Paper Search Console

Home Search Page About Contact

Journal Title

Title of Journal: J Neurol

Search In Journal Title:

Abbravation: Journal of Neurology

Search In Journal Abbravation:

Publisher

Steinkopff-Verlag

Search In Publisher:

DOI

10.1002/ange.201302596

Search In DOI:

ISSN

1432-1459

Search In ISSN:
Search In Title Of Papers:

APOE genotypes in Greek multiple sclerosis patient

Authors: Georgios Koutsis Marios Panas Georgia Karadima Dimitris Mandellos Constantinos Sfagos Constantin Potagas Demetris Vassilopoulos
Publish Date: 2007/03/07
Volume: 254, Issue: 3, Pages: 394-395
PDF Link

Abstract

Sirs Evidence on the influence of apolipoprotein E APOE polymorphisms on multiple sclerosis MS disease severity has been controversial Several studies have associated the ε4 polymorphism with more rapid progression 1 2 7 Others have not confirmed this 5 6 10 11 The MS severity score MSSS was recently developed as a powerful method for comparing disease progression in genetic association studies 4 In the present study we investigated the effect of APOE genotypes on disease severity in Greek MS patients a previously unstudied population using the MSSSAPOE genotypes were determined in 212 Greek patients 135 females 77 males with MS McDonald criteria under the care of the Neurology Department University of Athens 3 Only patients with disease duration of at least one year were included Mean patient age was 387 ± 104 years range 16–69 mean age at onset 301 ± 99 years range 10–64 mean disease duration 86 ± 67 years range 1–39 mean EDSS

Keywords:

References

.
Search In Abstract Of Papers:
Other Papers In This Journal:
  1. Toothbrushing-induced seizures at onset of cryptogenic partial epilepsy: a case report
  2. Associated and predictive factors of depressive symptoms in patients with Parkinson’s disease
  3. Sensory loss, pains, motor deficit and axonal regeneration in length-dependent diabetic polyneuropathy
  4. Walter Rudolf Hess (1881–1973)
  5. Current concepts and future approaches to vestibular rehabilitation
  6. Clinical features associated with REM sleep behavior disorder symptoms in the early stages of Parkinson’s disease
  7. Vestibular animal models: contributions to understanding physiology and disease
  8. Primary leptomeningeal lymphoma of the cauda equina: a rare cause of radiculopathy
  9. DWI and FLAIR imaging in herpes simplex encephalitis: a comparative and topographical analysis
  10. Interferon beta in secondary progressive multiple sclerosis
  11. Tissue damage within normal appearing white matter in early multiple sclerosis: assessment by the ratio of T1- and T2-weighted MR image intensity
  12. Diaphragm of the internal carotid artery: a novel cause of pulsatile tinnitus
  13. Retinal nerve fiber layer thickness in subgroups of multiple sclerosis, measured by optical coherence tomography and scanning laser polarimetry
  14. Tolvaptan treatment of severe stroke-like symptoms and bilateral subcortical diffusion restriction due to syndrome of inappropriate secretion of ADH after polytrauma
  15. Tolvaptan treatment of severe stroke-like symptoms and bilateral subcortical diffusion restriction due to syndrome of inappropriate secretion of ADH after polytrauma
  16. Detailing intra-lesional venous lumen shrinking in multiple sclerosis investigated by sFLAIR MRI at 7-T
  17. Neurological complications of Behçet’s syndrome
  18. Highly skewed inactivation of the wild-type X-chromosome in asymptomatic female carriers of spinal and bulbar muscular atrophy (Kennedy’s disease)
  19. Meningitis–retention syndrome
  20. Early MRI findings in Creutzfeldt-Jakob disease
  21. Causes and characteristics of horizontal positional nystagmus
  22. The comparison of clonidine, arginine and both combined: a growth hormone stimulation test to differentiate multiple system atrophy from idiopathic Parkinson’s disease
  23. Mastication-induced vertigo and nystagmus
  24. Need for extensive diagnostic work-up for patients with lacunar stroke
  25. Low testosterone and myasthenia gravis in males: a national record-linkage study
  26. Plasma levels of nitric oxide and stroke outcome
  27. High field MR imaging and 1 H-MR spectroscopy in clinically isolated syndromes suggestive of multiple sclerosis
  28. Patient-reported adverse effects of high-dose intravenous methylprednisolone treatment: a prospective web-based multi-center study in multiple sclerosis patients with a relapse
  29. Cesare Vigna (1819–1892)
  30. Cesare Vigna (1819–1892)
  31. Aquaporin-4 seropositivity in a patient with coeliac disease but normal neurological examination and imaging
  32. Repetitive magnetic stimulation A novel therapeutic approach for myofascial pain syndrome
  33. Downbeat positioning nystagmus is a common clinical feature despite variable phenotypes in an FHM1 family
  34. Psychological interventions for migraine: a systematic review
  35. Respiratory dysfunction in Charcot–Marie–Tooth disease type 1A
  36. Myoclonus-dystonia and epilepsy in a family with a novel epsilon-sarcoglycan mutation
  37. Epiretinal membrane: a treatable cause of visual disability in myotonic dystrophy type 1
  38. Spinocerebellar ataxia type 17 in a patient from an Indian kindred
  39. ‘Switching off’ SUNCT by sudden head movement: a new symptom
  40. A clinical, radiological and outcome study of status epilepticus from India
  41. The impact of subthalamic deep brain stimulation on caregivers of Parkinson’s disease patients: an exploratory study
  42. Management of respiratory symptoms in ALS
  43. Lower serum ceruloplasmin levels correlate with younger age of onset in Parkinson’s disease
  44. Opsoclonus–myoclonus–ataxia syndrome and HIV seroconversion
  45. Vascular risk factors are associated with faster decline of Alzheimer disease: a longitudinal SPECT study
  46. Electrophysiological features of late-onset transthyretin Met30 familial amyloid polyneuropathy unrelated to endemic foci
  47. Presenilin 2 mutation R71W in an Italian early-onset sporadic Alzheimer’s disease case
  48. Recovery from mild traumatic brain injury
  49. Modafinil for Parkinson’s disease fatigue
  50. Diagnosis and treatment of upper limb apraxia
  51. Familial aggregation in atypical Parkinson’s disease: a case control study in multiple system atrophy and progressive supranuclear palsy
  52. Thymectomy: role in the treatment of myasthenia gravis
  53. Long-term EMG recordings differentiate between parkinsonian and essential tremor
  54. Isolated recurrent myelitis in a 7-year-old child with serum aquaporin-4 IgG antibodies
  55. Cortical thinning in drug-naive Parkinson’s disease patients with depression
  56. Clinical phenotype and risk of levodopa-induced dyskinesia in Parkinson’s disease
  57. Frontal lobe function and behavioral changes in amyotrophic lateral sclerosis: a study from Southwest China
  58. Tic disorders: from pathophysiology to treatment
  59. Parkinson’s disease: news on tremor, subthalamic stimulation and impulse control disorders
  60. The use of multiattribute decision models in evaluating triptan treatment options in migraine
  61. Psychiatric disorders in idiopathic-isolated focal dystonia
  62. Domain-specific versus generalized cognitive screening in acute stroke
  63. Multiple sclerosis imaging: recent advances
  64. Hemifacial presentation of mitochondrial myopathy
  65. Teleneurology in stroke management: costs of service in different organizational models
  66. Small-fibre neuropathy related to bulbar and spinal-onset in patients with ALS
  67. Cerebral blood flow abnormalities in patients with neurally mediated syncope
  68. Specific electron transport chain abnormalities in amyotrophic lateral sclerosis
  69. Parkinson’s disease-related disorders in the impulsive-compulsive spectrum
  70. Accepting or declining non-invasive ventilation or gastrostomy in amyotrophic lateral sclerosis: patients’ perspectives
  71. Bladder dysfunction in subacute combined degeneration
  72. Predictors and prevalence of low bone mineral density in fully ambulatory persons with multiple sclerosis
  73. Missense exchanges in the TTBK2 gene mutated in SCA11
  74. Diffusion tensor imaging reveals widespread white matter abnormalities in children and adolescents with myotonic dystrophy type 1
  75. Prior medical conditions and the risk of amyotrophic lateral sclerosis
  76. An epidemiological study of neuromyelitis optica in Cuba
  77. Brachial neuritis caused by varicella-zoster diagnosed by changes in brachial plexus on MRI
  78. Subthalamic nucleus stimulation in Parkinson’s disease
  79. Dopaminergic medication does not improve stepping responses following backward and forward balance perturbations in patients with Parkinson’s disease
  80. Novel EXOSC3 mutation causes complicated hereditary spastic paraplegia
  81. A genome wide linkage disequilibrium screen in Parkinson’s disease
  82. Differential effect of Huntington's and Parkinson's diseases in programming motor sequences of varied lengths
  83. Accuracy of subjective and objective handwriting assessment for differentiating Parkinson’s disease from tremulous subjects without evidence of dopaminergic deficits (SWEDDs): an FP-CIT-validated study
  84. The utility of F wave chronodispersion in lumbosacral radiculopathy
  85. Accuracy of subjective and objective handwriting assessment for differentiating Parkinson’s disease from tremulous subjects without evidence of dopaminergic deficits (SWEDDs): an FP-CIT-validated study
  86. Recurrent rhabdomyolysis due to muscle β-enolase deficiency: very rare or underestimated?
  87. Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else?
  88. Paroxysmal raised intracranial pressure associated with spinal meningeal cysts
  89. The relationship between impairment of voluntary movements and cognitive impairment in Huntington’s disease
  90. Long-term domain-specific improvement following poor grade aneurysmal subarachnoid hemorrhage
Search Result: