DECRETO 3518 SIVIGILA PDF
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Repositorio Institucional EdocUR dc. Genetic, immune and vasoactive factors in the vascular dysfunction associated with hypertension in pregnancy. Expert Opin Ther Targets, 19 11 Vascular Health and Risk Management, 11, Glomerular endothelial cell differentiation. Kidney Int, 67 5 STOX1 gene in pre-eclampsia and intrauterine growth restriction. Bjog, 9 Increased placental production of leukotriene B4 in gestational hypertension.
Thromb Res, 60 5 The Notch effector Hey1 associates with myogenic target genes to repress myogenesis. J Biol Chem, 2 A homozygous donor splice-site sibigila in the meiotic gene MSH4 causes primary ovarian insufficiency. Hum Mol Genet, 26 16 Bioinformatics, 21 13 Nucl Acids Res Novel biomarkers for predicting preeclampsia. Trends Cardiovasc Med, 18 5 Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorder.
Neurol Sci, 34 12 Angiogenic factors in preeclampsia and related disorders. Cold Spring Harb Perspect Med, 2 Pre-eclampsia and cardiovascular disease. Cardiovascular Research, 4 Advances in the pathophysiology of pre-eclampsia and related podocyte injury.
Kidney international, 86 2 Etiology and pathogenesis of preeclampsia: Am Edcreto Obstet Gynecol, 5 Gateway-compatible yeast one-hybrid screens. CSH Protoc, 5.
Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis. Hum Mutat, 33 8 Nitroso-redox balance and mitochondrial homeostasis are regulated by STOX1, a pre-eclampsia-associated gene. Antioxid Redox Signal, 21 6 Preeclampsia-like symptoms induced in mice by fetoplacental expression of STOX1 are reversed by aspirin treatment.
Hypertension, 61 3 Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia. Scientific Reports, 6, Journal of Pregnancy, Screening for mutations of the FOXO4 gene in premature suvigila failure patients.
Reprod Biomed Online, 24 3 Reprod Biomed Online, 29 5 Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations. Fertil Steril, 1 A de novo 14q12q Am J Med Genet A, a 3 Br J Dermatol, 2 Current needs for human and medical genomics research infrastructure in low and middle income countries.
J Med Genet, 53 7 Altered global gene expression in first trimester placentas of women destined to develop preeclampsia. Placenta, 30 1 Downregulation of notch signaling pathway in late preterm and term placentas from pregnancies complicated by preeclampsia. PLoS One, 10 5e New approaches for managing preeclampsia: Clin Ther, 36 12 A new player in preeclampsia?
Angiogenic factors in preeclampsia: Curr Opin Nephrol Hypertens, 22 6 Genomic imprinting, development and disease–is pre-eclampsia caused by a maternally imprinted gene? Reprod Fertil Dev, 10 1dc. Potential markers of preeclampsia–a review. Reprod Biol Endocrinol, 7, A yeast one-hybrid and microfluidics-based pipeline to map mammalian gene regulatory networks. Molecular Systems Biology, 9, Asymmetric distribution of the C.
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Development, 11 Promoter architectures and developmental gene regulation. Biomarker development for presymptomatic molecular diagnosis of preeclampsia: Expert Rev Mol Diagn, 15 5 Ther Adv Cardiovasc Dis, 3 1 Electrophoretic mobility shift assay EMSA for detecting protein-nucleic acid interactions.
Nat Protoc, 2 8 Nutr Rev, 71 Suppl 1, S The Biology of Preeclampsia. Kidney international, 76 8 Evaluation of STOX1 as a preeclampsia candidate gene in a population-wide sample. Eur J Hum Genet, 15 4 Differentially expressed genes in the pre-eclamptic placenta: PLoS One, 8 7e In Mol Cell Biol Vol. Bioessays, 32 2 Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing.
Mol Cell Endocrinol, The molecular complexity of primary ovarian dscreto aetiology and the use of massively parallel sequencing. Identification of Quantitative Trait Loci responsible for embryonic lethality in mice assessed by ultrasonography.
Int J Dev Biol, 53 4 Mouse models for identifying genes modulating fertility parameters. Animal, 3 1 Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2.
Decreto 3518 de 2006 powerpoint download
J Med Genet, 46 7 Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans. Open Biol, 6 Improving the evaluation of milestones for students completing a clinical genetics elective. Genet Med, 19 BMP15 and premature ovarian failure: