Gabriele AL - Search Results

1

A simple and rapid nonisotopic method for sizing CAG repeats in the SCA1 gene.

Annesi G, Muglia M, Conforti FL, Leone O, Grandinetti C, Imbrogno E, Gabriele AL, Naso F, Brancati C. Annesi G, et al. Among authors: gabriele al. Hum Hered. 1997 Jan-Feb;47(1):47-51. doi: 10.1159/000154389. Hum Hered. 1997. PMID: 9017980

2

Nonisotopic method for accurate detection of (CAG)n repeats causing Huntington disease.

Muglia M, Leone O, Annesi G, Gabriele AL, Imbrogno E, Grandinetti C, Conforti FL, Naso F, Brancati C. Muglia M, et al. Among authors: gabriele al. Clin Chem. 1996 Oct;42(10):1601-3. Clin Chem. 1996. PMID: 8855141

3

Analysis of the (CAG)n repeat at the IT15 locus in a population from Calabria (southern Italy).

Leone O, Muglia M, Gabriele AL, Annesi G, Conforti FL, Imbrogno E, Imbrogno L, Brancati C. Leone O, et al. Among authors: gabriele al. Hum Biol. 1997 Oct;69(5):653-62. Hum Biol. 1997. PMID: 9299885 Clinical Trial.

4

Alpha-thalassemia in a southern Italian population (detection by a non-radioactive procedure).

Muglia M, Annesi G, Gabriele AL, Covello M, Brancati C. Muglia M, et al. Among authors: gabriele al. Hemoglobin. 1993 Jun;17(3):285-7. doi: 10.3109/03630269308998906. Hemoglobin. 1993. PMID: 8330983 No abstract available.

5

Hb Valletta [beta 87(F3)Thr-->Pro] due to an A-->C substitution at codon 87 in a Calabrian family with alpha-thalassemia.

Qualtieri A, Andreoli V, Crescibene L, De Marco EV, Muglia M, Gabriele AL, Annesi G, Brancati C. Qualtieri A, et al. Among authors: gabriele al. Hemoglobin. 1997 Jan;21(1):97-103. doi: 10.3109/03630269708997514. Hemoglobin. 1997. PMID: 9028827 No abstract available.

6

Identification of a new polymorphism (c134G>A) in the exon 2 of the myelin protein zero gene.

Muglia M, Toscano A, Gabriele AL, Magariello A, Patitucci A, Conforti FL, Mazzei R, Rodolico C, Gambardella A, Quattrone A. Muglia M, et al. Among authors: gabriele al. Hum Mutat. 2000 Mar;15(3):299. doi: 10.1002/(SICI)1098-1004(200003)15:3<299::AID-HUMU24>3.0.CO;2-Z. Hum Mutat. 2000. PMID: 10679959 No abstract available.

7

A simple method for diagnosis of autosomal recessive spinal muscular atrophy by denaturing high-performance liquid chromatography.

Mazzei R, Conforti FL, Muglia M, Sprovieri T, Patitucci A, Magariello A, Gabriele AL, Quattrone A. Mazzei R, et al. Among authors: gabriele al. J Child Neurol. 2003 Apr;18(4):269-71. doi: 10.1177/08830738030180041301. J Child Neurol. 2003. PMID: 12760430

8

Gene conversion events in adult-onset spinal muscular atrophy.

Mazzei R, Gambardella A, Conforti FL, Magariello A, Patitucci A, Gabriele AL, Sprovieri T, Labate A, Valentino P, Bono F, Bonavita S, Zappia M, Muglia M, Quattrone A. Mazzei R, et al. Among authors: gabriele al. Acta Neurol Scand. 2004 Feb;109(2):151-4. doi: 10.1034/j.1600-0404.2003.00181.x. Acta Neurol Scand. 2004. PMID: 14705979

9

Gene symbol: MECP2. Disease: Rett syndrome.

Conforti FL, Mazzei R, Patitucci A, Magariello A, Sprovieri T, Ungaro C, Gabriele AL, Muglia M, Del Giudice E, Quattrone A. Conforti FL, et al. Among authors: gabriele al. Hum Genet. 2006 Jul;119(6):675. Hum Genet. 2006. PMID: 17128467 No abstract available.

10

Gene symbol: MECP2. Disease: Rett syndrome.

Conforti FL, Mazzei R, Sprovieri T, Ungaro C, Patitucci A, Magariello A, Gabriele AL, Bravaccio C, Muglia M, Quattrone A. Conforti FL, et al. Among authors: gabriele al. Hum Genet. 2006 Jul;119(6):676. Hum Genet. 2006. PMID: 17128468 No abstract available.

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