Gabriele AL - Search Results

1

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.

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

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

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

A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy.

Conforti FL, Sprovieri T, Mazzei R, Ungaro C, La Bella V, Tessitore A, Patitucci A, Magariello A, Gabriele AL, Tedeschi G, Simone IL, Majorana G, Valentino P, Condino F, Bono F, Monsurrò MR, Muglia M, Quattrone A. Conforti FL, et al. Among authors: gabriele al. Neuromuscul Disord. 2008 Jan;18(1):68-70. doi: 10.1016/j.nmd.2007.07.003. Epub 2007 Aug 20. Neuromuscul Disord. 2008. PMID: 17703939

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

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.

8

Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy.

Muglia M, Zappia M, Timmerman V, Valentino P, Gabriele AL, Conforti FL, De Jonghe P, Ragno M, Mazzei R, Sabatelli M, Nicoletti G, Patitucci AM, Oliveri RL, Bono F, Gambardella A, Quattrone A. Muglia M, et al. Among authors: gabriele al. Neurology. 2001 Jan 9;56(1):100-3. doi: 10.1212/wnl.56.1.100. Neurology. 2001. PMID: 11148244

9

Juvenile Huntington's disease presenting as progressive myoclonic epilepsy.

Gambardella A, Muglia M, Labate A, Magariello A, Gabriele AL, Mazzei R, Pirritano D, Conforti FL, Patitucci A, Valentino P, Zappia M, Quattrone A. Gambardella A, et al. Among authors: gabriele al. Neurology. 2001 Aug 28;57(4):708-11. doi: 10.1212/wnl.57.4.708. Neurology. 2001. PMID: 11524486

10

Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus.

Muglia M, Criscuolo C, Magariello A, De Michele G, Scarano V, D'Adamo P, Ambrosio G, Gabriele AL, Patitucci A, Mazzei R, Conforti FL, Sprovieri T, Morgante L, Epifanio A, La Spina P, Valentino P, Gasparini P, Filla A, Quattrone A. Muglia M, et al. Among authors: gabriele al. Neurogenetics. 2004 Feb;5(1):49-54. doi: 10.1007/s10048-003-0167-7. Epub 2003 Dec 5. Neurogenetics. 2004. PMID: 14658060

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