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2. The phenotype of TNF receptor-associated autoinflammatory syndrome (TRAPS) at presentation: a series of 158 cases from the Eurofever/EUROTRAPS international registry. Issue 12 (21st August 2013)

3. A family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis. Issue 1 (December 2015)

4. Clinical and genetic features of Spanish patients with Mevalonate kinase deficiency. Issue 1 (December 2015)

5. Preliminary response to Janus kinase inhibition with baricitinib in chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperatures (CANDLE). Issue 1 (December 2015)

6. Clinical and genetic features of Spanish patients with Mevalonate kinase deficiency. Issue 1 (December 2015)

7. A family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis. Issue 1 (December 2015)

8. Preliminary response to Janus kinase inhibition with baricitinib in chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperatures (CANDLE). Issue 1 (December 2015)