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Daneshyari Developmental Neuroscience Journas Latest Articles

Developmental Neuroscience Research Articles

Subject Index
Fulltext Access 5 Pages 2006
Alteration of regional cerebral blood flow to thyrotropin-releasing hormone therapy in acute encephalitis and encephalopathy during childhood
Fulltext Access 5 Pages 2006
Paediatric and adult ataxias (update 5)
Fulltext Access 5 Pages 2006
Use of the bayley infant neurodevelopmental screener with premature infants
Fulltext Access 5 Pages 2006
Administration of secretin for autism alters dopamine metabolism in the central nervous system
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Neuro-otological features of Benign Paroxysmal Vertigo and Benign Paroxysmal Positioning Vertigo in children: A follow-up study
Fulltext Access 5 Pages 2006
Satoyoshi syndrome: A rare multisystemic disorder requiring systemic and symptomatic treatment
Fulltext Access 5 Pages 2006
IL-1β, IL-6 and TNF-α and outcomes of neonatal hypoxic ischemic encephalopathy
Fulltext Access 5 Pages 2006
Reflex periodic spasms induced by eating
Fulltext Access 5 Pages 2006
Glutaric aciduria types I and II
Fulltext Access 5 Pages 2006
Surgical treatment of two patients with infantile spasms in early infancy
Fulltext Access 5 Pages 2006
Development of the human magnocellular red nucleus: A morphological study
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Frontal horn cysts in normal neonates
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The significance of reduced respiratory chain enzyme activities: Clinical, biochemical and radiological associations
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TRH therapy in a patient with juvenile Alexander disease
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Tracheo-arterial fistula in tracheostomy patients with Duchenne muscular dystrophy
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Fluctuating hearing loss, episodic headache, and stroke with platelet hyperaggregability: Coexistence of auditory neuropathy and cochlear hearing loss
Fulltext Access 5 Pages 2006
Brain MRI findings of older patients with Pallister–Killian syndrome
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Cerebrospinal fluid interleukin-6 levels in patients with west syndrome
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Neurophysiologic and intellectual evaluation of beta-thalassemia patients
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Morphofunctional organization in three patients with unilateral polymicrogyria: Combined use of diffusion tensor imaging and functional magnetic resonance imaging
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Excitatory amino acids and magnesium sulfate in neonatal asphyxia
Fulltext Access 5 Pages 2006
Endogenous semicarbazide-sensitive amine oxidase (SSAO) inhibitor increases 1-methyl-4-phenylpyridinium ion (MPP+)-induced dopamine efflux by immobilization stress in rat striatum
Fulltext Access 5 Pages 2006
Huntingtin is localized in the nucleus during preimplanatation embryo development in mice
Fulltext Access 5 Pages 2006
Zinc uptake is mediated by M1 muscarinic acetylcholine receptors in differentiated SK-SH-SY5Y cells
Fulltext Access 5 Pages 2006
Familial inclusion body myositis in a mother and son with different ancestral MHC haplotypes
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Gene dosage sensitivity of a novel mutation in the intracellular domain of P0 associated with Charcot-Marie-Tooth disease type 1B
Fulltext Access 5 Pages 2006
A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis
Fulltext Access 5 Pages 2006
Eosinophilic fasciitis in a child mimicking a myopathy
Fulltext Access 5 Pages 2006
Carriers and patients with muscle–eye–brain disease can be rapidly diagnosed by enzymatic analysis of fibroblasts and lymphoblasts
Fulltext Access 5 Pages 2006
‘Cap myopathy’: Case report of a family
Fulltext Access 5 Pages 2006
So doctor, what exactly is wrong with my muscles? Glutaric aciduria type II presenting in a teenager
Fulltext Access 5 Pages 2006
Myosin storage (hyaline body) myopathy: A case report
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Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot–Marie–Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLE
Fulltext Access 5 Pages 2006
Long-term improvement of slow-channel congenital myasthenic syndrome with fluoxetine
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Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genes
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Sporadic inclusion body myositis in Japanese is associated with the MHC ancestral haplotype 52.1
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SOD1 gene mutations in Italian patients with Sporadic Amyotrophic Lateral Sclerosis (ALS)
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Expression of the α7, α4 and α3 nicotinic receptor subtype in the brain and adrenal medulla of transgenic mice carrying genes coding for human AChE and β-amyloid
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Extreme phenotypic variability in a German family with X-linked myotubular myopathy associated with E404K mutation in MTM1
Fulltext Access 5 Pages 2006
Development of polyglucosan inclusions in skeletal muscle
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Severe fascioscapulohumeral muscular dystrophy presenting with Coats’ disease and mental retardation
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Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation
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Decrement pattern in Lambert–Eaton myasthenic syndrome is different from myasthenia gravis
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Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2
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Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophy
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Myotilinopathy in a family with late onset myopathy
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Two cases of autosomal recessive generalized dystonia in childhood: 5 year follow-up and bilateral globus pallidus stimulation results
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+H-proton-magnetic resonance spectroscopic findings in a patient with acute hemicerebellitis presenting without localized signs: A case report
Fulltext Access 5 Pages 2006
Transient acute obstructive hydrocephalus of unknown origin in a 13-month-old infant
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Activation of Color-Selective areas of the Visual Cortex in a Blind Synesthete
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Two cases of spontaneous middle cerebral arterial dissection causing ischemic stroke
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Intrafamilial phenotypic and genetic heterogeneity of dystonia
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Predictors of delay in the diagnosis and clinical trial entry of amyotrophic lateral sclerosis patients: A population-based study
Fulltext Access 5 Pages 2006
Heterogeneous epileptogenicity and cortical function within malformations of cortical development: A case report
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CSF markers in Alzheimer disease patients are not related to the different degree of cognitive impairment
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Two new missense mutations of GAA in late onset glycogen storage disease type II
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Genetic analysis of LRRK2 mutations in patients with Parkinson disease
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MMP-2 and MMP-9 levels in peripheral blood after subarachnoid hemorrhage
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Variability of the systemic acute phase response after ischemic stroke
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Effect of arundic acid on serum S-100β in ischemic stroke
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Hand Actions and Speech Representation in Broca's Area
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The Language Faculty, Broca'S Region, and the Mirror System
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Interleukin-12 is reduced in cerebrospinal fluid of patients with Alzheimer's disease and frontotemporal dementia
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Pupillometry of Grapheme-Color Synaesthesia
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Color Congruity Effect: Where do Colors and Numbers Interact in Synesthesia?
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Williams Syndrome: Fractionations All the Way Down?
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Stretch That Net or Your Mind May Fall into Phrenology
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Stretching Ideas About the Brain That Haven't Changed my Mind
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Lexical Selection is Not a Competitive Process: A Reply to La Heij et al. (2006)
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A Method for Studies of Madness
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“A Rough Guide to the Mind” a Festschrift in Honour of Prof. John C. Marshall
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Visual Spatial Neglect in Multiple Sclerosis
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Variability of the Snarc Effect: Systematic Interindividual Differences or Just Random Error?
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How Images of the Brain can Constrain Cognitive Theory: the Case of Numerical Cognition
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Sohlh2 is a germ cell-specific bHLH transcription factor
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Caffeine modulates potassium currents in Drosophila neurons
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Ganglionary mechanisms of spasticity and ileus in cerebral hemorrhage: an experimental study
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Differential activities in adhesion and neurite growth of fibronectin type III repeats in the PTP-δ extracellular domain
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Instructions to Authors
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Spatiotemporal expression of zebrafish keratin 18 during early embryogenesis and the establishment of a keratin 18:RFP transgenic line
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Developmental expression of FoxJ1.2, FoxJ2, and FoxQ1 in Xenopus tropicalis
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Bruno-like protein is localized to zebrafish germ plasm during the early cleavage stages
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Expression of abdominal-A homeotic gene in ants with different abdominal morphologies
Fulltext Access 5 Pages 2006
Identification and developmental expression analysis of a novel homeobox gene closely linked to the mouse Twirler mutation
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Differential Effects of Transcranial Magnetic Stimulation of Left and Right Posterior Parietal Cortex on Mental Rotation Tasks
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Teashirt 3 expression in the chick embryo reveals a remarkable association with tendon development
Fulltext Access 5 Pages 2006
Tenectin, a novel extracellular matrix protein expressed during Drosophila melanogaster embryonic development
Fulltext Access 5 Pages 2006
CyNodal, the Japanese newt nodal-related gene, is expressed in the left side of the lateral plate mesoderm and diencephalon
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Expression analysis of the Epha1 receptor tyrosine kinase and its high-affinity ligands Efna1 and Efna3 during early mouse development
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Molecular characterization of the rostral-most somites in early somitic stages of the chick embryo
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Diffuse metabolic changes in the brain of patients with familial amyloid polyneuropathy. A proton MRSI study
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Should neurologists measure fibrinogen concentrations?
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Myopathy in thiamine deficiency: Analysis of a case
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Single nucleotide polymorphisms and functional analysis of MxA promoter region in multiple sclerosis
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Enhanced neuroprotective effect by combination of bromocriptine and Hypericum perforatum extract against MPTP-induced neurotoxicity in mice
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Cerebrovascular reactivity over time course in healthy subjects
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A functional FERM domain binding motif in neurofascin
Fulltext Access 6 Pages 2006
Pin1 allows for differential Tau dephosphorylation in neuronal cells
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Neurotrophic property of geniposide for inducing the neuronal differentiation of PC12 cells
Fulltext Access 6 Pages 2006
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