Cristina
Martín Higueras
Investigadora en el periodo 2020-2022
Publicaciones (23) Publicaciones de Cristina Martín Higueras
2024
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Multicenter Long-Term Real World Data on Treatment With Lumasiran in Patients With Primary Hyperoxaluria Type 1
Kidney International Reports, Vol. 9, Núm. 1, pp. 114-133
2023
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Correction to: Three Tesla magnetic resonance imaging detects oxalate osteopathy in patients with primary hyperoxaluria type I (Pediatric Nephrology, (2023), 38, 7, (2083-2092), 10.1007/s00467-022-05836-3)
Pediatric Nephrology
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Determinants of Kidney Failure in Primary Hyperoxaluria Type 1: Findings of the European Hyperoxaluria Consortium
Kidney International Reports, Vol. 8, Núm. 10, pp. 2029-2042
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Simple, fast and inexpensive quantification of glycolate in the urine of patients with primary hyperoxaluria type 1
Urolithiasis, Vol. 51, Núm. 1, pp. 49
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Three Tesla magnetic resonance imaging detects oxalate osteopathy in patients with primary hyperoxaluria type I
Pediatric Nephrology, Vol. 38, Núm. 7, pp. 2083-2092
2022
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Chronic liver disease and hepatic calcium-oxalate deposition in patients with primary hyperoxaluria type I
Scientific Reports, Vol. 12, Núm. 1
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Diet-related urine collections: assistance in categorization of hyperoxaluria
Urolithiasis, Vol. 50, Núm. 2, pp. 141-148
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Disorders of Oxalate Metabolism
Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases, Second Edition (Springer International Publishing), pp. 1319-1332
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Improving Treatment Options for Primary Hyperoxaluria
Drugs, Vol. 82, Núm. 10, pp. 1077-1094
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Nephrolithiasis and nephrocalcinosis in children and adolescents
Urologie, Vol. 61, Núm. 10, pp. 1099-1109
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New salicylic acid derivatives, double inhibitors of glycolate oxidase and lactate dehydrogenase, as effective agents decreasing oxalate production
European Journal of Medicinal Chemistry, Vol. 237
2021
2020
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Inherited conditions resulting in nephrolithiasis
Current opinion in pediatrics, Vol. 32, Núm. 2, pp. 273-283
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Is stiripentol truly effective for treating primary hyperoxaluria?
Clinical Kidney Journal, Vol. 14, Núm. 1, pp. 442-444
2019
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Systemic Alanine Glyoxylate Aminotransferase mRNA Improves Glyoxylate Metabolism in a Mouse Model of Primary Hyperoxaluria Type 1
Nucleic Acid Therapeutics, Vol. 29, Núm. 2, pp. 104-113
2018
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CRISPR/Cas9-mediated glycolate oxidase disruption is an efficacious and safe treatment for primary hyperoxaluria type I
Nature Communications, Vol. 9, Núm. 1
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Salicylic Acid Derivatives Inhibit Oxalate Production in Mouse Hepatocytes with Primary Hyperoxaluria Type 1
Journal of Medicinal Chemistry, Vol. 61, Núm. 16, pp. 7144-7167
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Specific Inhibition of Hepatic Lactate Dehydrogenase Reduces Oxalate Production in Mouse Models of Primary Hyperoxaluria
Molecular Therapy, Vol. 26, Núm. 8, pp. 1983-1995
2017
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Molecular therapy of primary hyperoxaluria
Journal of Inherited Metabolic Disease, Vol. 40, Núm. 4, pp. 481-489