Nadia Awni Sakati - bibliography

Related eponyms

Biography

Syrian paediatrician, born 1938, Damascus.

Bibliography

  • William L. Nyhan, Nadia A. Sakati:
    Genetic & Malformation Syndromes in Clinical Medicine.
    Chicago : Year Book Medical Publishers, 1976. 499 pages.
  • Kathryn J. Reid, Nadia Sakati, Lorraine L. Prichard, Lawrence J. Schneiderman, Oliver W. Jones, and Barbara K. Dixson:
    Genetic Counseling. An Evaluation of Public Health Genetic Clinics.
    The Western Journal of Medicine, San Francisco, January 1976, 124 (1): 6-12.
  • William L. Nyhan, Nadia A. Sakati:
    Diagnostic Recognition of Genetic Disease. Lea & Febiger, 1987.
  • Nabil K. Bissada, Nadia Sakati, Nicholas J. Y. Woodhouse, and Rafik R. Morcos.
    One-Stage Complete Genital Reconstruction for Patients with Congenital Adrenal Hyperplasia. The Journal of Urology, April 1987, 137: 703-705.
  • S. Sanjad, N. Sakati, Y. K. Abu-Osba:
    Congenital hypoparathyroidism with dysmorphic features: a new syndrome.
    Pediatric Research, Hagerstown, 1988, 23: A419.
  • S. Sanjad, N. Sakati, Y. K. Abu-Osba, R. Kaddora, R. D. G. Milner:
    A new sydrome of congenital hypoparathyrodism, seizure, growth failure and dysmorphic features. Archives of Disease in Childhood, London, 1991, 66: 193-196.
  • A. al –Rabeeah, A. al-Ashwal, A. al-Herbish, N. al-Jurayyan, N. Sakati, A. Abobakr:
    Persistent hyperinsulinemic hypoglycemia of infancy: experience with 28 cases.
    The Journal of Pediatric Surgery, New York, 1995, 30: 1119-1121
  • N. Attia, N. Sakati, A. Al Ashwal, R. Al Saif, M. Rashed, P. T. Ozand:
    Case Report. Isovaleric acidaemia appearing as diabetic ketoacidosis.
    Journal of Inherited Metabolic Disease, 1996, 19 (1): 85-86.
  • N. Attia, A. Zahrani, R. Saif, H. A. Kattan, N. Sakati, A. Al Ashwal, W. V. Tamborlane:
    Different faces of non-autoimmune diabetes of infancy.
    Short Communication. Acta Paediatrica, August 1998, 87 (1): 95.
  • Thaddeus E. Kelly, Susan Blanton, Ramla Saif, Sami A. Sanjad, and Nadia Sakati:
    Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome lq42-43.
    Journal of Medical Genetics, London, 2000, 37: 63-64. Biographical etc:
  • The Official ABMS [American Board of Medical Specialties] directory of board certified medical specialists. Edition 27, 1995. Providence N.J. : Marquis Who's Who 1994, page 2981.

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