Sfoglia per Autore
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.
Acanthosis Nigricans (AN), Glucose Tolerance and Turner Syndrome: Influence of GH-Therapy
2004 R. Bergamaschi; L. Mazzanti; E. Scarano; I. Neri; S. Strocchi; V. Rosetti; L. Castiglioni; F. Zappulla; A. Cicognani; E. Cacciari
Cardiofaciocutaneous Syndrome (CFC): A New Case with GH-Deficit and without Mental Retardation (MR)
2004 E. Scarano; L. Mazzanti; F. Mencarelli; V. Rosetti; F. Tamburrino; A. Cicognani; E. Cacciari
Gonadal dysgenesis and XY sex reversal in one patient with a deletion of the distal short arm of chromosome 9 (9p).
2004 A.Balsamo; M.Gennari; MC.Pittalis; P.Biso; L.Baldazzi; L.Mazzanti; R.De Castro; A.Cicognani.
Prevalence of Aortic Dilation in Turner Patients without Congenital Heart Disease (CHD) Studied at Echocardiography and Transthoracic MRI
2004 L. Mazzanti; D. Prandstraller; R. Bergamaschi; R. Fattori; E. Scarano; F. Mencarelli; S. Strocchi; V. Rosetti; D. Tassinari; A. Cicognani; E. Cacciari
EARLY TREATMENT WITH GH ALONE IN TURNER SYNDROME: PREPUBERTAL CATCH-UP GROWTH AND WANING EFFECT.
2004 Wasniewska M.; De Luca F.; Bergamaschi R.; Guarneri MP.; Mazzanti L.; Matarazzo P.; Petri A.; Crisafulli G.; Salzano G.; Lombardo F.
MOLECULAR AND CLINICAL ANALYSES OF GREIG CEPHALOPOLYSYNDACTYLY AND PALLISTER-HALL SYNDROMES: ROBUST PHENOTYPE PREDICTION FROM THE TYPE AND POSITION OF GLI3 MUTATIONS.
2005 Johnston J.J.; Olivos-Glander I.; Killoran C.; Elson E.; Turner J.T.; Peters K.F.; Abbott M.H.; Aughton D.J.; Aylsworth A.S.; Bamshad M.J.; Booth C.; Curry C.J.; David A.; Dinulos M.B.; Flannery D.B.; Fox M.A.; Graham J.M.; Grange D.K.; Guttmacher A.E.; Hannibal M.C.; Henn W.; Hennekam R.C.; Holmes L.B.; Hoyme H.E.; Leppig K.A.; Lin A.E.; Macleod P.; Manchester D.K.; Marcelis C.; Mazzanti L.; McCann E.; McDonald M.T.; Mendelsohn N.J.; Moeschler J.B.; Moghaddam B.; Neri G.; Newbury-Ecob R.; Pagon R.A.; Phillips J.A.; Sadler L.S.; Stoler J.M.; Tilstra D.; Walsh Vockley C.M.; Zackai E.H.; Zadeh T.M.; Brueton L.; Black G.C.; Biesecker L.G.
Glucose tolerance and insulin sensitivity in Turner patients treated with GH: Follow-up until the young adult age
2005 L. Mazzanti;R. Bergamaschi;E. Scarano;M. Bal;L. Castiglioni;C. Matteucci;F.Tamburrino;F. Zappulla ; A. Cicognani
Turner syndrome, insulin sensitivity and growth hormone treatment
2005 Mazzanti L.; Bergamaschi R.; Castiglioni L.; Zappulla F.; Pirazzoli P.; 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.
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.
Gonadoblastoma in Turner syndrome and Y-chromosome-derived material.
2005 Mazzanti L; Cicognani A; Baldazzi L; Bergamaschi R; Scarano E; Strocchi S; Nicoletti A; Mencarelli F; Pittalis M; Forabosco A; Cacciari E.
AUTOIMMUNE DISEASE IN TURNER SYNDROME.
2006 Mazzanti L.; Naeraa R.W.
GAIN OF FUNCTION RAF1 MUTATIONS CAUSE NOONAN AND LEOPARD SYNDROMES WITH HYPERTROPHIC CARDIOMYOPATHY.
2007 Pandit B.; Sarkozy A.; Pennacchio L.A.; Carta C.; Oishi K.; Martinelli S.; Pogna E.A.; Schackwitz W; Ustaszewska A.; Landstrom A.; Bos J.M.; Ommen S.R.; Esposito G.; Lepri F.; Faul C.; Mundel P.; Lòpez Siguero J.P.; Tenconi .; Selicorni A.; Rossi C.; Mazzanti L.; Torrente I.; Marino B.; Digilio M.C.; Zampino G.; Ackerman M.J.; Dallapiccola B.; Tartaglia M.; Gelb B.D.
A de novo nonsense mutation of PAX6 gene in a patient with aniridia, ataxia, and mental retardation
2007 Graziano C.; D'Elia AV.; Mazzanti L.; Moscano F.; Guidelli Guidi S.; Scarano E.; Turchetti D.; Franzoni E.; Romeo G.; Damante G.; Seri M.
Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16.
2007 Zollino M; Lecce R; Murdolo M; Orteschi D; Marangi G; Selicorni A; Midro A; Sorge G; Zampino G; Memo L; Battaglia D; Petersen M; Pandelia E; Gyftodimou Y; Faravelli F; Tenconi R; Garavelli L; Mazzanti L; Fischetto R; Cavalli P; Savasta S; Rodriguez L; Neri G.
CARE OF GIRLS AND WOMEN WITH TURNER SYNDROME: A GUIDLINE OF THE TURNER SYNDROME STUDY GROUP.
2007 TURNER SYNDROME STUDY GROUP. Bondy CA and Turner Sindrome Study Group: Turner Sindrome Consensus Study Group: Neus Baena; V. K. Bakalov; B.B. Biesecker; J.C. Carel; G.Conway; M. Davenport; C. Disteche; M. F. Karnis; J. A. Germak; C.H. Gravholt; J. Foodim; D. Gunther; O. Hovatta; A.M. Kappelgard; W. Kiess; K. Landin-Wilhelmsen; A. Lin; B. Lippe; M. Loscalzo; K. Lynch; L. Mazzanti; M. M. M. Mazzocco; E. McCauley; P. McDonough; S.M.P.F. de Muinck Keizer-Schrama; R. W. Naeraa; C. Quigley; R. Rosenfield; D. Rosing; J. Ross; D. Roulot; K. Rubin; P. Saenger; P. Schmidt; M. Silberbach; V. Sybert; D. L. Van Dyke; A. Zinn.
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
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| 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 | - |
| Acanthosis Nigricans (AN), Glucose Tolerance and Turner Syndrome: Influence of GH-Therapy |
R. Bergamaschi; L. Mazzanti; E. Scarano; I. Neri; S. Strocchi; V. Rosetti; L. Castiglioni; F. Za...ppulla; A. Cicognani; E. Cacciari |
2004-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| Cardiofaciocutaneous Syndrome (CFC): A New Case with GH-Deficit and without Mental Retardation (MR) |
E. Scarano; L. Mazzanti; F. Mencarelli; V. Rosetti; F. Tamburrino; A. Cicognani; E. Cacciari |
2004-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| Gonadal dysgenesis and XY sex reversal in one patient with a deletion of the distal short arm of chromosome 9 (9p). | A.Balsamo; M.Gennari; MC.Pittalis; P.Biso; L.Baldazzi; L.Mazzanti; R.De Castro; A.Cicognani. | 2004-01-01 | - | O.Hiort | 4.02 Riassunto (Abstract) | - |
| Prevalence of Aortic Dilation in Turner Patients without Congenital Heart Disease (CHD) Studied at Echocardiography and Transthoracic MRI |
L. Mazzanti; D. Prandstraller; R. Bergamaschi; R. Fattori; E. Scarano; F. Mencarelli; S. Strocch...i; V. Rosetti; D. Tassinari; A. Cicognani; E. Cacciari |
2004-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| EARLY TREATMENT WITH GH ALONE IN TURNER SYNDROME: PREPUBERTAL CATCH-UP GROWTH AND WANING EFFECT. | Wasniewska M.; De Luca F.; Bergamaschi R.; Guarneri MP.; Mazzanti L.; Matarazzo P.; Petri A.; Cri...safulli G.; Salzano G.; Lombardo F. | 2004-01-01 | EUROPEAN JOURNAL OF ENDOCRINOLOGY | - | 1.01 Articolo in rivista | - |
| MOLECULAR AND CLINICAL ANALYSES OF GREIG CEPHALOPOLYSYNDACTYLY AND PALLISTER-HALL SYNDROMES: ROBUST PHENOTYPE PREDICTION FROM THE TYPE AND POSITION OF GLI3 MUTATIONS. | Johnston J.J.; Olivos-Glander I.; Killoran C.; Elson E.; Turner J.T.; Peters K.F.; Abbott M.H.; A...ughton D.J.; Aylsworth A.S.; Bamshad M.J.; Booth C.; Curry C.J.; David A.; Dinulos M.B.; Flannery D.B.; Fox M.A.; Graham J.M.; Grange D.K.; Guttmacher A.E.; Hannibal M.C.; Henn W.; Hennekam R.C.; Holmes L.B.; Hoyme H.E.; Leppig K.A.; Lin A.E.; Macleod P.; Manchester D.K.; Marcelis C.; Mazzanti L.; McCann E.; McDonald M.T.; Mendelsohn N.J.; Moeschler J.B.; Moghaddam B.; Neri G.; Newbury-Ecob R.; Pagon R.A.; Phillips J.A.; Sadler L.S.; Stoler J.M.; Tilstra D.; Walsh Vockley C.M.; Zackai E.H.; Zadeh T.M.; Brueton L.; Black G.C.; Biesecker L.G. | 2005-01-01 | AMERICAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| Glucose tolerance and insulin sensitivity in Turner patients treated with GH: Follow-up until the young adult age |
L. Mazzanti;R. Bergamaschi;E. Scarano;M. Bal;L. Castiglioni;C. Matteucci;F.Tamburrino;F. Zappulla... ; A. Cicognani |
2005-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| Turner syndrome, insulin sensitivity and growth hormone treatment | Mazzanti L.; Bergamaschi R.; Castiglioni L.; Zappulla F.; Pirazzoli P.; Cicognani A. | 2005-01-01 | HORMONE RESEARCH | - | 1.01 Articolo in rivista | - |
| 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) | - |
| 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 | - |
| Gonadoblastoma in Turner syndrome and Y-chromosome-derived material. | Mazzanti L; Cicognani A; Baldazzi L; Bergamaschi R; Scarano E; Strocchi S; Nicoletti A; Mencarell...i F; Pittalis M; Forabosco A; Cacciari E. | 2005-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART A | - | 1.01 Articolo in rivista | - |
| AUTOIMMUNE DISEASE IN TURNER SYNDROME. | Mazzanti L.; Naeraa R.W. | 2006-01-01 | - | Elsevier | 2.01 Capitolo / saggio in libro | - |
| GAIN OF FUNCTION RAF1 MUTATIONS CAUSE NOONAN AND LEOPARD SYNDROMES WITH HYPERTROPHIC CARDIOMYOPATHY. | Pandit B.; Sarkozy A.; Pennacchio L.A.; Carta C.; Oishi K.; Martinelli S.; Pogna E.A.; Schackwitz... W; Ustaszewska A.; Landstrom A.; Bos J.M.; Ommen S.R.; Esposito G.; Lepri F.; Faul C.; Mundel P.; Lòpez Siguero J.P.; Tenconi .; Selicorni A.; Rossi C.; Mazzanti L.; Torrente I.; Marino B.; Digilio M.C.; Zampino G.; Ackerman M.J.; Dallapiccola B.; Tartaglia M.; Gelb B.D. | 2007-01-01 | NATURE GENETICS | - | 1.01 Articolo in rivista | - |
| A de novo nonsense mutation of PAX6 gene in a patient with aniridia, ataxia, and mental retardation | Graziano C.; D'Elia AV.; Mazzanti L.; Moscano F.; Guidelli Guidi S.; Scarano E.; Turchetti D.; Fr...anzoni E.; Romeo G.; Damante G.; Seri M. | 2007-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART A | - | 1.01 Articolo in rivista | - |
| Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16. | Zollino M; Lecce R; Murdolo M; Orteschi D; Marangi G; Selicorni A; Midro A; Sorge G; Zampino G; M...emo L; Battaglia D; Petersen M; Pandelia E; Gyftodimou Y; Faravelli F; Tenconi R; Garavelli L; Mazzanti L; Fischetto R; Cavalli P; Savasta S; Rodriguez L; Neri G. | 2007-01-01 | HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| CARE OF GIRLS AND WOMEN WITH TURNER SYNDROME: A GUIDLINE OF THE TURNER SYNDROME STUDY GROUP. |
TURNER SYNDROME STUDY GROUP. Bondy CA and Turner Sindrome Study Group: Turner Sindrome Consensus... Study Group: Neus Baena; V. K. Bakalov; B.B. Biesecker; J.C. Carel; G.Conway; M. Davenport; C. Disteche; M. F. Karnis; J. A. Germak; C.H. Gravholt; J. Foodim; D. Gunther; O. Hovatta; A.M. Kappelgard; W. Kiess; K. Landin-Wilhelmsen; A. Lin; B. Lippe; M. Loscalzo; K. Lynch; L. Mazzanti; M. M. M. Mazzocco; E. McCauley; P. McDonough; S.M.P.F. de Muinck Keizer-Schrama; R. W. Naeraa; C. Quigley; R. Rosenfield; D. Rosing; J. Ross; D. Roulot; K. Rubin; P. Saenger; P. Schmidt; M. Silberbach; V. Sybert; D. L. Van Dyke; A. Zinn. |
2007-01-01 | THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM | - | 1.01 Articolo in rivista | - |
| 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) | - |
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