NICOLETTI, ANNALISA
NICOLETTI, ANNALISA
DIPARTIMENTO DI SCIENZE PER LA QUALITA' DELLA VITA
Personale tecnico amm.vo
Nicoletti A.; A. L. NICOLETTI; NICOLETTI L.; A. NICOLETTI; Annalisa Nicoletti
First Description of Partial Atrioventricular Septal Defect in a Rabbit
2018 Di Girolamo, Nicola*; Palmieri, Chiara; Baron Toaldo, Marco; Nicoletti, Annalisa; Spattini, Giliola; Zeyen, Ulrich; Selleri, Paolo
NKX2.1-Related Disorders: a novel mutation with mild clinical presentation.
2015 Monti, Sara; Nicoletti, Annalisa; Cantasano, Antonella; Krude, H; Cassio, Alessandra
Copy number determination of hypothyroidism genes by MLPA analysis in patients with hypothyroidism and thyroid hypoplasia
2013 Annalisa Nicoletti; Alessandra Cassio; Ilaria Bettocchi; Soara Menabò; Angela Rizzello; Giuseppe A. Cangemi; Laura Mazzanti; Lilia Baldazzi
Current Loss-Of-Function Mutations in The Thyrotropin Receptor Gene: When to Investigate, Clinical Effects, and Treatment.
2013 Cassio, A; Nicoletti, A; Rizzello, A; Zazzetta, E; Bal, M; Baldazzi, L
Non classical CAH: molecular evaluation of 287 subjects from northern and southern Italy with comparison between genetical and hormonal results.
2013 Balsamo A.; Menabò S.; Wasniewska M.; Mirabelli S.; Nicoletti A.; Marsigli A.; Rinaldini D.; De Luca F.; Mazzanti L.; Baldazzi L.
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia.
2012 Menabò S; Balsamo A; Baldazzi L; Barbaro M; Nicoletti A; Conti V; Pirazzoli P; Wedell A; Cicognani A.
CYP21A2 AND CYP11B1: FIRST REPORT OF A DIGENIC INHERITANCE IN CAH.
2012 Menabò S.; Marsigli A.; Baldazzi L.; Nicoletti A.; Pirazzoli P.; Balsamo A.
Determination of BMP15 gene dosage in a woman with TS and spontaneous menarche.
2012 Nicoletti A; Mazzanti L.; Menabò S.; Scarano E.; Tamburrino F.; Cangemi G.; Pirazzoli P.; Baldazzi L
Molecular characterization to predict tetrahydrobiopterin (BH4) responsiveness in phenylalanine hydroxylase (PAH) deficiency
2012 I.Bettocchi; A.Nicoletti; F.Baronio; S.Monti; A.Rizzello; L.Baldazzi; A.Cassio; A.Pession; M.Bal
SHOX dosage and final height (FH) in Turner syndrome (TS) treated with GH-therapy
2011 Mazzanti L.; Nicoletti A.; Tamburrino F.; Scarano E.; Baldazzi L.; Ragni M.C.; Perri A.; De Angelis C.; Cicognani A.
Study of the NR5A1 gene in a cohort of Italian patients with 46,XY Disorders of Sex Development (DSD) without adrenal insufficiency: identification of 7 novel mutations.
2011 Baldazzi, Lilia; Balsamo, Antonio; Nicoletti, Annalisa; Menabo', Soara; Rinaldini, D.; Cangemi, GIUSEPPE ALESSANDRO; Balsamo, Claudia; Pirazzoli, Piero; Cicognani, Alessandro
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia
2010 Menabo', Soara; Balsamo, Antonio; Baldazzi, Lilia; Barbaro, M.; Nicoletti, Annalisa; Conti, Veronica; Pirazzoli, Piero; Wedell, A.; Cicognani, Alessandro
HESX1 gene analysis in a population of 45 patients with posterior pituitari ectopia (PPE) and GH deficiency (GHD): two novel mutations associated with a mild phenotype.
2010 Baldazzi L.; Zucchini S.; Menabò S.; Nicoletti A.; Baronio F.; Cangemi G; Pirazzoli P.; Cicognani A.
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence
2009 Bertelloni S.; Balsamo A.; Giordani L. ; Fischetto R.; Russo G.; Delvecchio M.; Gennari M.; Nicoletti A.; Maggio M.C.; Concolino D.; Cavallo L.; Cicognani A.; Chiumello G.; Hiort O.; Baroncelli G.I.; Faienza M.F.
Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA.
2009 Barbaro M.; Balsamo A.; Anderlid B.M.; Myhre A.G.; Gennari M.; Nicoletti A.; Pittalis M.C.; Oscarson M.; Wedell A.
Thyrotropin-stimulating hormone receptor gene analysis in pediatric patients with non-autoimmune subclinical hypothyroidism
2009 Nicoletti A; Bal M; De Marco G; Baldazzi L; Agretti P; Menabò S; Ballarini E; Cicognani A; Tonacchera M; Cassio A.
TSHR gene analysis in paediatric subjects with NASH (non autoimmune subclinical hypothyroidism) not selected by neonatal screening
2009 A.Nicoletti; M.Bal; A. Cassio; L.Baldazzi ; M.Tonacchera; S.Menabò; G.Sponza; E.Ballarini; A . Cicognani
Three new mutations in androgen receptor gene identified in patients with 46,XY SDS: Complications for genetic counselling
2008 Nicoletti A.; Baldazzi L.; Menabò S.; Gennari M.; Cangemi G.; Maccaferri M.; Cicognani A.
Three Novel AMHGene Mutations in a Patient with Persistent Mullerian Duct Syndrome and Normal AMH Serum Dosage.
2008 Menabò S; Balsamo A; Nicoletti A; Gennari M; Pirazzoli P; Cicognani A; Baldazzi L.
A molecular analysis of candidate genes for hypospadias in Italian subjects
2007 Nicoletti A.; Baldazzi L.; Menabò S.; Balsamo A.; Gennari M.; Buzi F.; Pasini A.; Cicognani A.