Rare C1q deficiency presenting as pediatric SLE: A case study of two consanguineous siblings Kerem Parlar; Berkay Akta¿; Sena Ladin Sicakyüz; Sezgin ¿ahin; Özgür Kasapçopur; Serdal U¿urlu;

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Uso de anifrolumab en un paciente con síndrome de Rowell crónico multirrefractario Carlota Navarro-Joven; María Alonso de Francisco; Margarita Pich-Aguilera Blasco; Rita María Cabeza Martínez; José Luis Andreu Sánchez; Hildegarda Godoy-Tundidor;