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2003, 1. ed., Tierra firme, ISBN 9789681668365, 460
Book
1993, American university studies. Series XXII, Latin American literature, ISBN 9780820419923, Volume 17, xiii, 278
Book
1976, 1. ed. --, Colección Novela nueva, 351 p., [2] leaves of plates
Book
1972, Poesía en el mundo, Volume no.101., 43
Book
Tissue Engineering Part B: Reviews, ISSN 1937-3368, 08/2015, Volume 21, Issue 4, pp. 345 - 353
Journal Article
Pediatric Transplantation, ISSN 1397-3142, 06/2019, Volume 23, Issue 4, pp. e13413 - n/a
FSGS is a potentially devastating form of nephrotic syndrome. Treatment of SRNS can be difficult, especially post‐transplantation. The current therapy of... 
FSGS | Renal Transplant | Ofatumumab | Transplants & implants | Hemodialysis | Rituximab | Monoclonal antibodies | Remission | Nephrotic syndrome | Transplantation | Plasmapheresis
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 2019, pp. 1 - 6
Malaria is a parasitic infection transmitted by mosquitos, resulting in significant morbidity and mortality. It affects 212 million worldwide, causing death in... 
Malaria | FEAST trial | Acute kidney injury | Blackwater fever | Kidneys | Infections | Inflammation | Children | Morbidity | Developing countries--LDCs
Journal Article
Journal Article
Oncotarget, ISSN 1949-2553, 2017, Volume 8, Issue 44, pp. 77385 - 77399
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Pediatric nephrology (Berlin, Germany), ISSN 0931-041X, 08/2019, pp. 1 - 2
Arthrogryposis, renal dysfunction, and cholestasis syndrome is a rare autosomal recessive disorder caused by mutations in the VPS33B and VIPAR genes. Most... 
Phenotypes | Renal function | Diabetes insipidus | Gallbladder diseases | Gene deletion | Fanconi syndrome | Renal tubular acidosis | Citric acid | Hereditary diseases | Hypercalciuria | Clonal deletion | Genetic analysis | Arthrogryposis | Mutation | Acidosis | Ultrasound | Cholestasis | Proteinuria
Journal Article
Pediatric nephrology (Berlin, Germany), ISSN 0931-041X, 08/2019, pp. 1 - 3
Journal Article
Molecular Therapy, ISSN 1525-0016, 05/2019, Volume 27, Issue 5, pp. 986 - 998
Gene editing constitutes a novel approach for precisely correcting disease-causing gene mutations. Frameshift mutations in COL7A1 causing recessive dystrophic... 
gene therapy | epidermal stem cells | CRISPR/Cas9 | epidermolysis bullosa | MEDICINE, RESEARCH & EXPERIMENTAL | DIAGNOSIS | CELLS | SAFETY | REGENERATION | TRANSPLANTATION | DELETION | EXON | DATABASE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | COL7A1 MUTATION | GENERATION
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