Results 121 to 130 of about 75,660 (223)
Brain atrophy patterns in anti-IgLON5 disease. [PDF]
BrainYogeshwar SM, Bartels F, Grüter T, Muñiz-Castrillo S, Picard G, Crijnen YS, Bernard E, Heidbreder A, Zekeridou A, Ringelstein M, Kraft A, Kovac S, Wandinger KP, de Vries JM, Boon AJW, Veenbergen S, Geis C, Penner L, Melzer N, Leypoldt F, Blaabjerg M, Pittock SJ, Gaig C, Sabater L, Santamaria J, Graus F, Dalmau J, Prüss H, Höftberger R, Schreiner B, McKeon A, Lewerenz J, Irani S, Mignot E, Titulaer MJ, Ayzenberg I, Honnorat J, Finke C, IgLON5 Imaging Consortium
. +38 moreeuropepmc +1 more sourceClinical and Electrophysiological Characterization of Essential Tremor in 18 Children and Adolescents. [PDF]
Tremor Other Hyperkinet Mov (N Y), 2023 Piarroux J, Dimopoulou E, Taieb G, Souvannanorath S, Roze E, Lion-François L, Spitz MA, Broussolle E, Laurencin C, Chanson JB, Belleville-Goffeney J, François-Heude MC, Meyer P, Khalil M, Dereure M, Doummar D, Chevassus H, Apartis E, Roubertie A. +18 moreeuropepmc +1 more sourceAcromegaly facial changes analysis using last generation artificial intelligence methodology: the AcroFace system. [PDF]
PituitaryRashwan HA, Marqués-Pamies M, Ruiz S, Gil J, Asensio-Wandosell D, Martínez-Momblán MA, Vázquez F, Salinas I, Ciriza R, Jordà M, Chanson P, Valassi E, Abdelnasser M, Puig D, Puig-Domingo M. +14 moreeuropepmc +1 more sourceClinical and Electrophysiological Characteristics of 23 French Patients With Neurolymphomatosis. [PDF]
Muscle NerveAsmani D, Chanson JB, Tard C, Svahn J, Pegat A, Magot A, Péréon Y, Camdessanché JP, Naudin S, Colin O, Taieb G, Coulibaly I, Magy L, Frachet S. +13 moreeuropepmc +1 more sourceDiagnosis of hereditary transthyretin amyloidosis in patients with suspected chronic inflammatory demyelinating polyneuropathy unresponsive to intravenous immunoglobulins: results of a retrospective study. [PDF]
Orphanet J Rare DisPéréon Y, Adams D, Camdessanché JP, Chanson JB, Cintas P, Magy L, Signaté A, Solé G, Svahn J, Tard C, Hababou C, Attarian S. +11 moreeuropepmc +1 more sourcePrevalence and predictors of uncommon features in FSHD1 patients: insights from the French FSHD registry. [PDF]
Orphanet J Rare DisSanson B, Slioui A, Garcia J, Klouvi L, Lejeune J, Stalens C, Guien C, Rabarimeriarijaona S, Bernard R, Nectoux J, Attarian S, Bédat-Millet AL, Bouhour F, Boyer FC, Chanson JB, Choumert A, Cintas P, De La Cruz E, Féasson L, Fournier M, Ghorab K, Jacquin-Piques A, Laforêt P, Magot A, Michaud M, Noury JB, Solé G, Spinazzi M, Stojkovic T, Tard C, Villa L, Béroud C, Sacconi S, French FSHD registry collaboration group. +33 moreeuropepmc +1 more source