PIRAZZOLI, PIERO

PIRAZZOLI, PIERO  

DIPARTIMENTO DI SCIENZE GINECOLOGICHE, OSTETRICHE E PEDIATRICHE  

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Risultati 1 - 20 di 34 (tempo di esecuzione: 0.036 secondi).
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 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 -
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) -
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 -
Interruption of GH Therapy on the Basis of GH Retesting at Puberty in Previously Diagnosed GHD Patients: Final Height Results S. Zucchini; F. Baronio; P. Pirazzoli; I. Bettocchi; M. Marsciani;
C. Retetangos; M. Bal; A. Cic...
ognani; E. Cacciari
2004-01-01 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 -
McCune-Albright syndrome in a boy may present with a monolateral macroorchidism as an early and isolated clinical manifestation. Arrigo T; Pirazzoli P; De Sanctis L; Leone O; Wasniewska M; Messina MF; De Luca F. 2006-01-01 HORMONE RESEARCH - 1.01 Articolo in rivista -
Mutational spectrum of SHOX gene in 25 Italian pediatric patients with Lèri-Weill dyschondrosteosis (LWD). Nicoletti A.; Mazzanti L.; Pirazzoli P.; Menabò S.; Boccone L.; Scarano E.; Cicognani A. 2011-01-01 HORMONE RESEARCH IN PAEDIATRICS Karger 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) -