Detalhe da pesquisa
1.
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.
Hum Mutat
; 40(7): 926-937, 2019 07.
Artigo
Inglês
| MEDLINE | ID: mdl-30927507
2.
New pathogenic variants in ARMC5 gene in a series of Italian patients affected by primary bilateral macronodular adrenocortical hyperplasia (PBMAH).
Mol Genet Genomic Med
; 11(4): e2126, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-36727580
3.
The Vobarno Study.
Panminerva Med
; 63(4): 458-463, 2021 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-33988330
4.
Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas.
JAMA
; 304(23): 2611-9, 2010 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-21156949
5.
Genetic polymorphism of the renin-angiotensin-aldosterone system and arterial hypertension in the Italian population: the GENIPER Project.
J Hypertens
; 21(10): 1853-60, 2003 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-14508191
6.
MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma.
Clin Cancer Res
; 18(10): 2828-37, 2012 May 15.
Artigo
Inglês
| MEDLINE | ID: mdl-22452945
7.
Functional alterations of mesenteric small resistance arteries in Milan hypertensive and normotensive rats.
Hypertens Res
; 32(7): 581-5, 2009 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-19407819
8.
Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas.
J Clin Endocrinol Metab
; 94(5): 1541-7, 2009 May.
Artigo
Inglês
| MEDLINE | ID: mdl-19223516
9.
Beta(2)-adrenergic receptor gene polymorphism, age, and cardiovascular phenotypes.
Hypertension
; 41(2): 361-7, 2003 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-12574108