Search Results - "Franques, Jerome"

Sensory Neuronopathy Revealing Severe Vitamin B12 Deficiency in a Patient with Anorexia Nervosa: An Often-Forgotten Reversible Cause by Franques, Jérôme, Chiche, Laurent, Mathis, Stéphane

“…Vitamin B12 (B12) deficiency is known to be associated with various neurological manifestations. Although central manifestations such as dementia or subacute…”
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Teaching NeuroImages: Cranial nerve hypertrophy in IgG4 anti-neurofascin 155 antibody–positive polyneuropathy by Franques, Jérôme, Chapon, Frédérique, Devaux, Jérôme, Mathis, Stéphane

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CANOMAD: a neurological monoclonal gammopathy of clinical significance that benefits from B-cell–targeted therapies by Le Cann, Marie, Bouhour, Françoise, Viala, Karine, Simon, Laurence, Tard, Céline, Rossi, Cédric, Morel, Guillaume, Lagrange, Emmeline, Magy, Laurent, Créange, Alain, Michaud, Maud, Franques, Jérôme, Echaniz-Laguna, Andoni, Antoine, Jean-Christophe, Baron, Marine, Arnulf, Bertrand, Puma, Angela, Delmont, Emilien, Maisonobe, Thierry, Leblond, Véronique, Roos-Weil, Damien

“…CANOMAD (chronic ataxic neuropathy, ophthalmoplegia, immunoglobulin M [IgM] paraprotein, cold agglutinins, and disialosyl antibodies) is a rare syndrome…”
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Characteristics of patients with vitamin B12-responsive neuropathy: a case series with systematic repeated electrophysiological assessment by Franques, Jérôme, Chiche, Laurent, De Paula, André Maues, Grapperon, Aude Marie, Attarian, Shahram, Pouget, Jean, Mathis, Stephane

“…Background: Vitamin B12 (B12) has a fundamental role in both central and peripheral nervous system function at all ages. Neurologic manifestations may be the…”
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Efficacy and safety of mexiletine in non-dystrophic myotonias: A randomised, double-blind, placebo-controlled, cross-over study by Vicart, Savine, Franques, Jérôme, Bouhour, Françoise, Magot, Armelle, Péréon, Yann, Sacconi, Sabrina, Nadaj-Pakleza, Aleksandra, Behin, Anthony, Zahr, Noël, Hézode, Marianne, Fournier, Emmanuel, Payan, Christine, Lacomblez, Lucette, Fontaine, Bertrand

“…•Myomex is a randomised, double-blind, placebo-controlled, cross-over study.•It assessed the efficacy and safety of mexiletine in nondystrophic…”
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Monoclonal gammopathy of undeterminated significance and endoneurial IgG deposition: A case report by Mathis, Stéphane, Franques, Jérôme, Richard, Laurence, Vallat, Jean-Michel

“…Monoclonal gammopathy of undeterminated significance is the most common form of plasma cell dyscrasia, usually considered as benign. In rare cases it may have…”
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A severe case of ipilimumab-induced guillain-barré syndrome revealed by an occlusive enteric neuropathy: a differential diagnosis for ipilimumab-induced colitis by Gaudy-Marqueste, Caroline, Monestier, Sandrine, Franques, Jérome, Cantais, Emmanuel, Richard, Marie-Aleth, Grob, Jean-Jacques

“…Ipilimumab is a fully human monoclonal antibody directed against cytotoxic T-lymphocyte antigen-4 recently approved for the treatment of metastatic melanoma…”
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Response to treatment in patients with lewis-sumner syndrome by Attarian, Shahram, Verschueren, Annie, Franques, Jérome, Salort-Campana, Emmanuelle, Jouve, Elisabeth, Pouget, Jean

“…Introduction: Our aim was to document the classification of Lewis–Sumner syndrome (L‐SS) based on the response to treatment and the pattern of progression over…”
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MRI and surgical lumbosacral trunk positioning palsy by Mathis, Stéphane, Chapon, Frédérique, Franques, Jérôme

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Predictive factors of efficacy of rituximab in patients with anti-MAG neuropathy by Gazzola, Sébastien, Delmont, Emilien, Franques, Jérôme, Boucraut, José, Salort-Campana, Emmanuelle, Verschueren, Annie, Sagui, Emmanuel, Hubert, Anne-Michèle, Pouget, Jean, Attarian, Shahram

“…Abstract Objective To identify factors associated with efficacy of rituximab (RTX) infusions in patients with anti-myelin associated glycoprotein (MAG)…”
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Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients by Molenaar, Joery P, Verhoeven, Jamie I, Rodenburg, Richard J, Kamsteeg, Erik J, Erasmus, Corrie E, Vicart, Savine, Behin, Anthony, Bassez, Guillaume, Magot, Armelle, Péréon, Yann, Brandom, Barbara W, Guglielmi, Valeria, Vattemi, Gaetano, Chevessier, Frédéric, Mathieu, Jean, Franques, Jérôme, Suetterlin, Karen, Hanna, Michael G, Guyant-Marechal, Lucie, Snoeck, Marc M, Roberts, Mark E, Kuntzer, Thierry, Fernandez-Torron, Roberto, Martínez-Arroyo, Amaia, Seeger, Juergen, Kusters, Benno, Treves, Susan, van Engelen, Baziel G, Eymard, Bruno, Voermans, Nicol C, Sternberg, Damien

“…Brody disease is an autosomal recessive myopathy characterized by exercise-induced muscle stiffness due to mutations in the ATP2A1 gene. Almost 50 years after…”
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Phenotypical variability and atypical presentations in a French cohort of Andersen–Tawil syndrome by Villar‐Quiles, Rocio Nur, Sternberg, Damien, Tredez, Grégoire, Beatriz Romero, Norma, Evangelista, Teresinha, Lafôret, Pascal, Cintas, Pascal, Sole, Guilhem, Sacconi, Sabrina, Bendahhou, Said, Franques, Jérôme, Cances, Claude, Noury, JB, Delmont, Emilien, Blondy, Patricia, Perrin, Laurence, Hezode, Marianne, Fournier, Emmanuel, Fontaine, Bertrand, Stojkovic, Tanya, Vicart, Savine

“…Background and purpose Andersen–Tawil syndrome (ATS) is a skeletal muscle channelopathy caused by KCNJ2 mutations, characterized by a clinical triad of…”
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An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth disease type 1A by Attarian, Shahram, Vallat, Jean-Michel, Magy, Laurent, Funalot, Benoît, Gonnaud, Pierre-Marie, Lacour, Arnaud, Péréon, Yann, Dubourg, Odile, Pouget, Jean, Micallef, Joëlle, Franques, Jérôme, Lefebvre, Marie-Noëlle, Ghorab, Karima, Al-Moussawi, Mahmoud, Tiffreau, Vincent, Preudhomme, Marguerite, Magot, Armelle, Leclair-Visonneau, Laurène, Stojkovic, Tanya, Bossi, Laura, Lehert, Philippe, Gilbert, Walter, Bertrand, Viviane, Mandel, Jonas, Milet, Aude, Hajj, Rodolphe, Boudiaf, Lamia, Scart-Grès, Catherine, Nabirotchkin, Serguei, Guedj, Mickael, Chumakov, Ilya, Cohen, Daniel

“…Charcot-Marie-Tooth type 1A disease (CMT1A) is a rare orphan inherited neuropathy caused by an autosomal dominant duplication of a gene encoding for the…”
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New strategy for improving the diagnostic sensitivity of repetitive nerve stimulation in myasthenia gravis by Bou Ali, Hanna, Salort‐Campana, Emmanuelle, Grapperon, Aude Marie, Gallard, Julien, Franques, Jerome, Sevy, Amandine, Delmont, Emilien, Verschueren, Annie, Pouget, Jean, Attarian, Shahram

“…ABSTRACT Introduction: The diagnostic sensitivity of repetitive nerve stimulation (RNS) in patients with myasthenia gravis (MG) varies as a function of the…”
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Improving molecular diagnosis of distal myopathies by targeted next-generation sequencing by Sevy, Amandine, Cerino, Mathieu, Gorokhova, Svetlana, Dionnet, Eugénie, Mathieu, Yves, Verschueren, Annie, Franques, Jérôme, Maues de Paula, André, Figarella-Branger, Dominique, Lagarde, Arnaud, Desvignes, Jean Pierre, Béroud, Christophe, Attarian, Shahram, Levy, Nicolas, Bartoli, Marc, Krahn, Martin, Campana-Salort, Emmanuelle, Pouget, Jean

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Identifying a therapeutic window in acute and subacute inflammatory sensory neuronopathies by Antoine, Jean-Christophe, Robert-Varvat, Florence, Maisonobe, Thierry, Créange, Alain, Franques, Jérôme, Mathis, Stéphane, Delmont, Emilien, Kuntzer, Thierry, Lefaucheur, Jean-Pascal, Pouget, Jean, Viala, Karine, Desnuelle, Claude, Echaniz-Laguna, Andoni, Rotolo, Francesco, Camdessanché, Jean-Philippe

“…Abstract Background Patients with inflammatory sensory neuronopathy (SNN) may benefit from immunomodulatory or immunosuppressant treatments if administered…”
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Proximal conduction block in the pharyngeal-cervical-brachial variant of guillain-barrÉ syndrome by Taieb, Guillaume, Grapperon, Aude-Marie, Duclos, Yann, Franques, Jérôme, Labauge, Pierre, Renard, Dimitri, Yuki, Nobuhiro, Attarian, Shahram

“…ABSTRACT Introduction: Conduction block (CB) has been included in the Rajabally criteria for axonal Guillain–Barré syndrome (GBS). Because the nerve roots may…”
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Correlation of Clinicoserologic and Pathologic Classifications of Inflammatory Myopathies: Study of 178 Cases and Guidelines for Diagnosis by Fernandez, Carla, Bardin, Nathalie, De Paula, André Maues, Salort-Campana, Emmanuelle, Benyamine, Audrey, Franques, Jérôme, Schleinitz, Nicolas, Weiller, Pierre-Jean, Pouget, Jean, Pellissier, Jean-François, Figarella-Branger, Dominique

“…The idiopathic inflammatory myopathies (IIM) are acquired muscle diseases characterized by muscle weakness and inflammation on muscle biopsy. Clinicoserologic…”
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Sudoscan as a noninvasive tool to assess sudomotor dysfunction in patients with Fabry disease: results from a case-control study by Sahuc, Pauline, Chiche, Laurent, Dussol, Bertrand, Pouget, Jean, Franques, Jérôme

“…Hypohidrosis is a frequent and early symptom in patients with Fabry disease. Studies have reported improved sweating in patients treated with…”
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FDG‐PET/CT is a pivotal imaging modality to diagnose rare intravascular large B‐cell lymphoma: case report and review of literature by Colavolpe, Cecile, Ebbo, Mikael, Trousse, Delphine, Khibri, Hajar, Franques, Jerome, Chetaille, Bruno, Coso, Diane, Ouvrier, Matthieu John, Gastaud, Lauris, Guedj, Eric, Schleinitz, Nicolas

“…Intravascular large B‐cell lymphoma (IVLBCL) remains a diagnostic challenge, because of non‐specific findings on clinical, laboratory, and imaging studies. We…”
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