Zobrazeno 1 - 10
of 109
pro vyhledávání: '"Schwingshandl, J"'
Publikováno v:
The British journal of dermatology. 130(2)
Hyperpigmented macules are a characteristic feature of neurofibromatosis and the McCune-Albright syndrome. Whereas neurofibromatosis 1 has an autosomal dominant mode of inheritance, it has been suggested that McCune-Albright syndrome is the result of
Autor:
Schwingshandl J, Sudi K, Eibl B, Wallner S, Borkenstein M, Schwingshandl, J, Sudi, K, Eibl, B, Wallner, S, Borkenstein, M
Publikováno v:
Archives of Disease in Childhood; Nov1999, Vol. 81 Issue 5, p426-428, 3p
Publikováno v:
Journal of Paediatrics & Child Health; Aug1993, Vol. 29 Issue 4, p315-318, 4p
Publikováno v:
Pediatric Cardiology; Jan1995, Vol. 16 Issue 1, p1-5, 5p
Publikováno v:
Diabetic Medicine; Oct1995, Vol. 12 Issue 10, p868-873, 6p
Autor:
Donaghue, Kim C., Pena, M.M., Fung, A.T.W., Bonney, M., Howard, N.J., Silink, M., Schwingshandl, J.
Publikováno v:
Diabetic Medicine; Oct1995, Vol. 12 Issue 10, p868-873, 6p
Autor:
Donaghue, K.C., Bonney, M., Simpson, J.M., Schwingshandl, J., Fung, A.T.W., Howard, N.J., Silinka, M.
Publikováno v:
Diabetic Medicine; Aug1993, Vol. 10 Issue 7, p664-671, 8p
Publikováno v:
Klinische Pädiatrie; 1987, Vol. 199 Issue 6, p449-452, 4p
Publikováno v:
Acta Diabetologica; 1994, Vol. 31 Issue 4, p205-209, 5p
Publikováno v:
European Journal of Pediatrics; 1996, Vol. 155 Issue 9, p787-790, 4p