1,017 results on '"Berciano, J."'
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2. Patología axonal en la fase precoz del síndrome de Guillain-Barré
3. Why do motor neurons degenerate? Actualisation in the pathogenesis of amyotrophic lateral sclerosis
4. ¿Por qué degeneran las motoneuronas? Actualización en la patogenia de la esclerosis lateral amiotrófica
5. The clinical and radiological profile of primary lateral sclerosis: an annotation on its pathological and clinical background
6. Olivopontocerebellar Atrophy
7. Guidelines for molecular diagnosis of Charcot-Marie-Tooth disease
8. Guía diagnóstica en el paciente con enfermedad de Charcot-Marie-Tooth
9. Multimodal neurophysiological study of SCA2 and SCA3 autosomal dominant hereditary spinocerebellar ataxias
10. Charcot-Marie-Tooth disease: a review with emphasis on the pathophysiology of pes cavus
11. Enfermedad de Charcot-Marie-Tooth: revisión con énfasis en la fisiopatología del pie cavo
12. Estudio neurofisiológico multimodal en las ataxias espinocerebelosas con herencia autosómica dominante de tipo SCA2 y SCA3
13. Changes in aminergic receptors in a PSP postmortem brain: correlation with pathological findings
14. Genetic risk score predicting accelerated progression from mild cognitive impairment to Alzheimer’s disease
15. Acute motor conduction block neuropathy pattern occurring in the course of an acute inflammatory demyelinating polyradiculoneuropathy
16. Serum uric acid and risk of dementia in Parkinsonʼs disease: 931
17. Clinical characteristics of long-term survivors in multiple system atrophy: An analysis of the EMSA-SG registry: 299
18. Antibodies against neurofascin-155 (NF155) in CIDP associated with disabling tremor, distal weakness and poor response to IVIg: OS3117
19. Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation
20. Reduced serum progranulin level might be associated with Parkinsonʼs disease risk
21. Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype
22. POLR3A-related spastic ataxia: new mutations and a look into the phenotype
23. Cholesteryl ester transfer protein (CETP) polymorphism modifies the Alzheimer's disease risk associated with APOE ε4 allele
24. The European Multiple System Atrophy-Study Group (EMSA-SG)
25. Charcot-Marie-Tooth disease type 1A duplication with severe paresis of the proximal lower limb muscles: a long-term follow-up study
26. The (alpha)-synuclein gene in multiple system atrophy
27. Eleventh meeting of The European Neurological Society21–25 April, 2001, Paris, France: Symposia and Free Communications
28. Primary brain lymphoma presenting as Parkinson's disease
29. Olivopontocerebellar Atrophy
30. Tenth Meeting of the European Neurological Society 18–22 June, 2000, Jerusalem, Israël: Programme of Symposia and Free Communications
31. Transcranial sonography, DaT-SPECT and olfactory function at the premotor stage of LRRK2 G2019S-associated Parkinsonʼs disease (PD): SC102
32. An early description of striatonigral degeneration
33. Linfoma primario del sistema nervioso central aparentando lesión del ángulo pontocerebeloso
34. Primary central nervous system lymphoma mimicking cerebellopontine angle lesion
35. Axonal pathology in early stages of Guillain-Barré syndrome
36. Leucoencefalopatía multifocal progresiva en un paciente inmunocompetente
37. Progressive multifocal leukoencephalopathy in an immunocompetent patient
38. The clinical and radiological profile of primary lateral sclerosis: an annotation on its pathological and clinical background
39. Synergistic effect of two oxidative stress-related genes (heme oxygenase-1 and GSK3β) on the risk of Parkinsonʼs disease
40. Serum heme oxygenase-1 levels are increased in Parkinsonʼs disease but not in Alzheimerʼs disease
41. Epistasis between tau phosphorylation regulating genes (CDK5R1 and GSK-3β) and Alzheimerʼs disease risk
42. SEVERE AND FATAL GUILLAIN-BARRé SYNDROME (GBS): SORTING OUT THE PATHOLOGICAL HALLMARK IN AN ELECTROPHYSIOLOGIC AXONAL CASE
43. Aromatase and interleukin-10 genetic variants interactively modulate Alzheimerʼs disease risk
44. Inflammation-related genes and the risk of Parkinsonʼs disease: a multilocus approach
45. Genetic interaction between two apolipoprotein E receptors increases Alzheimer's disease risk
46. Gene–gene interaction between 14-3-3 zeta and butyrylcholinesterase modulates Alzheimer′s disease risk
47. Meta-analysis of genetic variability in the β-amyloid production, aggregation and degradation metabolic pathways and the risk of Alzheimerʼs disease
48. Description of Restrictively Defined Acute Flaccid Myelitis
49. Schwann cell nuclear remodelling and formation of nuclear and coiled bodies in Guillain-Barré syndrome
50. Glial cell cytoplasmic inclusions in SCA2 do not express α–synuclein
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