M. Giacché

发表

Blood pressure evaluation by noninvasive and traditional methods. Consistencies and discrepancies among photoplethysmomanometry, office sphygmomanometry, and ambulatory monitoring. Effects of blood pressure measurement.

N. Musso, M. Giacché, G. Galbariggi, 1996, American journal of hypertension.

MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

M. Urioste, P. Chanson, M. Blok, 2012, Clinical Cancer Research.

Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas.

G. Arnaldi, B. Biondi, M. Castellano, 2009, The Journal of clinical endocrinology and metabolism.

Genetic polymorphism of the renin–angiotensin–aldosterone system and arterial hypertension in the Italian population: the GENIPER Project

C. Zoccali, M. Castellano, N. Glorioso, 2003, Journal of hypertension.

Aldosterone stimulation by angiotensin II : influence of gender, plasma renin, and familial resemblance.

S. Hunt, P. Hopkins, X. Jeunemaître, 2000, Hypertension.

Blood pressure response to angiotensin II, low-density lipoprotein cholesterol and polymorphisms of the angiotensin II type 1 receptor gene in hypertensive sibling pairs

S. Hunt, P. Hopkins, X. Jeunemaître, 2001, Journal of Molecular Medicine.

Characterization of the binding of the RNA-binding protein AUF1 to the human AT(1) receptor mRNA.

J. Port, M. Giacché, A. Pende, 1999, Biochemical and biophysical research communications.

Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas.

S. Gruber, C. Ricketts, M. Vikkula, 2010, JAMA.

A novel menin gene deletional mutation in a little series of Italian patients affected by apparently sporadic multiple endocrine neoplasia type 1 syndrome

M. Castellano, E. Agabiti Rosei, I. Pirola, 2012, Journal of Endocrinological Investigation.

&bgr;2-Adrenergic Receptor Gene Polymorphism, Age, and Cardiovascular Phenotypes

D. Rizzoni, M. Muiesan, M. Salvetti, 2003, Hypertension.

Genetic Mutation Screening in an Italian Cohort of Nonsyndromic Pheochromocytoma/Paraganglioma Patients

M. Castellano, C. Cappelli, F. Veglio, 2006, Annals of the New York Academy of Sciences.

Functional alterations of mesenteric small resistance arteries in Milan hypertensive and normotensive rats

E. Porteri, D. Rizzoni, M. Castellano, 2009, Hypertension Research.

p.Ser891Ala RET gene mutations in medullary thyroid cancer: Phenotypical and genealogical characterization of 28 apparently unrelated kindreds and founder effect uncovering in Northern Italy

M. Castellano, C. Cappelli, I. Pirola, 2019, Human mutation.

Hemlock poisoning due to plant misidentification

R. Zulli, P. Restani, C. Locatelli, 2009 .

New pathogenic variants in ARMC5 gene in a series of Italian patients affected by primary bilateral macronodular adrenocortical hyperplasia (PBMAH)

P. L. Poliani, L. Mori, M. Giacché, 2023, Molecular genetics & genomic medicine.

Beta(2)-adrenergic receptor gene polymorphism, age, and cardiovascular phenotypes.

D. Rizzoni, M. Muiesan, M. Salvetti, 2003, Hypertension.