MARÍA DEL CONSUELO
MODESTO CABALLERO
Publicaciones (60) Publicaciones de MARÍA DEL CONSUELO MODESTO CABALLERO
2022
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Intravenous iron treatment-induced hypophosphatemia
Medicina Clinica
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Transient migratory osteoporosis
Medicina Clinica, Vol. 158, Núm. 3, pp. 147
2021
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Clinical remission and subsequent relapse in patients with juvenile idiopathic arthritis: predictive factors according to therapeutic approach
Pediatric Rheumatology, Vol. 19, Núm. 1
2019
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American College of Rheumatology Provisional Criteria for Clinically Relevant Improvement in Children and Adolescents With Childhood-Onset Systemic Lupus Erythematosus
Arthritis Care and Research, Vol. 71, Núm. 5, pp. 579-590
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Anti-IL6-Receptor Tocilizumab in Refractory and Noninfectious Uveitic Cystoid Macular Edema: Multicenter Study of 25 Patients
American Journal of Ophthalmology, Vol. 200, pp. 85-94
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Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis
Scientific Reports, Vol. 9, Núm. 1
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Clinical characteristics and genetic analyses of 187 patients with undefined autoinflammatory diseases
Annals of the Rheumatic Diseases, Vol. 78, Núm. 10, pp. 1405-1411
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Síndrome d’activació macrofàgica com a forma de debut d’una artritis idiopàtica juvenil sistèmica
Pediatria catalana: butlletí de la Societat Catalana de Pediatria, Vol. 79, Núm. 3, pp. 89-93
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Unexpected relevant role of gene mosaicism in patients with primary immunodeficiency diseases
Journal of Allergy and Clinical Immunology, Vol. 143, Núm. 1, pp. 359-368
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Valoración inicial del paciente con sospecha de enfermedad reumática
Manual de pediatría (Ergon), pp. 1345-1348
2018
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Blau Syndrome–Associated Uveitis: Preliminary Results From an International Prospective Interventional Case Series
American Journal of Ophthalmology, Vol. 187, pp. 158-166
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S100A12 and S100A8/9 proteins are biomarkers of articular disease activity in Blau syndrome
Rheumatology (United Kingdom), Vol. 57, Núm. 7, pp. 1299-1304
2017
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Anti–Interleukin-6 Receptor Tocilizumab for Severe Juvenile Idiopathic Arthritis–Associated Uveitis Refractory to Anti–Tumor Necrosis Factor Therapy: A Multicenter Study of Twenty-Five Patients
Arthritis and Rheumatology, Vol. 69, Núm. 3, pp. 668-675
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Novel evidences of atypical manifestations in cryopyrin-associated periodic syndromes
Clinical and Experimental Rheumatology, Vol. 35, pp. S27-S31
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Preliminary Definitions for the Sonographic Features of Synovitis in Children
Arthritis Care and Research, Vol. 69, Núm. 8, pp. 1217-1223
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Subcutaneous tocilizumab may be less effective than intravenous tocilizumab in the treatment of juvenile idiopathic arthritis-Associated uveitis
Journal of Rheumatology
2016
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Efficacy of the Janus kinase 1/2 inhibitor ruxolitinib in the treatment of vasculopathy associated with TMEM173-activating mutations in 3 children
Journal of Allergy and Clinical Immunology, Vol. 138, Núm. 6, pp. 1752-1755
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The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From the Eurofever Registry
Arthritis and Rheumatology, Vol. 68, Núm. 11, pp. 2795-2805
2015
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Clinical and genetic features of Spanish patients with Mevalonate kinase deficiency
Pediatric Rheumatology, Vol. 13, Núm. 1
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Consensus of the Spanish society of pediatric rheumatology for transition management from pediatric to adult care in rheumatic patients with childhood onset
Rheumatology International, Vol. 35, Núm. 10, pp. 1615-1624