C. Consoli

发表

Gonosomal mosaicism for a nonsense mutation (R1947X) in the NF1 gene in segmental neurofibromatosis type 1.

D. Cooper, M. Upadhyaya, C. Moss, 2005, The Journal of investigative dermatology.

Effects of a short-term exercise training on serum factors involved in ventricular remodelling in chronic heart failure patients.

F. Iellamo, M. Volterrani, G. Caminiti, 2012, International journal of cardiology.

Unusual features in a patient with neurofibromatosis type 1: Multiple subcutaneous lipomas, a juvenile polyp in ascending colon, congenital intrahepatic portosystemic venous shunt, and horseshoe kidney

C. Eng, M. Upadhyaya, R. Pilarski, 2004, American journal of medical genetics. Part A.

Severity of left ventricular dysfunction in heart failure patients affects the degree of serum-induced cardiomyocyte apoptosis. Importance of inflammatory response and metabolism.

F. Iellamo, G. Rosano, L. Marlier, 2013, International journal of cardiology.

Sildenafil Reduces Insulin-Resistance in Human Endothelial Cells

M. Federici, D. Lauro, A. Fabbri, 2011, PloS one.

Salt intake induces epithelial-to-mesenchymal transition of the peritoneal membrane in rats.

W. van Biesen, R. Vanholder, A. Pletinck, 2010, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Three different pathological lesions in the NF1 gene originating de novo in a family with neurofibromatosis type 1

D. Cooper, M. Krawczak, E. Majounie, 2002, Human Genetics.

Molecular genetics of neurofibromatosis type 1 (NF1)

C. Consoli, 2006 .

Insulin resistance affects gene expression in endothelium.

M. Federici, R. Lauro, O. Porzio, 2007, Arteriosclerosis, thrombosis, and vascular biology.

The hippocampus in spontaneously hypertensive rats: an animal model of vascular dementia?

D. Tomassoni, R. Avola, Daniele Tomassoni, 2002, Mechanisms of Ageing and Development.

Maternal corticosterone influences behavior, stress response and corticosteroid receptors in the female rat

G. Cigliana, S. Scaccianoce, L. Angelucci, 2002, Pharmacology Biochemistry and Behavior.

An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation.

E. Haan, D. Baralle, D. Evans, 2007, American journal of human genetics.

Characterization of the somatic mutational spectrum of the neurofibromatosis type 1 (NF1) gene in neurofibromatosis patients with benign and malignant tumors

Christopher Potts, D. Cooper, A. von Deimling, 2004, Human mutation.

APC transcription studies and molecular diagnosis of familial adenomatous polyposis

M. Mort, J. Maynard, L. Thomas, 2020, European Journal of Human Genetics.

APC transcription studies and molecular diagnosis of familial adenomatous polyposis

M. Mort, J. Maynard, L. Thomas, 2019, European Journal of Human Genetics.

Glial fibrillary acidic protein immunoreactive astrocytes in developing rat hippocampus

E. Azmitia, D. Tomassoni, F. Amenta, 2002, Mechanisms of Ageing and Development.

A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features

M. Upadhyaya, M. Sağlam, P. Thompson, 2003, Clinical dysmorphology.

Peripheral blood mononuclear cells from mild cognitive impairment patients show deregulation of Bax and Sod1 mRNAs

Fabrizio Stocchi, Andrea Armani, F. Stocchi, 2009, Neuroscience Letters.

Maternal glucocorticoid hormone influences nerve growth factor expression in the developing rat brain

S. Scaccianoce, K. Lombardo, L. Angelucci, 2001, Neuroreport.