Giliberto F - Search Results

1

Neurofibromatosis type 2: molecular and clinical analyses in Argentine sporadic and familial cases.

Ferrer M, Schulze A, Gonzalez S, Ferreiro V, Ciavarelli P, Otero J, Giliberto F, Basso A, Szijan I. Ferrer M, et al. Among authors: giliberto f. Neurosci Lett. 2010 Aug 9;480(1):49-54. doi: 10.1016/j.neulet.2010.05.094. Epub 2010 Jun 8. Neurosci Lett. 2010. PMID: 20553997

2

Deletion patterns in Argentine patients with Duchenne and Becker muscular dystrophy.

Baranzini SE, Giliberto F, Herrera M, Bernath V, Barreiro C, Garcia Erro M, Grippo J, Szijan I. Baranzini SE, et al. Among authors: giliberto f. Neurol Res. 1998 Jul;20(5):409-414. doi: 10.1080/01616412.1998.11740539. Neurol Res. 1998. PMID: 9664586 Clinical Trial.

3

Carrier detection in Duchenne and Becker muscular dystrophy Argentine families.

Baranzini SE, Giliberto F, Dalamon V, Barreiro C, García-Erro M, Grippo J, Szijan I. Baranzini SE, et al. Among authors: giliberto f. Clin Genet. 1998 Dec;54(6):503-11. doi: 10.1111/j.1399-0004.1998.tb03771.x. Clin Genet. 1998. PMID: 9894797

4

Clinical, cytogenetic, and molecular testing of Argentine patients with retinoblastoma.

Arbetman A, Abdala M, Fandiño A, Herrera J, Baranzini S, Borelina D, Parma D, Manzitti J, Barreiro C, Giliberto F, Szijan I. Arbetman A, et al. Among authors: giliberto f. J AAPOS. 1998 Apr;2(2):102-7. doi: 10.1016/s1091-8531(98)90072-6. J AAPOS. 1998. PMID: 10530971

5

Direct deletion analysis in two Duchenne muscular dystrophy symptomatic females using polymorphic dinucleotide (CA)n loci within the dystrophin gene.

Giliberto F, Ferreiro V, Dalamón V, Surace E, Cotignola J, Esperante S, Borelina D, Baranzini S, Szijan I. Giliberto F, et al. J Biochem Mol Biol. 2003 Mar 31;36(2):179-84. doi: 10.5483/bmbrep.2003.36.2.179. J Biochem Mol Biol. 2003. PMID: 12689516

6

Supernumerary marker 15 chromosome in a patient with Prader-Willi syndrome.

Borelina D, Esperante S, Gutnisky V, Ferreiro V, Ferrer M, Giliberto F, Frechtel G, Francipane L, Szijan I. Borelina D, et al. Among authors: giliberto f. Clin Genet. 2004 Mar;65(3):242-3. doi: 10.1111/j.0009-9163.2004.00203.x. Clin Genet. 2004. PMID: 14756675 No abstract available.

7

Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy.

Giliberto F, Ferreiro V, Dalamon V, Szijan I. Giliberto F, et al. Neurol Res. 2004 Jan;26(1):83-7. doi: 10.1179/016164104773026589. Neurol Res. 2004. PMID: 14977063

8

Detection of germline mutations in argentine retinoblastoma patients: low and full penetrance retinoblastoma caused by the same germline truncating mutation.

Dalamón V, Surace E, Giliberto F, Ferreiro V, Fernandez C, Szijan I. Dalamón V, et al. Among authors: giliberto f. J Biochem Mol Biol. 2004 Mar 31;37(2):246-53. doi: 10.5483/bmbrep.2004.37.2.246. J Biochem Mol Biol. 2004. PMID: 15469703

9

Detection of germline mosaicism in two Duchenne muscular dystrophy families using polymorphic dinucleotide (CA)n repeat loci within the dystrophin gene.

Ferreiro V, Szijan I, Giliberto F. Ferreiro V, et al. Among authors: giliberto f. Mol Diagn. 2004;8(2):115-21. doi: 10.1007/BF03260054. Mol Diagn. 2004. PMID: 15527326

10

The role of polymorphic short tandem (CA)n repeat loci segregation analysis in the detection of Duchenne muscular dystrophy carriers and prenatal diagnosis.

Ferreiro V, Giliberto F, Francipane L, Szijan I. Ferreiro V, et al. Among authors: giliberto f. Mol Diagn. 2005;9(2):67-80. doi: 10.1007/BF03260074. Mol Diagn. 2005. PMID: 16137182

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