Rosaia L - Search Results

1

[Familial segregation of simple and complex chromosomal rearrangements].

Anichini C, Vivarelli R, Scarinci R, Berardi R, Rosaia L, Pucci L, Tomaccini D. Anichini C, et al. Among authors: rosaia l. Boll Soc Ital Biol Sper. 1992 Mar;68(3):183-6. Boll Soc Ital Biol Sper. 1992. PMID: 1389074 Italian.

2

[Correlation of the clinical phenotype with a pericentric inversion of chromosome 9].

Scarinci R, Anichini C, Vivarelli R, Berardi R, Pucci L, Rosaia L, Tomaccini D. Scarinci R, et al. Among authors: rosaia l. Boll Soc Ital Biol Sper. 1992 Mar;68(3):175-81. Boll Soc Ital Biol Sper. 1992. PMID: 1389073 Italian.

3

[Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18].

Vivarelli R, Paolieri M, Anichini C, Scarinci R, Berardi R, Rosaia L, Pucci L. Vivarelli R, et al. Among authors: rosaia l. Boll Soc Ital Biol Sper. 1992 Apr;68(4):263-9. Boll Soc Ital Biol Sper. 1992. PMID: 1463601 Italian.

4

Ectodermal dysplasia, primary hypothyroidism, and agenesis of the corpus callosum: variable expression of a single syndrome?

Silengo M, Silvestro L, Capizzi G, Lerone M, Seri M, Rosaia L, Romeo G. Silengo M, et al. Among authors: rosaia l. J Med Genet. 1998 Feb;35(2):157-8. doi: 10.1136/jmg.35.2.157. J Med Genet. 1998. PMID: 9507398 Free PMC article.

5

Malformations following methimazole exposure in utero: an open issue.

Ferraris S, Valenzise M, Lerone M, Divizia MT, Rosaia L, Blaid D, Nemelka O, Ferrero GB, Silengo M. Ferraris S, et al. Among authors: rosaia l. Birth Defects Res A Clin Mol Teratol. 2003 Dec;67(12):989-92. doi: 10.1002/bdra.10098. Birth Defects Res A Clin Mol Teratol. 2003. PMID: 14745920

6

Question mark ears, temporo-mandibular joint malformation and hypotonia: auriculo-condylar syndrome or a distinct entity?

Priolo M, Lerone M, Rosaia L, Calcagno EP, Sadeghi AK, Ghezzi F, Ravazzolo R, Silengo M. Priolo M, et al. Among authors: rosaia l. Clin Dysmorphol. 2000 Oct;9(4):277-80. doi: 10.1097/00019605-200009040-00009. Clin Dysmorphol. 2000. PMID: 11045585 Review.

7

Total anonychia congenita in a woman with normal intelligence: report of a further case.

Priolo M, Rosaia L, Seri M, Silengo MC, Ravazzolo R, Lerone M. Priolo M, et al. Among authors: rosaia l. Dermatology. 2000;200(1):84-5. doi: 10.1159/000018329. Dermatology. 2000. PMID: 10681628 Review. No abstract available.

8

Auriculo-condylar syndrome or new syndrome?

Divizia MT, Cordone A, Bado M, Rosaia L, Cirillo Silengo M, Ravazzolo R, Lerone M. Divizia MT, et al. Among authors: rosaia l. Clin Dysmorphol. 2002 Apr;11(2):143-4. doi: 10.1097/00019605-200204000-00015. Clin Dysmorphol. 2002. PMID: 12002148

9

Study of MECP2 gene in Rett syndrome variants and autistic girls.

Zappella M, Meloni I, Longo I, Canitano R, Hayek G, Rosaia L, Mari F, Renieri A. Zappella M, et al. Among authors: rosaia l. Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):102-7. doi: 10.1002/ajmg.b.10070. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12707946

10

Immunogenicity of anti-idiotypic antibodies and of their F(ab')2 fragments.

Tassi V, Ruggiero G, Rosaia L, Lorenzoni P, Ceccarini C, Tecce MF. Tassi V, et al. Among authors: rosaia l. Immunol Lett. 1991 Jan;27(1):39-43. doi: 10.1016/0165-2478(91)90241-2. Immunol Lett. 1991. PMID: 1708352

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