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Creutzfeldt-Jakob Disease as a Novel Cause of Wing-Beating Tremor

JAMA neurology, 2021-02, Vol.78 (2), p.249

Álvarez Bravo, Gary

2021

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Progressive multifocal leukoencephalopathy in a patient with relapsing multiple sclerosis treated with ocrelizumab: A case report

European journal of neurology, 2023-10, Vol.30 (10), p.3357-3361

2023

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Sphingosine-1-Phosphate (S1P) and S1P Signaling Pathway Modulators, from Current Insights to Future Perspectives

Cells (Basel, Switzerland), 2022-06, Vol.11 (13), p.2058

2022

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A new phenotype of myorhythmia: Oculofacial myorhythmia in a patient with Erdheim Chester disease

Parkinsonism & related disorders, 2023-11, Vol.116, p.105889, Article 105889

Álvarez-Bravo, Gary

2023

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Clinical and radiological features of cerebral amyloid angiopathy-related inflammation

Neurological sciences, 2021-12, Vol.42 (12), p.5353-5358

2021

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The nature of memory impairment in multiple sclerosis: understanding different patterns over the course of the disease

Frontiers in psychology, 2024-01, Vol.14, p.1269794-1269794

2024

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Clinical heterogeneity in patients with myoclonus associated to COVID-19

Neurological sciences, 2022-03, Vol.43 (3), p.1587-1592

2022

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Differences in metacognition between multiple sclerosis phenotypes: cognitive impairment and fatigue are key factors

Frontiers in psychology, 2023-08, Vol.14, p.1163112-1163112

2023

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Assessing the presence of oligoclonal IgM bands as a prognostic biomarker of cognitive decline in the early stages of multiple sclerosis

Brain and behavior, 2021-12, Vol.11 (12), p.e2405-n/a

2021

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The adult motor phenotype of Dravet syndrome is associated with mutation of the STXBP1 gene and responds well to cannabidiol treatment

Seizure (London, England), 2018-08, Vol.60, p.68-70

2018

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Hiperintensidad reversible en los pedúnculos cerebelosos medios. Un hallazgo infrecuente en la enfermedad de Marchiafava-Bignami

Revista de neurologiá, 2023-11, Vol.77 (9), p.227-228

2023

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Cerebellopathy secondary to anti-peroxidase antibody-mediated toxicity. A special case of Hashimoto encephalopathy

Journal of neuroimmunology, 2017-11, Vol.312, p.1-3

2017

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Iatrogenic Shapiro syndrome: a case report

Neurological sciences, 2024-03, Vol.45 (3), p.1267-1270

2024

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Reversible hyperintensity in middle cerebellar peduncles. An infrequent finding in Marchiafava-Bignami disease

Revista de neurologiá, 2023-11, Vol.77 (9), p.227-228

2023

Volltextzugriff (PDF)

A Novel Clinical Phenotype of Fragile X‐Associated Tremor/Ataxia Syndrome

Movement disorders clinical practice (Hoboken, N.J.), 2018-07, Vol.5 (4), p.430-432

2018

Volltextzugriff (PDF)

A new phenotype of myorhythmia: Oculofacial myorhythmia in a patient with Erdheim Chester disease

Parkinsonism & related disorders, 2023, Vol.116, p.105889-105889

Álvarez-Bravo, Gary

2023

Volltextzugriff (PDF)

Intravenous Fibrinolysis in Ischemic Stroke of Large Vessel after Reversing Effect of Dabigatran with Idarucizumab

Journal of stroke and cerebrovascular diseases, 2017-09, Vol.26 (9), p.e192-e193

2017

Volltextzugriff (PDF)

A Novel Clinical Phenotype of Fragile X-Associated Tremor/Ataxia Syndrome

Movement disorders clinical practice, 2018, Vol.5 (4), p.430-432

2018

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Creutzfeldt-Jakob Disease as a Novel Cause of Wing-Beating Tremor

Progressive multifocal leukoencephalopathy in a patient with relapsing multiple sclerosis treated with ocrelizumab: A case report

Sphingosine-1-Phosphate (S1P) and S1P Signaling Pathway Modulators, from Current Insights to Future Perspectives

A new phenotype of myorhythmia: Oculofacial myorhythmia in a patient with Erdheim Chester disease

Clinical and radiological features of cerebral amyloid angiopathy-related inflammation

The nature of memory impairment in multiple sclerosis: understanding different patterns over the course of the disease

Clinical heterogeneity in patients with myoclonus associated to COVID-19

Differences in metacognition between multiple sclerosis phenotypes: cognitive impairment and fatigue are key factors

Assessing the presence of oligoclonal IgM bands as a prognostic biomarker of cognitive decline in the early stages of multiple sclerosis

The adult motor phenotype of Dravet syndrome is associated with mutation of the STXBP1 gene and responds well to cannabidiol treatment

Hiperintensidad reversible en los pedúnculos cerebelosos medios. Un hallazgo infrecuente en la enfermedad de Marchiafava-Bignami

Cerebellopathy secondary to anti-peroxidase antibody-mediated toxicity. A special case of Hashimoto encephalopathy

Iatrogenic Shapiro syndrome: a case report

Reversible hyperintensity in middle cerebellar peduncles. An infrequent finding in Marchiafava-Bignami disease

COVID19-associated new-onset movement disorders: a follow-up study

A Novel Clinical Phenotype of Fragile X‐Associated Tremor/Ataxia Syndrome

A new phenotype of myorhythmia: Oculofacial myorhythmia in a patient with Erdheim Chester disease

Intravenous Fibrinolysis in Ischemic Stroke of Large Vessel after Reversing Effect of Dabigatran with Idarucizumab

A Novel Clinical Phenotype of Fragile X-Associated Tremor/Ataxia Syndrome

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