Cesar Bergadá, Argentine pediatric endocrinologist (Buenos Aires 08 June 1929 – Buenos Aires 08 April 2005)
Presented original hypothesis about anomalies of sexual differentiation
With I. Bergadá, G. Del Rey, P. Lapunzina, M. Fellous & S. Copelli. Familial occurrence of the IMAGe association: additional clinical variants and a proposed mode of inheritance. J. Clin. Endocr. Metab. 90:3186-90, 2005
Described Bergada syndrome or Rudimentary testes syndrome
With W.W. Cleveland, H.W. Jones Jr & L. Wilkins. Variants of embryonic testicular dysgenesis: bilateral anorchia and the syndrome of rudimentary testes. Acta Endocrinol 40:521-36, 1962.
DESCRIBED DISEASES
With S. Iorcansky, N. Altschuler & M. Cullen. Familial dysenzymatic goiter caused by failure in the binding of iodothyroxines. Rev. Arg. Endocr. Metab. 12(4):227-33, 1967
With V.A. Dahl. New endocrine system caused by the inadequate secretion of antidiuretic syndrome. Rev. Arg. Endocr. Metab. 10:148-50, 1964
With M. Cullen. Female pseudohermaphroditism without postnatal adrenal hyperplasia. Rev. Arg. Endocr. Metab. 4(4):352-71, 1958
DEVELOPED METHODS
With F. Gruneiro & A. Chiesa. The surface of epiphysis of the knee: an index of the onset of neonatal hypothyroidism (NH). Pediat. Res. 28(4), 1990
With C. Bianculli, B. Cano de Candas, J. Menendez & M. A. Rivarola. Urinary acid phosphatase as an auxiliary index of androgenic response. J. Pediatrics 89(2):325, 1976
With V.A. Dahl. The determination of urinary pregnanetriol. Rev. Arg. Endocr. Metabolismo 10:84-9, 1964