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Attainment of Inactive Disease Following Discontinuation of Adalimumab Monotherapy in Patients with Enthesitis-Related Arthritis: A Real-Life, Dual-Center Experience

Autor: Papailiou, S. Dasoula, F. Tsolia, M.N. Maritsi, D.N.

The optimum duration of treatment in patients with juvenile idiopathic arthritis (JIA), including enthesitis-related arthritis (ERA), is an area of pivotal concern for both parents and physicians. Novel medicines have managed to achieve remission of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::f99a2b6fbf75d0348358b4043ff35c0e
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3118509

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Aldosterone synthase deficiency type II: An unusual presentation of the first Greek case reported with confirmed genetic analysis

Autor: Papailiou, S. Vlachopapadopoulou, E.A. Sertedaki, A. Maritsi, D. Syggelos, N. Syggelou, A.

Objective. Aldosterone synthase deficiency (ASD) is a rare, autosomal recessive inherited disease with an overall clinical phenotype of failure to thrive, vomiting, severe dehydration, hyperkalemia, and hyponatremia. Mutations in the CYP11B2 gene enc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::57bcd244f346f87d2e83d2cdc976758f
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3078966

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A novel de novo KCNQ2 mutation in a child with treatment-resistant early-onset epileptic encephalopathy

Autor: Benetou, C. Papailiou, S. Maritsi, D. Anagnostopoulou, K. Kontos, H. Vartzelis, G.

Mutations in KCNQ2 gene, encoding for voltage-gated K+ channel subunit, may result in a wide spectrum of early-onset epileptic disorders. The phenotype of the disease varies from “benign familial neonatal seizures” to “severe epileptic encephal

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::8ab372304f06495aacf3d099c40ea6ab
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3106383

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