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Page 1
Hair anomalies as a sign of mitochondrial disease.
Silengo M, Valenzise M, Spada M, Ferrero GB, Ferraris S, Dassi P, Jarre L. Silengo M, et al. Among authors: ferrero gb. Eur J Pediatr. 2003 Jul;162(7-8):459-461. doi: 10.1007/s00431-003-1228-5. Epub 2003 Apr 24. Eur J Pediatr. 2003. PMID: 12712334
Tetrahydrobiopterin loading test in hyperphenylalaninemia.
Ponzone A, Guardamagna O, Ferraris S, Ferrero GB, Dianzani I, Cotton RG. Ponzone A, et al. Among authors: ferrero gb. Pediatr Res. 1991 Nov;30(5):435-8. doi: 10.1203/00006450-199111000-00008. Pediatr Res. 1991. PMID: 1754298
Monitoring treatment in tetrahydrobiopterin deficiency by serum prolactin.
Spada M, Ferraris S, Ferrero GB, Sartore M, Lanza C, Perfetto F, de Sanctis L, Dompé C, Blau N, Ponzone A. Spada M, et al. Among authors: ferrero gb. J Inherit Metab Dis. 1996;19(2):231-3. doi: 10.1007/BF01799437. J Inherit Metab Dis. 1996. PMID: 8739973 No abstract available.
Newborn feeding and screening for phenylketonuria.
Ponzone A, Spada M, Ferrero GB, Ponzone R, Ferraris S. Ponzone A, et al. Among authors: ferrero gb. Acta Paediatr. 1999 Mar;88(3):347-8. doi: 10.1080/08035259950170178. Acta Paediatr. 1999. PMID: 10229052 No abstract available.
Hair as a diagnostic tool in dysmorphology.
Silengo M, Valenzise M, Sorasio L, Ferrero GB. Silengo M, et al. Among authors: ferrero gb. Clin Genet. 2002 Oct;62(4):270-2. doi: 10.1034/j.1399-0004.2002.620403.x. Clin Genet. 2002. PMID: 12372052
Pachygyria and cerebellar hypoplasia in Goldberg-Shprintzen syndrome.
Silengo M, Ferrero GB, Tornetta L, Cortese MG, Canavese F, D'Alonzo G, Papalia F. Silengo M, et al. Among authors: ferrero gb. Am J Med Genet A. 2003 May 1;118A(4):388-90. doi: 10.1002/ajmg.a.20013. Am J Med Genet A. 2003. PMID: 12687674 No abstract available.
200 results