Concurrent Sexual Partnerships and Primary HIV Infectio ...
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Concurrent Sexual Partnerships ...
The combination of long-term concurrent sexual partnerships and high infectiousness early in HIV infection has been suggested as a key driver of the ...
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An Integrated Theoretical Appro ...
Research demonstrates a consistent association between substance use and sexual risk, particularly among men who have sex with men (MSM). The presen ...
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Online Social Networking Techno ...
This study evaluates associations between online social networking and sexual health behaviors among homeless youth in Los Angeles. We analyzed surv ...
179.26 KB
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HIV Interventions to Reduce HIV ...
We reviewed the literature to determine the effectiveness of HIV-related interventions in reducing HIV/AIDS stigma. Studies selected had randomized ...
280.97 KB
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Neurocognitive correlates of ad ...
We established a neuropsychological testing profile among Turkish adults presenting with ADHD controlling for general intelligence and comorbid psyc ...
248.74 KB
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ADHD and comorbid conduct probl ...
Attention-deficit/hyperactivity disorder (ADHD) is a common child and adolescent disorder that is associated with negative outcomes (e.g., emotional ...
232.54 KB
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Childhood obesity and parental ...
ADHD prevalence has risen in parallel with rising prevalence of pregnancy smoking and childhood obesity. The objective was to determine the epidemio ...
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A pilot study: differential eff ...
To examine the effects of methylphenidate- OROS (MPH-OROS) on working memory (WM) and attention functions in children with attention-deficit hypera ...
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Comparison of SHR, WKY and Wist ...
Spontaneously hypertensive rats (SHR) and its counterpart, the Wistar-Kyoto rats (WKY), are probably the most often used animal model of ADHD. Howev ...
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New neuropathological findings ...
Unverricht–Lundborg disease (EPM1A), also known as Baltic myoclonus, is the most common form of progressive myoclonic epilepsy. It is inherited as a ...
605.77 KB
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Four-repeat tauopathy clinicall ...
A man aged 55 with negative family history presented with progressive decline in spatial orientation and visual functions for 2 years. He showed imp ...
640.98 KB
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Superficial neurofibromas in th ...
First described in the past decade, schwannomatosis is a syndrome distinct from neurofibromatosis 2 (NF2). It is characterized by the development of ...
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Neuronal migration disorders in ...
Microcephalic osteodysplastic primordial dwarfism (MOPD) is a rare microlissencephaly syndrome, with at least two distinct phenotypic and genetic ty ...
1.22 MB
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PI3K/AKT pathway alterations ar ...
Pilocytic astrocytomas (PA) are well-differentiated gliomas having a favorable prognosis when compared with other diffuse or infiltrative astrocytom ...
1.18 MB
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Defects in amphiphysin 2 (BIN1) ...
Myotubular myopathy and centronuclear myopathies (CNM) are congenital myopathies characterized by generalized muscle weakness and mislocalization of ...
2.18 MB
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The application of in vitro cel ...
A key event in the pathogenesis of prion diseases is the conversion of the normal cellular isoform of the prion protein into the disease-associated ...
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Genome-wide comparison of pair ...
Array comparative genomic hybridization (aCGH) is a powerful tool for detecting DNA copy number alterations (CNA). Because diffuse malignant gliomas ...
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Mutation-specific IDH1 antibody ...
Isocitrate dehydrogenase 1 (IDH1) mutations are frequent in astrocytomas, oligoastrocytomas and oligodendrogliomas. We previously reported the gener ...
1.19 MB
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Cellular and sub-cellular patho ...
The transmissible spongiform encephalopathies (TSEs) or prion diseases of animals are characterised by CNS spongiform change, gliosis and the accumu ...
1.51 MB
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Preponderance of sonic hedgehog ...
Medulloblastoma (MB) represents approximately 4% of adult brain tumours, and as such is a poorly studied disease. Although many adult MB are treated ...
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Molecular biology and pathology ...
Prion diseases are believed to propagate by the mechanism involving self-perpetuating conformational conversion of the normal form of the prion prot ...
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Risk genotypes at TMEM106B are ...
TMEM106B has recently been identified as a genetic risk factor for frontotemporal lobar degeneration with TDP-43 inclusions (FTLD-TDP). Amyotrophic ...
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The spectrum and severity of FU ...
Neuronal intermediate filament inclusion disease (NIFID), a rare form of frontotemporal lobar degeneration (FTLD), is characterized neuropathologica ...
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Cytoplasmic accumulation of TDP ...
TDP-43, encoded by TARDBP, is a ubiquitously expressed, primarily nuclear protein. In recent years, TDP-43 has been identified as the major patholog ...
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Pathological correlates of fron ...
Frontotemporal lobar degeneration (FTLD) is generally recognised as a disorder with presenile onset (that is before 65 years of age) with only occas ...
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