Detalhe da pesquisa
1.
Research into New Molecular Mechanisms in Thrombotic Diseases Paves the Way for Innovative Therapeutic Approaches.
Int J Mol Sci
; 25(5)2024 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38473772
2.
Platelets, Protean Cells with All-Around Functions and Multifaceted Pharmacological Applications.
Int J Mol Sci
; 24(5)2023 Feb 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-36901997
3.
Decreased Gas6 and sAxl Plasma Levels Are Associated with Hair Loss in COVID-19 Survivors.
Int J Mol Sci
; 24(7)2023 Mar 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37047229
4.
Consumption of complement in a 26-year-old woman with severe thrombotic thrombocytopenia after ChAdOx1 nCov-19 vaccination.
J Autoimmun
; 124: 102728, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34592707
5.
Serum amyloid A in healthy subjects: assessment of reference value using ELISA method.
J Immunoassay Immunochem
; 42(2): 129-137, 2021 Mar 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33119992
6.
Hereditary Deficiency of the Second Component of Complement: Early Diagnosis and 21-Year Follow-Up of a Family.
Medicina (Kaunas)
; 56(3)2020 Mar 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32164349
7.
Novel GLI2 mutations identified in patients with Combined Pituitary Hormone Deficiency (CPHD): Evidence for a pathogenic effect by functional characterization.
Clin Endocrinol (Oxf)
; 90(3): 449-456, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30548673
8.
Improving clinical diagnosis in SHOX deficiency: the importance of growth velocity.
Pediatr Res
; 83(2): 438-444, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29211059
9.
Genetic variations at the human growth hormone receptor (GHR) gene locus are associated with idiopathic short stature.
J Cell Mol Med
; 21(11): 2985-2999, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28557176
10.
Variations in the high-mobility group-A2 gene (HMGA2) are associated with idiopathic short stature.
Pediatr Res
; 79(2): 258-61, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26536448
11.
Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort.
Clin Endocrinol (Oxf)
; 83(6): 849-60, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26147833
12.
Unexpectedly high prevalence of rare genetic disorders in kidney transplant recipients with an unknown causal nephropathy.
Clin Transplant
; 28(9): 995-1003, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24961278
13.
Chronic renal failure of unknown origin is caused by HNF1B mutations in 9% of adult patients: a single centre cohort analysis.
Nephrology (Carlton)
; 19(4): 202-9, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24387224
14.
Role of CES1 and ABCB1 Genetic Polymorphisms on Functional Response to Dabigatran in Patients with Atrial Fibrillation.
J Clin Med
; 13(9)2024 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38731074
15.
Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation.
Front Endocrinol (Lausanne)
; 15: 1382583, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38737552
16.
The changing landscape of neonatal diabetes mellitus in Italy between 2003-2022.
J Clin Endocrinol Metab
; 2024 Feb 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38408297
17.
Genes and Microbiota Interaction in Monogenic Autoimmune Disorders.
Biomedicines
; 11(4)2023 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37189745
18.
Case report: Better late than never, but sooner is better: switch from CSII to sulfonylureas in two patients with neonatal diabetes due to KCNJ11 variants.
Front Endocrinol (Lausanne)
; 14: 1143736, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37251668
19.
A new mutation in the CAVIN1/PTRF gene in two siblings with congenital generalized lipodystrophy type 4: case reports and review of the literature.
Front Endocrinol (Lausanne)
; 14: 1212729, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37501786
20.
Temporal correlation between the first melanoma and the first noncutaneous tumor in CKDN2A genotyped patients.
Melanoma Res
; 33(5): 425-430, 2023 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37352544