Sergio Bernasconi

Summary

Affiliation: University of Parma
Country: Italy

Publications

  1. ncbi Placental determinants of fetal growth: identification of key factors in the insulin-like growth factor and cytokine systems using artificial neural networks
    Maria E Street
    Department of Pediatrics, University of Parma, 43100 Parma, Italy
    BMC Pediatr 8:24. 2008
  2. ncbi SHOX gene in Leri-Weill syndrome and in idiopathic short stature
    S Bernasconi
    Department of Pediatrics, University of Parma, OORR, Italy
    J Endocrinol Invest 24:737-41. 2001
  3. ncbi A new era for "Italian Journal of Pediatrics"
    Sergio Bernasconi
    Department of Pediatrics, University of Parma, Parma, Italy
    Ital J Pediatr 34:1. 2008
  4. ncbi SHOX point mutations and deletions in Leri-Weill dyschondrosteosis
    C Falcinelli
    Cattedra di Genetica Medica, , Via del Pozzo 71, 41100 Modena, Italy
    J Med Genet 39:E33. 2002
  5. ncbi Genitourinary anomalies in Mowat-Wilson syndrome with deletion/mutation in the zinc finger homeo box 1B gene (ZFHX1B). Report of three Italian cases with hypospadias and review
    L Garavelli
    Department of Pediatrics and Genetic Unit, S Maria Nuova Hospital, Reggio Emilia, Italy
    Horm Res 63:187-92. 2005

Collaborators

Detail Information

Publications5

  1. ncbi Placental determinants of fetal growth: identification of key factors in the insulin-like growth factor and cytokine systems using artificial neural networks
    Maria E Street
    Department of Pediatrics, University of Parma, 43100 Parma, Italy
    BMC Pediatr 8:24. 2008
    ....
  2. ncbi SHOX gene in Leri-Weill syndrome and in idiopathic short stature
    S Bernasconi
    Department of Pediatrics, University of Parma, OORR, Italy
    J Endocrinol Invest 24:737-41. 2001
  3. ncbi A new era for "Italian Journal of Pediatrics"
    Sergio Bernasconi
    Department of Pediatrics, University of Parma, Parma, Italy
    Ital J Pediatr 34:1. 2008
    ..Readers will also benefit from free online access to the journal via the website and a range of full text archives...
  4. ncbi SHOX point mutations and deletions in Leri-Weill dyschondrosteosis
    C Falcinelli
    Cattedra di Genetica Medica, , Via del Pozzo 71, 41100 Modena, Italy
    J Med Genet 39:E33. 2002
  5. ncbi Genitourinary anomalies in Mowat-Wilson syndrome with deletion/mutation in the zinc finger homeo box 1B gene (ZFHX1B). Report of three Italian cases with hypospadias and review
    L Garavelli
    Department of Pediatrics and Genetic Unit, S Maria Nuova Hospital, Reggio Emilia, Italy
    Horm Res 63:187-92. 2005
    ..MWS should be considered by endocrinologists in patients with hypospadias associated with developmental delays/mental retardation, in particular in the presence of a distinct facial phenotype...