Search

Search Results

• 

  Protein tyrosine phosphatase non-receptor type 22 C1858T gene polymorphism in children with Down syndrome and autoimmune thyroid diseases

  Muhammad Faizi, Nur Rochmah, Soetjipto Soetjipto, Anang Endaryanto, Sukmawati Basuki, Yuni Hisbiyah, Rayi Kurnia Perwitasari

  22-02-2023

  Published: 22 February 2023

  872

  PDF: 418

  HTML: 18

• A not very essential obesity: the Rohhad Syndrome. Description of two cases and review of the literature

  V. Ramistella, M. Wasniewska, M. Valenzise, D. Corica, S. Cantucci, E. Pitrolo, M. Romeo, F. De Luca

  31-08-2013

  Published: 31 August 2013

  1949

  PDF: 5244
• 

  Kearns-Sayre syndrome with facial and white matter extensive involvement: a (mitochondrial and nuclear gene related?) neurocristopathy?

  Agostino Berio, Attilia Piazzi, Carlo Enrico Traverso

  15-12-2017

  Published: 15 December 2017

  1816

  PDF: 979

  HTML: 296