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International Journal of Obesity (2005)|September 13, 2013
The energy intake modulates the association of the -55CT polymorphism of UCP3 with body weight in type 2 diabetic patientsE Lapice, A Monticelli, S Cocozza, et al.
Diabetes|April 1, 1992
NIDDM associated with mutation in tyrosine kinase domain of insulin receptor geneS Cocozza, A Porcellini, G Riccardi, et al.
Clinical Neurology and Neurosurgery|February 1, 1997
Pleomorphic xanthoastrocytoma: clinical, imaging and pathological features of four casesA Bucciero, M De Caro, V De Stefano, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 4, 2009
Transcriptional regulator Id2 controls survival of hepatic NKT cellsLaurel A Monticelli, Yang Yang, Jamie Knell, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|April 20, 2016
The combination of UCP3-55CT and PPARγ2Pro12Ala polymorphisms affects BMI and substrate oxidation in two diabetic populationsE Lapice, A Monticelli, S Cocozza, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 14, 1999
Relation between trinucleotide GAA repeat length and sensory neuropathy in Friedreich's ataxiaL Santoro, G De Michele, A Perretti, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1994
Isolation of a new gene in the Friedreich ataxia candidate region on human chromosome 9 by cDNA direct selectionM Pandolfo, A Pizzuti, E Redolfi, et al.
European Journal of Clinical Investigation|December 1, 1988
Polymorphism at the 5' end flanking region of the insulin gene is associated with reduced insulin secretion in healthy individualsS Cocozza, G Riccardi, A Monticelli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 18, 2004
Real time PCR quantification of frataxin mRNA in the peripheral blood leucocytes of Friedreich ataxia patients and carriersL Pianese, M Turano, M S Lo Casale, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Linkage disequilibrium analysis of Friedreich's ataxia in 140 Caucasian families: positioning of the disease locus and evaluation of allelic heterogeneityG Sirugo, S Cocozza, A Brice, et al.
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