-
381
-
382
Absceso esplénico. Una causa poco frecuente de choque séptico y trombocitopenia
Published 2023-10-01Get full text
Article -
383
LAS PLANTAS VASCULARES Y VEGETACIÓN DE LA BARRANCA TEPECAPA EN EL MUNICIPIO DE TLAYACAPAN, MORELOS, MÉXICO
Published 2014-01-01Get full text
Article -
384
-
385
Bis(methyl xanthato)-κS;κ2S:S′-(triphenylphosphane-κP)palladium(II)
Published 2011-11-01Get full text
Article -
386
Nuevas especies de Licaria, Ocotea y Persea (Lauraceae) de México
Published 2005-01-01Get full text
Article -
387
IL-17 Inhibition: Emerging Perspectives in the Future Management of Axial Spondyloarthritis
Published 2015-07-01Get full text
Article -
388
Strategies and performance of New Mexican emerging multinational enterprises
Published 2010Get full text
Book Section -
389
Tamoxifen for the treatment of myeloproliferative neoplasms: A Phase II clinical trial and exploratory analysis
Published 2023-11-01“…TAMARIN Phase-II, multicenter, single-arm clinical trial assessed tamoxifen’s safety and activity in patients with stable MPNs, no prior thrombotic events and mutated JAK2 V617F , CALR ins5 or CALR del52 peripheral blood allele burden ≥20% (EudraCT 2015-005497-38). 38 patients were recruited over 112w and 32 completed 24w-treatment. The study’s A’herns success criteria were met as the primary outcome ( ≥ 50% reduction in mutant allele burden at 24w) was observed in 3/38 patients. …”
Get full text
Article -
390
Monogenic signs of susceptibility to ischemic stroke: literature review
Published 2016-03-01“…These syndromes include: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL, mutation in the NOTCH3 gene); cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL, mutation in the HTRA1 gene); Fabry disease (FD, GLA D313Y mutation); COL4A1-related brain small vessel disease associated with mutation in the gene encoding IVα1 collagen; Ehlers Danlos syndrome (EDS) caused by mutation in the COL3A1 gene; hereditary endotheliopathy with retinopathy, nephropathy and stroke (HERNS, mutation in the TREX1 gene); sickle cell disease (SCD, mutation in the beta-globin gene); homocystinuria - hereditary metabolic disorder associated with mutations in the MTHFR, MTRR, MTR CBS genes of the folate cycle; neurofibromatosis type 1 (NF1, mutation in the gene NF1); hereditary hemorrhagic telangiectasia (HHT, mutations in the ENG, ALK1 or SMAD4 genes); hereditary cerebral amyloid angiopathy (CAA, mutation in the APP gene); cerebral cavernous malformations (CCM, mutations in the CCM1, CCM2 or CCM3 genes); mithochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS, mutations in the MT-ND1, MT-ND5, MT-TH, MT-TL1, MT-TV genes).The study of the genetic profile permits to personify medical tactics in ischemic stroke.…”
Get full text
Article -
391
-
392
Influence of Anodic Conditions on Self-ordered Growth of Highly Aligned Titanium Oxide Nanopores
Published 2007-01-01Get full text
Article -
393
Simulated Annealing Hyper-Heuristic for a Shelf Space Allocation on Symmetrical Planograms Problem
Published 2021-06-01Get full text
Article -
394
-
395
Aislamiento e identificación de hongos nematófagos nativos de zonas arroceras de Costa Rica
Published 2011-01-01Get full text
Article -
396
UN MODELO PARA GESTIONAR EL CONOCIMIENTO CONSIDERANDO LA CULTURA ORGANIZACIONAL EN LAS PYME’S
Published 2021-11-01Get full text
Article -
397
Especies raras de hongos anamorfos saprobios en el estado de Tabasco
Published 2011-01-01Get full text
Article -
398
Salmonella Mississippi: An unusual cause of renal abscess in an immunocompetent patient
Published 2022-11-01Get full text
Article -
399
Evaluación agronómica de germoplasma de soya (Glycine max L. Merr.) En Cuba
Published 2003-01-01Get full text
Article -
400