Casula L - Search Results

1

History, geography and population structure influence the distribution and heritability of blood and anthropometric quantitative traits in nine Sardinian genetic isolates.

Portas L, Murgia F, Biino G, Concas MP, Casula L, Milia S, Whalen MB, Vaccargiu S, Cosso M, Parracciani D, Frongia B, Pirastu M. Portas L, et al. Among authors: casula l. Genet Res (Camb). 2010 Jun;92(3):199-208. doi: 10.1017/S001667231000025X. Genet Res (Camb). 2010. PMID: 20667164

2

Genetic architecture of hand quantitative ultrasound measures: a population-based study in a Sardinian genetic isolate.

Biino G, Casula L, de Terlizzi F, Adamo M, Vaccargiu S, Francavilla M, Loi D, Casti A, Atzori M, Cosso M, Marras F, Cepollaro C, Brandi ML, Pirastu M. Biino G, et al. Among authors: casula l. Bone. 2010 Apr;46(4):1197-203. doi: 10.1016/j.bone.2009.11.033. Epub 2009 Dec 30. Bone. 2010. PMID: 20004756

3

Analysis of 12,517 inhabitants of a Sardinian geographic isolate reveals that predispositions to thrombocytopenia and thrombocytosis are inherited traits.

Biino G, Balduini CL, Casula L, Cavallo P, Vaccargiu S, Parracciani D, Serra D, Portas L, Murgia F, Pirastu M. Biino G, et al. Among authors: casula l. Haematologica. 2011 Jan;96(1):96-101. doi: 10.3324/haematol.2010.029934. Epub 2010 Sep 7. Haematologica. 2011. PMID: 20823129 Free PMC article.

4

Epidemiology of osteoporosis in an isolated Sardinian population by using quantitative ultrasound.

Biino G, Casula L, de Terlizzi F, Adamo M, Vaccargiu S, Francavilla M, Loi D, Casti A, Atzori M, Pirastu M. Biino G, et al. Among authors: casula l. Am J Epidemiol. 2011 Aug 15;174(4):432-9. doi: 10.1093/aje/kwr106. Epub 2011 Jun 27. Am J Epidemiol. 2011. PMID: 21709133

5

A strategy analysis for genetic association studies with known inbreeding.

Cabras S, Castellanos ME, Biino G, Persico I, Sassu A, Casula L, Del Giacco S, Bertolino F, Pirastu M, Pirastu N. Cabras S, et al. Among authors: casula l. BMC Genet. 2011 Jul 18;12:63. doi: 10.1186/1471-2156-12-63. BMC Genet. 2011. PMID: 21767363 Free PMC article.

6

Illegitimate recombination produced a duplication within the FVIII gene in a patient with mild hemophilia A.

Murru S, Casula L, Pecorara M, Mori P, Cao A, Pirastu M. Murru S, et al. Among authors: casula l. Genomics. 1990 May;7(1):115-8. doi: 10.1016/0888-7543(90)90526-z. Genomics. 1990. PMID: 2159433

7

A spontaneous mutation produced a novel elongated beta-globin chain structural variant (Hb Agnana) with a thalassemia-like phenotype.

Ristaldi MS, Pirastu M, Murru S, Casula L, Loudianos G, Cao A, Sciarratta GV, Agosti S, Parodi MI, Leone D, et al. Ristaldi MS, et al. Among authors: casula l. Blood. 1990 Mar 15;75(6):1378-9. Blood. 1990. PMID: 2310835 Free article. No abstract available.

8

A genetic epidemiology study of congenital adrenal hyperplasia in Italy.

Gialluisi A, Menabò S, Baldazzi L, Casula L, Meloni A, Farci MC, Mariotti S, Balestrino L, Ortolano R, Murru S, Carcassi C, Loche S, Balsamo A, Romeo G. Gialluisi A, et al. Among authors: casula l. Clin Genet. 2018 Feb;93(2):223-227. doi: 10.1111/cge.13078. Epub 2017 Oct 17. Clin Genet. 2018. PMID: 28644547

9

Recurrent mutations and three novel rearrangements in the factor VIII gene of hemophilia A patients of Italian descent.

Casula L, Murru S, Pecorara M, Ristaldi MS, Restagno G, Mancuso G, Morfini M, De Biasi R, Baudo F, Carbonara A, et al. Casula L, et al. Blood. 1990 Feb 1;75(3):662-70. Blood. 1990. PMID: 2105106 Free article.

10

A DNA fragment from Xq21 replaces a deleted region containing the entire FVIII gene in a severe hemophilia A patient.

Murru S, Casula L, Casarino L, Moi P, Rocchi M, Loi A, Figus A, Mannella M, Poddie D, Kenwrick S, et al. Murru S, et al. Among authors: casula l. Genomics. 1994 Sep 15;23(2):352-61. doi: 10.1006/geno.1994.1511. Genomics. 1994. PMID: 7835884

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