PERSANI, LUCA

PERSANI, LUCA  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

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Risultati 1 - 20 di 360 (tempo di esecuzione: 0.004 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
2012 European thyroid association guidelines for the management of familial and persistent sporadic non-autoimmune hyperthyroidism caused by thyroid-stimulating hormone receptor germline mutations. 1-ott-2012 L. Persani + Article (author) -
2018 European Thyroid Association (ETA) Guidelines on the Diagnosis and Management of Central Hypothyroidism 1-ott-2018 Persani, LucaBonomi, Marco + Article (author) -
8-Chloro-cyclic AMP and protein kinase A I-selective cyclic AMP analogs inhibit cancer cell growth through different mechanisms 1-giu-2011 D. CalebiroE. GrassiM. BorghiL. Persani + Article (author) -
8-Cl-cAMP and PKA I-selective cAMP analogs effectively inhibit undifferentiated thyroid cancer cell growth 1-gen-2016 E.S. GrassiM.O. BorghiG. VitaleL. Persani + Article (author) -
A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH) 1-gen-2009 G. WeberD. CalebiroP. Beck PeccozL. Persani + Article (author) -
A balanced reciprocal translocation t(10;15)(q22.3;q26.1) interrupting ACAN gene in a family with proportionate short stature 1-ago-2018 M. CrippaS. GiangiobbeR. VillaI. BestettiL. FattiTAURINO, JACOPOL. LarizzaL. PersaniF. BelliniP. Finelli + Article (author) -
A clinical research integration special program (CRISP) for young women with primary ovarian insufficiency 1-dic-2014 L. PersaniR. Rossetti + Article (author) -
A design thinking approach to primary ovarian insufficiency 1-mar-2017 L. Persani + Article (author) -
A family with complete resistance to thyrotropin-releasing hormone 1-gen-2009 M. BonomiM. BusnelliP. Beck-PeccozC. DolciL. Persani + Article (author) -
A Frequent Oligogenic Involvement in Congenital Hypothyroidism 1-lug-2017 F. MarelliM. BonomiL. Persani + Article (author) -
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure 1-gen-2009 A. MarozziL. PersaniR. Rossetti + Article (author) -
A Meta-Analysis of Thyroid-Related Traits Reveals Novel Loci and Gender-Specific Differences in the Regulation of Thyroid Function 1-feb-2013 L. FugazzolaL. Persani + Article (author) -
A new variant in signal peptide of the human luteinizing hormone receptor (LHCGR) affects receptor biogenesis causing leydig cell hypoplasia 1-nov-2015 V. VezzoliR. MinariI. BassiL. PersaniM. Bonomi + Article (author) -
A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidism 1-set-2001 M. C. ProverbioP. Beck-PeccozL. Persani + Article (author) -
A novel germline mutation of ADA2 gene in two “discordant” homozygous female twins affected by adenosine deaminase 2 deficiency: description of the bone-related phenotype 3-ago-2021 Vai, SilviaChiodini, IacopoPersani, Luca + Article (author) -
A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome 1-dic-2018 Bonomi, MarcoPersani, Luca + Article (author) -
A novel mutation in the BMP15 gene causing defective protein secretion is associated with both increased ovulation rate and sterility in Lacaune sheep 1-gen-2007 E. Di PasqualeL. Persani + Article (author) -
A novel splice variant involving the 5’ untranslated region of thyroid hormone receptor beta1 (TRbeta1) 1-gen-2004 D. MannavolaP. Beck-PeccozL. Persani + Article (author) -
A novel splice variant involving the 5’ untranslated region of thyroid hormone receptor β1 (TRβ1) 1-apr-2004 D. MannavolaP. Beck-PeccozL. Persani + Article (author) -
A rare genetic disorder causing persistent severe neonatal hypoglycaemia the diagnostic workup 19-lug-2012 G. FrancescatoL. Persani + Article (author) -