Vademecum histórico y bibliográfico, de la anatomía, fisiología, higiene, terapéutica y materia médica, cirugía, medicina, medicina legal y obstrecticia (sic), formado con presencia de las tablas sinópticas de los doctores Choulant, Kurt Sprengel, Black, Victor Broussais, Montffalcon, Decembiers y otros historiadores, y añadido hasta nuestros dias /

Mode of access: Internet.

Catalogue des livres provenans de la bibliothèque de M.L.D.D.L.V. : disposé et mis en ordre, avec une table alphabétique des auteurs /

Later editions of the catalog were pub. as follows: a) 1772, b) 1777, c) 1780 (each in 1 v.) / by G. Debure, cousin of the compiler of the present work. d) 1. ptie., 1783 (in 4 v.) / by G. Debure; 2. ptie., 1784 / by J.L. Lyon; e) reissued 1788 in 6 v.

Répertoire du Théâtre François, ou, Recueil des tragédies et comédies restées au théâtre depuis Rotrou pour faire suite aux éditions in-octavo de Corneille, Molière, Racine, Regnard, Crébillon, et au théatre de Voltaire,

"Nouvelle ed."

In the Supreme Court of the United States, October term, 1948 : American Communications Association, C.I.O., Joseph P. Selly, etc., et al., appelants v. Charles T. Douds, individually and as regional director of the National Labor Relations Board, second region, on appeal from the District Court of the United States for the Southern District of New York : brief for appellee.

"No. 336."

National Labor Relations Board petitioner v. National Maritime Union of America, affiliated with the Congress of Industrial Organizations, and Joseph Curran, Jack Lawrenson, Josh Lawrence, Chester Young, Harold McCormick, Michael McBride, and Charles Monroe, respondents; on petition for enforcement of an order of the National Labor Relations Board; brief for the National Labor Relations Board.

Cover title.

Y callaron el tambor de Joseph Bara, hubo cuchilla de afeitar nacional ,coclí, coclí, Su Majestad, ... al que lo ví, lo vi : nación, ley y jaque al rey 4

Fondo Margaritainés Restrepo

Cerebral Cortex Involvement In Machado-joseph Disease.

Machado-Joseph disease (MJD/SCA3) is the most frequent spinocerebellar ataxia, characterized by brainstem, basal ganglia and cerebellar damage. Few magnetic resonance imaging based studies have investigated damage in the cerebral cortex. The objective was to determine whether patients with MJD/SCA3 have cerebral cortex atrophy, to identify regions more susceptible to damage and to look for the clinical and neuropsychological correlates of such lesions. Forty-nine patients with MJD/SCA3 (mean age 47.7 ± 13.0 years, 27 men) and 49 matched healthy controls were enrolled. All subjects underwent magnetic resonance imaging scans in a 3 T device, and three-dimensional T1 images were used for volumetric analyses. Measurement of cortical thickness and volume was performed using the FreeSurfer software. Groups were compared using ancova with age, gender and estimated intracranial volume as covariates, and a general linear model was used to assess correlations between atrophy and clinical variables. Mean CAG expansion, Scale for Assessment and Rating of Ataxia (SARA) score and age at onset were 72.1 ± 4.2, 14.7 ± 7.3 and 37.5 ± 12.5 years, respectively. The main findings were (i) bilateral paracentral cortex atrophy, as well as the caudal middle frontal gyrus, superior and transverse temporal gyri, and lateral occipital cortex in the left hemisphere and supramarginal gyrus in the right hemisphere; (ii) volumetric reduction of basal ganglia and hippocampi; (iii) a significant correlation between SARA and brainstem and precentral gyrus atrophy. Furthermore, some of the affected cortical regions showed significant correlations with neuropsychological data. Patients with MJD/SCA3 have widespread cortical and subcortical atrophy. These structural findings correlate with clinical manifestations of the disease, which support the concept that cognitive/motor impairment and cerebral damage are related in disease.

Spinal Cord Damage In Machado-joseph Disease.

Machado-Joseph disease (SCA3) is the most frequent spinocerebellar ataxia worldwide and characterized by remarkable phenotypic heterogeneity. MRI-based studies in SCA3 focused in the cerebellum and connections, but little is known about cord damage in the disease and its clinical relevance. To evaluate the spinal cord damage in SCA3 through quantitative analysis of MRI scans. A group of 48 patients with SCA3 and 48 age and gender-matched healthy controls underwent MRI on a 3T scanner. We used T1-weighted 3D images to estimate the cervical spinal cord area (CA) and eccentricity (CE) at three C2/C3 levels based on a semi-automatic image segmentation protocol. The scale for assessment and rating of ataxia (SARA) was employed to quantify disease severity. The two groups-SCA3 and controls-were significantly different regarding CA (49.5 ± 7.3 vs 67.2 ± 6.3 mm(2), p < 0.001) and CE values (0.79 ± 0.06 vs 0.75 ± 0.05, p = 0.005). In addition, CA presented a significant correlation with SARA scores in the patient group (p = 0.010). CE was not associated with SARA scores (p = 0.857). In the multiple variable regression, we found that disease duration was the only variable associated with CA (coefficient = -0.629, p = 0.025). SCA3 is characterized by cervical cord atrophy and antero-posterior flattening. In addition, the spinal cord areas did correlate with disease severity. This suggests that quantitative analyses of the spinal cord MRI might be a useful biomarker in SCA3.

Machado-Joseph disease versus hereditary spastic paraplegia: case report

Machado-Joseph disease (MJD) is the most common autosomal dominant spinocerebellar ataxia and presents great phenotypic variability. MJD presenting with spastic paraparesis was recently described in Japanese patients. We report the case of 41-year-old woman with the phenotype of complicated hereditary spastic paraplegia. Her father died at the age of 56 years due to an undiagnosed progressive neurological disease that presented parkinsonism. She had an expanded allele with 66 CAG repeats and a normal allele with 22 repeats in the gene of MJD. MJD should be considered in the differential diagnosis of autosomal dominant complicated HSP. A patient with the phenotype of complicated HSP and relatives with other clinical features of a neurodegenerative disease should raise the suspicion of MJD.

Functional and Evolutionary Insights from the Genomes of Three Parasitoid Nasonia Species

We report here genome sequences and comparative analyses of three closely related parasitoid wasps: Nasonia vitripennis, N. giraulti, and N. longicornis. Parasitoids are important regulators of arthropod populations, including major agricultural pests and disease vectors, and Nasonia is an emerging genetic model, particularly for evolutionary and developmental genetics. Key findings include the identification of a functional DNA methylation tool kit; hymenopteran-specific genes including diverse venoms; lateral gene transfers among Pox viruses, Wolbachia, and Nasonia; and the rapid evolution of genes involved in nuclear-mitochondrial interactions that are implicated in speciation. Newly developed genome resources advance Nasonia for genetic research, accelerate mapping and cloning of quantitative trait loci, and will ultimately provide tools and knowledge for further increasing the utility of parasitoids as pest insect-control agents.

The Genome Sequence of Taurine Cattle: A Window to Ruminant Biology and Evolution

To understand the biology and evolution of ruminants, the cattle genome was sequenced to about sevenfold coverage. The cattle genome contains a minimum of 22,000 genes, with a core set of 14,345 orthologs shared among seven mammalian species of which 1217 are absent or undetected in noneutherian (marsupial or monotreme) genomes. Cattle-specific evolutionary breakpoint regions in chromosomes have a higher density of segmental duplications, enrichment of repetitive elements, and species-specific variations in genes associated with lactation and immune responsiveness. Genes involved in metabolism are generally highly conserved, although five metabolic genes are deleted or extensively diverged from their human orthologs. The cattle genome sequence thus provides a resource for understanding mammalian evolution and accelerating livestock genetic improvement for milk and meat production.

Simuliidae (Diptera: Culicomorpha) no Brasil: V - Sobre o Simulium (Chirostilbia) friedlanderi sp.n. e a revisão do Simulium (C.) laneportoi Vargas, 1941

Uma espécie nova, Simulium friedlanderi, do subgênero Simulium (Chirostilbia) Enderlein é descrita, sendo a mesma procedente do norte da Província Hidrogeológica do Centro-Oeste, subprovíncia Alto Paraguai. Simulium (Chirostilbia) laneportoi Vargas, 1941 é revisada, sendo o Simulium (C.) dekeyseri Shelley e Py-Daniel, 1981 colocada em sua sinonimia, e apresentando uma distribuição geográfica tanto no norte da Província Hidrogeológica do Centro-Oeste, subprovíncia Alto Paraguai, como no sudeste da Província Hidrogeológica do Escudo Central. São apresentadas chaves diferenciativas para larvas e pupas do grupo pertinax.

Manipulus Rubiacearum - V. A revision of the genus Capirona.

The taxonomic histort of the genus Capirona is presented. Complete synonymies, descriptions, common names, distributions and discussions are given for Capirona and its two species C. descorticans and C. leiophloea. The generic distribution is the Amazon valley and eastern Guianas and coincides with that of the genus Hevea. C. descorticans is know from the western and southeastern Amazon valley; C. leiophloea is reported from the eastern Guianas and the northeastern Amazon valley. The zone of contact between the two species is along the southern edge oh the Amazon River and the lower drainage of the Rio Tapajoz in Pará, Brazil.