcholine receptors in vivo

artículo científico publicado en 2006

G.P.130

Grey and white matter loss along cerebral midline structures in myotonic dystrophy type 2.

artículo científico publicado en 2008

Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia

artículo científico publicado en 2017

In Vivo Voxel-Based Morphometry in Multiple System Atrophy of the Cerebellar Type ⬇️

artículo científico publicado el 1 de octubre de 2003

In vitro evaluation of nicotinic acetylcholine receptors with 2-[18F]F-A85380 in Parkinson's disease

artículo científico publicado en 2006

In vivo voxel-based relaxometry in amyotrophic lateral sclerosis

artículo científico publicado en 2009

Investigation of Visual System Involvement in Spinocerebellar Ataxia Type 14

scientific article published on 27 April 2020

Longitudinal changes in brains of patients with fluent primary progressive aphasia

artículo científico publicado en 2013

Neurochemical Differences in Spinocerebellar Ataxia Type 14 and 1

artículo científico publicado en 2020

Neuropsychological features of patients with spinocerebellar ataxia (SCA) types 1, 2, 3, and 6.

artículo científico publicado en 2010

Never neglect inspecting the leg in movement disorders

artículo científico publicado en 2012

Progressive cognitive dysfunction in spinocerebellar ataxia type 3.

artículo científico publicado en 2013

REM sleep behavioral disorder in pure autonomic failure (PAF).

artículo científico publicado en 2006

Reference values for the Cerebellar Cognitive Affective Syndrome Scale: age and education matter

artículo científico publicado en 2020

Reply to: Cognitive dysfunction in spinocerebellar ataxia type 3: variable topographies and patterns.

artículo científico publicado en 2013

Reply: Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis

artículo científico publicado en 2019

Reply: POLR3A variants in hereditary spastic paraplegia and ataxia

artículo científico publicado en 2017

Smoking upregulates alpha4beta2* nicotinic acetylcholine receptors in the human brain

artículo científico publicado en 2007

Stochastic resonance therapy in Parkinson's disease

artículo científico publicado en 2011

Structural and functional MRI abnormalities of cerebellar cortex and nuclei in SCA3, SCA6 and Friedreich's ataxia

artículo científico publicado en 2015

Studying variability in human brain aging in a population-based German cohort—rationale and design of 1000BRAINS

artículo científico publicado en 2014

The brain in myotonic dystrophy 1 and 2: evidence for a predominant white matter disease

artículo científico publicado en 2011

The genetics of spinocerebellar ataxias

artículo científico publicado en 2013

The time course of neurolinguistic and neuropsychological symptoms in three cases of logopenic primary progressive aphasia

artículo científico

Tracking the brain in myotonic dystrophies: A 5-year longitudinal follow-up study

Validation of a German version of the Cerebellar Cognitive Affective/ Schmahmann Syndrome Scale: preliminary version and study protocol

artículo científico publicado en 2020

Voxel-based analysis of multiple-system atrophy of cerebellar type: complementary results by combining voxel-based morphometry and voxel-based relaxometry

artículo científico publicado en 2005

Lista de obras de Martina Minnerop

A randomized pilot study of stochastic vibration therapy in spinocerebellar ataxia

Accuracy and repeatability of two methods of gait analysis - GaitRite™ und Mobility Lab™ - in subjects with cerebellar ataxia

Alexithymia in healthy young men: a voxel-based morphometric study

Ataxia with oculomotor apraxia type 2: novel mutations in six patients with juvenile age of onset and elevated serum alpha-fetoprotein.

Autosomal recessive cerebellar ataxia 3 due to homozygote c.132dupA mutation within the ANO10 gene

Bell's palsy: combined treatment of famciclovir and prednisone is superior to prednisone alone

Brain morphometry shows effects of long-term musical practice in middle-aged keyboard players.

CNS infection with Chlamydia pneumoniae complicated by multiple strokes

Callosal tissue loss in multiple system atrophy--a one-year follow-up study

Cerebellar Involvement in DYT-THAP1 Dystonia

Cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency

Cerebellar pathology in Friedreich's ataxia: atrophied dentate nuclei with normal iron content.

Clinical and neurophysiological profile of four German families with spinocerebellar ataxia type 14

Current Progress in CNS Imaging of Myotonic Dystrophy

Cytoarchitectonic mapping of the human brain cerebellar nuclei in stereotaxic space and delineation of their co-activation patterns

Derivation of Fiber Orientations From Oblique Views Through Human Brain Sections in 3D-Polarized Light Imaging

Dopamine transporter positron emission tomography in spinocerebellar ataxias type 1, 2, 3, and 6.

Dual task effect on postural control in patients with degenerative cerebellar disorders

Early signs of VCP-related frontotemporal dementia: a neuropsychological, FDG-PET and fMRI study

Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2.

Expanded phenotype and hippocampal involvement in a novel compound heterozygosity of adult PLA2G6 associated neurodegeneration (PARK14).

Experience in a short-term trial with 4-aminopyridine in cerebellar ataxia.

Feasibility of 2-deoxy-2-[18F]fluoro-D-glucose- A85380-PET for imaging of human cardiac nicotinic acetylcholine receptors in vivo

G.P.130

Grey and white matter loss along cerebral midline structures in myotonic dystrophy type 2.

Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia

In Vivo Voxel-Based Morphometry in Multiple System Atrophy of the Cerebellar Type ⬇️

In vitro evaluation of nicotinic acetylcholine receptors with 2-[18F]F-A85380 in Parkinson's disease

In vivo voxel-based relaxometry in amyotrophic lateral sclerosis

Investigation of Visual System Involvement in Spinocerebellar Ataxia Type 14

Longitudinal changes in brains of patients with fluent primary progressive aphasia

Neurochemical Differences in Spinocerebellar Ataxia Type 14 and 1

Neuropsychological features of patients with spinocerebellar ataxia (SCA) types 1, 2, 3, and 6.

Never neglect inspecting the leg in movement disorders

Progressive cognitive dysfunction in spinocerebellar ataxia type 3.

REM sleep behavioral disorder in pure autonomic failure (PAF).

Reference values for the Cerebellar Cognitive Affective Syndrome Scale: age and education matter

Reply to: Cognitive dysfunction in spinocerebellar ataxia type 3: variable topographies and patterns.

Reply: Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis

Reply: POLR3A variants in hereditary spastic paraplegia and ataxia

Smoking upregulates alpha4beta2* nicotinic acetylcholine receptors in the human brain

Stochastic resonance therapy in Parkinson's disease

Structural and functional MRI abnormalities of cerebellar cortex and nuclei in SCA3, SCA6 and Friedreich's ataxia

Studying variability in human brain aging in a population-based German cohort—rationale and design of 1000BRAINS

The brain in myotonic dystrophy 1 and 2: evidence for a predominant white matter disease

The genetics of spinocerebellar ataxias

The time course of neurolinguistic and neuropsychological symptoms in three cases of logopenic primary progressive aphasia

Tracking the brain in myotonic dystrophies: A 5-year longitudinal follow-up study

Validation of a German version of the Cerebellar Cognitive Affective/ Schmahmann Syndrome Scale: preliminary version and study protocol

Voxel-based analysis of multiple-system atrophy of cerebellar type: complementary results by combining voxel-based morphometry and voxel-based relaxometry