Search Results - "Ana Perdomo"
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Teaching Strategies for Developing Clinical Reasoning Skills in Nursing Students: A Systematic Review of Randomised Controlled Trials
Published in Healthcare (Basel) (30-12-2023)“…Clinical reasoning (CR) is a holistic and recursive cognitive process. It allows nursing students to accurately perceive patients' situations and choose the…”
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4-Phenylbutyric Acid Treatment Reduces Low-Molecular-Weight Proteinuria in a Clcn5 Knock-in Mouse Model for Dent Disease-1
Published in International journal of molecular sciences (01-08-2024)“…Dent disease-1 (DD-1) is a rare X-linked tubular disorder characterized by low-molecular-weight proteinuria (LMWP), hypercalciuria, nephrolithiasis and…”
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Mesenchymal Stromal Cells from Perinatal Tissues as an Alternative for Ex Vivo Expansion of Hematopoietic Progenitor and Stem Cells from Umbilical Cord Blood
Published in International journal of molecular sciences (01-11-2023)“…Umbilical cord blood (UCB) serves as a source of hematopoietic stem and progenitor cells (HSPCs) utilized in the regeneration of hematopoietic and immune…”
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Real-time quantification of proteins secreted of conditioned media from mesenchymal stromal cells (MSC) in co-culture with hematopoietic progenitor cells
Published in Sensing and Bio-Sensing Research (01-02-2024)“…The interaction of mesenchymal stromal cells (MSC) in co-cultures with hematopoietic progenitor cells (HPC) in ex-vivo models induce the secretion of…”
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A new strategy for umbilical cord blood collection developed at the first Colombian public cord blood bank increases total nucleated cell content
Published in Transfusion (Philadelphia, Pa.) (01-09-2017)“…BACKGROUND The total nucleated cell dosage of umbilical cord blood (UCB) is an important factor in determining successful allogeneic hematopoietic stem cell…”
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Hypomagnesaemia with varying degrees of extrarenal symptoms as a consequence of heterozygous CNNM2 variants
Published in Scientific reports (22-03-2024)“…Variants in the CNNM2 gene are causative for hypomagnesaemia, seizures and intellectual disability, although the phenotypes can be variable. This study aims to…”
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Teaching and Learning Clinical Reasoning in Nursing Education: A Student Training Course
Published in Healthcare (Basel) (19-06-2024)“…Clinical reasoning is an essential component of nursing. It has emerged as a concept that integrates the core competencies of quality and safety education for…”
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Hereditary kidney diseases associated with hypomagnesemia
Published in Kidney research and clinical practice (01-12-2021)“…In the kidney, a set of proteins expressed in the epithelial cells of the thick ascending loop of Henle and the distal convoluted tubule directly or indirectly…”
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Epidemiology of inflammatory bowel disease in Mexico and Colombia: Analysis of health databases, mathematical modelling and a case-series study
Published in PloS one (27-01-2020)“…Ulcerative Colitis (UC) and Crohn's Disease (CD) have a major impact on quality of life and medical costs. The aim of the study was to estimate the prevalence,…”
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Characterization of a novel HLA‐C allele, HLA‐C01:166, in a Colombian Umbilical Cord Blood Bank Donor
Published in HLA : immune response genetics (01-10-2019)“…HLA‐C*01:166 has a nonsynonymous nucleotide substitution in the position 256 position (C/T) when compared to C*01:02:01:01…”
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Identification of the novel HLA‐B18:147 allele in two Colombian umbilical cord blood bank samples
Published in HLA (01-09-2019)“…HLA‐B*18:147 differs from HLA‐B*18:01:01:01 by one nucleotide substitution…”
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“Learning a Way of Thinking”—World Café on Clinical Reasoning in Nursing and Midwifery Education and Practice across Five European Union Countries
Published in Healthcare (Basel) (01-11-2023)“…Clinical reasoning is a key attribute of nursing and midwifery professionals. As a part of the Erasmus plus project, we designed a study with the aim of…”
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New HLA‐C alleles identified in two donors from the Colombian public umbilical cord blood bank
Published in HLA (01-10-2018)“…Two novel HLA‐class I alleles discovered: HLA‐C*08:162 and HLA‐C*03:296:02…”
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Human Leukocyte Antigen and Red Blood Cells Impact Umbilical Cord Blood CD34 + Cell Viability after Thawing
Published in International journal of molecular sciences (30-09-2019)“…Hematopoietic progenitor cell (HPC) transplantation is a treatment option for malignant and nonmalignant diseases. Umbilical cord blood (UCB) is an important…”
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Characterization of pre-mRNA Splicing Defects Caused by CLCN5 and OCRL Mutations and Identification of Novel Variants Associated with Dent Disease
Published in Biomedicines (01-11-2023)“…Dent disease (DD) is an X-linked renal tubulopathy characterized by low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, nephrolithiasis and…”
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Conductive extracellular matrix derived/chitosan methacrylate/ graphene oxide-pegylated hybrid hydrogel for cell expansion
Published in Frontiers in bioengineering and biotechnology (17-06-2024)“…Electrical stimulation has emerged as a cornerstone technique in the rapidly evolving field of biomedical engineering, particularly within the realms of tissue…”
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Effectiveness and Safety of Ustekinumab for Moderate to Severely Active Crohn's Disease: Results from an Early Access Program in Brazil
Published in Journal of clinical medicine (31-10-2022)“…This prospective, observational, open-label study aimed to provide access to ustekinumab prior to market authorization and assess its safety and effectiveness…”
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Clinical Outcomes of Unrelated Umbilical Cord Blood Graft vs. Haploidentical Donor Transplantation: Critical Issues for an Adequate Comparison
Published in Frontiers in medicine (28-10-2021)“…Unrelated umbilical cord blood (UCB) and haploidentical grafts have been used for allogeneic hematopoietic stem and progenitor cell (HSPC) transplantation in…”
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Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis
Published in Molecular genetics & genomic medicine (01-11-2020)“…Background Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is an autosomal recessive tubulopathy characterized by excessive urinary…”
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