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1. Clinical, paraclinical and outcome features of 166 patients with acute anti-GQ1b antibody syndrome

4. Neuropathies related to hepatitis E virus infection: A prospective, matched case–control study

5. Motor unit number index as an individual biomarker: Reference limits of intra-individual variability over time in healthy subjects

6. Electrophysiological features of chronic inflammatory demyelinating polyradiculoneuropathy associated with IgG4 antibodies targeting neurofascin 155 or contactin 1 glycoproteins

7. Immune checkpoint inhibitor-related myositis and myocarditis: diagnostic pitfalls and imaging contribution in a real-world, institutional case series

9. Antibodies against the node of Ranvier: a real-life evaluation of incidence, clinical features and response to treatment based on a prospective analysis of 1500 sera

10. Genotype–phenotype correlations in recessive titinopathies

11. A multicenter cross-sectional French study of the impact of COVID-19 on neuromuscular diseases

13. Successful autologous hematopoietic stem cell transplantation in a refractory anti‐Caspr1 antibody nodopathy.

16. The emerging spectrum of foetal acetylcholine receptor antibody-associated disorders (FARAD)

17. Neuropathies related to hepatitis E virus infection: A prospective, matched case–control study.

19. EGR2 gene‐linked hereditary neuropathies present with a bimodal age distribution at symptoms onset.

21. Anti‐disialosyl‐immunoglobulin M chronic autoimmune neuropathies: a nationwide multicenter retrospective study

26. Early-onset leukoencephalomyelopathy due to a biallelic NDUFV1 variant in a mid-forties patient

29. Serum neurofilament light chain as a reliable biomarker of hereditary transthyretin‐related amyloidosis—A Swiss reference center experience.

32. Testing the validity of a set of diagnostic criteria for sensory neuronopathies: a francophone collaborative study

37. Deep phenotyping of an international series of patients with late‐onset dysferlinopathy

38. Implication of folate deficiency in CYP2U1 loss of function

41. Charcot–Marie–Tooth disease misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy: An international multicentric retrospective study

44. Guillain-Barr�� syndrome after SARS-CoV-2 infection in an international prospective cohort study

45. Implication of folate deficiency in CYP2U1 loss of function

46. Charcot-Marie-Tooth disease misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy: An international multicentric retrospective study.

47. Iatrogenic immune-mediated neuropathies: diagnostic, epidemiological and mechanistic uncertainties for causality and implications for clinical practice.

48. Guillain-Barré syndrome after SARS-CoV-2 infection in an international prospective cohort study

49. Guillain-Barré syndrome after SARS-CoV-2 infection in an international prospective cohort study

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