Search Results - "Ruxandra Iancu Ferfoglia"

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    Sporadic late onset nemaline myopathy with monoclonal gammopathy of undetermined significance: two cases with long term stability by Truffert, André, Iancu Ferfoglia, Ruxandra, Lobrinus, Johannes Alexander, Samii, Kaveh, Kohler, André

    Published in European journal of translational myology (16-09-2020)
    “…Monoclonal gammopathy of undetermined significance (MGUS) associated to sporadic late onset nemaline myopathy (SLONM) is a rare and severely disabling…”
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    Journal Article
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    Long-term efficacy of rituximab in IgM anti-myelin-associated glycoprotein neuropathy: RIMAG follow-up study by Iancu Ferfoglia, Ruxandra, Guimarães-Costa, Raquel, Viala, Karine, Musset, Lucile, Neil, Jean, Marin, Benoit, Léger, Jean-Marc

    Published in Journal of the peripheral nervous system (01-03-2016)
    “…The Rituximab vs. Placebo in Polyneuropathy Associated With Anti‐MAG IgM Monoclonal Gammopathy (RIMAG) study showed no improvement using the inflammatory…”
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    Journal Article
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    The pathogenesis of multifocal motor neuropathy and an update on current management options by Léger, Jean-Marc, Guimarães-Costa, Raquel, Iancu Ferfoglia, Ruxandra

    “…Multifocal motor neuropathy (MMN) is a rare and disabling disease. Several experimental studies and clinical data are strongly suggestive of an immune-mediated…”
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    Book Review Journal Article
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    Impaired conduction of Ia sensory fibers in multifocal motor neuropathy: An electrophysiological demonstration by Sukockienė, Eglė, Magistris, Michel R., Iancu Ferfoglia, Ruxandra, Lascano, Agustina M., Truffert, André

    Published in Clinical neurophysiology practice (01-01-2020)
    “…•Tendon areflexia may be observed in otherwise asymptomatic lower limbs, in patients with Multifocal Motor Neuropathy.•Sensory afferent pathways can be…”
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    Journal Article
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    Gait Performance and Use of Mental Imagery as a Measure of Disease Progression in Amyotrophic Lateral Sclerosis by Iancu Ferfoglia, Ruxandra, Heritier Barras, Anne-Chantal, Pollak, Pierre, Janssens, Jean-Paul, Pradat, Pierre-Francois, Allali, Gilles

    Published in European neurology (01-01-2016)
    “…Gait and balance are key determinants of disease status in amyotrophic lateral sclerosis (ALS). This study aims at testing the relationship between the imagery…”
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    Journal Article
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    Combined tendon reflex and motor evoked potential recordings in amyotrophic lateral sclerosis by Truffert, André, Sukockienė, Eglė, Desmaison, Annaïck, Ališauskienė, Miglė, Iancu Ferfoglia, Ruxandra, Guy, Nathalie

    Published in Clinical neurophysiology (01-03-2023)
    “…[Display omitted] •Combined tendon reflex and MEP recordings improve ALS diagnosis.•Corticospinal conduction time to lower limbs increases in…”
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    Journal Article
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    Does executive functioning contribute to locomotion in amyotrophic lateral sclerosis patients? by SukockienĖ, EglĖ, Allali, Gilles, Janssens, Jean-Paul, Iancu Ferfoglia, Ruxandra

    “…Amyotrophic lateral sclerosis (ALS) is associated with co-existing motor and cognitive impairment in almost half of the patients; however, the relationship…”
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    Journal Article
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    Longitudinal Timed Up and Go Assessment in Amyotrophic Lateral Sclerosis: A Pilot Study by Sukockienė, Eglė, Ferfoglia, Ruxandra Iancu, Poncet, Antoine, Janssens, Jean-Paul, Allali, Gilles

    Published in European neurology (2021)
    “…Progressive loss of walking ability in amyotrophic lateral sclerosis (ALS) has been scarcely studied as a potential predictive factor for survival in motor…”
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    Journal Article
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    Sporadic late onset nemaline myopathy with monoclonal gammopathy of undetermined significance: two cases with long term stability by Truffert, André, Iancu Ferfoglia, Ruxandra, Lobrinus, Johannes Alexander, Samii, Kaveh, Kohler, André

    Published in European journal of translational myology (16-09-2020)
    “…Monoclonal gammopathy of undetermined significance (MGUS) associated to sporadic late onset nemaline myopathy (SLONM) is a rare and severely disabling…”
    Get full text
    Journal Article
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    Should patients with ALS gain weight during their follow-up? by Héritier, Anne-Chantal, M.D, Janssens, Jean-Paul, M.D, Adler, Dan, M.D, Ferfoglia, Ruxandra Iancu, M.D, Genton, Laurence, M.D

    “…Abstract It was recently postulated that a nutritional intervention aiming at achieving weight gain might increase survival in ALS patients. This article…”
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    Journal Article
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    Is tracheostomy still an option in amyotrophic lateral sclerosis? by Anne-Chantal Heritier-Barras, Dan Adler, Ruxandra Iancu Ferfoglia, Bara Ricou, Yvan Gasche, Igor Leuchter, Samia Hurst, Monica Escher-Imhof, Pierre Pollak, Jean-Paul Janssens

    Published in Swiss medical weekly (07-08-2013)
    “…QUESTION UNDER STUDY: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease with a poor prognosis. Survival and quality of life of ALS…”
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    Journal Article
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    Minimal supportive treatment in natalizumab-related PML in a MS patient by Lalive, Patrice H, Bridel, Claire, Ferfoglia, Ruxandra Iancu, Kaiser, Laurent, Du Pasquier, Renaud, Barkhof, Frederik, Haller, Sven

    “…A second spinal tap revealed a positive JCV DNA by PCR and confirmed the diagnosis of PML. Since the spontaneous washout of NTZ is expected to be completed 3…”
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    Journal Article
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    Paraneoplastic neurological syndromes: an update by Zekeridou, Anastasia, Ferfoglia, Ruxandra Iancu, Du Pasquier, Renaud, Lalive, Patrice H

    Published in Revue médicale suisse (27-04-2016)
    “…Paraneoplastic neurological syndromes are a group of neurological syndromes secondary to an underlying malignancy. Associated autoantibodies can be classified…”
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    Journal Article
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    Is tracheostomy still an option in amyotrophic lateral sclerosis? Reflections of a multidisciplinary work group by Heritier Barras, Anne-Chantal, Adler, Dan, Iancu Ferfoglia, Ruxandra, Ricou, Bara, Gasche, Yvan, Leuchter, Igor, Hurst, Samia, Escher, Monica, Pollak, Pierre, Janssens, Jean-Paul

    Published in Swiss medical weekly (2013)
    “…Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease with a poor prognosis. Survival and quality of life of ALS patients have…”
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    Journal Article