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Daneshyari Developmental Neuroscience Journas Latest Articles

Developmental Neuroscience Research Articles

Asymmetric expression of Syndecan-2 in early chick embryogenesis
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Xenopus genetics and genomics
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Plenary Abstracts
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NMDA receptors contribute to the survival promoting effect of high potassium in cultured cerebellar granule cells
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Putative mechanisms of action of statins in multiple sclerosis - comparison to interferon-β and glatiramer acetate
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Prevalence and pathogenic role of cerebrovascular lesions in Alzheimer disease
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Predictors of reversible mild cognitive impairment after stroke: a 2-year follow-up study
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Chronic inflammatory demyelinating polyneuropathy in a patient with hyperIgEaemia
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Comparison of age of onset and development of motor complications between smokers and non-smokers in Parkinson's disease
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Intravascular lymphomatosis presenting with sudden hearing loss
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Transcranial color-coded sonography for vertebrobasilar disorders in end-stage renal disease
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Utilization of the multiple sclerosis functional composite in follow-up: relationship to disease phenotype, disability and treatment strategies
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Expression of ABCA2 protein in human vestibular schwannoma and peripheral nerve
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Diffusion-weighted MRI in familial Creutzfeldt-Jakob disease with the codon 200 mutation in the prion protein gene
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Accrual of MRI white matter abnormalities in elderly with normal and impaired mobility
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Patterns of memory impairment and perseverative behavior discriminate early Alzheimer's disease from subcortical vascular dementia
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Can glatiramer acetate reduce brain atrophy development in multiple sclerosis?
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Vitamin B12, demyelination, remyelination and repair in multiple sclerosis
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Mechanisms of CNS remyelination-the key to therapeutic advances
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Axonal signals in central nervous system myelination, demyelination and remyelination
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Intravenous immunoglobulin treatment of multiple sclerosis and its animal model, experimental autoimmune encephalomyelitis
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Cortical lesions and brain atrophy in MS
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Overcoming inhibitors in myelin to promote axonal regeneration
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Cannabinoids and neuroprotection in CNS inflammatory disease
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The relation between MRI measures of inflammation and neurodegeneration in multiple sclerosis
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Abnormalities on ECG and telemetry predict stroke outcome at 3 months
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Pilot study to examine the effect of antibiotic therapy on MRI outcomes in RRMS
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Neuroanatomic observations of the brain in autism: a review and future directions
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Dephosphorylation and internalization of cell adhesion molecule L1 induced by theta burst stimulation in rat hippocampus
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Anomic Alexia of Kanji in a Patient with Anomic Aphasia
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George Combe - Phrenologist, Philosopher, Psychologist (1788-1858)
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The Neurobiology of Developmental Disorders
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Paradox Lost: Illusion Regained
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Cerebral white matter injury in the newborn following Escherichia coli meningitis
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Peripheral neuropathy-a novel finding in dyskeratosis congenita
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Acute demyelinating encephalomyelitis (ADEM), cryptococcal reactivation and disseminated Herpes simplex in an HIV infected child following HAART
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Honorary membership of the European Paediatric Neurology Society
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CNS malformations: Gene locations of known human mutations
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Prevalence of pyridoxine dependent seizures in south Indian children with early onset intractable epilepsy: A hospital based prospective study
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The acoustic cortex in vascular dementia: a Golgi and electron microscope study
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Instructions to Authors
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The regulation of β-secretase by cholesterol and statins in Alzheimer's disease
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Non-human primate SPECT model for determining cerebral perfusion effects of cerebrovasoactive drugs acting via multiple modes of pharmacological action
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[11C]Vinpocetine: a prospective peripheral benzodiazepine receptor ligand for primate PET studies
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Cognitive functioning after repetitive transcranial magnetic stimulation in patients with cerebrovascular disease without dementia: a pilot study of seven patients
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Does blood pressure lowering treatment prevents dementia or cognitive decline in patients with cardiovascular and cerebrovascular disease?
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Differential cognitive outcomes in the Hypertensive Old People in Edinburgh study
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Gait slowing as a predictor of incident dementia: 6-year longitudinal data from the Sydney Older Persons Study
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Multiple sclerosis in Iraq: Does it have the same features encountered in Western countries?
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Methods of detecting potential causes of vascular cognitive impairment after coronary artery bypass grafting
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Maternal ethanol administration inhibits 5-hydroxytryptamine synthesis and tryptophan hydroxylase expression in the dorsal raphe of rat offspring
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Dilated cardiomyopathy may be an early sign of the C826A Fukutin-related protein mutation
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A rapid PCR method for genotyping the Largemyd mouse, a model of glycosylation-deficient congenital muscular dystrophy
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Non-progressive leukoencephalopathy with bilateral anterior temporal cysts: a case report and review of the literature
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Congenital bilateral perisylvian syndrome with partial epilepsy. Case report with long-term follow-up
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Oxidative nucleotide damage and superoxide dismutase expression in the brains of xeroderma pigmentosum group A and Cockayne syndrome
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Possible antenatal and perinatal related factors in development of cystic periventricular leukomalacia
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Learning ability in children with Rett syndrome
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Early motor disturbances in Rett syndrome and its pathophysiological importance
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Predictive value of the early clinical signs in Rett disorder
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Perturbations in the development of infants with Rett disorder and the implications for early diagnosis
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Acute onset of abducens nerve palsy in a child with prior history of otitis media: a misleading sign of Gradenigo syndrome
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Prognosis of Bell's palsy in children-analysis of 29 cases
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An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene
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Clinical experience with Topiramate to counteract neuroleptic induced weight gain in 10 individuals with autistic spectrum disorders
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Lateralization of the frontal lobe functions elicited by a cognitive bias task is a fundamental process. Lesion study
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Acute respiratory distress syndrome in children with severe motor and intellectual disabilities
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Autonomic dysfunction in cases of spinal muscular atrophy type 1 with long survival
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Epilepsy and neurological findings in 11 individuals with 1p36 deletion syndrome
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The inv dup(15) or idic(15) syndrome: A clinically recognisable neurogenetic disorder
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Natural history of X-linked adrenoleukodystrophy in Japan
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Differences between attention-deficit disorder with and without hyperactivity: a 1H-magnetic resonance spectroscopy study
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Comparison of two low dose ACTH therapies for West syndrome: their efficacy and side effect
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Mutation analysis of methyl-CpG binding protein family genes in autistic patients
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Zonisamide for West syndrome: a comparison of clinical responses among different titration rate
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Lymphocyte-specific protein tyrosine kinase is a novel risk gene for Alzheimer disease
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Mannitol in intracerebral hemorrhage: A randomized controlled study
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Frontal nonconvulsive status epilepticus manifesting somatic hallucinations
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Pectoralis major motor evoked potentials in cervical spondylosis
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Approaching an individual methotrexate regimen in leptomeningeal carcinomatosis
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Prevalence and risk factors of post-polio syndrome in a cohort of polio survivors
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Spinocerebellar ataxia type 6 in Mainland China: Molecular and clinical features in four families
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Unilateral retrobulbar optic neuritis due to varicella zoster virus in a patient with AIDS: A case report and review of the literature
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Decreased β-amyloid peptide42 in cerebrospinal fluid of patients with progressive supranuclear palsy and corticobasal degeneration
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Extrathymic malignancies in patients with myasthenia gravis
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MEP recruitment curves in multiple sclerosis and hereditary spastic paraplegia
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CADASIL with NOTCH3 S180C presenting anticipation of onset age and hallucinations
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A test for the evaluation of the lateral cutaneous branch of the iliohypogastric nerve using somatosensory evoked potentials
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International Child Neurology Association: Current role and future perspectives
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Late-onset pure cerebellar ataxia: Differentiating those with and without identifiable mutations
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Thalidomide neuropathy in childhood
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Author Index
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Co-segregation of LMNA and PMP22 gene mutations in the same family
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Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophy
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A family with a novel frameshift mutation in the PMP22 gene (c.433_434insC) causing a phenotype of hereditary neuropathy with liability to pressure palsies
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Comparison of different techniques for detecting 17p12 duplication in CMT1A
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Recurrent somatic mosaicism for D4Z4 contractions in a family with facioscapulohumeral muscular dystrophy
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129th ENMC International Workshop: Clinical Trials for Chronic Inflammatory Demyelinating Polyradiculoneuropathy and Multifocal Motor Neuropathy, 27th October 2004, Schiphol airport, The Netherlands
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The genes encoding for D4Z4 binding proteins HMGB2, YY1, NCL, and MYOD1 are excluded as candidate genes for FSHD1B
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A novel ANT1 gene mutation with probable germline mosaicism in autosomal dominant progressive external ophthalmoplegia
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