Search Results - "Gugenheim, Michel"

Neurologic manifestations associated with COVID-19: a multicentre registry by Meppiel, Elodie, Peiffer-Smadja, Nathan, Maury, Alexandra, Bekri, Imen, Delorme, Cécile, Desestret, Virginie, Gorza, Lucas, Hautecloque-Raysz, Geoffroy, Landre, Sophie, Lannuzel, Annie, Moulin, Solène, Perrin, Peggy, Petitgas, Paul, SellaI, François, Wang, Adrien, Tattevin, Pierre, de Broucker, Thomas, Abgrall, Sophie, Alby-Laurent, Fanny, Allou, Thibault, Amevigbe, Joséphine, Amarguellay, Hanifa, Alloussi, Nabil, Baille, Guillaume, Barbaz, Mathilde, Bekri, Imen, Bencherif, Lamia, Bensaadi, Samia, Beraud, Guillaume, Bizot, Alexandra, Bottin, Laure, Bruneel, Fabrice, Camdessanche, Jean-Philippe, Chauffier, Jeanne, Csajaghy, Jean-Philippe, De Broucker, Chloé, De Broucker, Thomas, Defebvre, Luc, Delorme, Cécile, Dembloque, Elodie, Derache, Nathalie, Dereeper, Olivier, Derollez, Céline, Descotes-Genon, Cécile, Desestret, Virginie, Devaux, Mathilde, Dubuc, Lydie, Edan, Gilles, Fickl, Andréa, Fraisse, Thibault, Gugenheim, Michel, Hankiewicz, Karolina, Hansmann, Yves, Hautecloque-Raysz, Geoffroy, Henry, Carole, Jobard, Stéphanie, Jouan, Fanny, Kwiatkowski, Arnaud, Lalu, Thibault, Landre, Sophie, Lannuzel, Annie, Leguilloux, Johan, Lejeune, Camille, Liegeois, Clémence, Mahy, Sophie, Marey, Jonathan, Maury, Alexandra, Meppiel, Elodie, Michel, Laure, Mitri, Rita, Moulin, Chloé, Moulin, Solène, Peiffer-Smadja, Nathan, Omarjee, Asma, Ozsancak, Canan, Perrin, Peggy, Petitgas, Paul, Pico, Fernando, Poupard, Marie, Rabier, Valérie, Rizzato, Camille, Roos, Caroline, Saison, Julien, Sayre, Naomi, Sedillot, Nicolas, Sellal, François, Servan, Jérôme, Storey, Caroline, Suchet, Laurent, Tarteret, Paul, Tattevin, Pierre, Thiebaut, Mathilde, Vaduva, Claudia, Varlan, David, Wang, Adrien, Zarrouk, Virginie

“…To provide an overview of the spectrum, characteristics and outcomes of neurologic manifestations associated with severe acute respiratory syndrome coronavirus…”
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Polyneuropathy in autosomal dominant cerebellar ataxias: Phenotype-genotype correlation by Kubis, Nathalie, Dürr, Alexandra, Gugenheim, Michel, Chneiweiss, Hervé, Mazzetti, Pilar, Brice, Alexis, Bouche, Pierre

“…Autosomal dominant cerebellar ataxias (ADCAs) are clinically and genetically heterogeneous neurodegenerative disorders. The aim of this study was to evaluate…”
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Feasibility and benefits of home initiation of subcutaneous apomorphine infusion for patients with Parkinson’s disease: the APOKADO study by Zagnoli, Fabien, Leblanc, Amélie, Viakhireva-Dovganyuk, Irina, Delabrousse-Mayoux, Jean-Philippe, Pouyet, Alain, Ziegler, Marc, Sogni, Laura, Patat, Marie, Bouillot, Régis, Vérin, Marc

“…Continuous subcutaneous apomorphine infusion (CSAI) is used to treat patients with Parkinson’s disease (PD) who are experiencing motor fluctuations. However,…”
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An amyotrophic lateral sclerosis-like syndrome revealing an amyloid polyneuropathy associated with a novel transthyretin mutation by Lozeron, Pierre, Lacroix, Catherine, Theaudin, Marie, Richer, Anne, Gugenheim, Michel, Adams, David, Misrahi, Micheline

“…Abstract Objective: Familial amyloid polyneuropathy (FAP) is typically a predominantly sensory and autonomic neuropathy with progressive and late motor…”
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Pratiques de prise en charge médicamenteuse des migraines par des médecins généralistes by Lucas, Christian, Raclot, Valentin, Gugenheim, Michel, Lefebvre, Hélène, Braithwaite, Ben, Ducros, Anne

“…De nouvelles recommandations de prise en charge de la migraine sont disponibles depuis 2021. Un état des lieux des pratiques chez les médecins généralistes…”
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Prise en charge en soins primaires des patients migraineux inéligibles ou résistants aux triptans : une étude française en vie réelle – étude France-Mig by Raclot, Valentin, Gugenheim, Michel, Casarotto, Emilie, Bretin, Oriane, Lefebvre, Hélène, Squara, Pierre-Alexandre, Lanteri-Minet, Michel

“…Les patients migraineux peuvent présenter une contre-indication ou une résistance aux triptans. Leur prévalence et leur profil sont peu documentés, notamment…”
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Pratiques de prise en charge médicamenteuse des migraines et perception des nouveaux traitements par des médecins neurologues by Ducros, Anne, Gugenheim, Michel, Raclot, Valentin, Lefebvre, Hélène, Braithwaite, Ben, Lucas, Christian

“…De nouvelles recommandations de prise en charge de la migraine sont disponibles depuis 2021. Un état des lieux des pratiques chez les médecins neurologues…”
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Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication: Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases by BIROUK, N, GOUIDER, R, LE GUERN, E, GUGENHEIM, M, TARDIEU, S, MAISONOBE, T, LE FORESTIER, N, AGID, Y, BRICE, A, BOUCHE, P

“…A clinical and electrophysiological study was performed in 119 Type 1A Charcot-Marie-Tooth disease (CMT1A) patients with proven 17p11.2 duplication. Onset of…”
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Peripheral neuropathy associated with essential mixed cryoglobulinaemia: a role for hepatitis C virus infection? by Apartis, E, Léger, J M, Musset, L, Gugenheim, M, Cacoub, P, Lyon-Caen, O, Pierrot-Deseilligny, C, Hauw, J J, Bouche, P

“…BACKGROUND--The prevalence of hepatitis C virus (HCV) infection has been estimated at 43 to 84% in patients with essential mixed cryoglobulinaemia in recent…”
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Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication by Nazha Birouk, Gouider, Riadh, Eric Le Guern, Gugenheim, Michel

“…A clinical and electrophysiological study was performed in 119 Type 1A Charcot-Marie-Tooth disease (CMT1A) patients with proven 17p11.2 duplication. Onset of…”
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A de Novo Case of Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) of Maternal Origin: A New Mechanism for Deletion in 17p11.2? by LeGuern, Eric, Gouider, Riadh, Ravisé, Nicole, Lopes, Judith, Tardieu, Sandrine, Gugenheim, Michel, Abbas, Nacer, Bouche, Pierre, Agid, Yves, Brice, Alexis

“…Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal dominant neuropathy, most often associated with a deletion of the 17p11.2…”
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An amyotrophic lateral sclerosis-like syndrome revealing an amyloid polyneuropathy associated with a novel transthyretin mutation by Lozeron, Pierre, Lacroix, Catherine, Theaudin, Marie, Richer, Anne, Gugenheim, Michel, Adams, David, Misrahi, Micheline

“…Objective: Familial amyloid polyneuropathy (FAP) is typically a predominantly sensory and autonomic neuropathy with progressive and late motor involvement…”
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Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11-Xq21 microsatellites in a new large family: three new markers are closely linked to the gene by Le Guern, E, Ravise, N, Gugenheim, M, Vignal, A, Penet, C, Bouche, P, Weissenbach, J, Agid, Y, Brice, A

“…X-linked dominant inheritance was suspected in a large family with Charcot-Marie-Tooth disease since no male to male transmission was observed, and since the…”
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