Ricard Rojas‐García

Universitat Autònoma de Barcelona — Spain

Medicine · Health Sciences

40h-index5.6kcitations120works3.12yr avg
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Research Topics

Peripheral Neuropathies and Disorders(41), Amyotrophic Lateral Sclerosis Research(26), Myasthenia Gravis and Thymoma(23), Hereditary Neurological Disorders(23), Neurogenetic and Muscular Disorders Research(23)

Publications120 total

Challenges in myasthenia gravis diagnosis: an analysis of the diagnostic process of myasthenia gravis in a specialized clinic
Neuromuscular Disorders·2025
Novel DES mutation presenting with isolated restrictive respiratory failure. Expanding the clinical spectrum
Neurología (English Edition)·2025Open Access
Novel DES mutation presenting with isolated restrictive respiratory failure. Expanding the clinical spectrum
Neurología·2025Open Access
A Novel <scp><i>CHMP2B</i></scp> Splicing Variant in Atypical Presentation of Familial Frontotemporal Lobar Degeneration
Annals of Clinical and Translational Neurology·2025· 1 citedOpen Access
Amiloidosis hereditaria por transtirretina por la variante Val142Ile en España
Revista Española de Cardiología·2025· 2 cited
Single-cell RNA sequencing highlights the role of distinct natural killer subsets in sporadic amyotrophic lateral sclerosis
Journal of Neuroinflammation·2025· 7 citedOpen Access
Hereditary transthyretin amyloidosis caused by the Val142Ile variant in Spain
Revista Española de Cardiología (English Edition)·2025
Single-cell RNA sequencing highlights the role of distinct natural killer subsets in amyotrophic lateral sclerosis
2024Open Access
Persistent symptoms, exacerbations and drug side effects despite treatment in myasthenia gravis
European Journal of Neurology·2024· 8 citedOpen Access
Identification of a pathogenic mutation in<i>ARPP21</i>in patients with amyotrophic lateral sclerosis
Journal of Neurology Neurosurgery & Psychiatry·2024· 5 citedOpen Access
Inter-laboratory comparison of routine autoantibody detection methods for autoimmune neuropathies and myasthenia gravis
Journal of Neurology·2024· 4 cited
Clinicopathological correlates in the frontotemporal lobar degeneration–motor neuron disease spectrum
Brain·2024· 10 citedOpen Access
Muscle magnetic resonance imaging of a large cohort of distal hereditary motor neuropathies reveals characteristic features useful for diagnosis
Neuromuscular Disorders·2023· 8 citedOpen Access
Antibodies against the flotillin-1/2 complex in patients with multiple sclerosis
Brain Communications·2023· 2 citedOpen Access
Profiling TREM2 expression in amyotrophic lateral sclerosis
Brain Behavior and Immunity·2023· 28 citedOpen Access
Leptospirosis‐induced acute acquired inflammatory neuropathy
Journal of the Peripheral Nervous System·2022· 1 cited
Phenotype and clinical outcomes of Glu89Lys hereditary transthyretin amyloidosis: a new endemic variant in Spain
Amyloid·2022· 13 citedOpen Access
Validation of a Set of Instruments to Assess Patient- and Caregiver-Oriented Measurements in Spinal Muscular Atrophy: Results of the SMA-TOOL Study
Neurology and Therapy·2022· 23 citedOpen Access
Antibodies against the flotillin-1/2 complex in patients with multiple sclerosis
2022Open Access
Rituximab in myasthenia gravis: efficacy, associated infections and risk of induced hypogammaglobulinemia
Neuromuscular Disorders·2022· 21 cited
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Frequent Co-authors

Isabel Illa(31), Eduard Gallardo(23), Jordi Díaz‐Manera(22), Luís Querol(18), Elena Cortés‐Vicente(12), Jordi Clarimón(12), Janina Turón‐Sans(12), Noemí de Luna(11), Rafael Blesa(10), Alberto Lleó(10), Julio Pardo(9), Teresa Sevilla(9), Adolfo López de Munaín(8), Carmen Paradas(8), Carlos Casasnovas(8), Daniel Alcolea(8), Juan Fortea(8), José Luís Muñoz-Blanco(7), Oriol Dols‐Icardo(7), Xavier Suárez‐Calvet(6)