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4. Phenotype Presentation and Molecular Diagnostic Yield in Non-5q Spinal Muscular Atrophy

Author

Fernández-Eulate, Gorka, primary, Theuriet, Julian, additional, Record, Christopher J., additional, Querin, Giorgia, additional, Masingue, Marion, additional, Leonard-Louis, Sarah, additional, Behin, Anthony, additional, Le Forestier, Nadine, additional, Pegat, Antoine, additional, Michaud, Maud, additional, Chanson, Jean-Baptiste, additional, Nadaj-Pakleza, Aleksandra, additional, Tard, Celine, additional, Bedat-Millet, Anne-Laure, additional, Sole, Guilhem, additional, Spinazzi, Marco, additional, Salort-Campana, Emmanuelle, additional, Echaniz-Laguna, Andoni, additional, Poinsignon, Vianney, additional, Latour, Philippe, additional, Reilly, Mary M., additional, Bouhour, Francoise, additional, and Stojkovic, Tanya, additional

Published
2023
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7. Extrapyramidal deficits in ALS: a combined biomechanical and neuroimaging study

Author

Feron, Maryse, Couillandre, Annabelle, Mseddi, Eya, Termoz, Nicolas, Abidi, Malek, Bardinet, Eric, Delgadillo, Daniel, Lenglet, Timothée, Querin, Giorgia, Welter, Marie-Laure, Le Forestier, Nadine, Salachas, François, Bruneteau, Gaelle, del Mar Amador, Maria, Debs, Rabab, Lacomblez, Lucette, Meininger, Vincent, Pélégrini-Issac, Mélanie, Bede, Peter, Pradat, Pierre-François, and de Marco, Giovanni

Published
2018
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8. Genetic screening of ANXA11 revealed novel mutations linked to amyotrophic lateral sclerosis

Author

Teyssou, Elisa, Muratet, François, Amador, Maria-Del-Mar, Ferrien, Mélanie, Lautrette, Géraldine, Machat, Selma, Boillée, Séverine, Larmonier, Thierry, Saker, Safaa, Leguern, Eric, Cazeneuve, Cécile, Marie, Yannick, Guegan, Justine, Gyorgy, Beata, Cintas, Pascal, Meininger, Vincent, Le Forestier, Nadine, Salachas, François, Couratier, Philippe, Camu, William, Seilhean, Danielle, and Millecamps, Stéphanie

Published
2021
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10. Detection of ATXN2 Expansions in an Exome Dataset: An Underdiagnosed Cause of Parkinsonism.

Author

Casse, Fanny, Courtin, Thomas, Tesson, Christelle, Ferrien, Mélanie, Noël, Sandrine, Fauret‐Amsellem, Anne‐Laure, Gareau, Thomas, Guegan, Justine, Anheim, Mathieu, Mariani, Louise‐Laure, Le Forestier, Nadine, Tranchant, Christine, Corvol, Jean‐Christophe, Lesage, Suzanne, and Brice, Alexis

Subjects
PARKINSON'S disease, PARKINSONIAN disorders, SPINOCEREBELLAR ataxia, POLYMERASE chain reaction
Abstract

Background: CAG‐repeat expansions in Ataxin 2 (ATXN2) are known to cause spinocerebellar ataxia type 2 (SCA2), but CAA interrupted expansions may also result in autosomal dominant Parkinson's disease (AD PD). However, because of technical limitations, such expansions are not explored in whole exome sequencing (WES) data. Objectives: To identify ATXN2 expansions using WES data from PD cases. Methods: We explored WES data from a cohort of 477 index cases with PD using ExpansionHunter (Illumina DRAGEN Bio‐IT Platform, San Diego, CA). Putative expansions were confirmed by combining polymerase chain reaction and fragment length analysis followed by sub‐cloning and sequencing methods. Results: Using ExpansionHunter, we identified three patients from two families with AD PD carrying either ATXN2 22/39 or 22/37 repeats, both interrupted by four CAA repeats. Conclusion: These findings demonstrate the usefulness of WES to detect pathogenic CAG repeat expansions, which were found in 1.7% of AD PD in the ATXN2 gene in our exome dataset. [ABSTRACT FROM AUTHOR]

Published
2023
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12. Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles

Author

Le Gall, Laura, primary, Duddy, William J., additional, Martinat, Cecile, additional, Mariot, Virginie, additional, Connolly, Owen, additional, Milla, Vanessa, additional, Anakor, Ekene, additional, Ouandaogo, Zamalou G., additional, Millecamps, Stephanie, additional, Lainé, Jeanne, additional, Vijayakumar, Udaya Geetha, additional, Knoblach, Susan, additional, Raoul, Cedric, additional, Lucas, Olivier, additional, Loeffler, Jean Philippe, additional, Bede, Peter, additional, Behin, Anthony, additional, Blasco, Helene, additional, Bruneteau, Gaelle, additional, Del Mar Amador, Maria, additional, Devos, David, additional, Henriques, Alexandre, additional, Hesters, Adele, additional, Lacomblez, Lucette, additional, Laforet, Pascal, additional, Langlet, Timothee, additional, Leblanc, Pascal, additional, Le Forestier, Nadine, additional, Maisonobe, Thierry, additional, Meininger, Vincent, additional, Robelin, Laura, additional, Salachas, Francois, additional, Stojkovic, Tanya, additional, Querin, Giorgia, additional, Dumonceaux, Julie, additional, Butler Browne, Gillian, additional, González De Aguilar, Jose‐Luis, additional, Duguez, Stephanie, additional, and Pradat, Pierre Francois, additional

Published
2022
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15. Muscle cells of sporadic ALS patients secrete neurotoxic vesicles

Author

Gall, Laura Le, primary, Duddy, William J, additional, Martinat, Cecile, additional, Mariot, Virginie, additional, Connolly, Owen, additional, Milla, Vanessa, additional, Anakor, Ekene, additional, Ouandaogo, Zamalou G, additional, Millecamps, Stephanie, additional, Lainé, Jeanne, additional, Vijayakumar, Udaya Geetha, additional, Knoblach, Susan, additional, Raoul, Cedric, additional, Lucas, Olivier, additional, Loeffler, Jean Philippe, additional, Bede, Peter, additional, Behin, Anthony, additional, Blasco, Helene, additional, Bruneteau, Gaelle, additional, Del Mar Amador, Maria, additional, Devos, David, additional, Henriques, Alexandre, additional, Hesters, Adele, additional, Lacomblez, Lucette, additional, Laforet, Pascal, additional, Langlet, Timothee, additional, Leblanc, Pascal, additional, Le Forestier, Nadine, additional, Maisonobe, Thierry, additional, Meininger, Vincent, additional, Robelin, Laura, additional, Salachas, Francois, additional, Stojkovic, Tanya, additional, Querin, Giorgia, additional, Dumonceaux, Julie, additional, Browne, Gillian Butler, additional, González De Aguilar, Jose-Luis, additional, Duguez, Stephanie, additional, and Pradat, Pierre Francois, additional

Published
2021
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17. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes

Author

Millecamps, Stéphanie, Boillée, Séverine, Le Ber, Isabelle, Seilhean, Danielle, Teyssou, Elisa, Giraudeau, Marine, Moigneu, Carine, Vandenberghe, Nadia, Danel-Brunaud, Véronique, Corcia, Philippe, Pradat, Pierre-François, Le Forestier, Nadine, Lacomblez, Lucette, Bruneteau, Gaelle, Camu, William, Brice, Alexis, Cazeneuve, Cécile, LeGuern, Eric, Meininger, Vincent, and Salachas, François

Published
2012
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20. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations

Author

Millecamps, Stéphanie, Salachas, François, Cazeneuve, Cécile, Gordon, Paul, Bricka, Bernard, Camuzat, Agnès, Guillot-Noël, Léna, Russaouen, Odile, Bruneteau, Gaëlle, Pradat, Pierre-François, Le Forestier, Nadine, Vandenberghe, Nadia, Danel-Brunaud, Véronique, Guy, Nathalie, Thauvin-Robinet, Christel, Lacomblez, Lucette, Couratier, Philippe, Hannequin, Didier, Seilhean, Danielle, Le Ber, Isabelle, Corcia, Philippe, Camu, William, Brice, Alexis, Rouleau, Guy, LeGuern, Eric, and Meininger, Vincent

Published
2010
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23. Lewis-Sumner Syndrome and Tangier Disease

Author

Théaudin, Marie, Couvert, Philippe, Fournier, Emmanuel, Bouige, Daniel, Bruckert, Eric, Perrotte, Paul, Vaschalde, Yvan, Maisonobe, Thierry, Bonnefont-Rousselot, Dominique, Carrié, Alain, and Le Forestier, Nadine

Published
2008

24. Caractérisation des macrophages dans les formes familiales et sporadiques de Sclérose Latérale Amyotrophique (SLA)

Author

Ribon, M., Hesters, A., Chiot, A., Amador, M.D.M., Bruneteau, G., Lenglet, T., Pradat, P.F., Le Forestier, Nadine, Couratier, Philippe, Millecamps, Stéphanie, Bohl, D., Lobsiger, C.S., Salachas, F., Boillée, S., Service de Neurophysiologie [CHU Pitié-Salpêtrière], CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Service de Neurologie [CHU Limoges], CHU Limoges, Neuroépidémiologie Tropicale (NET), Institut Génomique, Environnement, Immunité, Santé, Thérapeutique (GEIST), and Université de Limoges (UNILIM)-Université de Limoges (UNILIM)-CHU Limoges-Institut d'Epidémiologie Neurologique et de Neurologie Tropicale-Institut National de la Santé et de la Recherche Médicale (INSERM)

Subjects
[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2019

25. The spinal and cerebral profile of adult spinal-muscular atrophy: A multimodal imaging study

Author

Querin, Giorgia, El Mendili, Mohamed-Mounir, Lenglet, Timothée, Behin, Anthony, Stojkovic, Tanya, Salachas, François, Devos, David, Le Forestier, Nadine, Del Mar Amador, Maria, Debs, Rabab, Lacomblez, Lucette, Meininger, Vincent, Bruneteau, Gaëlle, Cohen-Adad, Julien, Lehéricy, Stéphane, Laforet, Pascal, Blancho, Sophie, Benali, Habib, Catala, Martin, Li, Menghan, Marchand-Pauvert, Véronique, Hogrel, Jean-Yves, Bede, Peter, Pradat, Pierre-François, Querin, Giorgia, El Mendili, Mohamed-Mounir, Lenglet, Timothée, Behin, Anthony, Stojkovic, Tanya, Salachas, François, Devos, David, Le Forestier, Nadine, Del Mar Amador, Maria, Debs, Rabab, Lacomblez, Lucette, Meininger, Vincent, Bruneteau, Gaëlle, Cohen-Adad, Julien, Lehéricy, Stéphane, Laforet, Pascal, Blancho, Sophie, Benali, Habib, Catala, Martin, Li, Menghan, Marchand-Pauvert, Véronique, Hogrel, Jean-Yves, Bede, Peter, and Pradat, Pierre-François

Abstract

Spinal muscular atrophy (SMA) type III and IV are autosomal recessive, slowly progressive lower motor neuron syndromes. Nevertheless, wider cerebral involvement has been consistently reported in mouse models. The objective of this study is the characterisation of spinal and cerebral pathology in adult forms of SMA using multimodal quantitative imaging. METHODS: Twenty-five type III and IV adult SMA patients and 25 age-matched healthy controls were enrolled in a spinal cord and brain imaging study. Structural measures of grey and white matter involvement and diffusion parameters of white matter integrity were evaluated at each cervical spinal level. Whole-brain and region-of-interest analyses were also conducted in the brain to explore cortical thickness, grey matter density and tract-based white matter alterations. RESULTS: In the spinal cord, considerable grey matter atrophy was detected between C2-C6 vertebral levels. In the brain, increased grey matter density was detected in motor and extra-motor regions of SMA patients. No white matter pathology was identified neither at brain and spinal level. CONCLUSIONS: Adult forms of SMA are associated with selective grey matter degeneration in the spinal cord with preserved white matter integrity. The observed increased grey matter density in the motor cortex may represent adaptive reorganisation.

Published
2019

27. Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis

Author

Millecamps, Stéphanie, Corcia, Philippe, Cazeneuve, Cécile, Boillée, Séverine, Seilhean, Danielle, Danel-Brunaud, Véronique, Vandenberghe, Nadia, Pradat, Pierre-François, Le Forestier, Nadine, Lacomblez, Lucette, Bruneteau, Gaëlle, Camu, William, Brice, Alexis, Meininger, Vincent, LeGuern, Eric, and Salachas, François

Published
2012
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28. Cursive Eye-Writing With Smooth-Pursuit Eye-Movement Is Possible in Subjects With Amyotrophic Lateral Sclerosis

Author

Lenglet, Timothée, primary, Mirault, Jonathan, additional, Veyrat-Masson, Marie, additional, Funkiewiez, Aurélie, additional, Amador, Maria del Mar, additional, Bruneteau, Gaelle, additional, Le Forestier, Nadine, additional, Pradat, Pierre-Francois, additional, Salachas, Francois, additional, Vacher, Yannick, additional, Lacomblez, Lucette, additional, and Lorenceau, Jean, additional

Published
2019
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29. The spinal and cerebral profile of adult spinal-muscular atrophy: A multimodal imaging study

Author

Querin, Giorgia, primary, El Mendili, Mohamed-Mounir, additional, Lenglet, Timothée, additional, Behin, Anthony, additional, Stojkovic, Tanya, additional, Salachas, François, additional, Devos, David, additional, Le Forestier, Nadine, additional, del Mar Amador, Maria, additional, Debs, Rabab, additional, Lacomblez, Lucette, additional, Meininger, Vincent, additional, Bruneteau, Gaëlle, additional, Cohen-Adad, Julien, additional, Lehéricy, Stéphane, additional, Laforêt, Pascal, additional, Blancho, Sophie, additional, Benali, Habib, additional, Catala, Martin, additional, Li, Menghan, additional, Marchand-Pauvert, Véronique, additional, Hogrel, Jean-Yves, additional, Bede, Peter, additional, and Pradat, Pierre-François, additional

Published
2019
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30. Emotional feeling in patients suffering from amyotrophic lateral sclerosis

Author

Unglik, Johanna, additional, Bungener, Catherine, additional, Delgadillo, Daniel, additional, Salachas, François, additional, Pradat, Pierre François, additional, Bruneteau, Gaëlle, additional, Lenglet, Timothée, additional, Le Forestier, Nadine, additional, Couratier, Philippe, additional, Vacher, Yannick, additional, and Lacomblez, Lucette, additional

Published
2018
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31. Screening of OPTN in French familial amyotrophic lateral sclerosis

Author

Millecamps, Stéphanie, Boillée, Séverine, Chabrol, Elodie, Camu, William, Cazeneuve, Cécile, Salachas, François, Pradat, Pierre-François, Danel-Brunaud, Véronique, Vandenberghe, Nadia, Corcia, Philippe, Le Forestier, Nadine, Lacomblez, Lucette, Bruneteau, Gaëlle, Seilhean, Danielle, Brice, Alexis, Feingold, Josué, Meininger, Vincent, and LeGuern, Eric

Published
2011
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33. The French national protocol for Kennedy's disease (SBMA): consensus diagnostic and management recommendations.

Author

Pradat, Pierre-François, Bernard, Emilien, Corcia, Philippe, Couratier, Philippe, Jublanc, Christel, Querin, Giorgia, Morélot Panzini, Capucine, Salachas, François, Vial, Christophe, Wahbi, Karim, Bede, Peter, Desnuelle, Claude, on behalf of the French Kennedy's Disease Writing Group, Le Forestier, Nadine, Echaniz-Laguna, Andoni, Sorarù, Gianni, Perez, Thierry, Ramos, Cédric, Goizet, Cyril, and Desport, Jean Claude

Subjects
MEDICAL personnel, ASPIRATION pneumonia, SPINAL muscular atrophy, BRUGADA syndrome, MOTOR neuron diseases, NEUROMUSCULAR diseases, ANDROGEN receptors, ADRENERGIC receptors
Abstract

Background: Kennedy's disease (KD), also known as spinal and bulbar muscular atrophy (SBMA), is a rare, adult-onset, X-linked recessive neuromuscular disease caused by CAG expansions in exon 1 of the androgen receptor gene (AR). The objective of the French national diagnostic and management protocol is to provide evidence-based best practice recommendations and outline an optimised care pathway for patients with KD, based on a systematic literature review and consensus multidisciplinary observations.Results: The initial evaluation, confirmation of the diagnosis, and management should ideally take place in a tertiary referral centre for motor neuron diseases, and involve an experienced multidisciplinary team of neurologists, endocrinologists, cardiologists and allied healthcare professionals. The diagnosis should be suspected in an adult male presenting with slowly progressive lower motor neuron symptoms, typically affecting the lower limbs at onset. Bulbar involvement (dysarthria and dysphagia) is often a later manifestation of the disease. Gynecomastia is not a constant feature, but is suggestive of a suspected diagnosis, which is further supported by electromyography showing diffuse motor neuron involvement often with asymptomatic sensory changes. A suspected diagnosis is confirmed by genetic testing. The multidisciplinary assessment should ascertain extra-neurological involvement such as cardiac repolarisation abnormalities (Brugada syndrome), signs of androgen resistance, genitourinary abnormalities, endocrine and metabolic changes (glucose intolerance, hyperlipidemia). In the absence of effective disease modifying therapies, the mainstay of management is symptomatic support using rehabilitation strategies (physiotherapy and speech therapy). Nutritional evaluation by an expert dietician is essential, and enteral nutrition (gastrostomy) may be required. Respiratory management centres on the detection and treatment of bronchial obstructions, as well as screening for aspiration pneumonia (chest physiotherapy, drainage, positioning, breath stacking, mechanical insufflation-exsufflation, cough assist machnie, antibiotics). Non-invasive mechanical ventilation is seldom needed. Symptomatic pharmaceutical therapy includes pain management, endocrine and metabolic interventions. There is no evidence for androgen substitution therapy.Conclusion: The French national Kennedy's disease protocol provides management recommendations for patients with KD. In a low-incidence condition, sharing and integrating regional expertise, multidisciplinary experience and defining consensus best-practice recommendations is particularly important. Well-coordinated collaborative efforts will ultimately pave the way to the development of evidence-based international guidelines. [ABSTRACT FROM AUTHOR]

Published
2020
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36. Correction: Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA

Author

El Mendili, Mohamed-Mounir, primary, Lenglet, Timothée, additional, Stojkovic, Tanya, additional, Behin, Anthony, additional, Guimarães-Costa, Raquel, additional, Salachas, François, additional, Meininger, Vincent, additional, Bruneteau, Gaelle, additional, Le Forestier, Nadine, additional, Laforêt, Pascal, additional, Lehéricy, Stéphane, additional, Benali, Habib, additional, and Pradat, Pierre-François, additional

Published
2016
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37. Les Passeurs de mots. Une éthique philosophique du soin : à propos d’une enquête nationale au sein des Centres SLA de France

Author

Le Forestier, Nadine, Département de Recherche en Ethique, Université Paris-Sud - Paris 11 (UP11), Université Paris Sud - Paris XI, Claude Debru, and Vincent Meininger

Subjects
Philosophie morale, Philosophy of morality, Philosophy of language, Formation médicale, Proche, [SDV.ETH]Life Sciences [q-bio]/Ethics, Annonce diagnostique, Caregivers, Palliative care, Soins palliatifs, Training of Doctor, ALS, SLA, Announcement of the diagnosis, Philosophie du langage
Abstract

The teaching of Doctor-Patient relationship, in particular in making announcement of the diagnosis, makes progress in the Faculties of Medicine. But in practice, communicating the thruth of a disease with fatal issue remains a distressing time because still badly told. Amyotrophic Lateral Sclerosis, a motor neuron disease, is the most pejorative diagnosis to make in Neurology. In the controversy surrounding the time of the announcement of the diagnosis, and, by examining the results of 203 ALS Patients’ and their Caregivers’ questionnaires, we compare with the results of 38 ALS Centre Neurologists’ interviews. Through bringing an epistemological, ethical and philosophical analysis into focus, we argue that, in the rational multidisciplinary of the care in a rapid and incurable disease, the evolution of the clearly medical information changes the Doctor-Patient relationship into a moral injunction of presence for the Caregivers and the families. Only through the training of Doctors and a certain conception of Patient information in palliative care can the harmful consequences of such a trend be limited.; La dynamique professionnelle pour améliorer la qualité du soin montre qu’en dépit des progrès de l’enseignement sur la relation Soigné-Soignant, le temps du verbe médical est encore sacrifié au chevet des Malades. Depuis une vingtaine d’années, en neurologie, l’annonce diagnostique, ce faire-savoir, a surtout été analysée dans le registre des maladies avec atteinte cognitive. Ce travail de thèse se propose d’étudier, d’un point de vue épistémologique, philosophique, et éthique, le conflit des libertés en jeu lors de l’annonce diagnostique d’une maladie incurable paralysante évolutive telle que la Sclérose Latérale Amyotrophique (SLA). Guidée par la confrontation des vécus et des représentations recueillis auprès des Médecins des Centres SLA (38 entretiens), et à travers une enquête de terrain, des Patients et de leurs Proches, au moyen de questionnaires (203 questionnaires d’une quarantaine de questions), notre approche révèle que, dans l’impératif d’une information qui se veut avoir la vertu de conserver le plus longtemps possible l’autonomie du Patient, les angles de vulnérabilités du triangle relationnel Médecin-Patient-Proche s’affrontent dans une sous-estimation de la perception du Proche de son devoir d’engagement. Au travers d’une relecture philosophique des réponses des trois identités concernées, et d’une expérience professionnelle, nous comprenons que l’évolution rationnelle multidisciplinaire de la démarche de soin face à la maladie incurable transforme la clarté de l’information médicale en une injonction morale de présence du tiers. Parce qu’il s’agit d’impuissance, mais en aucun cas d’incapacité, nous proposons que tout Médecin, présent et à venir, apprenne à interroger en toute lucidité la pertinence de ses propositions de soins dés l’instant où il s’est engagé à annoncer l’incurabilité. Pour qu’un nouvel esprit du temps lui soit insufflé, quelle que soit son orientation, l’apprentissage systématique des soins palliatifs lui permettra de rester soucieux de ses choix, dans le clair-obscur des intentions humaines, et de reconnaître ses imperfections tout en se donnant le défi de la collaboration thérapeutique pour accompagner.

Published
2014

38. Émotions ressenties chez des patients atteints de sclérose latérale amyotrophique.

Author

Unglik, Johanna, Bungener, Catherine, Delgadillo, Daniel, Salachas, François, Pradat, Pierre François, Bruneteau, Gaëlle, Lenglet, Timothée, Le Forestier, Nadine, Couratier, Philippe, Vacher, Yannick, and Lacomblez, Lucette

Abstract

Copyright of Gériatrie et Psychologie Neuropsychiatrie du Vieillissement is the property of John Libbey Eurotext Ltd. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Published
2018
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39. Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA

Author

El Mendili, Mohamed-Mounir, primary, Lenglet, Timothée, additional, Stojkovic, Tanya, additional, Behin, Anthony, additional, Guimarães-Costa, Raquel, additional, Salachas, François, additional, Meininger, Vincent, additional, Bruneteau, Gaelle, additional, Le Forestier, Nadine, additional, Laforêt, Pascal, additional, Lehéricy, Stéphane, additional, Benali, Habib, additional, and Pradat, Pierre-François, additional

Published
2016
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40. Plasma Peptide Biomarker Discovery for Amyotrophic Lateral Sclerosis by MALDI –TOF Mass Spectrometry Profiling

Author

Conraux, Laurence, primary, Pech, Catherine, additional, Guerraoui, Halim, additional, Loyaux, Denis, additional, Ferrara, Pascual, additional, Guillemot, Jean-Claude, additional, Meininger, Vincent, additional, Pradat, Pierre-François, additional, Salachas, François, additional, Bruneteau, Gaëlle, additional, Le Forestier, Nadine, additional, and Lacomblez, Lucette, additional

Published
2013
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41. Validation of robust tools to measure sialorrhea in amyotrophic lateral sclerosis: A study in a large French cohort

Author

Abdelnour-Mallet, Maya, primary, Tezenas Du Montcel, Sophie, additional, Cazzolli, Pamela A., additional, Assouline, Avi, additional, Pointon, Christine, additional, Leveque, Nathalie, additional, Dominique, Henri, additional, Elmazria, Hassan, additional, Rothmayer, Michaela, additional, Lenglet, Timothee, additional, Bruneteau, Gaelle, additional, le Forestier, Nadine, additional, Delanian, Sylvie, additional, Gonzalez-Bermejo, Jesus, additional, Salachas, François, additional, Brooks, Benjamin Rix, additional, and Pradat, Pierre François, additional

Published
2012
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44. Phenotype difference between ALS patients with expanded repeats inC9ORF72and patients with mutations in other ALS-related genes

Author

Millecamps, Stéphanie, primary, Boillée, Séverine, additional, Le Ber, Isabelle, additional, Seilhean, Danielle, additional, Teyssou, Elisa, additional, Giraudeau, Marine, additional, Moigneu, Carine, additional, Vandenberghe, Nadia, additional, Danel-Brunaud, Véronique, additional, Corcia, Philippe, additional, Pradat, Pierre-François, additional, Le Forestier, Nadine, additional, Lacomblez, Lucette, additional, Bruneteau, Gaelle, additional, Camu, William, additional, Brice, Alexis, additional, Cazeneuve, Cécile, additional, LeGuern, Eric, additional, Meininger, Vincent, additional, and Salachas, François, additional

Published
2012
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45. Safety of home parenteral nutrition in patients with amyotrophic lateral sclerosis: A French national survey

Author

Abdelnour-Mallet, Maya, primary, Verschueren, Annie, additional, Guy, Nathalie, additional, Soriani, Marie-Hélène, additional, Chalbi, Myriam, additional, Gordon, Paul, additional, Salachas, François, additional, Bruneteau, Gaelle, additional, le Forestier, Nadine, additional, Lenglet, Timothée, additional, Desnuelle, Claude, additional, Clavelou, Pierre, additional, Pouget, Jean, additional, Meininger, Vincent, additional, and Pradat, Pierre-François, additional

Published
2010
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46. Impaired glucose tolerance in patients with amyotrophic lateral sclerosis

Author

Pradat, Pierre-Francois, primary, Bruneteau, Gaelle, additional, Gordon, Paul H., additional, Dupuis, Luc, additional, Bonnefont-Rousselot, Dominique, additional, Simon, Dominique, additional, Salachas, Francois, additional, Corcia, Philippe, additional, Frochot, Vincent, additional, Lacorte, Jean-Marc, additional, Jardel, Claude, additional, Coussieu, Christiane, additional, Le Forestier, Nadine, additional, Lacomblez, Lucette, additional, Loeffler, Jean-Philippe, additional, and Meininger, Vincent, additional

Published
2010
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47. Causes of death in a post‐mortem series of ALS patients

Author

Corcia, Philippe, primary, Pradat, Pierre‐François, additional, Salachas, François, additional, Bruneteau, Gaëlle, additional, le Forestier, Nadine, additional, Seilhean, Danielle, additional, Hauw, Jean‐Jacques, additional, and Meininger, Vincent, additional

Published
2008
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48. Muscle Nogo-a expression is a prognostic marker in lower motor neuron syndromes

Author

Pradat, Pierre-François, primary, Bruneteau, Gaelle, additional, Gonzalez de Aguilar, Jose-Luis, additional, Dupuis, Luc, additional, Jokic, Natasa, additional, Salachas, François, additional, Le Forestier, Nadine, additional, Echaniz-Laguna, Andoni, additional, Dubourg, Odile, additional, Hauw, Jean-Jacques, additional, Tranchant, Christine, additional, Loeffler, Jean-Philippe, additional, and Meininger, Vincent, additional

Published
2007
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50. Neuropsychological changes in patients with primary lateral sclerosis

Author

Piquard, Ambre, primary, Le Forestier, Nadine, additional, Baudoin‐Madec, Véronique, additional, Delgadillo, Daniel, additional, Salachas, François, additional, Pradat, Pierre‐François, additional, Derouesné, Christlan, additional, Meininger, Vincent, additional, and Lacomblez, Lucette, additional

Published
2006
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