McCune-Albright Syndrome: A Clinical Longitudinal Study of 32 Patients

C. de Sanctis,; R. Lala,; P. Matarazzo,; A. Balsamo,; R. Bergamaschi,; M. Cappa,; M. Cisternino,; V. de Sanctis,; M. Lucci,; A. Franzese,; L. Ghizzoni,; A.M. Pasquino,; M. Segni,; F. Rigon,; G. Saggese,; S. Bertelloni,; F. Buzi,

doi:10.1515/JPEM.1999.12.6.817

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McCune-Albright Syndrome: A Clinical Longitudinal Study of 32 Patients

C. de Sanctis, , R. Lala, , P. Matarazzo, , A. Balsamo, , R. Bergamaschi, , M. Cappa, , M. Cisternino, , V. de Sanctis, , M. Lucci, , A. Franzese, , L. Ghizzoni, , A.M. Pasquino, , M. Segni, , F. Rigon, , G. Saggese, , S. Bertelloni, and F. Buzi,

Published/Copyright: November 1, 1999

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From the journal Journal of Pediatric Endocrinology and Metabolism Volume 12 Issue 6

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de Sanctis,, C., Lala,, R., Matarazzo,, P., Balsamo,, A., Bergamaschi,, R., Cappa,, M., Cisternino,, M., de Sanctis,, V., Lucci,, M., Franzese,, A., Ghizzoni,, L., Pasquino,, A.M., Segni,, M., Rigon,, F., Saggese,, G., Bertelloni,, S. and Buzi,, F.. "McCune-Albright Syndrome: A Clinical Longitudinal Study of 32 Patients" Journal of Pediatric Endocrinology and Metabolism, vol. 12, no. 6, 1999, pp. 817-826. https://doi.org/10.1515/JPEM.1999.12.6.817

de Sanctis,, C., Lala,, R., Matarazzo,, P., Balsamo,, A., Bergamaschi,, R., Cappa,, M., Cisternino,, M., de Sanctis,, V., Lucci,, M., Franzese,, A., Ghizzoni,, L., Pasquino,, A., Segni,, M., Rigon,, F., Saggese,, G., Bertelloni,, S. & Buzi,, F. (1999). McCune-Albright Syndrome: A Clinical Longitudinal Study of 32 Patients. Journal of Pediatric Endocrinology and Metabolism, 12(6), 817-826. https://doi.org/10.1515/JPEM.1999.12.6.817

de Sanctis,, C., Lala,, R., Matarazzo,, P., Balsamo,, A., Bergamaschi,, R., Cappa,, M., Cisternino,, M., de Sanctis,, V., Lucci,, M., Franzese,, A., Ghizzoni,, L., Pasquino,, A., Segni,, M., Rigon,, F., Saggese,, G., Bertelloni,, S. and Buzi,, F. (1999) McCune-Albright Syndrome: A Clinical Longitudinal Study of 32 Patients. Journal of Pediatric Endocrinology and Metabolism, Vol. 12 (Issue 6), pp. 817-826. https://doi.org/10.1515/JPEM.1999.12.6.817

de Sanctis,, C., Lala,, R., Matarazzo,, P., Balsamo,, A., Bergamaschi,, R., Cappa,, M., Cisternino,, M., de Sanctis,, V., Lucci,, M., Franzese,, A., Ghizzoni,, L., Pasquino,, A.M., Segni,, M., Rigon,, F., Saggese,, G., Bertelloni,, S. and Buzi,, F.. "McCune-Albright Syndrome: A Clinical Longitudinal Study of 32 Patients" Journal of Pediatric Endocrinology and Metabolism 12, no. 6 (1999): 817-826. https://doi.org/10.1515/JPEM.1999.12.6.817

de Sanctis, C, Lala, R, Matarazzo, P, Balsamo, A, Bergamaschi, R, Cappa, M, Cisternino, M, de Sanctis, V, Lucci, M, Franzese, A, Ghizzoni, L, Pasquino, A, Segni, M, Rigon, F, Saggese, G, Bertelloni, S, Buzi, F. McCune-Albright Syndrome: A Clinical Longitudinal Study of 32 Patients. Journal of Pediatric Endocrinology and Metabolism. 1999;12(6): 817-826. https://doi.org/10.1515/JPEM.1999.12.6.817

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Articles in the same Issue

TABLE OF CONTENTS
Body Composition Measurement: A Hierarchy of Methods
McCune-Albright Syndrome: A Clinical Longitudinal Study of 32 Patients
Ullrich-Turner Syndrome: Relevance of Searching for Y Chromosome Fragments
Effects of 12 Months rhGH Treatment on Bone and Collagen Turnover in Children with Constitutional Growth Delay
Leptin Concentrations in Precocious Puberty or Untimely Puberty With and Without GnRH Analogue Therapy
Arginine Infusion and/or Acute Changes of Growth Hormone Levels do Not Acutely Alter Leptin Serum Levels
Changes in Leptin, Insulin, and Body Composition in Obese Children During a Weight Reduction Program
Diurnal Rhythm in Serum Leptin
Developmental Outcome of Offspring of Pregestational Diabetic Mothers
Successful Therapy with Calcium Channel Blocker (Nifedipine) in Persistent Neonatal Hyperinsulinemic Hypoglycemia of Infancy
Correlation among Markers of Renal Osteodystrophy in Pediatric Hemodialysis Patients
HLA-DQ Genotype in Early Onset Insulin Dependent Diabetes Mellitus
A Boy Presenting with Familial Short Stature - Diagnosis Gitelman Syndrome
Virilising 21-Hydroxylase Deficiency: Timing of Newborn Screening and Confirmatory Tests can be Crucial
Prediabetes: An Unusual Case
Pituitary Gigantism Causing Diabetic Ketoacidosis
BOOK REVIEWS. CALENDAR. INDEX

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https://doi.org/10.1515/JPEM.1999.12.6.817

Articles in the same Issue

TABLE OF CONTENTS
Body Composition Measurement: A Hierarchy of Methods
McCune-Albright Syndrome: A Clinical Longitudinal Study of 32 Patients
Ullrich-Turner Syndrome: Relevance of Searching for Y Chromosome Fragments
Effects of 12 Months rhGH Treatment on Bone and Collagen Turnover in Children with Constitutional Growth Delay
Leptin Concentrations in Precocious Puberty or Untimely Puberty With and Without GnRH Analogue Therapy
Arginine Infusion and/or Acute Changes of Growth Hormone Levels do Not Acutely Alter Leptin Serum Levels
Changes in Leptin, Insulin, and Body Composition in Obese Children During a Weight Reduction Program
Diurnal Rhythm in Serum Leptin
Developmental Outcome of Offspring of Pregestational Diabetic Mothers
Successful Therapy with Calcium Channel Blocker (Nifedipine) in Persistent Neonatal Hyperinsulinemic Hypoglycemia of Infancy
Correlation among Markers of Renal Osteodystrophy in Pediatric Hemodialysis Patients
HLA-DQ Genotype in Early Onset Insulin Dependent Diabetes Mellitus
A Boy Presenting with Familial Short Stature - Diagnosis Gitelman Syndrome
Virilising 21-Hydroxylase Deficiency: Timing of Newborn Screening and Confirmatory Tests can be Crucial
Prediabetes: An Unusual Case
Pituitary Gigantism Causing Diabetic Ketoacidosis
BOOK REVIEWS. CALENDAR. INDEX