Xin ke chong jiao zeng bu Yuan ji huo fa shi xue quan shu : 24 juan /

Chong kan ben.

Jing xun tang cong shu : shi qi zhong yi bai ling jiu juan /

Juan qian xu ci hang you ti "bing bu shi lang jian du cha yuan you fu du yu shi xun fu Shanxi Xi'an deng chu di fang zan li jun wu jian li liang xiang qin ci yi pin ding dai Bi Yuan zhuan".

Kun xue ji wen ji zheng : 20 juan, bu yi : 1 juan /

Double leaves, oriental style, in case.

Li xue zong zhuan : 26 juan.

Blockprint.

Preexposure Chemoprophylaxis for HIV Prevention in Men Who Have Sex with Men.

Background: Antiretroviral chemoprophylaxis before exposure is a promising approach for the prevention of human immunodeficiency virus (HIV) acquisition. Methods: We randomly assigned 2499 HIV-seronegative men or transgender women who have sex with men to receive a combination of two oral antiretroviral drugs, emtricitabine and tenofovir disoproxil fumarate (FTC-TDF), or placebo once daily. All subjects received HIV testing, risk-reduction counseling, condoms, and management of sexually transmitted infections. Results: The study subjects were followed for 3324 person-years (median, 1.2 years; maximum, 2.8 years). Of these subjects, 10 were found to have been infected with HIV at enrollment, and 100 became infected during follow-up (36 in the FTC-TDF group and 64 in the placebo group), indicating a 44% reduction in the incidence of HIV (95% confidence interval, 15 to 63; P=0.005). In the FTC-TDF group, the study drug was detected in 22 of 43 of seronegative subjects (51%) and in 3 of 34 HIV-infected subjects (9%) (P<0.001). Nausea was reported more frequently during the first 4 weeks in the FTC-TDF group than in the placebo group (P<0.001). The two groups had similar rates of serious adverse events (P=0.57). Conclusions: Oral FTC-TDF provided protection against the acquisition of HIV infection among the subjects. Detectable blood levels strongly correlated with the prophylactic effect. (Funded by the National Institutes of Health and the Bill and Melinda Gates Foundation; ClinicalTrials.gov number, NCT00458393.) N Engl J Med 2010;363:2587-99.

Genome-wide meta-analysis of common variant differences between men and women.

The male-to-female sex ratio at birth is constant across world populations with an average of 1.06 (106 male to 100 female live births) for populations of European descent. The sex ratio is considered to be affected by numerous biological and environmental factors and to have a heritable component. The aim of this study was to investigate the presence of common allele modest effects at autosomal and chromosome X variants that could explain the observed sex ratio at birth. We conducted a large-scale genome-wide association scan (GWAS) meta-analysis across 51 studies, comprising overall 114 863 individuals (61 094 women and 53 769 men) of European ancestry and 2 623 828 common (minor allele frequency >0.05) single-nucleotide polymorphisms (SNPs). Allele frequencies were compared between men and women for directly-typed and imputed variants within each study. Forward-time simulations for unlinked, neutral, autosomal, common loci were performed under the demographic model for European populations with a fixed sex ratio and a random mating scheme to assess the probability of detecting significant allele frequency differences. We do not detect any genome-wide significant (P < 5 × 10(-8)) common SNP differences between men and women in this well-powered meta-analysis. The simulated data provided results entirely consistent with these findings. This large-scale investigation across ~115 000 individuals shows no detectable contribution from common genetic variants to the observed skew in the sex ratio. The absence of sex-specific differences is useful in guiding genetic association study design, for example when using mixed controls for sex-biased traits.

Early white matter alterations in men predisposed to FXTAS revealed by MT imaging.

Introduction: The Fragile X - associated Tremor Ataxia Syndrome (FXTAS) is a recently described, and under-diagnosed, late onset (≈ 60y) neurodegenerative disorder affecting male carriers of a premutation in the Fragile X Mental Retardation 1 (FMR1) gene. The premutation is an CGG (Cytosine-Guanine-Guanine) expansion (55 to 200 CGG repeats) in the proximal region of the FMR1 gene. Patients with FXTAS primarily present with cerebellar ataxia and intention tremor. Neuroradiological features of FXTAS include prominent white matter disease in the periventricular, subcortical, middle cerebellar peduncles and deep white matter of the cerebellum on T2-weighted or FLAIR MR imaging (Jacquemmont 2007, Loesch 2007, Brunberg 2002, Cohen 2006). We hypothesize that a significant white matter alteration is present in younger individuals many years prior to clinical symptoms and/or the presence of visible lesions on conventional MR sequences and might be detectable by magnetization transfer (MT) imaging. Methods: Eleven asymptomatic premutation carriers (mean age = 55 years) and seven intra-familial controls participated to the study. A standardized neurological examination was performed on all participants and a neuropsychological evaluation was carried out before MR scanning performed on a 3T Siemens Trio. The protocol included a sagittal T1-weighted 3D gradient-echo sequence (MPRAGE, 160 slices, 1 mm^3 isotropic voxels) and a gradient-echo MTI (FA 30, TE 15, matrix size 256*256, pixel size 1*1 mm, 36 slices (thickness 2mm), MT pulse duration 7.68 ms, FA 500, frequency offset 1.5 kHz). MTI was performed by acquiring consecutively two set of images; first with and then without the MT saturation pulse. MT images were coregistered to the T1 acquisition. The MTR for every intracranial voxel was calculated as follows: MTR = (M0 - MS)/M0*100%, creating a MTR map for each subject. As first analysis, the whole white matter (WM) was used to mask the MTR image in order to create an histogram of the MTR distribution in the whole tissue class over the two groups examined. Then, for each subject, we performed a segmentation and parcellation of the brain by means of Freesurfer software, starting from the high resolution T1-weighted anatomical acquisition. Cortical parcellations was used to assign a label to the underlying white matter by the construction of a Voronoi diagram in the WM voxels of the MR volume based on distance to the nearest cortical parcellation label. This procedure allowed us to subdivide the cerebral WM in 78 ROIs according to the cortical parcellation (see example in Fig 1). The cerebellum, by the same procedure, was subdivided in 5 ROIs (2 per each hemisphere and one corresponding to the brainstem). For each subject, we calculated the mean value of MTR within each ROI and averaged over controls and patients. Significant differences between the two groups were tested using a two sample T-test (p<0.01). Results: Neurological examination showed that no patient met the clinical criteria of Fragile X Tremor and Ataxia Syndrome yet. Nonetheless, premutation carriers showed some subtle neurological signs of the disorder. In fact, premutation carriers showed a significant increase of tremor (CRST, T-test p=0.007) and increase of ataxia (ICARS, p=0.004) when compared to controls. The neuropsychological evaluation was normal in both groups. To obtain general characterizations of myelination for each subject and premutation carriers, we first computed the distribution of MTR values across the total white matter volume and averaged for each group. We tested the equality of the two distributions with the non parametric Kolmogorov-Smirnov test and we rejected the null-hypothesis at a p=0.03 (fig. 2). As expected, when comparing the asymptomatic permutation carriers with control subjects, the peak value and peak position of the MTR values within the whole WM were decreased and the width of the distribution curve was increased (p<0.01). These three changes point to an alteration of the global myelin status of the premutation carriers. Subsequently, to analyze the regional myelination and white matter integrity of the same group, we performed a ROI analysis of MTR data. The ROI-based analysis showed a decrease of mean MTR value in premutation carriers compared to controls in bilateral orbito-frontal and inferior frontal WM, entorhinal and cingulum regions and cerebellum (Fig 3). The detection of these differences in these regions failed with other conventional MR techniques. Conclusions: These preliminary data confirm that in premutation carriers, there are indeed alterations in "normal appearing white matter" (NAWM) and these alterations are visible with the MT technique. These results indicate that MT imaging may be a relevant approach to detect both global and local alterations within NAWM in "asymptomatic" carriers of premutations in the Fragile X Mental Retardation 1 (FMR1) gene. The sensitivity of MT in the detection of these alterations might point towards a specific physiopathological mechanism linked to an underlying myelin disorder. ROI-based analyses show that the frontal, parahippocampal and cerebellar regions are already significantly affected before the onset of symptoms. A larger sample will allow us to determine the minimum CGG expansion and age associated with these subclinical white matter alterations.

許嘉祿傳Xu jia lu zhuan.Vie de Charles Xu.

Par He Shi zheng (1675).

新刻正原本第八才子. 花箋Xin ke zheng yuan ben di ba cai zi — Hua jian.Le Hua jian ji nouvellement gravé.

Recueil de chansons publiées par Zhong Yang xue. Édition faite à la salle Han jing, à la capitale provinciale (Canton) en 1840. Deux illustrations.4 livres.

繡像白圭全傳Xiu xiang bai gui quan zhuan.Histoire illustrée de la tablette blanche.

Par Cui Xiang chuan, de Bai ling ; le titre porte l'indication : édition du 10e romancier de génie par Ji Xiao lan. Ce dernier, postnom Yun, originaire de Xian, a vécu de 1724 à 1805. Préface de Qing chuan ju shi. Portraits des personnages. Édition de la salle Yong an.Livre préliminaire + 4 sections (16 hui).

幾何要法Ji he yao fa.Principes de géométrie.

Par le P. Giulio Aleni (1582-1649) ; rédigé par Qu Shi gu, de Hai yu. Préface par Zheng Hong you, de Lu an (1631). Publié avec autorisation du P. Emmanuel Diaz (1574-1659), à la Mission du Fu jian.

崇禎曆書 。測量全義Chong zheng li shu. — Ce liang quan yi.Collection relative au calendrier, années Chong zheng : traité de la mesure des lignes, surfaces et volumes,.

Même ouvrage.Livres 3 et 5. — Comparer Cat. imp., liv. 106, f. 21 (Xin fa suan shu, 100 livres).

崇禎曆書 。割圓八線表Chong zheng li shu. — Ge yuan ba xian biao.Collection relative au calendrier, années Chong zheng : explication et tables des sinus, etc.

Par le P. Jean Terenz (1576-1630) ; publié par les PP. Rho et Schall, sous la direction de Xu Guang qi. Édition antérieure à 1644.1 livre. — Comparer Cat. imp., liv. 106, f. 21 (Xin fa suan shu, 100 livres).

高厚蒙求Gao hou mong qiu.Collection de traités scientifiques.

Contient : I天學入門Tian xue ru men.Éléments de cosmographie ; II海域大觀Hai yu da guan.Éléments de géographie ; III天地圖儀Tian di tu yi.Des cartes célestes et terrestres ; IV日晷圖法Ri gui tu fa.Figure et explication du cadran solaire et d'autres instruments ; V自鳴鐘表圖法Zi ming zhong biao tu fa.Figure et explication des horloges européennes

崇禎曆書 。日躔曆指Chong zheng li shu. — Ri chan li zhi.Collection relative au calendrier, années Chong zheng : théorie du mouvement du soleil.

Comparer aussi Cat. imp., liv. 106, f. 21 (Xin fa suan shu, 100 livres).Par les PP. Giacomo Rho (1590-1638), Nicolao Longobardi et Adam Schall ; publié sous la direction de Xu Guang qi. Édition antérieure à 1644. Texte et figures.