Publicaciones (83) Publicaciones de GERMAN MORIS DE LA TASSA

2024

  1. Alternative splicing expands the clinical spectrum of NDUFS6-related mitochondrial disorders

    Genetics in Medicine, Vol. 26, Núm. 6

  2. Description of clinical and genetic features of 122 patients included in the Spanish Pompe registry

    Neuromuscular Disorders, Vol. 34, pp. 1-8

2023

  1. Hydrocephalus and myasthenia gravis: neurological manifestations in autoimmune polyendocrine syndrome type II

    Acta Neurologica Belgica

2022

  1. Drug-refractory myasthenia gravis: Clinical characteristics, treatments, and outcome

    Annals of Clinical and Translational Neurology, Vol. 9, Núm. 2, pp. 122-131

  2. Metrics of progression and prognosis in untreated adults with thymidine kinase 2 deficiency: An observational study

    Neuromuscular Disorders, Vol. 32, Núm. 9, pp. 728-735

  3. Muscle MRI characteristic pattern for late-onset TK2 deficiency diagnosis

    Journal of Neurology, Vol. 269, Núm. 7, pp. 3550-3562

  4. Smoking is associated with age at disease onset in Parkinson's disease

    Parkinsonism & related disorders, Vol. 97, pp. 79-83

2021

  1. Cancer in Parkinson's Disease: An Approximation to the Main Risk Factors

    Neurodegenerative Diseases, Vol. 21, Núm. 1-2, pp. 36-41

  2. Natural History, Phenotypic Spectrum, and Discriminative Features of Multisystemic RFC1 Disease

    Neurology, Vol. 96, Núm. 9, pp. e1369-e1382

  3. Recurrent rhabdomyolysis and exercise intolerance: A new phenotype of late-onset thymidine kinase 2 deficiency

    Molecular Genetics and Metabolism Reports, Vol. 26

2020

  1. Cervical myelopathy as a form of presentation of Whipple disease

    Neurologia

  2. Clinical and therapeutic features of myasthenia gravis in adults based on age at onset

    Neurology, Vol. 94, Núm. 11, pp. e1171-e1180

  3. Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease

    Neurologia, Vol. 35, Núm. 3, pp. 185-206

2019

  1. Current treatment practice of Guillain-Barré syndrome

    Neurology, Vol. 93, Núm. 1, pp. E59-E76

  2. HTT gene intermediate alleles in neurodegeneration: evidence for association with Alzheimer's disease

    Neurobiology of Aging, Vol. 76, pp. 215.e9-215.e14

  3. La anosognosia en la enfermedad de Alzheimer influye negativamente en los síntomas depresivos del cuidador

    RqR Enfermería Comunitaria, Vol. 7, Núm. 2, pp. 5-16

  4. Late-onset thymidine kinase 2 deficiency: A review of 18 cases

    Orphanet Journal of Rare Diseases, Vol. 14, Núm. 1

  5. Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy

    Journal of Neurology, Neurosurgery and Psychiatry, Vol. 90, Núm. 5, pp. 576-585

  6. Neuroinvasion of influenza A/H3N2: a fatal case in an immunocompetent adult

    Journal of NeuroVirology, Vol. 25, Núm. 2, pp. 275-279

  7. PDGF-BB serum levels are decreased in adult onset Pompe patients

    Scientific Reports, Vol. 9, Núm. 1