Search

Your search keyword '"T Maisonobe"' showing total 346 results

Search Constraints

Start Over You searched for: Author "T Maisonobe" Remove constraint Author: "T Maisonobe"
346 results on '"T Maisonobe"'

Search Results

201. Antisynthetase syndrome with anti-Jo1 antibodies in 48 patients: pulmonary involvement predicts disease-modifying antirheumatic drug use.

202. Adult polyglucosan body disease: Natural History and Key Magnetic Resonance Imaging Findings.

203. Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulin.

204. Regional difference and similarity of familial amyloidosis with polyneuropathy in France.

205. [Neurologic paraneoplastic syndrome with anti-CV2/CRMP5 antibodies revealing a small cell lung cancer. Effectiveness of the lung cancer treatment].

206. Characteristics of clinical and electrophysiological pattern of Charcot-Marie-Tooth 4C.

207. Inflammatory myopathies with anti-Ku antibodies: a prognosis dependent on associated lung disease.

208. Eosinophilic fasciitis (Shulman disease): new insights into the therapeutic management from a series of 34 patients.

209. Heterogeneous spectrum of neuropathies in Waldenström's macroglobulinemia: a diagnostic strategy to optimize their management.

210. Genotype-phenotype relationship in 2 SMA III patients with novel mutations in the Tudor domain.

211. A phase I trial of adeno-associated virus serotype 1-γ-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2C.

212. Long-term observational study of sporadic inclusion body myositis.

213. A new electrode placement for recording the compound motor action potential of the first dorsal interosseous muscle.

214. Diagnostic value of markers of muscle degeneration in sporadic inclusion body myositis.

215. Late onset radiation-induced camptocormia.

217. Mononeuropathy multiplex associated with acute parvovirus B19 infection: characteristics, treatment and outcome.

218. Non-anti-MAG DADS neuropathy as a variant of CIDP: clinical, electrophysiological, laboratory features and response to treatment in 10 cases.

219. Distal muscle involvement in granulomatous myositis can mimic inclusion body myositis.

220. Lambert-Eaton myasthenic syndrome and follicular thymic hyperplasia in systemic lupus erythematosus.

221. A novel MYH7 mutation occurring independently in French and Norwegian Laing distal myopathy families and de novo in one Finnish patient.

222. Hepatitis C virus-associated polyarteritis nodosa.

223. Peripheral neuropathies associated with primary Sjögren syndrome: immunologic profiles of nonataxic sensory neuropathy and sensorimotor neuropathy.

224. Defects in amphiphysin 2 (BIN1) and triads in several forms of centronuclear myopathies.

225. Nodes of ranvier and paranodes in chronic acquired neuropathies.

226. Neuropathy in Wolfram syndrome.

227. Systemic vasculitis in patients with hepatitis C virus infection with and without detectable mixed cryoglobulinemia.

228. Interleukin-25: a cytokine linking eosinophils and adaptive immunity in Churg-Strauss syndrome.

229. [Management of muscle and nerve biopsies: expert guidelines from two French professional societies, Société française de myologie et de l'Association française contre les myopathies].

230. [Cryoglobulinemic peripheral neuropathy in hepatitis C virus infection: clinical and anatomical correlations of 22 cases].

231. [Chronic inflammatory demyelinating polyradiculoneuropathy: clinical heterogeneity and therapeutic perspectives].

232. A current view of the diagnosis, clinical variants, response to treatment and prognosis of chronic inflammatory demyelinating polyradiculoneuropathy.

234. [Sensory neuropathy and autoimmune diseases].

235. Identification and characterization of a novel XK splice site mutation in a patient with McLeod syndrome.

236. [Multifocal motor neuropathy: a retrospective study of sensory nerve conduction velocities in long-term follow-up of 21 patients].

237. Significant clinical improvement in radiation-induced lumbosacral polyradiculopathy by a treatment combining pentoxifylline, tocopherol, and clodronate (Pentoclo).

238. Postradiation lumbosacral radiculopathy with spinal root cavernomas mimicking carcinomatous meningitis.

239. Two further cases of spondyloenchondrodysplasia (SPENCD) with immune dysregulation.

241. Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene.

242. Lewis-Sumner syndrome and Tangier disease.

243. Neuropathy in lymphoma: a relationship between the pattern of neuropathy, type of lymphoma and prognosis?

244. Distal inflammatory myopathy: unusual presentation of polymyositis or new entity?

245. [Are idiopathic neuropathies autoimmune in origin?].

246. Complete fatty degeneration of lumbar erector spinae muscles caused by a primary dysferlinopathy.

247. Intravenous immunoglobulin as short- and long-term therapy of multifocal motor neuropathy: a retrospective study of response to IVIg and of its predictive criteria in 40 patients.

248. [Multifocal motor neuropathy: a retrospective study of the response to high-dose intravenous immunoglobulin (IVIg) and current perspectives for diagnosis and treatment].

249. [Chronic inflammatory demyelinating polyneuropathy (CIDP) revealing an associated disease diagnostic and therapeutic pitfalls].

250. Severe colchicine-induced bilateral optico-neuromyopathy.

Catalog

Books, media, physical & digital resources