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2. Atypical hemolytic–uremic syndrome: recurrent phenotypic expression of a patient with MCP gene mutation combined with risk haplotypes. Issue 2 (March 2019)

3. Combined study of ADAMTS13 and complement genes in the diagnosis of thrombotic microangiopathies using next‐generation sequencing. Issue 1 (23rd June 2017)

4. Familial thrombotic risk based on the genetic background of Protein C Deficiency in a Portuguese Study. (13th March 2015)

6. Multicentric evaluation of the new HemosIL Acustar® chemiluminescence ADAMTS13 activity assay. (2nd December 2020)