A covariant constituent-quark formalism for mesons

Using the framework of the Covariant Spectator Theory (CST) [1] we are developing a covariant model formulated in Minkowski space to study mesonic structure and spectra. Treating mesons as effective $q\bar{q}$ states, we focused in [2] on the nonrelativistic bound-state problem in momentum space with a linear confining potential. Although integrable, this kernel has singularities which are difficult to handle numerically. In [2] we reformulate it into a form in which all singularities are explicitely removed. The resulting equations are then easier to solve and yield accurate and stable solutions. In the present work, the same method is applied to the relativistic case, improving upon the results of the one-channel spectator equation (1CSE) given in [3].Comment: 6 pages, 5 figures, Presented at EEF70, Workshop on Unquenched Hadron Spectroscopy: Non-Perturbative Models and Methods of QCD vs. Experimen

Correction to: Northerly wind trends along the Portuguese marine coast since 1950

All figure captions are not accurate. Also, there is a repeated error in most figures because the vertical scales incorrectly show Wind Strenght instead of Wind Strength and in Fig. 4 (mid-panel) 2003 instead of 2004.info:eu-repo/semantics/publishedVersio

Congenital Volkmann ischemic contracture – A case report

A contractura isquémica congénita de Volkmann é uma entidade rara, observada em recém-nascidos logo após o parto, caracterizada clinicamente por uma placa necrótica que atinge, geralmente, um dos membros superiores e que se faz acompanhar de paralisia flácida. Ocorre no período intrauterino e surge devido a compressão mecânica do membro. O seu mau posicionamento, a constrição por banda aminiótica, a existência de oligoâmnios e de distocias são alguns dos possíveis factores implicados. A compressão conduz a um síndrome de compartimento que induz isquemia e necrose da pele, músculos e nervos. O tratamento é cirúrgico, implicando desbridamento da placa de necrose e eventual recurso a um enxerto cutâneo. Relatamos o caso clínico de um recém-nascido de 2 dias de vida com uma contractura isquémica congénita de Volkmann do membro superior esquerdo, induzida pela presença de oligoâmnios

Avaliação da Estereopsia em Crianças sob Terapêutica Oclusiva por Ambliopia e Relação desta com a Acuidade Visual

Introdução: A ambliopia é a principal causa de diminuição da acuidade visual em crianças. O diagnóstico e tratamento precoces são fundamentais para o sucesso terapêutico. A oclusão continua a ser o tratamento mais utilizado nesta patologia. Objectivos: Este estudo teve como objectivo a avaliação da estereopsia em crianças com ambliopia sob terapêutica oclusiva e a sua relação com a acuidade visual. Material e Métodos: Estudo prospectivo que incluiu 35 crianças com ambliopia, por anisometropia, estrabismo ou ambos, a fazer terapêutica oclusiva. Em cada consulta foi avaliada a melhor acuidade visual corrigida (MAVC) e a estereopsia para perto. Resultados: A idade média no início do estudo era de 6,17 anos (intervalo 3-9 anos) e o seguimento médio foi de 17 meses (intervalo 6-24 meses). Após tratamento com oclusão houve uma melhoria da MAVC média de 0,5 para 0,84 (p<0,001) e da estereopsia para perto de 1148 para 415 segundos de arco (p<0,001). Observou-se uma correlação linear significativa entre a melhoria da AV e da estereopsia (0,001<p<0,01). Conclusão: Podemos dizer que, em crianças com ambliopia, após tratamento com oclusão, a melhoria da acuidade visual está relacionada com uma melhoria da estereopsia

Reconstruction of velopharyngeal sphincter in secondary Cleft Palate: surgical alternative

Cir Pediatr. 2006 Apr;19(2):106-10. [Reconstruction of velopharyngeal sphincter in secondary Cleft Palate: surgical alternative] [Article in Spanish] Recamán M, Bonet B, Leitão J, Mesquita A. Hospital Central e Especializado de Crianças Maria Pia, Serviço de Cirurgía Plástica. [email protected] Abstract There are numerous surgical procedures for the repair of Cleft Palate (CP). Since 1998, in children with CP we use a modified Wardill-Kilner technique, with a large section of the nasal mucous layer at the level of the muscular insertion on the hard palate and lateral nasopharingeal wall, obtaining a push-back and reorientation of the muscular fibres without dissection, diminishing this way the risks of haemorrhages and fibrosis, simplifying the intervention. It allows a lower operative time and a short internment. The aim of our study was to evaluate the results of this operative procedure specially in the development of the speech in 73 children operated on from 1998 until 2000 in our hospital. We verify a competence of the velopharingeal sphincter with ideal results in speech in 88,8% of the cases. PMID: 16846134 [PubMed - indexed for MEDLIN

Maculopatia Torpedo numa Criança Caucasiana de 5 Anos de Idade com Ambliopia Anisometrópica: Relato de Caso

The aim of this study is to report a clinical case of asymptomatic female Caucasian children with torpedo maculopathy. A 5-year-old girl was referred to our clinic for routine evaluation. The ophthalmic examination revealed best-corrected visual acuity of 20/20 in both eyes, without any changes in the biomicroscopy. Fundus examination showed normal findings in one eye, whereas in the contralateral eye it disclosed, in the temporal sector of the macular region, a whitish, atrophic, oval chorioretinal lesion with clearly defined margins. Posterior evaluations documented the stability of the lesion. Torpedo maculopathy diagnosis is based on its characteristic shape and peculiar location. The differential diagnosis has to be established versus choroidal lesions (melanoma and nevus), congenital or iatrogenic hyperplasia of the retinal pigment epithelium (RPE) and particularly versus the congenital pigmented lesions associated with Gardner's syndrome

Consulta de Diabetes Ocular. Primeiros Resultados do Rastreio da Retinopatia Diabética por Câmara Não Midriática

Introdução: a retinopatia diabética (RD) é, nos países industrializados, uma das principais causas de cegueira. A perda de visão na RD diminui com o diagnóstico precoce e instituição terapêutica2 adequada possibilitados por programas de rastreio sistemático. O rastreio efectuado por fotografias do polo posterior com câmara não midriática é simples e apresenta boa sensibilidade e especificidade3. Material e Métodos: estudo prospectivo, observacional, dos doentes diabéticos sem seguimento oftalmológico regular, seguidos na consulta de Medicina do Centro Hospitalar de Lisboa Central desde Setembro de 2008 a Julho de 2009. Incluíram-se 86 doentes. Um ortoptista fez a aquisição de imagens do polo posterior com uma câmara não midriática e a impressão de fotografias compostas, coloridas, que foram posteriormente analisadas por um oftalmologista da consulta de Diabetes Ocular. Resultados: foram excluídos 7 olhos (4,2%) por não existir qualidade de imagem. Identificou-se a existência de RD em 26% dos 165 olhos incluídos ( 28% dos doentes), apresentando 21% RD não proliferativa e 5% proliferativa. Apurou-se uma relação estatisticamente significativa entre a existência de RD, a idade (p= 0,253 x 10-1) e a duração da diabetes (p= 7,16 x 10-5). Relativamente ao encaminhamento, 57,8% foram referenciados para rastreio anual e 42,2% para a Consulta Geral de Oftalmologia. Todos os excluídos foram igualmente encaminhados para a Consulta Geral de Oftalmologia. Conclusões: a percentagem de doentes rastreados que apresentou RD foi elevada (28%). O rastreio sistemático da população diabética com câmara não midriática pareceu-nos ser um método simples e eficaz no despiste da RD

Alteration of the conserved residue tyrosine-158 to histidine renders human O6-alkylguanine-DNA alkyltransferase insensitive to the inhibitor O6- benzylguanine

The DNA repair protein O6-alkylguanine-DNA alkyltransferase (AGT) protects cells from alkylation damage. O6-Benzylguanine (BG) is a potent inactivator of human AGT (ED50 of 0.1 μM) that is currently undergoing clinical trials to enhance chemotherapy by alkylating agents. In a screen of AGT mutants randomly mutated at position glycine-160, we found that the double mutant Y158H/G160A protected Escherichia coli from killing by N- methyl-N'-nitro-N-nitrosoguanidine (MNNG) even in the presence of BG and that the AGT activity of this mutant was strongly resistant to BG (ED50 of 180 μM). Because the single mutant G160A was not resistant to BG, this suggested that the presence of the charged histidine residue at position 158 was responsible. This hypothesis was confirmed by the construction of the single mutation Y158H. The Y158H-mutant AGT was slightly less active than wild-type AGT for the repair of mcthylated DNA in vitro, but it protected E. coli from killing by MNNG even in the presence of BG and had an ED50 for the inactivation by BG of 620 μM. In contrast, mutant Y158F had an ED50 of 0.2 μM. Previous studies (M. Xu-Welliver et al., Cancer Res., 58: 1936-1945, 1998) have shown that mutant P140K is highly resistant to BG (ED50 of > 1200 μM). Models of human AGT suggest that the side chain of the lysine inserted into this mutant is close to tyrosine-158 and that the positively charged lysine side-chain may interfere with BG binding. The double mutants P140K/Y158H and P140K/Y158F resembled P140K and Y158H in being highly resistant to BG, but the use of a sensitive assay for reaction of BG with AGT indicated that their abilities to react were in the order P140K/Y158H < P140K < P140K/Y158F. These results confirm that the presence of a positively charged residue close to the active site of human AGT renders it highly resistant to BG without substantially affecting activity toward methylated DNA substrates. Such mutants may limit the value of BG therapy if they arise in malignant cells during chemotherapy, but the mutant sequences may be useful for gene therapy approaches in which BG-resistant human AGTs are used to prevent hematopoietic toxicity. At least 28 AGT sequences (from 25 species) have now been described. In 25 of these, the position equivalent to 158 in the human AGT is also a tyrosine, and in the other 3, it is a phenylalanine. The importance of an aromatic ring side chain at this position is emphasized by previous studies (S. Edara et al., Carcinogenesis, 16: 1637- 1642, 1995), which show that the replacement by alanine renders human AGT inactive. Our results show that histidine can also substitute for tyrosine at this position

In vitro efficacy of nitro- and bromo-thiazolyl-salicylamide compounds (thiazolides) against Besnoitia besnoiti infection in Vero cells

Nitazoxanide (NTZ) and its deacetylated metabolite tizoxanide (TIZ) exhibit considerable in vitro activity against Besnoitia besnoiti tachyzoites grown in Vero cells. Real-time-PCR was used to assess B. besnoiti tachyzoite adhesion, invasion, and intracellular proliferation in vitro. A number of NTZ-derivatives, including Rm4822 and Rm4803, were generated, in which the thiazole-ring-associated nitro-group was replaced by a bromo-moiety. We here show that replacement of the nitro-group on the thiazole ring with a bromo (as it occurs in Rm4822) does not impair the efficacy of the drug, but methylation of the salicylate ring at the ortho-position in a bromo-derivative (Rm4803) results in complete abrogation of the antiparasitic activity. Treatment of extracellular B. besnoiti tachyzoites with NTZ has an inhibitory effect on host cell invasion, while treatments with TIZ, Rm4822 do not. TEM demonstrates that the effects of Rm4822 treatment upon the parasites are similar to the damage induced by NTZ. This includes increased vacuolization of the parasite cytoplasm, and loss of the structural integrity of the parasitophorous vacuole and its membrane. Thus, Rm4822, due to the absence of a potentially mutagenic nitro-group, may represent an important potential addition to the anti-parasitic arsenal for food animal production, especially in cattl