Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Ruxandra Iancu-Ferfoglia"'
Autor:
Eglė Sukockienė, Ruxandra Iancu-Ferfoglia, Monique Boegli, Catherine Lefranc-Barranco, André Truffert, Anne-Chantal Héritier-Barras, Laurence Genton, Igor Leuchter, Dan Adler, Jean-Paul Janssens, Monica Escher
Publikováno v:
Swiss Medical Weekly, Vol 151, Iss 1112 (2021)
INTRODUCTION Although recommended, the implementation of early advance care planning is suboptimal in amyotrophic lateral sclerosis (ALS) patients. Barriers to advance care planning include healthcare professionals’ and patients’ reluctance, and
Externí odkaz:
https://doaj.org/article/63cbad6eb92e431dac3b22abc5e124b6
Autor:
André Truffert, Eglė Sukockienė, Annaïck Desmaison, Miglė Ališauskienė, Ruxandra Iancu Ferfoglia, Nathalie Guy
Publikováno v:
Clinical Neurophysiology. 147:88-98
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2bcda7a8127bb0ddfaf823aaec1ba393
https://doi.org/10.1016/j.clinph.2022.12.013
https://doi.org/10.1016/j.clinph.2022.12.013
Autor:
André Truffert, Ruxandra Iancu Ferfoglia, Johannes Alexander Lobrinus, Kaveh Samii, André Kohler
Publikováno v:
European Journal of Translational Myology (2020)
Monoclonal gammopathy of undetermined significance (MGUS) associated to sporadic late onset nemaline myopathy (SLONM) is a rare and severely disabling condition of quickly progressive limb girdle acquired myopathy. It is believed by some authors to b
Externí odkaz:
https://doaj.org/article/68779f81851747d48b67d3b4d3b92a7a
Autor:
Marcus Weitz, Jan Kern, Peter Huppke, Ruxandra Iancu Ferfoglia, Klaus-Peter Wandinger, Elisabeth Probst-Müller, Steffen Syrbe, Tilman Polster, Ingo Borggraefe, Annette Weichselbaum, Robert Steinfeld, Andreas Ziegler, Julien Bally, Silvia Schmid, Christian G. Bien, Frank Leypoldt, Susi Strozzi, Georg M. Stettner, Corinna I. Bien
Publikováno v:
Neurology. 94:e2290-e2301
ObjectiveTo delineate autoimmune disease in association with contactin-associated protein 2 (CASPR2) antibodies in childhood, we reviewed the clinical phenotype of children with CASPR2 antibodies.MethodsRetrospective assessment of patients recruited
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db91599e0c31763bc65b7d939b8183e1
https://doi.org/10.1212/wnl.0000000000009523
https://doi.org/10.1212/wnl.0000000000009523
Autor:
Eglė Sukockienė, André Truffert, Michel R. Magistris, Agustina M. Lascano, Ruxandra Iancu Ferfoglia
Publikováno v:
Clinical Neurophysiology Practice, Vol 5, Iss, Pp 152-156 (2020)
Clinical Neurophysiology Practice
Clinical Neurophysiology Practice
Highlights • Tendon areflexia may be observed in otherwise asymptomatic lower limbs, in patients with Multifocal Motor Neuropathy. • Sensory afferent pathways can be assessed electrophysiologically by recording T (tendon) and H (Hoffmann) waves.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74a90432aa22842a74ca4dd42ab662ef
http://www.sciencedirect.com/science/article/pii/S2467981X20300226
http://www.sciencedirect.com/science/article/pii/S2467981X20300226
Publikováno v:
European neurology. 84(5)
Progressive loss of walking ability in amyotrophic lateral sclerosis (ALS) has been scarcely studied as a potential predictive factor for survival in motor neuron disease. We aimed to assess the progression of gait decline and its association with mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c76d68303e7b9332260dfaf72305ed1e
https://pubmed.ncbi.nlm.nih.gov/34167113
https://pubmed.ncbi.nlm.nih.gov/34167113
Autor:
Kaveh Samii, Johannes Alexander Lobrinus, André Truffert, Ruxandra Iancu Ferfoglia, André Kohler
Publikováno v:
European Journal of Translational Myology
European Journal of Translational Myology, Vol. 30, No 3 (2020) P. 9225
European Journal of Translational Myology (2020)
European Journal of Translational Myology, Vol. 30, No 3 (2020) P. 9225
European Journal of Translational Myology (2020)
Monoclonal gammopathy of undetermined significance (MGUS) associated to sporadic late onset nemaline myopathy (SLONM) is a rare and severely disabling condition of quickly progressive limb girdle acquired myopathy. It is believed by some authors to b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31018dec58d84b3b37935e4ace59ae5d
https://pubmed.ncbi.nlm.nih.gov/33117509
https://pubmed.ncbi.nlm.nih.gov/33117509
Autor:
Dan Adler, Eglė Sukockienė, Patrick Pasquina, Anne-Chantal Héritier Barras, V. Viatte, Monica Escher, Antoine Poncet, Jean-Paul Janssens, Ninon S. Horié, Laurence Genton, André Truffert, Igor Leuchter, Ruxandra Iancu Ferfoglia
Publikováno v:
Swiss Medical Weekly, Vol. 150 (2020) P. w20258
Over a four-year period, ALS patients complied with the modalities of the multidisciplinary management follow-up without any drop-outs. The multidisciplinary management structure also contributes to increasing the experience and knowledge of the clin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c93521b65bc017a3f1dbab6251aa3165
https://pubmed.ncbi.nlm.nih.gov/32579697
https://pubmed.ncbi.nlm.nih.gov/32579697
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Autor:
Philippe Petiot, Emilien Delmont, Laurent Magy, Andreas J. Steck, Armelle Magot, Antoine Gueguen, Karine Viala, Jean-Christophe Antoine, Arnaud Lacour, Karine Ferraud, Thierry Kuntzer, Juliette Svahn, Christophe Vial, Cécile Cauquil, Jean-Philippe Camdessanché, Aline Zarea, Andoni Echaniz-Laguna, Jean-Marc Léger, Ruxandra Iancu Ferfoglia
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 89:499-505
ObjectiveTo assess the clinicopathological and therapeutic features of patients with low (≥1000 to MethodsWe retrospectively and prospectively analysed standardised report forms and medical records of 202 patients from 14 neuromuscular centres.Resu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a93da206dee5fc1d1e286fd118ab9101
https://doi.org/10.1136/jnnp-2017-316715
https://doi.org/10.1136/jnnp-2017-316715