PIRAZZOLI, PIERO
PIRAZZOLI, PIERO
DIPARTIMENTO DI SCIENZE GINECOLOGICHE, OSTETRICHE E PEDIATRICHE
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.
A NOVEL FRAME-SHIFT MUTATION IN THE SHOX GENE IN A SUBJECT WITH LERI-WEIL DYSCHONDROSTEOSIS.
2005 Nicoletti A.; Baldazzi L.; Antelli A.; Mazzanti L.; Baronio F.; Menabò S.; Pirazzoli P.
A novel frame-shift mutation in the SHOX gene in a subject with Léri-Weill dyschondrosteosis
2005 Nicoletti A.; Baldazzi L.; Antelli A.; Mazzanti L.; Baronio F.; Menabò S.; Pirazzoli P.; Cicognani A.
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.
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia
2010 S. Menabo;A.Balsamo; L. Baldazzi; M. Barbaro; A. Nicoletti; V.Conti; P. Pirazzoli; A. Wedell; A. Cicognani
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.
Active and total ghrelin concentrations in the newborn
2005 Pirazzoli P; Lanari M; Zucchini S; Gennari M; Pagotto U; De Iasio R; Pasquali R; Cassio A; Cicognani A; Cacciari E.
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
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.
FINAL HEIGHT IN A PATIENT WITH LARON SYNDROME AFTER LONG TERM THERAPY WITH rhIGF-1 AND SHORT TERM THERAPY WITH LHRH-ANALOGUE AND OXANDROLONE DURING PUBERTY.
2005 Zucchini S.; Scarano E.; Baldazzi L.; Mazzanti L.; Pirazzoli P.; Cacciari E.
Final Height Related to Growth Hormone Levels (Stimulated and Physiological) Evaluated in Short Children Before and After Growth Hormone Therapy
2004 P. Pirazzoli; F. Baronio; S. Zucchini; S. Gualandi; A. Pasini; A. Cassio; S. Salardi; A. Cicognani; E. Cacciari
Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patients with congenital adrenal hyperplasia.
2004 Barbaro M; Lajic S; Baldazzi L; Balsamo A; Pirazzoli P; Cicognani A; Wedell A; Cacciari E
Functional studies of two novel and two rare mutations in the 21-hydroxylase gene.
2006 Barbaro M; Baldazzi L; Balsamo A; Lajic S; Robins T; Barp L; Pirazzoli P; Cacciari E; Cicognani A; Wedell 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.
Helicobacter pylori and type 1 diabetes mellitus in children
1999 Salardi S.; Cacciari E.; Menegatti M.; Landi F.; Mazzanti L.; Stella F.A.; Pirazzoli P.; Vaira D.
Helicobacter pylori and type 1 diabetes mellitus in children
1999 Salardi S.; Cacciari E.; Menegatti M.; Landi F.; Mazzanti L.; Stella F.A.; Pirazzoli P.; Vaira D.
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.
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
Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
---|---|---|---|---|---|---|
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) | - |
A NOVEL FRAME-SHIFT MUTATION IN THE SHOX GENE IN A SUBJECT WITH LERI-WEIL DYSCHONDROSTEOSIS. | Nicoletti A.; Baldazzi L.; Antelli A.; Mazzanti L.; Baronio F.; Menabò S.; Pirazzoli P. | 2005-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
A novel frame-shift mutation in the SHOX gene in a subject with Léri-Weill dyschondrosteosis | Nicoletti A.; Baldazzi L.; Antelli A.; Mazzanti L.; Baronio F.; Menabò S.; Pirazzoli P.; Cicognan...i A. | 2005-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
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 | - |
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia | S. Menabo;A.Balsamo; L. Baldazzi; M. Barbaro; A. Nicoletti; V.Conti; P. Pirazzoli; A. Wedell; A. ...Cicognani | 2010-01-01 | 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. | 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 | - |
Active and total ghrelin concentrations in the newborn | Pirazzoli P; Lanari M; Zucchini S; Gennari M; Pagotto U; De Iasio R; Pasquali R; Cassio A; Cicogn...ani A; Cacciari E. | 2005-01-01 | JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | - | 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 | - |
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 | - |
FINAL HEIGHT IN A PATIENT WITH LARON SYNDROME AFTER LONG TERM THERAPY WITH rhIGF-1 AND SHORT TERM THERAPY WITH LHRH-ANALOGUE AND OXANDROLONE DURING PUBERTY. | Zucchini S.; Scarano E.; Baldazzi L.; Mazzanti L.; Pirazzoli P.; Cacciari E. | 2005-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | - |
Final Height Related to Growth Hormone Levels (Stimulated and Physiological) Evaluated in Short Children Before and After Growth Hormone Therapy |
P. Pirazzoli; F. Baronio; S. Zucchini; S. Gualandi; A. Pasini; A. Cassio; S. Salardi; A. Cicogna...ni; E. Cacciari |
2004-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patients with congenital adrenal hyperplasia. | Barbaro M; Lajic S; Baldazzi L; Balsamo A; Pirazzoli P; Cicognani A; Wedell A; Cacciari E | 2004-01-01 | THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM | - | 1.01 Articolo in rivista | - |
Functional studies of two novel and two rare mutations in the 21-hydroxylase gene. | Barbaro M; Baldazzi L; Balsamo A; Lajic S; Robins T; Barp L; Pirazzoli P; Cacciari E; Cicognani A...; Wedell A. | 2006-01-01 | JOURNAL OF MOLECULAR MEDICINE | - | 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) | - |
Helicobacter pylori and type 1 diabetes mellitus in children | Salardi S.; Cacciari E.; Menegatti M.; Landi F.; Mazzanti L.; Stella F.A.; Pirazzoli P.; Vaira D. | 1999-01-01 | JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION | - | 1.01 Articolo in rivista | - |
Helicobacter pylori and type 1 diabetes mellitus in children | Salardi S.; Cacciari E.; Menegatti M.; Landi F.; Mazzanti L.; Stella F.A.; Pirazzoli P.; Vaira D. | 1999-01-01 | JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION | - | 1.01 Articolo in rivista | - |
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) | - |
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 | - |