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1.
J Eur Acad Dermatol Venereol ; 35(3): 712-720, 2021 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-32896010

RESUMO

BACKGROUND: There is increasing use of anti-osteoporotic agents (AOA) worldwide for prevention or management of patients with osteoporosis. However, there have been reports of severe cutaneous adverse reactions (SCAR) induced by AOA. A recent study showed weak association between HLA and strontium ranelate (SR)-SCAR. OBJECTIVE: To characterize patients with AOA-SCAR and investigate the HLA association and utility of in vitro diagnostic methods. METHODS: We enrolled 16 cases with AOA-cutaneous adverse drug reactions (cADR), including SCAR (n = 10: 8 with Stevens-Johnson syndrome [SJS] and 2 with drug rash with eosinophilia and systemic symptoms [DRESS]) and maculopapular exanthema (MPE) (n = 6) from Taiwan and Hong Kong. We analysed the clinical characteristics, outcomes, HLA alleles and in vitro testing of AOA-SCAR, and tolerability to alternative drugs. We further performed literature review and meta-analysis on the HLA association of AOA-SCAR. RESULTS: Our data showed strontium ranelate is the most common causality of AOA-SCAR in Asian populations. There was no cross-hypersensitivity of SR-SCAR with other AOA. HLA genotyping showed that SR-SJS was most significantly associated with HLA-A*33:03 (Pc = 5.17 × 10-3 , OR: 25.97, 95% CI: 3.08-219.33). Meta-analysis showed that HLA-A*33:03 was associated with SR-SJS (P = 5.01 × 10-5 ; sensitivity: 85.7%) in Asians. The sensitivity of lymphocyte activation test (LAT) for identifying the culprit drug of SR-SJS was 83.3%. CONCLUSIONS: Strontium ranelate is identified as the most notorious AOA associated with SCAR. The HLA-A*33:03 genetic allele and LAT testing may add benefits to the diagnosis of SR-SCAR in patients whose reaction developed while taking multiple drugs.


Assuntos
Síndrome de Stevens-Johnson , Alelos , Anticonvulsivantes , Povo Asiático , Antígenos HLA-B/genética , Hong Kong , Humanos , Taiwan
2.
Genet Mol Res ; 15(3)2016 Sep 16.
Artigo em Inglês | MEDLINE | ID: mdl-27706730

RESUMO

Long-term radiation exposure is hazardous to health; late-onset effects of exposure to ionizing radiation (IR) pose risks to the lens, and are associated with other non-cancerous diseases. Individuals occupationally exposed to low-dose IR are prone to developing eye cataracts. Cytogenetic evaluations suggest that IR is associated with chromosomal aberrations in occupationally exposed individuals. However, data regarding the association between chromosomal aberrations in cataract patients and occupational exposure to IR is scarce. Therefore, we aimed to report the characteristics of chromosomal aberrations in cataract patients from a Chinese population, occupationally exposed to IR. We found that the average age and frequency of numerical chromosomal aberrations were significantly lower in the exposed patients as compared with that in the non-exposed patients. In addition, the frequencies of dicentric and acentric chromosomes were significantly higher in the exposed patients as compared with those in the non-exposed patients. Therefore, chronic occupational exposure to IR affects cataract development in the Chinese population. The age of cataract patients exposed to IR was significantly lower than the age of cataract onset in normal individuals. Based on this study, we suggest that there is an urgent need for improved radiation safety and eye protection in individuals exposed to IR in the work place.


Assuntos
Catarata/genética , Aberrações Cromossômicas/efeitos da radiação , Cristalino/efeitos da radiação , Exposição Ocupacional , Idoso , Catarata/etiologia , Catarata/patologia , China , Relação Dose-Resposta à Radiação , Feminino , Humanos , Cristalino/patologia , Masculino , Pessoa de Meia-Idade , Radiação Ionizante
3.
Genet Mol Res ; 15(1)2016 Mar 22.
Artigo em Inglês | MEDLINE | ID: mdl-27050976

RESUMO

Long-term radiation exposure affects human health. Ionizing radiation has long been known to raise the risk of cancer. In addition to high doses of radiation, low-dose ionizing radiation might increase the risk of cardiovascular disease, lens opacity, and some other non-cancerous diseases. Low- and high-dose exposures to ionizing radiation elicit different signaling events at the molecular level, and may involve different response mechanisms. The health risks arising from exposure to low doses of ionizing radiation should be re-evaluated. Health workers exposed to ionizing radiation experience low-dose radiation and have an increased risk of hematological malignancies. Reproductive function is sensitive to changes in the physical environment, including ionizing radiation. However, data is scarce regarding the association between occupational radiation exposure and risk to human fertility. Sperm DNA integrity is a functional parameter of male fertility evaluation. Hence, we aimed to report sperm quality and DNA damage in men from Jilin Province, China, who were occupationally exposed to ionizing radiation. Sperm motility and normal morphology were significantly lower in the exposed compared with the non-exposed men. There was no statistically significant difference in sperm concentration between exposed and non-exposed men. The sperm DNA fragmentation index was significantly higher in the exposed than the non-exposed men. Chronic long-term exposure to low doses of ionizing radiation could affect sperm motility, normal morphology, and the sperm DNA fragmentation index in the Chinese population. Sperm quality and DNA integrity are functional parameters that could be used to evaluate occupational exposure to ionizing radiation.


Assuntos
Fragmentação do DNA/efeitos da radiação , Exposição Ocupacional/efeitos adversos , Radiação Ionizante , Motilidade dos Espermatozoides/efeitos da radiação , Espermatozoides/efeitos da radiação , Adulto , Estudos de Casos e Controles , China , Humanos , Masculino
4.
Transplant Proc ; 40(8): 2525-6, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-18929788

RESUMO

Hepatic arterial thrombosis is a critical complication in living donor liver transplantation (LDLT). Two separate branches of the right hepatic artery (RHA) are sometimes observed and addressed by anastomosis of the larger branch first, then checking backflow from the smaller branch. If not good, the smaller branch must be reconstructed. We used the cystic artery as a conduit for the reconstruction. Meticulous dissection was performed to identify all branches of the hepatic artery in the donor operation. The length of cystic artery preserved was as long as possible. The cystic arterial stump was anastomosed to the stump of the posterior branch the of RHA under microscopic guidance on the back table. Patency was checked through the stump of the anterior branch of the RHA. With this technique, only one orifice, the stump of right anterior hepatic artery, was used for hepatic artery reconstruction. We have performed this technique in two patients. Both had good arterial flow after living donor liver transplantation. This innovative technique is easy and safe, and requires only one anastomosis, which, in theory, decreases the adds of developing hepatic arterial thrombosis.


Assuntos
Artéria Hepática/cirurgia , Transplante de Fígado/métodos , Doadores Vivos , Procedimentos de Cirurgia Plástica , Anastomose Cirúrgica , Dissecação/métodos , Lateralidade Funcional , Artéria Hepática/anatomia & histologia , Humanos , Complicações Pós-Operatórias/patologia , Trombose/patologia
5.
Epidemiol Psychiatr Sci ; 27(2): 176-185, 2018 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-27974084

RESUMO

AIMS: Poor insight is prevalent in patients with schizophrenia and has been associated with acute illness severity, medication non-adherence and poor treatment outcomes. Paradoxically, high insight has been associated with various undesirable outcomes, including low self-esteem, depression and low subjective quality of life (QoL) in patients with schizophrenia. Despite the growing body of studies conducted in Western countries supporting the pernicious effects of improved insight in psychosis, which bases on the level of self-stigma, the effects are unclear in non-Western societies. The current study examined the role of self-stigma in the relationship between insight and psychosocial outcomes in a Chinese population. METHODS: A total of 170 outpatients with schizophrenia spectrum disorders were recruited from two general university hospitals. Sociodemographic data and clinical variables were recorded and self-report scales were employed to measure self-stigma, depression, insight, self-esteem and subjective QoL. Structural equation modelling (SEM) was used to analyse the cross-sectional data. RESULTS: High levels of self-stigma were reported by 39% of the participants (n = 67). The influences of insight, self-stigma, self-esteem and depression on subjective QoL were confirmed by the SEM results. Our model with the closest fit to the data (χ 2 = 33.28; df = 20; p = 0.03; χ 2/df = 1.66; CFI = 0.98; TLI = 0.97; RMSEA = 0.06) demonstrated that self-stigma might fully mediate the association of insight with low self-esteem, depression and poor subjective QoL. High insight into illness contributed to self-stigma, which caused low self-esteem and depression and, consequently, low QoL. Notably, insight did not directly affect self-esteem, depression or QoL. Furthermore, the association of insight with poor psychosocial outcomes was not moderated by self-stigma. CONCLUSIONS: Our findings support the mediating model of insight relevant to the poor psychosocial outcomes of individuals diagnosed with schizophrenia in non-Western societies, in which self-stigma plays a pivotal role. These findings elucidate the direct and indirect effects of insight on psychosocial outcomes and imply that identifying and correcting self-stigma in people with schizophrenia could be beneficial. Additional studies are required to identify whether several other neurocognitive or psychosocial variables mediate or moderate the association of insight with self-esteem, depression and QoL in patients with schizophrenia. Studies with detailed longitudinal assessments are necessary to confirm our findings.


Assuntos
Qualidade de Vida/psicologia , Psicologia do Esquizofrênico , Autoimagem , Estigma Social , Adolescente , Adulto , Estudos Transversais , Depressão/etiologia , Feminino , Humanos , Análise de Classes Latentes , Masculino , Pessoa de Meia-Idade , Pacientes Ambulatoriais , Esquizofrenia/diagnóstico , Autorrelato , Adulto Jovem
6.
Oncogene ; 37(5): 589-600, 2018 02 01.
Artigo em Inglês | MEDLINE | ID: mdl-28991224

RESUMO

Growing evidence indicates that resistin-an obesity-related cytokine-is upregulated in breast cancer patients, yet its impact on breast cancer behavior remains to be ascertained. Similarly, Toll-like receptor 4 (TLR4) has been implicated in breast cancer progression, however, its clinically relevant endogenous ligand remains elusive. In this study, we observed that high serum resistin levels in breast cancer patients positively correlated with tumor stage, size and lymph node metastasis. These findings were replicated in animal models of breast cancer tumorigenesis and metastasis. Resistin was found to promote epithelial-mesenchymal transition and stemness in breast cancer cells-mechanisms critical to tumorigenesis and metastasis-through a TLR4/nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB)/signal transducer and activator of transcription 3 (STAT3) signaling pathway and negated by TLR4-specific antibody and antagonist. These findings provide clear evidence that resistin is a clinically relevant endogenous ligand for TLR4, which promotes tumor progression via TLR4/NF-κB/STAT3 signaling, providing insights into a novel therapeutic target in breast cancer.


Assuntos
Neoplasias da Mama/patologia , Transição Epitelial-Mesenquimal , Células-Tronco Neoplásicas/patologia , Resistina/metabolismo , Receptor 4 Toll-Like/metabolismo , Animais , Mama/patologia , Neoplasias da Mama/sangue , Carcinogênese/patologia , Linhagem Celular Tumoral , Progressão da Doença , Feminino , Humanos , Metástase Linfática , Pessoa de Meia-Idade , NF-kappa B , Estadiamento de Neoplasias , Resistina/sangue , Fator de Transcrição STAT3/metabolismo , Transdução de Sinais , Regulação para Cima , Ensaios Antitumorais Modelo de Xenoenxerto , Peixe-Zebra
7.
J Med Genet ; 43(8): 653-9, 2006 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16571646

RESUMO

BACKGROUND: Andersen-Tawil syndrome (ATS) is a rare inherited disorder, characterised by periodic paralysis, cardiac dysarrhythmias, and dysmorphic features, and is caused by mutations in the gene KCNJ2, which encodes the inward rectifier potassium channel, Kir2.1. This study sought to analyse KCNJ2 in patients with familial ATS and to determine the functional characteristics of the mutated gene. METHODS AND RESULTS: We screened a family with inherited ATS for the mutation in KCNJ2, using direct DNA sequencing. A missense mutation (T75R) of Kir2.1, located in the highly conserved cytoplasmic N-terminal domain, was identified in three affected members of this family. Using the Xenopus oocyte expression system and whole cell voltage clamp analyses, we found that the T75R mutant was non-functional and possessed a strong dominant negative effect when co-expressed with the same amount of wild type Kir2.1. Transgenic (Tg) mice expressing the mutated form of Kir2.1 in the heart had prolonged QTc intervals compared with mice expressing the wild type protein. Ventricular tachyarrhythmias were observed in 5 of 14 T75R-Tg mice compared with 1 of 7 Wt-Tg and none of 6 non-transgenic littermates. In three of five T75R-Tg mice with ventricular tachycardia, their ECG disclosed bidirectional tachycardia as in our proband. CONCLUSIONS: The in vitro studies revealed that the T75R mutant of Kir2.1 had a strong dominant negative effect in the Xenopus oocyte expression system. It still preserved the ability to co-assemble and traffic to the cell membrane in mammalian cells. For in vivo studies, the T75R-Tg mice had bidirectional ventricular tachycardia after induction and longer QT intervals.


Assuntos
Síndrome de Andersen/genética , Predisposição Genética para Doença , Mutação/genética , Canais de Potássio Corretores do Fluxo de Internalização/genética , Adolescente , Animais , Análise Mutacional de DNA , Eletrocardiografia , Eletrofisiologia , Feminino , Humanos , Camundongos , Camundongos Transgênicos , Miocárdio/citologia , Miocárdio/patologia , Miócitos Cardíacos/citologia , Xenopus
8.
Int J Cardiol ; 72(3): 221-7, 2000 Feb 15.
Artigo em Inglês | MEDLINE | ID: mdl-10716130

RESUMO

From 1993 to 1998, a total of 100 consecutive pediatric patients with tachycardia (45 male and 55 female, aged 1 year 10 months to 17 years, 11+/-4 year) who underwent electrophysiological study were reviewed. Eleven of them were younger than 5 years. Two had tachycardia-related cerebrovascular accident. Congenital heart disease was found in 12 patients. After propofol anesthesia, the clinical tachycardia could not be induced in three (two atrial tachycardia and one AV nodal re-entrant tachycardia) and became nonsustained in five (atrial tachycardia). Mechanical ablation occurred in three and two had subsequent recurrences. Among the 85 cases who received radiofrequency ablation, the overall final success rate of RF ablation for all diagnoses was 94% with a diagnosis-specific success rate ranging from 100 to 57%. Tachycardia cardiomyopathy was noted in four (three atrial tachycardia and one junctional ectopic tachycardia) and all regressed after successful ablation. Success in two patients with left posterioseptal accessory pathway could only be achieved by delivering the energy at the middle cardiac vein. Two patients with right atrial isomerism had an 'AV nodal-to-AV nodal tachycardia' which was eliminated by ablation. Total recurrence rate was 13% but final success was achieved in all during re-study except the three patients who refused re-intervention. The atrial tachycardia developed in postoperative congenital heart disease was associated with the lowest success rate (57%) and highest recurrence rate (25%). Procedure-related complications occurred in four; two with transient brachial palsy, one with first-degree AV block and one with blood loss requiring blood transfusion. In conclusion, the experience of this single center confirmed the efficacy and safety of radiofrequency catheter ablation in treating pediatric arrhythmias, but the limitations in postoperative arrhythmias and the effects of propofol on tachycardia induction (especially the atrial tachycardia) need to be improved.


Assuntos
Ablação por Cateter , Cardiopatias Congênitas , Taquicardia/cirurgia , Anestésicos Intravenosos , Estimulação Cardíaca Artificial , Estudos de Casos e Controles , Criança , Eletrofisiologia , Feminino , Cardiopatias Congênitas/complicações , Humanos , Masculino , Propofol , Recidiva , Estudos Retrospectivos , Taquicardia/etiologia
9.
Acta Paediatr Taiwan ; 42(1): 46-8, 2001.
Artigo em Inglês | MEDLINE | ID: mdl-11270186

RESUMO

A very low-birth-weight neonate developed chylus-like urine after receiving parenteral nutrition (PN) via percutaneous central venous catheters (CVC) for 7 weeks. A perirenal fluid collection could be seen under sonography. This kind of complication has not been described in literature. After withdrawing the CVC for 5 cm, the urine cleared up. For patients under prolonged PN via CVC and repeated change dressing of the CVC, close monitoring and regular evaluation of the position of the catheter tip are warranted.


Assuntos
Cateterismo Venoso Central/efeitos adversos , Quilo , Nutrição Parenteral/efeitos adversos , Humanos , Recém-Nascido , Masculino , Urina
10.
Neotrop Entomol ; 43(3): 209-17, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-27193616

RESUMO

Two new species of the tetrigid genus Xistra Bolivar from China, namely Xistra oculata Li, Deng et Zheng n. sp. and Xistra brachynota Li, Deng et Zheng n. sp. are described. An updated key to all known species of the genus is given.


Assuntos
Ortópteros/classificação , Animais , China
11.
Eur J Pediatr Surg ; 21(5): 304-9, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21751122

RESUMO

OBJECTIVE: Aim of the study was to further evaluate the role of caspase 8 and death receptors (DR) in the TRAIL-induced apoptosis of neuroblastoma (NB) cell lines. METHODS: Caspase 8 mRNA expression was monitored by RT-PCR. Caspase 8, DR5 and DR4 protein expression were monitored by Western blot analysis. The effects of IFNγ, TRAIL, IFNγ+TRAIL, caspase 8 inhibitor+TRAIL and IFNγ+chemotherapeutic agents+TRAIL on the growth and apoptosis of NB cells were detected with MTT and flow cytometry. The relative caspase 8 activity was measured with colorimetric assay. RESULTS: Caspase 8 expression was induced by IFNγ in the NB cell line SKNDZ. TRAIL alone did not induce apoptosis compared with controls but a combination of IFNγ+TRAIL and IFNγ+chemotherapeutic agents+TRAIL significantly induced cell apoptosis in SY5Y cells. Etoposide and doxorubicin induced DR5 but not DR4 in NB cell lines. SKNDZ cells expressing caspase 8 after treatment with IFNγ were still resistant to TRAIL but sensitive to TRAIL after the induction of DR5. CONCLUSIONS: Sensitization of NB cells to TRAIL may be mediated by the upregulation of caspase 8 with IFNγ and DR5 with chemotherapeutic agents. This suggests that caspase 8 and death receptors play a very important role in TRAIL-induced apoptosis of NB cells and a combination of IFNγ, TRAIL and chemotherapeutic agents may be a new and interesting anticancer treatment strategy for NB.


Assuntos
Antineoplásicos/farmacologia , Caspase 8/biossíntese , Interferon gama/farmacologia , Neuroblastoma/tratamento farmacológico , Receptores do Ligante Indutor de Apoptose Relacionado a TNF/biossíntese , Apoptose/efeitos dos fármacos , Linhagem Celular Tumoral , Doxorrubicina/farmacologia , Etoposídeo/farmacologia , Humanos , RNA Mensageiro , Ligante Indutor de Apoptose Relacionado a TNF/metabolismo , Regulação para Cima
12.
Neurology ; 77(23): 2025-33, 2011 Dec 06.
Artigo em Inglês | MEDLINE | ID: mdl-22116946

RESUMO

OBJECTIVE: Ethnicity has been shown to be a contributing risk factor regarding antiepileptic drug (AED)-induced severe cutaneous adverse drug reactions (SCARs). To increase the clinical and epidemiologic information in Asians, we investigated the characteristics, outcome, and tolerability toward alternative drugs for AED-induced SCARs. METHODS: A total of 154 patients with AED-induced SCARs, including Stevens-Johnson syndrome (SJS), toxic epidermal necrosis (TEN), and drug rash with eosinophilia and systemic symptoms (DRESS), were analyzed for demographic characteristics, causative AEDs, latent period, organ involvement, complications, and mortality. Tolerability toward alternative AEDs was followed for patients after AED-SCARs episodes. RESULTS: Carbamazepine (CBZ) and phenytoin (PHT) were the most common causative AEDs for SJS/TEN (67.8%) and DRESS (43.6%), respectively. No SCARs case was caused by nonaromatic AEDs, e.g., valproic acid (VPA) and topiramate (TPM). The liver was the most frequently involved internal organ in AED-DRESS, whereas ocular complications were more commonly seen in AED-SJS/TEN. The mortality of AED-SJS/TEN and -DRESS was 6.1% and 7.7%, respectively. By following alternative AED usage of patients after AED-SCARs episodes, we noted that most patients were tolerant of nonaromatic AEDs. One case of oxcarbazepine-SJS had cross-hypersensitivity to lamotrigine (LTG) and further developed into DRESS. CONCLUSION: CBZ, PHT, and LTG were the major causative AEDs for SCARs. The mortality of PHT-SCARs was higher than CBZ-SCARs due to complicated comorbidity in patients. Nonaromatic AEDs were safe alternatives for patients with aromatic AED-induced SCARs.


Assuntos
Anticonvulsivantes/efeitos adversos , Carbamazepina/efeitos adversos , Fenitoína/efeitos adversos , Síndrome de Stevens-Johnson/induzido quimicamente , Síndrome de Stevens-Johnson/etiologia , Triazinas/efeitos adversos , Adulto , Povo Asiático/etnologia , Exantema/induzido quimicamente , Exantema/mortalidade , Feminino , Seguimentos , Humanos , Lamotrigina , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Fatores de Risco , Índice de Gravidade de Doença , Síndrome de Stevens-Johnson/etnologia , Síndrome de Stevens-Johnson/mortalidade , Taiwan/epidemiologia
15.
Optom Vis Sci ; 68(1): 12-21, 1991 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-2023710

RESUMO

We compared the theoretical peripheral power errors and oblique astigmatism of eyes corrected with commercially available intraocular lenses (IOL's) with experimental data of normal phakic eyes. The peripheral power errors and the oblique astigmatism of the pseudophakic eye are larger than those of phakic eyes. The most sensitive component of the optical system of the pseudophakic eye to the peripheral power errors is the shape of the IOL, but only if the lens is away from the iris. The corneal and the retinal surfaces do not affect the peripheral power errors and oblique astigmatism significantly. A plano-convex lens with the flat surface facing the cornea gives the least peripheral power errors and oblique astigmatism and thus the value closest to the experimental data of phakic eyes. However, this design does not give the minimum spherical aberration. Therefore, eyes corrected with IOL's are expected to have poorer peripheral retinal image quality than normal phakic eyes.


Assuntos
Astigmatismo/etiologia , Lentes Intraoculares/efeitos adversos , Campos Visuais , Humanos , Modelos Biológicos , Óptica e Fotônica , Refração Ocular
16.
Ophthalmic Physiol Opt ; 8(3): 287-94, 1988.
Artigo em Inglês | MEDLINE | ID: mdl-3269508

RESUMO

Seidel aberration theory shows that the spherical aberration of a spherically surfaced intra-ocular lens cannot be made zero but only minimized and that the optimum shape is independent of the aberration of the rest of the eye (i.e. the cornea). The optimum shape of an intra-ocular lens correcting for spherical aberration is almost plano-convex with the more curved surface facing the cornea. The resulting total Seidel spherical aberration of the whole eye cannot be made zero unless the cornea has an asphericity much higher than the population mean.


Assuntos
Lentes Intraoculares , Óptica e Fotônica , Desenho de Equipamento , Humanos , Matemática , Modelos Biológicos
17.
Ophthalmic Physiol Opt ; 10(1): 54-66, 1990 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-2330216

RESUMO

While a spherically surfaced intra-ocular lens cannot be designed to give zero spherical aberration for the whole eye, aspherizing one surface of an intra-ocular lens can produce zero Seidel spherical aberration in a pseudophakic eye or set it to any desired level provided the corneal asphericity is known and this does not change with the operation. Equations for determining the asphericities are given. Asphericities for five lens shapes; the minimum spherical aberration lens and its reverse form, the equi-biconvex lens, the plano-convex lens and its reverse form are determined. The Seidel aberrations of eyes with aspherized intra-ocular lenses were compared with that of eyes with spherical intra-ocular lenses. While aspherizing eliminates the Seidel spherical aberration, some residual higher order spherical aberration exists and the amount of this residual spherical aberration depends upon the lens shape. However, this residual aberration can be reduced but not made zero by modifying the asphericity. For currently used plano-convex lenses, only the curves surface can be aspherized. The effect of variations in the anterior corneal asphericity on the necessary lens asphericity was also investigated.


Assuntos
Lentes Intraoculares , Córnea/fisiopatologia , Humanos , Óptica e Fotônica , Complicações Pós-Operatórias/fisiopatologia
18.
J Virol ; 75(9): 4357-66, 2001 May.
Artigo em Inglês | MEDLINE | ID: mdl-11287584

RESUMO

The function of the N terminus of the murine leukemia virus (MuLV) surface (SU) protein was examined. A series of five chimeric envelope proteins (Env) were generated in which the N terminus of amphotropic 4070A was replaced by equivalent sequences from ecotropic Moloney MuLV (M-MuLV). Viral titers of these chimeras indicate that exchange with homologous sequences could be tolerated, up to V17eco/T15ampho (crossover III). Constructs encoding the first 28 amino acids (aa) of ecotropic M-MuLV resulted in Env expression and binding to the receptor; however, the virus titer was reduced 5- to 45-fold, indicating a postbinding block. Additional exchange beyond the first 28 aa of ecotropic MuLV Env resulted in defective protein expression. These N-terminal chimeras were also introduced into the AE4 chimeric Env backbone containing the amphotropic receptor binding domain joined at the hinge region to the ecotropic SU C terminus. In this backbone, introduction of the first 17 aa of the ecotropic Env protein significantly increased the titer compared to that of its parental chimera AE4, implying a functional coordination between the N terminus of SU and the C terminus of the SU and/or transmembrane proteins. These data functionally dissect the N-terminal sequence of the MuLV Env protein and identify differential effects on receptor-mediated entry.


Assuntos
Vírus da Leucemia Murina/fisiologia , Proteínas do Envelope Viral/fisiologia , Sequência de Aminoácidos , Animais , Linhagem Celular , Cães , Vírus da Leucemia Murina/genética , Camundongos , Dados de Sequência Molecular , Proteínas do Envelope Viral/genética
19.
Pacing Clin Electrophysiol ; 23(10 Pt 1): 1564-6, 2000 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11060880

RESUMO

We report on 16-year-old, female identical twins who both have atrioventricular reentrant tachycardia caused by the same left lateral atrioventricular accessory pathway. The Kent pathway in twin A was a unidirectional retrograde accessory pathway. A manifest Kent pathway was demonstrated in twin B. Both pathways were successfully ablated by radiofrequency (RF) energy and without recurrence. In addition, innocent dual AV nodal pathways were shown in both patients. These findings suggest that genetic factors may play a role in the pathogenesis of the formation of accessory atrioventricular pathways and dual AV nodal pathways.


Assuntos
Doenças em Gêmeos , Taquicardia por Reentrada no Nó Atrioventricular/genética , Taquicardia Paroxística/genética , Taquicardia Supraventricular/genética , Adolescente , Ablação por Cateter , Eletrocardiografia , Técnicas Eletrofisiológicas Cardíacas , Feminino , Humanos , Taquicardia por Reentrada no Nó Atrioventricular/diagnóstico , Taquicardia Paroxística/diagnóstico , Taquicardia Paroxística/cirurgia , Taquicardia Supraventricular/diagnóstico , Taquicardia Supraventricular/cirurgia , Síndrome de Wolff-Parkinson-White/genética
20.
J Gastroenterol Hepatol ; 7(4): 363-6, 1992.
Artigo em Inglês | MEDLINE | ID: mdl-1515559

RESUMO

The value of serum C-reactive protein, lactate dehydrogenase isoenzymes and erythrocyte sedimentation rate in predicting the outcome of acute pancreatitis was evaluated for 57 episodes in 54 patients. Serum C-reactive protein levels on day 2, 4 and 7 after admission were significantly higher in 19 episodes of severe attacks than in 38 episodes of mild attacks (13.71 +/- 9.68, 9.00 +/- 7.54, 6.02 +/- 3.83 vs 4.78 +/- 3.91, 3.30 +/- 3.61, 1.43 +/- 2.08 mg/dL; P less than 0.0001, P less than 0.005, P less than 0.0001, respectively). The sensitivity, specificity and accuracy of predicting a severe attack were 94, 76 and 82% using C-reactive protein greater than or equal to 8 mg/dL on day 2; 67, 92 and 84% using C-reactive protein greater than or equal to 5 mg/dL on day 7; and 59, 76 and 70% using Ranson's criteria greater than or equal to 3. Increases in LDH-4 and LDH-5 isoenzymes were found in both groups, with LDH-4 being slightly higher in severe attacks than in mild attacks. There was no significant difference of erythrocyte sedimentation rate between both groups. When compared with Ranson's criteria, lactate dehydrogenase isoenzymes and erythrocyte sedimentation rate, C-reactive protein is more valuable in the early assessment of the severity of acute pancreatitis.


Assuntos
Proteína C-Reativa/análise , L-Lactato Desidrogenase/sangue , Pancreatite/metabolismo , Doença Aguda , Feminino , Humanos , Isoenzimas , Masculino , Pessoa de Meia-Idade , Pancreatite/sangue , Prognóstico , Estudos Prospectivos
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