# عنوان نوع فایل سایز فایل بازدید دانلود امتیاز قیمت (تومان)
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Long-term open-label response to atomoxetine in adult ADHD:influence of sex, emotional dysregulation, and double-blind response to atomoxetine
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Mothers of children with attention deficit/hyperactivity disorder:relationship among parenting stress, parental practices and child behaviour
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Olfactory and gustatory sensitivity in adults with attention-deficit/hyperactivity disorder
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Antecedents of ADHD: a historical account of diagnostic concepts
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Globular glial tauopathies (GGT) presenting with motor neuron disease or frontotemporal dementia: an emerging group of 4-repeat tauopathies
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Peroxisomal alterations in Alzheimer’s disease
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Macrophage migration inhibitory factor (MIF) expression in human malignant gliomas contributes to immune escape and tumour progression
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Vasculitis-like neuropathy in amyotrophic lateral sclerosis unresponsive to treatment
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Enhancement of endogenous neurogenesis in ephrin-B3 deficient I ce after transient focal cerebral ischemia
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Postsynaptic degeneration as revealed by PSD-95 reduction occurs after advanced Ab and tau pathology in transgenic mouse models of Alzheimer’s disease
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Widespread non-central nervous system organ pathology in fragile X premutation carriers with fragile X-associated tremor/ataxia syndrome and CGG knock-in mice
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The cerebellar component of Friedreich’s ataxia
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Factors affecting Ab plasma levels and their utility as biomarkers in ADNI
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The spinal muscular atrophy mouse model, SMAD7, displays altered axonal transport without global neurofilament alterations
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Cholinergic imbalance in the multiple sclerosis hippocampus
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Cell stress induces TDP-43 pathological changes associated with ERK1/2 dysfunction: implications in ALS
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Spindle cell oncocytoma of the pituitary gland with follicle-like component: organotypic differentiation to support its origin from folliculo-stellate cells
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SOCS3 promoter methylation is mutually exclusive to EGFR amplification in gliomas and promotes glioma cell invasion through STAT3 and FAK activation
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The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene
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A distinct region of the MGMT CpG island critical for transcriptional regulation is preferentially methylated in glioblastoma cells and xenografts
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Analysis of BRAF V600E mutation in 1,320 nervous system tumors reveals high mutation frequencies in pleomorphic xanthoastrocytoma, ganglioglioma and extra-cerebellar pilocytic astrocytoma
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Pediatric and adult sonic hedgehog medulloblastomas are clinically and molecularly distinct
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Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation
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A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy
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Granular expression of prolyl-peptidyl isomerase PIN1 is a constant and specific feature of Alzheimer’s disease pathology and is independent of tau, Ab and TDP-43 pathology
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Long-term open-label response to atomoxetine in adult ADHD:influence of sex, emotional dysregulation, and double-blind response to atomoxetine

Long-term open-label response t ...

A three-year open-label study of atomoxetine in adults with ADHD followed two multicenter, double-blind trials. In the double-blind trials, female g ...

دانلود 2
216.72 KB
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Mothers of children with attention deficit/hyperactivity disorder:relationship among parenting stress, parental practices and child behaviour

Mothers of children with attent ...

This study focuses on mothers of children diagnosed with attention deficit/hyperactivity disorder (ADHD) and sets out (1) to characterize dimensions ...

203.01 KB
رایگان
Olfactory and gustatory sensitivity in adults with attention-deficit/hyperactivity disorder

Olfactory and gustatory sensiti ...

Recently, research on olfactory functions in attention-deficit/hyperactivity disorder (ADHD) has become prominent, whereas gustation has never been ...

282.43 KB
رایگان
Antecedents of ADHD: a historical account of diagnostic concepts

Antecedents of ADHD: a historic ...

The concept of ADHD has evolved gradually and still carries some traces of its origins. The idea of uncontrolled behaviour as a medical problem aros ...

دانلود 1
198.11 KB
رایگان
Globular glial tauopathies (GGT) presenting with motor neuron disease or frontotemporal dementia: an emerging group of 4-repeat tauopathies

Globular glial tauopathies (GGT ...

A number of recent studies have described cases with tau-positive globular oligodendroglial inclusions (GOIs) and such cases have overlapping pathol ...

941.23 KB
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Peroxisomal alterations in Alzheimer’s disease

Peroxisomal alterations in Alzh ...

In Alzheimer’s disease (AD), lipid alterations are present early during disease progression. As some of these alterations point towards a peroxisoma ...

627.39 KB
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Macrophage migration inhibitory factor (MIF) expression in human malignant gliomas contributes to immune escape and tumour progression

Macrophage migration inhibitory ...

Macrophage migration inhibitory factor (MIF), which inhibits apoptosis and promotes angiogenesis, is expressed in cancers suppressing immune surveil ...

878.46 KB
رایگان
Vasculitis-like neuropathy in amyotrophic lateral sclerosis unresponsive to treatment

Vasculitis-like neuropathy in a ...

Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disease with variable involvement of other systems. A pathogenetic role of immune-mediat ...

1.47 MB
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Enhancement of endogenous neurogenesis in ephrin-B3 deficient I ce after transient focal cerebral ischemia

Enhancement of endogenous neuro ...

Cerebral ischemia stimulates endogenous neurogenesis. However, the functional relevance of this phenomenon remains unclear because of poor survival ...

743.82 KB
رایگان
Postsynaptic degeneration as revealed by PSD-95 reduction occurs after advanced Ab and tau pathology in transgenic mouse models of Alzheimer’s disease

Postsynaptic degeneration as re ...

Impairment of synaptic plasticity underlies memory dysfunction inAlzheimer’s disease (AD). Molecules involved in this plasticity such as PSD-95, a m ...

885.84 KB
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Widespread non-central nervous system organ pathology in fragile X premutation carriers with fragile X-associated tremor/ataxia syndrome and CGG knock-in mice

Widespread non-central nervous ...

Fragile X-associated tremor/ataxia syndrome (FXTAS) is an adult-onset neurodegenerative disorder generally presenting with intention tremor and gait ...

545.66 KB
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The cerebellar component of Friedreich’s ataxia

The cerebellar component of Fri ...

Lack of frataxin in Friedreich’s ataxia (FRDA) causes a complex neurological and pathological phenotype. Progressive atrophy of the dentate nucleus ...

1.41 MB
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Factors affecting Ab plasma levels and their utility as biomarkers in ADNI

Factors affecting Ab plasma lev ...

Previous studies of Ab plasma as a biomarker for Alzheimer’s disease (AD) obtained conflicting results. We here included 715 subjects with baseline ...

411.18 KB
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The spinal muscular atrophy mouse model, SMAD7, displays altered axonal transport without global neurofilament alterations

The spinal muscular atrophy mou ...

Spinal muscular atrophy (SMA) is a neurodegenerative disease resulting from decreased levels of survival motor neuron 1 (SMN1) protein. Reduced SMN1 ...

783.03 KB
رایگان
Cholinergic imbalance in the multiple sclerosis hippocampus

Cholinergic imbalance in the mu ...

Hippocampal pathology was shown to be extensive in multiple sclerosis (MS) and is associated with memory impairment. In this post-mortem study, we ...

658.29 KB
رایگان
Cell stress induces TDP-43 pathological changes associated with ERK1/2 dysfunction: implications in ALS

Cell stress induces TDP-43 path ...

TDP-43 has been implicated in the pathogenesis of amyotrophic lateral sclerosis and other neurodegenerative diseases. Here we demonstrate, using ne ...

1.33 MB
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Spindle cell oncocytoma of the pituitary gland with follicle-like component: organotypic differentiation to support its origin from folliculo-stellate cells

Spindle cell oncocytoma of the ...

Spindle cell oncocytoma (SCO) is a rare, nonadenomatous tumor originating from the anterior pituitary gland. Composed of fusiform, mitochondrion-ric ...

593.01 KB
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SOCS3 promoter methylation is mutually exclusive to EGFR amplification in gliomas and promotes glioma cell invasion  through STAT3 and FAK activation

SOCS3 promoter methylation is m ...

The suppressor of cytokine signaling 3 (SOCS3) gene is one of eight structurally related genes of the SOCS family and has been suggested to function ...

692.36 KB
رایگان
The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene

The most common type of FTLD-FU ...

rontotemporal lobar degeneration (FTLD) is clinically, pathologically and genetically heterogeneous. Recent descriptions of a pathological sub-type ...

481.03 KB
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A distinct region of the MGMT CpG island critical for transcriptional regulation is preferentially methylated in glioblastoma cells and xenografts

A distinct region of the MGMT C ...

O6-Methylguanine-DNA methyltransferase (MGMT) is a DNA repair protein that removes alkyl DNA adducts such as those induced by alkylating agents. Los ...

686.11 KB
رایگان
Analysis of BRAF V600E mutation in 1,320 nervous system tumors reveals high mutation frequencies in pleomorphic xanthoastrocytoma, ganglioglioma and extra-cerebellar pilocytic astrocytoma

Analysis of BRAF V600E mutation ...

Missense mutations of the V600E type constitute the vast majority of tumor-associated somatic alterations in the v-RAF murine sarcoma viral oncogene ...

360.69 KB
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Pediatric and adult sonic hedgehog medulloblastomas are clinically and molecularly distinct

Pediatric and adult sonic hedge ...

Recent integrative genomic approaches have defined molecular subgroups of medulloblastoma that are genetically and clinically distinct. Sonic hedgeh ...

811.59 KB
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Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation

Pathological heterogeneity in a ...

Mutations in the gene encoding the fused in sarcoma (FUS) protein are responsible for*3% of familial amyotrophic lateral sclerosis (ALS) and\1% of s ...

725.88 KB
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A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy

A new phenotype of mitochondria ...

Axial myopathy is a rare neuromuscular disease that is characterized by paraspinal muscle atrophy and abnormal posture, most notably camptocormia (a ...

738.08 KB
رایگان
Granular expression of prolyl-peptidyl isomerase PIN1 is a constant and specific feature of Alzheimer’s disease pathology and is independent of tau, Ab and TDP-43 pathology

Granular expression of prolyl-p ...

Alzheimer’s disease (AD) manifests with progressive memory loss and decline of spatial awareness and motor skills. Neurofibrillary tangles (NFTs) re ...

839.93 KB
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