Selicorni A - Search Results

1

Additional case of Tsukahara's syndrome or new syndrome: further delineation of the association of microcephaly and radio-ulnar synostosis.

Selicorni A, Ferrarini A, Cagnoli G, Fratoni A, Bottigelli M, Milani D. Selicorni A, et al. Am J Med Genet A. 2005 Jan 15;132A(2):189-90. doi: 10.1002/ajmg.a.30415. Am J Med Genet A. 2005. PMID: 15578583 Review.

2

X-linked mental retardation with marfanoid habitus: first report of four Italian patients.

Lalatta F, Livini E, Selicorni A, Briscioli V, Vita A, Lugo F, Zollino M, Gurrieri F, Neri G. Lalatta F, et al. Among authors: selicorni a. Am J Med Genet. 1991 Feb-Mar;38(2-3):228-32. doi: 10.1002/ajmg.1320380211. Am J Med Genet. 1991. PMID: 2018063

3

Variability of the Brachmann-de Lange syndrome.

Selicorni A, Lalatta F, Livini E, Briscioli V, Piguzzi T, Bagozzi DC, Mastroiacovo P, Zampino G, Gaeta G, Pugliese A, et al. Selicorni A, et al. Am J Med Genet. 1993 Nov 15;47(7):977-82. doi: 10.1002/ajmg.1320470708. Am J Med Genet. 1993. PMID: 8291540

4

Trisomy 10qter confirmed by in situ hybridisation.

Briscioli V, Floridia G, Rossi E, Selicorni A, Lalatta F, Zuffardi O. Briscioli V, et al. Among authors: selicorni a. J Med Genet. 1993 Jul;30(7):601-3. doi: 10.1136/jmg.30.7.601. J Med Genet. 1993. PMID: 8411036 Free PMC article.

5

Cardio-facio-cutaneous (CFC) syndrome: report of an adult without mental retardation.

Manoukian S, Lalatta F, Selicorni A, Tadini G, Cavalli R, Neri G. Manoukian S, et al. Among authors: selicorni a. Am J Med Genet. 1996 May 17;63(2):382-5. doi: 10.1002/(SICI)1096-8628(19960517)63:2<382::AID-AJMG11>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8725790

6

Biliary atresia and Kabuki syndrome: another case with long-term follow-up.

Selicorni A, Colombo C, Bonato S, Milani D, Giunta AM, Bedeschi MF. Selicorni A, et al. Am J Med Genet. 2001 May 1;100(3):251. doi: 10.1002/ajmg.1253. Am J Med Genet. 2001. PMID: 11343312 No abstract available.

7

Right pulmonary agenesis with ipsilateral microtia: a new laterality association or part of the oculoauriculovertebral spectrum?

Milani D, Selicorni A. Milani D, et al. Among authors: selicorni a. Prenat Diagn. 2002 Nov;22(11):1053-4; author reply 1054-5. doi: 10.1002/pd.446. Prenat Diagn. 2002. PMID: 12424776 No abstract available.

8

Renal tract ultrasonography and calcium homeostasis in Williams-Beuren syndrome.

Sforzini C, Milani D, Fossali E, Barbato A, Grumieri G, Bianchetti MG, Selicorni A. Sforzini C, et al. Among authors: selicorni a. Pediatr Nephrol. 2002 Nov;17(11):899-902. doi: 10.1007/s00467-002-0889-z. Epub 2002 Oct 9. Pediatr Nephrol. 2002. PMID: 12432430 Clinical Trial.

9

Oligoyric microcephaly in a child with Williams syndrome.

Faravelli F, D'Arrigo S, Bagnasco I, Selicorni A, D'Incerti L, Riva D, Pantaleoni C. Faravelli F, et al. Among authors: selicorni a. Am J Med Genet A. 2003 Mar 1;117A(2):169-71. doi: 10.1002/ajmg.a.10892. Am J Med Genet A. 2003. PMID: 12567416

10

Gastroesophageal reflux and Cornelia de Lange syndrome: typical and atypical symptoms.

Luzzani S, Macchini F, Valadè A, Milani D, Selicorni A. Luzzani S, et al. Among authors: selicorni a. Am J Med Genet A. 2003 Jun 15;119A(3):283-7. doi: 10.1002/ajmg.a.20191. Am J Med Genet A. 2003. PMID: 12784293

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