Lymphology

Bertelli, M

• Vol 45, No 1 (2012) - Articles
  CLINICAL AND GENETIC STUDY OF 46 ITALIAN PATIENTS WITH PRIMARY LYMPHEDEMA
  Abstract  PDF
• Vol 49, No 1 (2016) - Articles
  A RARE CASE OF EMBERGER SYNDROME CAUSED BY A DE NOVO MUTATION IN THE GATA2 GENE
  Abstract  PDF
• Vol 49, No 2 (2016) - Articles
  GENETIC SCREENING IN A LARGE COHORT OF ITALIAN PATIENTS AFFECTED BY PRIMARY LYMPHEDEMA USING A NEXT GENERATION SEQUENCING (NGS) APPROACH
  Abstract  PDF
• Vol 53, No 1 (2020) - Articles
  CYP26B1 AND ITS IMPLICATIONS IN LYMPHANGIOGENESIS: LITERATURE REVIEW AND STUDY OF RARE VARIANTS IN TWO FAMILIES
  Abstract  PDF
• Vol 53, No 2 (2020) - Articles
  REVIEW OF THE FUNCTION OF SEMA3A IN LYMPHATIC VESSEL MATURATION AND ITS POTENTIAL AS A CANDIDATE GENE FOR LYMPHEDEMA: ANALYSIS OF THREE FAMILIES WITH RARE CAUSATIVE VARIANTS
  Abstract  PDF
• Vol 53, No 3 (2020) - Articles
  RARE PECAM1 VARIANTS IN THREE FAMILIES WITH LYMPHEDEMA
  Abstract  PDF