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Page 1
Pitt-Hopkins syndrome: report of a case with a TCF4 gene mutation.
Taddeucci G, Bonuccelli A, Mantellassi I, Orsini A, Tarantino E. Taddeucci G, et al. Among authors: tarantino e. Ital J Pediatr. 2010 Feb 2;36:12. doi: 10.1186/1824-7288-36-12. Ital J Pediatr. 2010. PMID: 20205897 Free PMC article.
[Gardner syndrome].
Tarantino E, Meozzi A, Villirillo A, Lamesa G, Taddeucci G. Tarantino E, et al. Pediatr Med Chir. 1995 Sep-Oct;17(5):473-7. Pediatr Med Chir. 1995. PMID: 8685009 Italian.
Radiological findings in a case of Menkes' disease.
Pinto F, Calderazzi A, Canapicchi R, Taddeucci G, Tarantino E. Pinto F, et al. Among authors: tarantino e. Childs Nerv Syst. 1995 Feb;11(2):112-4. doi: 10.1007/BF00303816. Childs Nerv Syst. 1995. PMID: 7758009
Further delineation of Pitt-Hopkins syndrome: phenotypic and genotypic description of 16 novel patients.
Zweier C, Sticht H, Bijlsma EK, Clayton-Smith J, Boonen SE, Fryer A, Greally MT, Hoffmann L, den Hollander NS, Jongmans M, Kant SG, King MD, Lynch SA, McKee S, Midro AT, Park SM, Ricotti V, Tarantino E, Wessels M, Peippo M, Rauch A. Zweier C, et al. Among authors: tarantino e. J Med Genet. 2008 Nov;45(11):738-44. doi: 10.1136/jmg.2008.060129. Epub 2008 Aug 26. J Med Genet. 2008. PMID: 18728071
Aarskog-Scott syndrome: clinical update and report of nine novel mutations of the FGD1 gene.
Orrico A, Galli L, Faivre L, Clayton-Smith J, Azzarello-Burri SM, Hertz JM, Jacquemont S, Taurisano R, Arroyo Carrera I, Tarantino E, Devriendt K, Melis D, Thelle T, Meinhardt U, Sorrentino V. Orrico A, et al. Among authors: tarantino e. Am J Med Genet A. 2010 Feb;152A(2):313-8. doi: 10.1002/ajmg.a.33199. Am J Med Genet A. 2010. PMID: 20082460
[Peutz-Jeghers syndrome].
Meozzi A, Tarantino E, Villirillo A, Crimaldi G, Ughi C. Meozzi A, et al. Among authors: tarantino e. Pediatr Med Chir. 1995 Sep-Oct;17(5):479-82. Pediatr Med Chir. 1995. PMID: 8685010 Italian.
69 results