GERMAN
MORIS DE LA TASSA
Profesor Asociado en CC. Salud - LOSU
Hospital de la Santa Creu i Sant Pau
Barcelona, EspañaPublicaciones en colaboración con investigadores/as de Hospital de la Santa Creu i Sant Pau (12)
2024
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Description of clinical and genetic features of 122 patients included in the Spanish Pompe registry
Neuromuscular Disorders, Vol. 34, pp. 1-8
2022
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Drug-refractory myasthenia gravis: Clinical characteristics, treatments, and outcome
Annals of Clinical and Translational Neurology, Vol. 9, Núm. 2, pp. 122-131
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Muscle MRI characteristic pattern for late-onset TK2 deficiency diagnosis
Journal of Neurology, Vol. 269, Núm. 7, pp. 3550-3562
2020
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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
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Late-onset thymidine kinase 2 deficiency: A review of 18 cases
Orphanet Journal of Rare Diseases, Vol. 14, Núm. 1
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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
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PDGF-BB serum levels are decreased in adult onset Pompe patients
Scientific Reports, Vol. 9, Núm. 1
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Study of the effect of anti-rhGAA antibodies at low and intermediate titers in late onset Pompe patients treated with ERT
Molecular Genetics and Metabolism, Vol. 128, Núm. 1-2, pp. 129-136
2018
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Regional variation of Guillain-Barré syndrome
Brain, Vol. 141, Núm. 10, pp. 2866-2877
2017
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International Guillain-Barré Syndrome Outcome Study: protocol of a prospective observational cohort study on clinical and biological predictors of disease course and outcome in Guillain-Barré syndrome
Journal of the Peripheral Nervous System, Vol. 22, Núm. 2, pp. 68-76
2015
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Autoimmune post-herpes simplex encephalitis of adults and teenagers
Neurology, Vol. 85, Núm. 20, pp. 1736-1743
1998
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The distinctive headache of the occipital condyle syndrome: A report of four cases
Headache, Vol. 38, Núm. 4, pp. 308-311