Monticelli A - Search Results

1

Mutations in insulin-receptor gene. Val996 allele in white NIDDM patients.

Porcellini A, Cocozza S, Monticelli A, Pianese L, Riccardi G, Ferrara A, Varrone S. Porcellini A, et al. Among authors: monticelli a. Diabetes Care. 1992 Apr;15(4):591-2. doi: 10.2337/diacare.15.4.591. Diabetes Care. 1992. PMID: 1499491 Free article. No abstract available.

2

NIDDM associated with mutation in tyrosine kinase domain of insulin receptor gene.

Cocozza S, Porcellini A, Riccardi G, Monticelli A, Condorelli G, Ferrara A, Pianese L, Miele C, Capaldo B, Beguinot F, et al. Cocozza S, et al. Among authors: monticelli a. Diabetes. 1992 Apr;41(4):521-6. doi: 10.2337/diab.41.4.521. Diabetes. 1992. PMID: 1607076

3

DNA polymorphism of the insulin gene, diabetes, and severe obesity.

Isernia C, Contaldo F, Scalfi L, Cocozza S, Monticelli A, Pellegrino A. Isernia C, et al. Among authors: monticelli a. Diabetes Care. 1988 Jun;11(6):511-2. doi: 10.2337/diacare.11.6.511. Diabetes Care. 1988. PMID: 3042318 No abstract available.

4

Pro12Ala polymorphism of the PPARgamma2 locus modulates the relationship between energy intake and body weight in type 2 diabetic patients.

Vaccaro O, Lapice E, Monticelli A, Giacchetti M, Castaldo I, Galasso R, Pinelli M, Donnarumma G, Rivellese AA, Cocozza S, Riccardi G. Vaccaro O, et al. Among authors: monticelli a. Diabetes Care. 2007 May;30(5):1156-61. doi: 10.2337/dc06-1153. Epub 2007 Jan 26. Diabetes Care. 2007. PMID: 17259473

5

Polymorphism at the 5' end flanking region of the insulin gene is associated with reduced insulin secretion in healthy individuals.

Cocozza S, Riccardi G, Monticelli A, Capaldo B, Genovese S, Krogh V, Celentano E, Farinaro E, Varrone S, Avvedimento VE. Cocozza S, et al. Among authors: monticelli a. Eur J Clin Invest. 1988 Dec;18(6):582-6. doi: 10.1111/j.1365-2362.1988.tb01271.x. Eur J Clin Invest. 1988. PMID: 3147185

6

Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's ataxia.

De Michele G, Cavalcanti F, Criscuolo C, Pianese L, Monticelli A, Filla A, Cocozza S. De Michele G, et al. Among authors: monticelli a. Hum Mol Genet. 1998 Nov;7(12):1901-6. doi: 10.1093/hmg/7.12.1901. Hum Mol Genet. 1998. PMID: 9811933

7

Atypical Friedreich ataxia phenotype associated with a novel missense mutation in the X25 gene.

De Michele G, Filla A, Cavalcanti F, Tammaro A, Monticelli A, Pianese L, Di Salle F, Perreti A, Santoro L, Caruso G, Cocozza S. De Michele G, et al. Among authors: monticelli a. Neurology. 2000 Jan 25;54(2):496-9. doi: 10.1212/wnl.54.2.496. Neurology. 2000. PMID: 10668723

8

Friedreich's disease. A linkage study in southern and central Italy.

Cavalcanti F, Cocozza S, Filla A, De Michele G, Pianese L, Porcellini A, Monticelli A, Pandolfo M, Banfi S, Varrone S, et al. Cavalcanti F, et al. Among authors: monticelli a. Acta Neurol (Napoli). 1992 Aug-Dec;14(4-6):519-23. Acta Neurol (Napoli). 1992. PMID: 1363458

9

New clues on the origin of the Friedreich ataxia expanded alleles from the analysis of new polymorphisms closely linked to the mutation.

Monticelli A, Giacchetti M, De Biase I, Pianese L, Turano M, Pandolfo M, Cocozza S. Monticelli A, et al. Hum Genet. 2004 Apr;114(5):458-63. doi: 10.1007/s00439-004-1089-7. Epub 2004 Feb 7. Hum Genet. 2004. PMID: 14767759

10

A dinucleotide repeat polymorphism (D9S202) in the Friedreich's ataxia region on chromosome 9q13-q21.1.

Pandolfo M, Munaro M, Cocozza S, Redolfi EM, Pianese L, Cavalcanti F, Monticelli A, Di Donato S. Pandolfo M, et al. Among authors: monticelli a. Hum Mol Genet. 1993 Jun;2(6):822. doi: 10.1093/hmg/2.6.822. Hum Mol Genet. 1993. PMID: 8353506 No abstract available.

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