Giampaolo Trivellin
Giampaolo Trivellin
Humanitas Clinical and Research Center - IRCCS
Zweryfikowany adres z
Cytowane przez
Cytowane przez
Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation
G Trivellin, AF Daly, FR Faucz, B Yuan, L Rostomyan, DO Larco, ...
New England Journal of Medicine 371 (25), 2363-2374, 2014
Characterization of aryl hydrocarbon receptor interacting protein (AIP) mutations in familial isolated pituitary adenoma families
S Igreja, HS Chahal, P King, GB Bolger, U Srirangalingam, L Guasti, ...
Human mutation 31 (8), 950-960, 2010
Somatostatin analogs modulate AIP in somatotroph adenomas: the role of the ZAC1 pathway
HS Chahal, G Trivellin, CA Leontiou, N Alband, RC Fowkes, A Tahir, ...
The Journal of Clinical Endocrinology & Metabolism 97 (8), E1411-E1420, 2012
Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patients
L Rostomyan, AF Daly, P Petrossians, E Nachev, AR Lila, AL Lecoq, ...
Endocrine-related cancer 22 (5), 745-757, 2015
AIP and its interacting partners.
G Trivellin, M Korbonits
The Journal of endocrinology 210 (2), 137-155, 2011
Macronodular Adrenal Hyperplasia due to Mutations in an Armadillo Repeat Containing 5 (ARMC5) Gene: A Clinical and Genetic Investigation
FR Faucz, M Zilbermint, MB Lodish, E Szarek, G Trivellin, N Sinaii, ...
The Journal of Clinical Endocrinology & Metabolism 99 (6), E1113-E1119, 2014
X-linked acrogigantism syndrome: clinical profile and therapeutic responses
A Beckers, MB Lodish, G Trivellin, L Rostomyan, M Lee, FR Faucz, ...
Endocrine-related cancer 22 (3), 353-367, 2015
Landscape of Familial Isolated and Young-Onset Pituitary Adenomas: Prospective Diagnosis in AIP Mutation Carriers
LC Hernández-Ramírez, P Gabrovska, J Dénes, K Stals, G Trivellin, ...
The Journal of Clinical Endocrinology & Metabolism 100 (9), E1242-E1254, 2015
A Novel Mutation in the Upstream Open Reading Frame of the CDKN1B Gene Causes a MEN4 Phenotype
G Occhi, D Regazzo, G Trivellin, F Boaretto, D Ciato, S Bobisse, S Ferasin, ...
PLoS genetics 9 (3), e1003350, 2013
Germline or somatic GPR101 duplication leads to X-linked acrogigantism: a clinico-pathological and genetic study
D Iacovazzo, R Caswell, B Bunce, S Jose, B Yuan, ...
Acta neuropathologica communications 4 (1), 1-12, 2016
MicroRNA miR-107 is overexpressed in pituitary adenomas and inhibits the expression of aryl hydrocarbon receptor-interacting protein in vitro
G Trivellin, H Butz, J Delhove, S Igreja, HS Chahal, V Zivkovic, T McKay, ...
American Journal of Physiology-Endocrinology and Metabolism, 2012
Somatic mosaicism underlies X-linked acrogigantism (XLAG) syndrome in sporadic male subjects
AF Daly, B Yuan, F Fina, JH Caberg, G Trivellin, L Rostomyan, ...
Endocrine-related cancer 23 (4), 221, 2016
Genetics of pituitary adenomas
MR Gadelha, G Trivellin, LCH Ramírez, M Korbonits
Endocrine Tumor Syndromes and Their Genetics 41, 111-140, 2013
Structure of the TPR domain of AIP: lack of client protein interaction with the C-terminal α-7 helix of the TPR domain of AIP is sufficient for pituitary adenoma predisposition
RML Morgan, LC Hernández-Ramírez, G Trivellin, L Zhou, SM Roe, ...
PloS one 7 (12), e53339, 2012
MEN1, MEN4, and carney complex: pathology and molecular genetics
MH Schernthaner-Reiter, G Trivellin, CA Stratakis
Neuroendocrinology 103 (1), 18-31, 2016
GHRH excess and blockade in X-LAG syndrome
AF Daly, PA Lysy, C Desfilles, L Rostomyan, A Mohamed, JH Caberg, ...
Endocrine-related cancer 23 (3), 161-170, 2016
Regulation of aryl hydrocarbon receptor interacting protein (AIP) protein expression by MiR-34a in sporadic somatotropinomas
J Denes, L Kasuki, G Trivellin, LM Colli, CM Takiya, CE Stiles, S Barry, ...
PloS one 10 (2), e0117107, 2015
Prevalence of AIP mutations in a large series of sporadic Italian acromegalic patients and evaluation of CDKN1B status in acromegalic patients with multiple endocrine neoplasia
G Occhi, G Trivellin, F Ceccato, P De Lazzari, G Giorgi, S Dematte, ...
European Journal of Endocrinology 163 (3), 369, 2010
The R304X mutation of the aryl hydrocarbon receptor interacting protein gene in familial isolated pituitary adenomas: mutational hot-spot or founder effect?
G Occhi, ML Jaffrain-Rea, G Trivellin, N Albiger, F Ceccato, E De Menis, ...
Journal of Endocrinological Investigation 33 (11), 800-805, 2010
Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing’s disease
LC Hernández-Ramírez, R Gam, N Valdés, MB Lodish, N Pankratz, ...
Endocrine-related cancer 24 (8), 379-392, 2017
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