Lituania M - Search Results

1

Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome.

Grasso M, Perroni L, Colella S, Piombo G, Argusti A, Lituania M, Buscaglia M, Giussani U, Grimoldi MG, Bricarelli FD. Grasso M, et al. Among authors: lituania m. Am J Med Genet. 1996 Jul 12;64(1):187-90. doi: 10.1002/(SICI)1096-8628(19960712)64:1<187::AID-AJMG33>3.0.CO;2-H. Am J Med Genet. 1996. PMID: 8826473

2

A familial case of achondrogenesis type II caused by a dominant COL2A1 mutation and "patchy" expression in the mosaic father.

Forzano F, Lituania M, Viassolo A, Superti-Furga V, Wildhardt G, Zabel B, Faravelli F. Forzano F, et al. Among authors: lituania m. Am J Med Genet A. 2007 Dec 1;143A(23):2815-20. doi: 10.1002/ajmg.a.32047. Am J Med Genet A. 2007. PMID: 17994563

3

Multipotent mesenchymal stromal cells from amniotic fluid: solid perspectives for clinical application.

Sessarego N, Parodi A, Podestà M, Benvenuto F, Mogni M, Raviolo V, Lituania M, Kunkl A, Ferlazzo G, Bricarelli FD, Uccelli A, Frassoni F. Sessarego N, et al. Among authors: lituania m. Haematologica. 2008 Mar;93(3):339-46. doi: 10.3324/haematol.11869. Epub 2008 Feb 11. Haematologica. 2008. PMID: 18268281 Free article.

4

Genetic amniocentesis: 505 cases performed before the sixteenth week of gestation.

Stripparo L, Buscaglia M, Longatti L, Ghisoni L, Dambrosio F, Guerneri S, Rosella F, Lituania M, Cordone M, De Biasio P, et al. Stripparo L, et al. Among authors: lituania m. Prenat Diagn. 1990 Jun;10(6):359-64. doi: 10.1002/pd.1970100603. Prenat Diagn. 1990. PMID: 2217077

5

Holoprosencephaly and primary craniosynostosis: the Genoa syndrome.

Camera G, Lituania M, Cohen MM Jr. Camera G, et al. Among authors: lituania m. Am J Med Genet. 1993 Dec 1;47(8):1161-5. doi: 10.1002/ajmg.1320470806. Am J Med Genet. 1993. PMID: 8291548

6

Autosomal dominant polycystic kidney disease: prenatal diagnosis by DNA analysis and sonography at 14 weeks.

Ceccherini I, Lituania M, Cordone MS, Perfumo F, Gusmano R, Callea F, Archidiacono N, Romeo G. Ceccherini I, et al. Among authors: lituania m. Prenat Diagn. 1989 Nov;9(11):751-8. doi: 10.1002/pd.1970091103. Prenat Diagn. 1989. PMID: 2575745

7

Prenatal diagnosis of a rare heteropagus.

Lituania M, Cordone M, Zampatti C, Passamonti U, Santi F. Lituania M, et al. Prenat Diagn. 1988 Sep;8(7):547-51. doi: 10.1002/pd.1970080710. Prenat Diagn. 1988. PMID: 3065772

8

Holoprosencephaly: prenatal diagnosis by sonography and magnetic resonance imaging.

Tomà P, Costa A, Magnano GM, Cariati M, Lituania M. Tomà P, et al. Among authors: lituania m. Prenat Diagn. 1990 Jul;10(7):429-36. doi: 10.1002/pd.1970100704. Prenat Diagn. 1990. PMID: 2235902

9

Schizencephaly: prenatal diagnosis by computed sonography and magnetic resonance imaging.

Lituania M, Passamonti U, Cordone MS, Magnano GM, Toma P. Lituania M, et al. Prenat Diagn. 1989 Sep;9(9):649-55. doi: 10.1002/pd.1970090908. Prenat Diagn. 1989. PMID: 2678087

10

Fetal aortic root dilation: a prenatal feature of the Loeys-Dietz syndrome.

Viassolo V, Lituania M, Marasini M, Dietz H, Benelli F, Forzano F, Faravelli F. Viassolo V, et al. Among authors: lituania m. Prenat Diagn. 2006 Nov;26(11):1081-3. doi: 10.1002/pd.1565. Prenat Diagn. 2006. PMID: 16981219

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