Results 71 to 80 of about 602,595 (256)

Evolutionarily conserved herpesviral protein interaction networks. [PDF]

open access: yes, 2009
Herpesviruses constitute a family of large DNA viruses widely spread in vertebrates and causing a variety of different diseases. They possess dsDNA genomes ranging from 120 to 240 kbp encoding between 70 to 170 open reading frames. We previously reported
Bandyopadhyay, Sourav   +79 more
core   +1 more source

Pityriasis Rosea in a Pregnancy

open access: yesGynecology Obstetrics & Reproductive Medicine, 2012
A pregnant woman with Pitriasis rosea whose lesion onset is in first trimester is presented. No interventions were undertaken and her eruption remitted completely 6-7 weeks. We found no evidence of active infection for HHV-6 and HHV-7.
Abdullah Karaer   +2 more
doaj  

Herpesvirus-6 Infection and First Febrile Seizures

open access: yesPediatric Neurology Briefs, 1995
The association between acute human herpesvirus-6 (HHV-6) infection and first febrile convulsions was investigated prospectively in 42 children evaluated by virologic and serologic methods at the North Shore University Hospital-Cornell University Medical
J Gordon Millichap
doaj   +1 more source

Gene expression studies of lytic infection and chromosomal integration of human herpesvirus 6.

open access: yes, 2008
Human herpesvirus 6 (HHV-6) was discovered in 1986 in patients with lymphoproliferative diseases and it has a predominant tropism for CD4+ T cells in vitro and in vivo.
Tsao, E.H.F.
core  

Human Herpesvirus-6 in Mesial Temporal Lobe Epilepsy

open access: yesPediatric Neurology Briefs, 2003
Brain samples obtained from surgical resections in 8 patients with mesial temporal lobe epilepsy (MTLE) and 7 patients with neocortical epilepsy (NE) were quantitatively analyzed for HHV-6 in a study at the National Institute of Neurological Disorders ...
J Gordon Millichap
doaj   +1 more source

Emerging Paediatric Uses of Dupilumab Beyond Approvals

open access: yesClinical &Experimental Allergy, EarlyView.
Dupilumab, through IL‐4Rα blockade, shows promising efficacy beyond approved indications in paediatric diseases driven by T2 inflammation. Emerging evidence—mainly from small studies—supports improvements in disease severity and quality of life, highlighting its potential as a targeted, steroid‐sparing therapy while underscoring the need for ...
Simone Foti Randazzese   +11 more
wiley   +1 more source

Pityriasis Rosea is Associated with Systemic Active Infection with Both Human Herpesvirus-7 and Human Herpesvirus-6

open access: yes, 2002
Pityriasis rosea is a common skin disease that has been suspected to have a viral etiology. We performed nested polymerase chain reaction to detect human herpesvirus-7, human herpesvirus-6, and cytomegalovirus DNA in lesional skin, nonlesional skin ...
Kawamura, Tatsuyoshi   +6 more
core   +1 more source

Perceived costs as drivers of wildlife management preferences in rural Tanzanian communities

open access: yesConservation Biology, EarlyView.
Abstract Effectively managing human–wildlife interactions is crucial for fostering coexistence on shared landscapes. Management options are most effective when aligned with the preferences of people directly affected by wildlife, yet little is known about how socioecological factors influence these preferences.
Christian Kiffner   +10 more
wiley   +1 more source

CNS Complications of Primary Human Herpesvirus-6 Infection

open access: yesPediatric Neurology Briefs, 2007
Central nervous system manifestations of primary human herpesvirus-6 (HHV-6) are described in 9 children, ages 3 to 24 months, with HHV-6 DNA in the cerebrospinal fluid, in a prospective study at the University of Helsinki, and other centers in Finland.
J Gordon Millichap
doaj   +1 more source

Clinical and genetic characterization of intellectual disability

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
This study examines the etiological factors and comorbidities in a large cohort of Finnish patients with intellectual disability. Genetic causes—including chromosomal abnormalities and pathogenic gene variants—were more frequently identified in individuals with moderate to profound intellectual disability.
Aarni Venetvaara   +14 more
wiley   +1 more source

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