Miguel Ángel
García González
Publications (42) Miguel Ángel García González publications
2024
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Gene editing: a near future for the treatment of genetic kidney diseases
Kidney International
2023
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Changes of Erythrocyte Fatty Acids after Supplementation with Highly Concentrated Docosahexaenoic Acid (DHA) in Pediatric Cystic Fibrosis: A Randomized Double-Blind Controlled Trial
Journal of Clinical Medicine, Vol. 12, Núm. 11
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Genetic testing in focal segmental glomerulosclerosis: in whom and when?
Clinical Kidney Journal, Vol. 16, Núm. 11, pp. 2011-2022
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SARS-CoV-2 infection in children with cystic fibrosis: A cross-sectional multicenter study in Spain. New waves, new knowledge
Pediatric Pulmonology, Vol. 58, Núm. 11, pp. 3195-3205
2022
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Genetic Kidney Diseases (GKDs) Modeling Using Genome Editing Technologies
Cells, Vol. 11, Núm. 9
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Long-term outcome of omalizumab-assisted desensitisation to cow's milk and eggs in patients refractory to conventional oral immunotherapy: real-life study
Allergologia et Immunopathologia, Vol. 50, Núm. 3, pp. 1-7
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Quantitative Proteomic Study Unmasks Fibrinogen Pathway in Polycystic Liver Disease
Biomedicines, Vol. 10, Núm. 2
2021
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Molecular basis, diagnostic challenges and therapeutic approaches of alport syndrome: A primer for clinicians
International Journal of Molecular Sciences, Vol. 22, Núm. 20
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Molecular basis, diagnostic challenges and therapeutic approaches of bartter and gitelman syndromes: A primer for clinicians
International Journal of Molecular Sciences, Vol. 22, Núm. 21
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Molecular pathophysiology of autosomal recessive polycystic kidney disease
International Journal of Molecular Sciences, Vol. 22, Núm. 12
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Protein Extraction From FFPE Kidney Tissue Samples: A Review of the Literature and Characterization of Techniques
Frontiers in Medicine, Vol. 8
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Tweak signaling pathway blockade slows cyst growth and disease progression in autosomal dominant polycystic kidney disease
Journal of the American Society of Nephrology, Vol. 32, Núm. 8, pp. 1913-1932
2020
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Association of single nucleotide polymorphisms with renal cell carcinoma in Algerian population
African Journal of Urology, Vol. 26, Núm. 1
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CystAnalyser: A new software tool for the automatic detection and quantification of cysts in polycystic kidney and liver disease, and other cystic disorders
PLoS Computational Biology, Vol. 16, Núm. 10
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First-Days Reduction of Plasma and Skin Advanced Glycation End Products is Related to Outcome in Septic Patients
Shock, Vol. 53, Núm. 4, pp. 400-406
2019
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Dietary care for ADPKD patients: Current status and future directions
Nutrients, Vol. 11, Núm. 7
2018
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Autosomal Dominant Tubulointerstitial Kidney Disease: Clinical Presentation of Patients With ADTKD-UMOD and ADTKD-MUC1
American Journal of Kidney Diseases, Vol. 72, Núm. 3, pp. 411-418
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Overview of autosomal dominant polycystic kidney disease in the south of Spain
Nefrologia, Vol. 38, Núm. 2, pp. 220-221
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Pkd2 deletion during embryo development does not alter mesonephric programmed cell senescence
International Journal of Developmental Biology, Vol. 62, Núm. 9-10, pp. 637-640
2017
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NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology
Scientific Reports, Vol. 7, Núm. 1