PIRAZZOLI, PIERO
PIRAZZOLI, PIERO
DIPARTIMENTO DI SCIENZE GINECOLOGICHE, OSTETRICHE E PEDIATRICHE
High prevalence of precocious puberty and obesity in childhood narcolepsy with cataplexy.
2013 F. Poli;F. Pizza;E. Mignot;R. Ferri;U. Pagotto;S. Taheri;E. Finotti;F. Bernardi;P. Pirazzoli;A. Cicognani;A. Balsamo;L. Nobili;O. Bruni;G. Plazzi
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
Mutational spectrum of SHOX gene in 25 Italian pediatric patients with Lèri-Weill dyschondrosteosis (LWD).
2011 Nicoletti, A.; Mazzanti, Laura; Pirazzoli, Piero; Menabo', Soara; Boccone, L.; Scarano, E.; 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.
The SHOX gene: a new indication for GH treatment
2010 Cicognani A.; Pirazzoli P.; Nicoletti A.; Baronio F.; Conti V.; Bonetti S.
A novel PRKAR1A mutation associated with hepatocellular carcinoma in a young patient and a variable Carney complex phenotype in affected subjects in older generations.
2008 Gennari M; Stratakis CA; Hovarth A; Pirazzoli P; Cicognani A.
Genotypic and phenotypic variability in 54 subjects with congenital hypopituitarism
2008 Zucchini S.; Baldazzi L.; Pirazzoli P.; Menabò S.; Conti V.; Sponza G.; Costa M.; Cicognani A.
INTRAVENOUS HIGH-DOSE IMMUNOGLOBULIN TREATMENT IN RECENT ONSET CHILDHOOD NARCOLEPSY WITH CATAPLEXY
2008 G.PLAZZI; F.POLI;C.FRANCESCHINI; A. PARMEGGIANI; P. PIRAZZOLI; F. BERNARDI; E. MIGNOT; A. CICOGNANI; P. MONTAGNA
ORTICARIA ACUTA IN BAMBINI CHE AFFERISCONO IN PRONTO SOCCORSO
2008 Belotti T.; Ricci G.; Pirazzoli P.; Dondi A.; Bendandi B.; Giannetti A.; Cipriani F.; Savorelli G.; Masi M.
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.
Thyroid status in children and adolescents after bone marrow transplantation(BMT) with and without total body irradiation (TBI)conditioning
2008 Baronio, Federico; A., Pasini; Cassio, Alessandra; Pirazzoli, Piero; S., Sonetti; DE CRISTOFARO, Enrico; Cicognani, Alessandro
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and in their unaffected father
2007 P. Pirazzoli; A. Nicoletti; M. Gennari; L. Baldazzi; A. Balsamo; F. Mencarelli; A. Cicognani
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and their unaffected father
2007 Pirazzoli P.; Nicoletti A.; Gennari M.; Baldazzi L.; Balsamo A.; Mencarelli F.; Cicognani A.
Noonan syndrome and PTPN11 mutations: clinical findings and growth follow-up with long-term GH therapy
2007 Laura Mazzanti; Emanuela Scarano; Rosalba Bergamaschi; Cesare Rossi; Chiara Matteucci; Federica Tamburrino; Piero Pirazzoli; Francesca Mencarelli; Alessandro Cicognani
Rare Syndromes and Hormones Noonan syndrome and PTPN11 mutations: clinical findings and growth follow-up with long-term GH therapy
2007 L. Mazzanti; E. Scarano; R. Bergamaschi; C.Rossi; C. Matteucci; F. Tamburrino; P. Pirazzoli; F. Mencarelli; A. Cicognani
Effect on adult height of pubertal growth hormone retesting and withdrawal of therapy in patients with previously diagnosed growth hormone deficiency.
2006 Zucchini S.; Pirazzoli P.; Baronio F.; Gennari M.; Bal M.O.; Balsamo A.; Gualandi S.; Cicognani A.
Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
---|---|---|---|---|---|---|
High prevalence of precocious puberty and obesity in childhood narcolepsy with cataplexy. | F. Poli;F. Pizza;E. Mignot;R. Ferri;U. Pagotto;S. Taheri;E. Finotti;F. Bernardi;P. Pirazzoli;A. C...icognani;A. Balsamo;L. Nobili;O. Bruni;G. Plazzi | 2013-01-01 | SLEEP | - | 1.01 Articolo in rivista | - |
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia. | Menabò S; Balsamo A; Baldazzi L; Barbaro M; Nicoletti A; Conti V; Pirazzoli P; Wedell A; Cicognan...i A. | 2012-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | - |
CYP21A2 AND CYP11B1: FIRST REPORT OF A DIGENIC INHERITANCE IN CAH. | Menabò S.; Marsigli A.; Baldazzi L.; Nicoletti A.; Pirazzoli P.; Balsamo A. | 2012-01-01 | HORMONE RESEARCH IN PAEDIATRICS | - | 4.02 Riassunto (Abstract) | - |
Determination of BMP15 gene dosage in a woman with TS and spontaneous menarche. | Nicoletti A; Mazzanti L.; Menabò S.; Scarano E.; Tamburrino F.; Cangemi G.; Pirazzoli P.; Baldazzi L | 2012-01-01 | HORMONE RESEARCH IN PAEDIATRICS | - | 1.06 Abstract in rivista | - |
Mutational spectrum of SHOX gene in 25 Italian pediatric patients with Lèri-Weill dyschondrosteosis (LWD). | Nicoletti, A.; Mazzanti, Laura; Pirazzoli, Piero; Menabo', Soara; Boccone, L.; Scarano, E.; Cicog...nani, A. | 2011-01-01 | HORMONE RESEARCH IN PAEDIATRICS | Karger | 4.02 Riassunto (Abstract) | - |
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. | Baldazzi, Lilia; Balsamo, Antonio; Nicoletti, Annalisa; Menabo', Soara; Rinaldini, D.; Cangemi, G...IUSEPPE ALESSANDRO; Balsamo, Claudia; Pirazzoli, Piero; Cicognani, Alessandro | 2011-01-01 | HORMONE RESEARCH IN PAEDIATRICS | - | 4.02 Riassunto (Abstract) | - |
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia | Menabo', Soara; Balsamo, Antonio; Baldazzi, Lilia; Barbaro, M.; Nicoletti, Annalisa; Conti, Veron...ica; Pirazzoli, Piero; Wedell, A.; Cicognani, Alessandro | 2010-01-01 | HORMONE RESEARCH IN PAEDIATRICS | - | 4.02 Riassunto (Abstract) | - |
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. | Baldazzi L.; Zucchini S.; Menabò S.; Nicoletti A.; Baronio F.; Cangemi G; Pirazzoli P.; Cicognani A. | 2010-01-01 | HORMONE RESEARCH IN PAEDIATRICS | - | 4.02 Riassunto (Abstract) | - |
The SHOX gene: a new indication for GH treatment | Cicognani A.; Pirazzoli P.; Nicoletti A.; Baronio F.; Conti V.; Bonetti S. | 2010-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | - |
A novel PRKAR1A mutation associated with hepatocellular carcinoma in a young patient and a variable Carney complex phenotype in affected subjects in older generations. | Gennari M; Stratakis CA; Hovarth A; Pirazzoli P; Cicognani A. | 2008-01-01 | CLINICAL ENDOCRINOLOGY | - | 1.01 Articolo in rivista | - |
Genotypic and phenotypic variability in 54 subjects with congenital hypopituitarism | Zucchini S.; Baldazzi L.; Pirazzoli P.; Menabò S.; Conti V.; Sponza G.; Costa M.; Cicognani A. | 2008-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
INTRAVENOUS HIGH-DOSE IMMUNOGLOBULIN TREATMENT IN RECENT ONSET CHILDHOOD NARCOLEPSY WITH CATAPLEXY | G.PLAZZI; F.POLI;C.FRANCESCHINI; A. PARMEGGIANI; P. PIRAZZOLI; F. BERNARDI; E. MIGNOT; A. CICOGNA...NI; P. MONTAGNA | 2008-01-01 | JOURNAL OF NEUROLOGY | - | 1.01 Articolo in rivista | - |
ORTICARIA ACUTA IN BAMBINI CHE AFFERISCONO IN PRONTO SOCCORSO | Belotti T.; Ricci G.; Pirazzoli P.; Dondi A.; Bendandi B.; Giannetti A.; Cipriani F.; Savorelli G....; Masi M. | 2008-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
Three Novel AMHGene Mutations in a Patient with Persistent Mullerian Duct Syndrome and Normal AMH Serum Dosage. | Menabò S; Balsamo A; Nicoletti A; Gennari M; Pirazzoli P; Cicognani A; Baldazzi L. | 2008-01-01 | HORMONE RESEARCH | - | 1.01 Articolo in rivista | - |
Thyroid status in children and adolescents after bone marrow transplantation(BMT) with and without total body irradiation (TBI)conditioning | Baronio, Federico; A., Pasini; Cassio, Alessandra; Pirazzoli, Piero; S., Sonetti; DE CRISTOFARO, ...Enrico; Cicognani, Alessandro | 2008-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and in their unaffected father |
P. Pirazzoli; A. Nicoletti; M. Gennari; L. Baldazzi; A. Balsamo; F. Mencarelli; A. Cicognani |
2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and their unaffected father | Pirazzoli P.; Nicoletti A.; Gennari M.; Baldazzi L.; Balsamo A.; Mencarelli F.; Cicognani A. | 2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
Noonan syndrome and PTPN11 mutations: clinical findings and growth follow-up with long-term GH therapy |
Laura Mazzanti; Emanuela Scarano; Rosalba Bergamaschi; Cesare Rossi; Chiara Matteucci; Federica ...Tamburrino; Piero Pirazzoli; Francesca Mencarelli; Alessandro Cicognani |
2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
Rare Syndromes and Hormones Noonan syndrome and PTPN11 mutations: clinical findings and growth follow-up with long-term GH therapy |
L. Mazzanti; E. Scarano; R. Bergamaschi; C.Rossi; C. Matteucci; F. Tamburrino; P. Pirazzoli; F.... Mencarelli; A. Cicognani |
2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
Effect on adult height of pubertal growth hormone retesting and withdrawal of therapy in patients with previously diagnosed growth hormone deficiency. | Zucchini S.; Pirazzoli P.; Baronio F.; Gennari M.; Bal M.O.; Balsamo A.; Gualandi S.; Cicognani A. | 2006-01-01 | THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM | - | 1.01 Articolo in rivista | - |