Organización de Osakidetza
Organización Sanitaria Integrada Araba
Publications (14) Publications auxquelles un chercheur a participé
2017
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Efectividad de la mensajería móvil para el control glucémico en pacientes diabéticos en atención primaria. Ensayo clínico aleatorizado
Atencion Primaria
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Eficacia y seguridad de la ketamina en depresión bipolar: una revisión sistemática
Revista de Psiquiatria y Salud Mental
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Eosinophilic gastroenteritis: three clinical cases with different presentations
Gastroenterologia y Hepatologia
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Erratum to «Pseudopseudohypoparathyroidism vs. progressive osseous heteroplasia in absence of family history» (Medicina Clinica (2015) 145(10) (e25–e27)(S0025775315001116)(10.1016/j.medcli.2015.02.009))
Medicina Clinica
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Erratum to: Online information seeking by patients with bipolar disorder: results from an international multisite survey (Int J Bipolar Disord, (2016), 4, (1), 10.1186/s40345-016-0058-0)
International Journal of Bipolar Disorders
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Identificación de pacientes con lupus eritematoso sistémico: problemas y soluciones
Revista Clinica Espanola
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Improved classification of leukemic B-cell lymphoproliferative disorders using a transcriptional and genetic classifier
Haematologica
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Microangiopatía trombótica tumoral pulmonar: El reto de un diagnóstico precoz
Revista de Patologia Respiratoria
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Prevalence of amyloid deposits determined by fine-needle aspiration of abdominal fat in patients with psoriasis
Journal of the European Academy of Dermatology and Venereology
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SCIENTIFIC LETTERS
ENDOCRINOLOGIA DIABETES Y NUTRICION
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Sex differences in the association between obstructive sleep apnea and hypertension-what's next?
Journal of Thoracic Disease
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Skin metastasis as the first clinical manifestation of breast carcinoma
Revista de Senologia y Patologia Mamaria
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The Challenge of Assessing Adherence to Subcutaneous Biological Drugs in Immune-Mediated Inflammatory Diseases. Letter to the Editor Regarding Michetti P, Weinman J, Mrowietz U, et al. Adv Ther (2017);34:91–108. doi:10.1007/s12325-016-0441-3
Advances in Therapy
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The p.R56* mutation in PTHLH causes variable brachydactyly type E
American Journal of Medical Genetics, Part A