761 results on '"Maisonobe T"'
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2. Neurodystrophic hand dermatitis – Sannino-Barduagni syndrome
3. Neuropathie multiple d’aggravation lente au retour de voyages humanitaires chez une femme de 76 ans
4. Sensory neuronopathy as a major clinical feature of mitochondrial trifunctional protein deficiency in adults
5. La lèpre autochtone existe en France : un diagnostic à ne pas manquer
6. Paranodopathie à anticorps anti-neurofascine 155 : atteinte conjointe du système nerveux central et périphérique. À propos d’un cas et revue de la littérature
7. Myofibrillar myopathies: State of the art, present and future challenges
8. Hommage au Pr Emmanuel Fournier (1959–2022)
9. P11.66.A Immune checkpoint inhibitors related peripheral nerve disorders: clinical and electrophysiological particularities
10. Segmental somatosensory-evoked potentials as a diagnostic tool in chronic inflammatory demyelinating polyneuropathies, and other sensory neuropathies
11. Mitochondrial Damage in HIV Patients treated with Highly Active Antiretroviral Therapy
12. Phenotypic spectrum of Charcot−Marie−Tooth disease due to LITAF/SIMPLE mutations: a study of 18 patients
13. Neuropathies post-radiques : un dommage collatéral chez les patients cancéreux long-survivants
14. A new electrode placement for recording the compound motor action potential of the first dorsal interosseous muscle
15. Troubles de la mémoire d’installation progressive chez un homme de 62 ans
16. Myotoxicité liée aux inhibiteurs de points de contrôle immunitaire: trouble de l’appareil musculaire et/ou de la jonction neuromusculaire?
17. Précision diagnostique de l’électroneuromyogramme dans les myosites
18. Performances de l’IRM musculaire pour le diagnostic des myopathies auto-immunes : étude prospective multicentrique (DARWIM)
19. Neurolymphomatosis related to direct epineural invasion of the superficial peroneal nerve from subcutaneous B-cell lymphoma
20. Corrélations anatomocliniques des neuropathies périphériques cryoglobulinémiques secondaires à l’hépatite C. Série consécutive de 22 cas
21. Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes (Nature Genetics, (2020), 52, 5, (473-481), 10.1038/s41588-020-0615-4)
22. Neuropathies sensitives et maladies auto-immunes : Stratégie diagnostique à propos d’une observation
23. Neuropathie motrice multifocale : existe-t-il une altération de la conduction sensitive au long cours ? Une étude rétrospective chez 21 patients
24. Movement disorders spectrum in adults with ataxia telangiectasia: 137
25. Myofiber HLA-DR expression: a distinctive biomarker for antisynthetase myositis: OS1213
26. Une cause rare d’altération de l’état général : cardiopathie et myopathie aux antipaludéens de synthèse
27. Neuropathy in lymphoma: a relationship between the pattern of neuropathy, type of lymphoma and prognosis?
28. Recommendations on diagnostic strategies for chronic inflammatory demyelinating polyradiculoneuropathy
29. Polyradiculonévrite inflammatoire démyélinisante chronique et maladie associée : problèmes diagnostiques et thérapeutiques
30. Parkinson's disease with camptocormia
31. Dysimmunité paranéoplasique dans les tumeurs à cellules dendritiques folliculaires : au-delà du syndrome auto-immun multi-organe paranéoplasique
32. Limites histologiques des polyradiculonévrites chroniques
33. Non-anti-MAG DADS neuropathy as a variant of CIDP: clinical, electrophysiological, laboratory features and response to treatment in 10 cases
34. Comparison of Lewis–Sumner syndrome with chronic inflammatory demyelinating polyradiculoneuropathy patients in a tertiary care centre
35. EP.58A late onset case of Becker muscular dystrophy
36. Two further cases of spondyloenchondrodysplasia (SPENCD) with immune dysregulation
37. DADS NEUROPATHY WITHOUT ANTI-MAG ANTIBODIES: A DISTINCT ENTITY?
38. Complete fatty degeneration of lumbar erector spinae muscles caused by a primary dysferlinopathy
39. 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
40. Encephalopathy associated with a reversible splenial lesion in riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency
41. BVES loss-of-function mutations in limb-girdle muscular dystrophy 2X with cardiac conduction disorders
42. Hyperhidrosis: a new and often early symptom in Fabry disease. International experience and data from the Fabry Outcome Survey
43. PERIPHERAL NEUROPATHY IN LYMPHOMA: DIFFERENT PATTERNS OF PRESENTATION ARE RELATED TO THE TYPE OF LYMPHOMA AND ARE PREDICTIVE OF THE OUTCOME
44. ARE INTRAVENOUS IMMUNOGLOBULINS (IVIG) A LONGTERM THERAPY OF MULTIFOCAL MOTOR NEUROPATHY? A RETROSPECTIVE STUDY OF RESPONSE TO IVIG AND ITS PREDICTIVE CRITERIA IN 40 PATIENTS
45. ABNORMAL MEDIAN-NORMAL SURAL SENSORY RESPONSE IN ANTI-MAG POLYNEUROPATHY
46. Familial inflammatory inclusion body myositis
47. Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11
48. Danon’s disease as a cause of hypertrophic cardiomyopathy: a systematic survey
49. Follow-up study and response to treatment in 23 patients with Lewis–Sumner syndrome
50. Phenotypical features of 12 Moroccan families with autosomal recessive Charcot-Marie-Tooth disease associated with mutations in GDAP1 gene: SC315
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