Baiget M - Search Results

1

F8 gene dosage defects in atypical patients with severe haemophilia A.

Venceslá Á, Baena M, Garrido RP, Núñez R, Velasco F, Rosell J, Villar A, Jiménez-Yuste V, Baiget M, Tizzano EF. Venceslá Á, et al. Among authors: baiget m. Haemophilia. 2012 Sep;18(5):708-13. doi: 10.1111/j.1365-2516.2012.02818.x. Epub 2012 May 23. Haemophilia. 2012. PMID: 22621702

2

Modifier genes in haemophilia: their expansion in the human genome.

Tizzano EF, Cornet M, Domènech M, Baiget M. Tizzano EF, et al. Among authors: baiget m. Haemophilia. 2002 May;8(3):250-4. doi: 10.1046/j.1365-2516.2002.00623.x. Haemophilia. 2002. PMID: 12010419 Review.

3

Exclusion of mosaicism in Spanish haemophilia A families with inversion of intron 22.

Tizzano EF, Cornet M, Domènech M, Baiget M. Tizzano EF, et al. Among authors: baiget m. Haemophilia. 2003 Sep;9(5):584-7. doi: 10.1046/j.1365-2516.2003.00813.x. Haemophilia. 2003. PMID: 14511298

4

Utility of a (GT) dinucleotide repeat in intron 1 of the factor 8 gene for haemophilia A carrier diagnosis.

Tizzano E, Venceslá A, Cornet M, Baena M, Baiget M. Tizzano E, et al. Among authors: baiget m. Haemophilia. 2005 Mar;11(2):142-4. doi: 10.1111/j.1365-2516.2005.01071.x. Haemophilia. 2005. PMID: 15810916

5

Application of intron 9 and intron 25 dinucleotide repeats of the factor VIII gene for carrier diagnosis in haemophilia A.

Venceslá A, Baena M, Fares Taie L, Cornet M, Baiget M, Tizzano EF. Venceslá A, et al. Among authors: baiget m. Haemophilia. 2008 May;14(3):489-93. doi: 10.1111/j.1365-2516.2008.01698.x. Epub 2008 Apr 1. Haemophilia. 2008. PMID: 18384354

6

Severe haemophilia A in a female resulting from an inherited gross deletion and a de novo codon deletion in the F8 gene.

Venceslá A, Fuentes-Prior P, Baena M, Quintana M, Baiget M, Tizzano EF. Venceslá A, et al. Among authors: baiget m. Haemophilia. 2008 Sep;14(5):1094-8. doi: 10.1111/j.1365-2516.2008.01816.x. Epub 2008 Jul 25. Haemophilia. 2008. PMID: 18665854 Review.

7

Detection of novel mutations in the SMN Tudor domain in type I SMA patients.

Cuscó I, Barceló MJ, del Río E, Baiget M, Tizzano EF. Cuscó I, et al. Among authors: baiget m. Neurology. 2004 Jul 13;63(1):146-9. doi: 10.1212/01.wnl.0000132634.48815.13. Neurology. 2004. PMID: 15249625

8

Inversion of intron 22 in isolated cases of severe hemophilia A.

Tizzano EF, Domènech M, Baiget M. Tizzano EF, et al. Among authors: baiget m. Thromb Haemost. 1995 Jan;73(1):6-9. Thromb Haemost. 1995. PMID: 7740498

9

Severe mental retardation in a young boy with an in-frame deletion in the dystrophin gene.

Colomer J, Gallano P, Nicholson LV, Tizzano E, Baiget M. Colomer J, et al. Among authors: baiget m. Eur J Pediatr. 1994 Jul;153(7):492-4. doi: 10.1007/BF01957003. Eur J Pediatr. 1994. PMID: 7957365

10

Cramps and minimal EMG abnormalities as preclinical manifestations of spinal muscular atrophy patients with homozygous deletions of the SMN gene.

Bussaglia E, Tizzano EF, Illa I, Cervera C, Baiget M. Bussaglia E, et al. Among authors: baiget m. Neurology. 1997 May;48(5):1443-5. doi: 10.1212/wnl.48.5.1443. Neurology. 1997. PMID: 9153488

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