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1.
Phys Rev Lett ; 99(16): 162502, 2007 Oct 19.
Artigo em Inglês | MEDLINE | ID: mdl-17995243

RESUMO

The time delay in fission induced by bombardment of W with 180 MeV 32S, 240-255 MeV 48Ti, and 315-375 MeV 58Ni has been measured by observation of crystal blocking. There is a clear narrowing and a small increase in the minimum yield of the angular dips for fission compared with scaled dips for elastically scattered ions. This is interpreted as a fission delay of about 2 as, only weakly dependent on energy and atomic number. The delay is longer by 1 to 2 orders of magnitude than obtained from standard interpretations of measurements of prescission neutrons and giant-dipole-resonance gamma rays and from calculations of the nuclear dynamics in heavy-ion reactions.

2.
J Cutan Pathol ; 29(6): 359-61, 2002 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12135467

RESUMO

BACKGROUND: In a previous study we detected virions with electron microscopy features of human herpes viruses in the supernatant of cocultured mononuclear cells from patients with acute pityriasis rosea. Because of their morphology and of polymerase chain reaction studies, we ascribed them to human herpes virus 7. OBJECTIVE: To find such virions in the lesional skin of pityriasis rosea patients. METHODS: Skin specimens from lesions of 21 patients with acute pityriasis rosea were examined by elecron microscopy. RESULTS: In 15 (71%) patients, human herpes virus particles in various stages of morphogenesis were detected. Mature enveloped virions appeared as typical human herpes virus virions, measuring about 160-200 nm in diameter and containing an electrodense cylindrical core, a capsid, an envelope with typical spikes and a very distinct tegument layer between the capsid and the envelope. They were very similar to those we reported in the supernatant of co-cultured circulating mononuclear cells from patients with pityriasis rosea. CONCLUSION: Our results confirm our previous findings and provides further evidence of a viral etiology for pityriasis rosea.


Assuntos
Herpesvirus Humano 7/isolamento & purificação , Pitiríase Rósea/etiologia , Infecções por Roseolovirus/complicações , Herpesvirus Humano 7/ultraestrutura , Humanos , Microscopia Eletrônica , Pitiríase Rósea/patologia , Infecções por Roseolovirus/patologia , Pele/patologia , Vírion/ultraestrutura
4.
Dermatology ; 195(4): 374-8, 1997.
Artigo em Inglês | MEDLINE | ID: mdl-9529560

RESUMO

BACKGROUND: Clinical evidence suggests a viral etiology for pityriasis rosea (PR). OBJECTIVE: To evaluate human herpesvirus (HHV)-6 and HHV-7 as candidates for the etiology of PR. METHODS: Blood and skin tissue from 12 patients with acute PR, and 12 patients with other dermatoses were studied, as well as blood samples from 25 healthy persons. Serum interferon (IFN)-alpha and IFN-gamma were analyzed by ELISA. Analysis of morphological changes in cocultured peripheral blood mononuclear cells (PBMC) and electron microscopy (EM) to identify viral particles were performed. Polymerase chain reaction (PCR) with specific primers for HHV-6 and HHV-7 DNA sequences was performed on the plasma and PBMC of patients and healthy controls and on the skin of patients with PR and other skin diseases. RESULTS: PR plasma contained detectable IFN-alpha and IFN-gamma, whereas plasma from controls did not. PBMC from PR patients showed ballooning cells and syncytia after 7 days in culture whereas PBMC from controls and recovered PR patients did not. This cytopathic effect was also documented in a PR patient who relapsed and in Sup-T1 cell cultures inoculated with the cell-free supernatant from centrifuged cultured PBMC; in this supernatant, herpesvirus, virions were detected by EM, PCR identified HHV-7 DNA in PBMC, plasma and skin from all patients with active PR and in the PBMC only of 5 patients tested 10-14 months later. Weaker signals of HHV-7 DNA were detected in PBMC of 11 controls, but not in their plasma. Skin was negative for HHV-7 in all control specimens. CONCLUSIONS: Although the detection of HHV-7 DNA in PBMC and tissues does not prove directly a causal role, HHV-7 DNA in cell-free plasma corresponds to active replication which supports a causal relationship. We propose that PR is a clinical presentation of HHV-7 reactivation.


Assuntos
Infecções por Herpesviridae , Herpesvirus Humano 7/isolamento & purificação , Pitiríase Rósea/virologia , Células Cultivadas , Meios de Cultivo Condicionados , Primers do DNA , DNA Viral/análise , DNA Viral/genética , Ensaio de Imunoadsorção Enzimática , Seguimentos , Células Gigantes/patologia , Infecções por Herpesviridae/sangue , Infecções por Herpesviridae/patologia , Herpesvirus Humano 6/genética , Herpesvirus Humano 6/isolamento & purificação , Herpesvirus Humano 7/genética , Humanos , Interferon-alfa/sangue , Interferon gama/sangue , Leucócitos Mononucleares/patologia , Microscopia Eletrônica , Pitiríase Rósea/sangue , Pitiríase Rósea/patologia , Reação em Cadeia da Polimerase , Recidiva , Pele/patologia , Pele/virologia , Dermatopatias/sangue , Dermatopatias/patologia , Linfócitos T Reguladores/patologia , Viremia/virologia , Vírion/ultraestrutura , Ativação Viral , Replicação Viral
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