Zobrazeno 1 - 10
of 131
pro vyhledávání: '"I. Penisson-Besnier"'
Autor:
P, Laforêt, K, Laloui, B, Granger, D, Hamroun, N, Taouagh, J-Y, Hogrel, D, Orlikowski, F, Bouhour, A, Lacour, E, Salort-Campana, I, Penisson-Besnier, S, Sacconi, F, Zagnoli, F, Chapon, B, Eymard, C, Desnuelle, J, Pouget, D, Vincent
Publikováno v:
Revue Neurologique. 169:595-602
Pompe disease is a rare autosomal recessive muscle lysosomal glycogenosis, characterised by limb-girdle muscle weakness and frequent respiratory involvement. The French Pompe registry was created in 2004 with the initial aim of studying the natural h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::168b913bde13165fa65af14534581b91
https://doi.org/10.1016/j.neurol.2013.07.002
https://doi.org/10.1016/j.neurol.2013.07.002
Autor:
G. Drossard, B. Lebrun-Vignes, M. Steff, Y. Le Corre, I. Penisson-Besnier, C. Le Clec’h, S. Michalak
Publikováno v:
La Revue de Médecine Interne. 30:720-723
We report a case of Epstein Barr virus-associated large B cell lymphoproliferative disorder, with an abdominal cutaneous localization, in an adult treated for 10 years with immunosuppressive agents for a dermatomyositis. This is the third case of imm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3a6dee2bebb285dfa11e8c70106bacf
https://doi.org/10.1016/j.revmed.2008.10.022
https://doi.org/10.1016/j.revmed.2008.10.022
Publikováno v:
Autoimmunity. 26:189-194
It has been suggested that inflammation may be a possible cause of Alzheimer's disease (AD). Increased anti-NGF autoantibody levels and increased NGF frequency in serum have previously been associated with inflammatory responses. In this study no cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59171915434830a6509101f3c7562682
https://doi.org/10.3109/08916939708994740
https://doi.org/10.3109/08916939708994740
Autor:
C. Vuillerot, P. Rippert, S. Roche, C. Bérard, F. Margirier, C. de Lattre, I. Poirot, A. Berruyer, V. Tiffreau, M. Fournier-Mehouas, F. Bouhour, J.-A. Urtizberea, A. Renders, R. Ecochard, A. Le Flem, A. Barrière, A.P. Rouyer, S. Fontaine, J.-P. Vadot, E. Luc Pupat, Y. Chartier, D. Vincent-Genod, F. Girardot, V. Manel, F. Aubert, G. Rode, D. Denis, V. Germa, S. Quijano, N. Pelligrini, M.C. d’Anjou, L. Féasson, S. Chabrier, A. Furby, C. Goyet, M.C. Delmas, M. Campech, F. Robert, H. Hovart, J.-M. Cuisset, I. Badoil, C. Fafin, V. Tanant, S. Sacconi, J.-P. Gayraud, A. Carpentier, S. Vanderschueren, I. Bourdeauducq, D. Salicio-Castillo, A.M. Cobo, M.C. Commare, V. Farigoule, C. Huzar, B. Berger, V. Humbertclaude, F. Rumeau, E. Viehweger, C. Payet-Laury, I. Penisson-Besnier, V. Kinet, D. Laridant, V. Spehrs-Ciaffi, G. Bassez, N. Goemans, D. Pichancourt, L. Jezequel, N. Vedrenne
Publikováno v:
Annals of physical and rehabilitation medicine
Annals of physical and rehabilitation medicine, 2013, 56, pp.673--86. ⟨10.1016/j.rehab.2013.10.002⟩
Annals of Physical and Rehabilitation Medicine, Vol. 56, no.9-10, p. 673-686 (2013)
Annals of physical and rehabilitation medicine, 2013, 56, pp.673--86. ⟨10.1016/j.rehab.2013.10.002⟩
Annals of Physical and Rehabilitation Medicine, Vol. 56, no.9-10, p. 673-686 (2013)
ObjectiveTo develop a classification for neuromuscular disease patients in each of the three motor function domains (D1: standing and transfers; D2: axial and proximal function; D3: distal function).Materials and methodsA draft classification was dev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2da813f7ea18788fc9997957c88e3bb4
https://hal.archives-ouvertes.fr/hal-02446479
https://hal.archives-ouvertes.fr/hal-02446479
Autor:
E, Uro-Soste, C, Fernandez, F-J, Authier, G, Bassez, C, Butori, F, Chapon, M-B, Delisle, O, Dubourg, L, Feasson, R, Gherardi, C, Lacroix, A, Laquerriere, F, Letournel, L, Magy, T, Maisonobe, P, Marcorelles, C-A, Maurage, P, Mezin, J-M, Mussini, I, Penisson-Besnier, N-B, Romero, N, Streichenberger, J-M, Vallat, G, Viennet, A, Vital, T, Voit, W, Boucharef, D, Figarella-Branger
Publikováno v:
Revue neurologique. 166(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3c6ec7205abf970de76ef9b79304d1ef
https://pubmed.ncbi.nlm.nih.gov/20626090
https://pubmed.ncbi.nlm.nih.gov/20626090
Autor:
J. Emile, K. Josi, C. Desnuelle, Dubas F, Patrick Lestienne, I. Penisson-Besnier, Françoise Degoul
Publikováno v:
Journal of the Neurological Sciences. 110:144-148
A new family of myoclonic epilepsy with ragged-red fibers (MERRF) was studied at clinical, histological, biochemical and molecular genetic levels. There was a remarkable variation in the age of onset, the clinical presentation and the severity of sym
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee8881eedb7fd03142dd4a0d8e0ad9c9
https://doi.org/10.1016/0022-510x(92)90021-c
https://doi.org/10.1016/0022-510x(92)90021-c
Autor:
Furby A, Guillaume Bassez, Beauvais K, Jean-Pascal Lefaucheur, Créange A, J.-M. Mussini, I. Penisson-Besnier, Bruno Eymard, Anthony Behin, Marcorelles P
Publikováno v:
Journal of Neurology, Neurosurgery and Psychiatry
Journal of Neurology, Neurosurgery and Psychiatry, BMJ Publishing Group, 2009, 81 (1), pp.101. ⟨10.1136/jnnp.2008.167577⟩
Journal of Neurology, Neurosurgery and Psychiatry, BMJ Publishing Group, 2009, 81 (1), pp.101. ⟨10.1136/jnnp.2008.167577⟩
International audience; Patients with cervical or mediastinal Hodgkin's disease (HD) classically underwent chemotherapy plus extended-field radiation therapy. We report six patients who gradually developed severe atrophy and weakness of cervical para
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd0181c55a6b35d39de680b75ccaec94
https://hal.archives-ouvertes.fr/hal-00552743/document
https://hal.archives-ouvertes.fr/hal-00552743/document
Autor:
Franck Letournel, Pascale Marcorelles, C Le Clec'h, I. Penisson-Besnier, Christian Lavigne, Anne Croue
Publikováno v:
Clinical Neuropathology
Clinical Neuropathology, Dustri-Verlag, 2009, 29 (6), pp.357-360
Clinical Neuropathology, Dustri-Verlag, 2009, 29 (6), pp.357-360
International audience; Dermatomyositis was diagnosed on clinical and muscle histological criteria in a 42-year-old woman. Despite treatment, the patient complained of deterioration of her muscle condition. Since her symptoms were discordant with the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::951ab9579982c52e15cd510315385dd8
https://hal.univ-angers.fr/hal-03403263
https://hal.univ-angers.fr/hal-03403263
Autor:
M, Steff, Y, Le Corre, I, Penisson-Besnier, S, Michalak, G, Drossard, B, Lebrun-Vignes, C, Le Clec'h
Publikováno v:
La Revue de medecine interne. 30(8)
We report a case of Epstein Barr virus-associated large B cell lymphoproliferative disorder, with an abdominal cutaneous localization, in an adult treated for 10 years with immunosuppressive agents for a dermatomyositis. This is the third case of imm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9571517736db8e09186def1c88e87fc2
https://pubmed.ncbi.nlm.nih.gov/19027995
https://pubmed.ncbi.nlm.nih.gov/19027995
Autor:
R, Ben Yaou, H-M, Bécane, L, Demay, P, Laforet, D, Hannequin, P-A, Bohu, V, Drouin-Garraud, X, Ferrer, J-M, Mussini, E, Ollagnon, P, Petiot, I, Penisson-Besnier, N, Streichenberger, A, Toutain, P, Richard, B, Eymard, G, Bonne
Publikováno v:
Revue neurologique. 161(1)
Limb girdle muscular dystrophy type 1b (LGMD1B), due to LMNA gene mutations, is a relatively rare form of LGMD characterized by proximal muscle involvement associated with heart involvement comprising atrio-ventricular conduction blocks and dilated c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2ce208b001e8a0d8ec9e80675bc40d41
https://pubmed.ncbi.nlm.nih.gov/15678000
https://pubmed.ncbi.nlm.nih.gov/15678000