Stefano Stagi

Summary

Country: Italy

Publications

  1. doi request reprint Partial growth hormone deficiency and changed bone quality and mass in type I trichorhinophalangeal syndrome
    Stefano Stagi
    Pediatric Endocrinology Unit, University of Florence, A Meyer Children s Hospital, Florence, Italy
    Am J Med Genet A 146:1598-604. 2008
  2. pmc The ever-expanding conundrum of primary osteoporosis: aetiopathogenesis, diagnosis, and treatment
    Stefano Stagi
    Health Sciences Department, University of Florence, Anna Meyer Children s University Hospital, Florence, Italy
    Ital J Pediatr 40:55. 2014
  3. pmc Coeliac disease and risk for other autoimmune diseases in patients with Williams-Beuren syndrome
    Stefano Stagi
    Department of Health Sciences, University of Florence, Anna Meyer Children s University Hospital, Florence, Italy
    BMC Med Genet 15:61. 2014
  4. ncbi request reprint Vitamin D levels and effects of vitamin D replacement in children with periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome
    Stefano Stagi
    Health s Sciences Department, University of Florence, Anna Meyer Children s University Hospital, Florence, Italy Electronic address
    Int J Pediatr Otorhinolaryngol 78:964-8. 2014
  5. pmc Kawasaki disease in a girl with Turner syndrome: a remarkable association
    Stefano Stagi
    Department of Health Sciences, University of Florence, Anna Meyer Children s University Hospital, Florence, Italy
    Ital J Pediatr 40:24. 2014
  6. pmc Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype
    Stefano Stagi
    Health s Sciences Department, University of Florence, Anna Meyer Children s University Hospital, Florence, Italy
    BMC Med Genet 15:16. 2014
  7. doi request reprint Thyroid function and morphology in subjects with microdeletion of chromosome 22q11 (del(22)(q11))
    Stefano Stagi
    Paediatric Endocrinology Unit, University of Florence, Anna Meyer Children s Hospital, Florence, Italy
    Clin Endocrinol (Oxf) 72:839-44. 2010
  8. ncbi request reprint Growth hormone neurosecretory dysfunction in a boy with hypohidrotic/anhidrotic ectodermal dysplasia: definition of short stature, molecular characterization and long-term hGH replacement treatment to final height
    S Stagi
    Paediatric Endocrinology Unit, University of Florence, Anna Meyer Children s Hospital, Florence, Italy
    J Pediatr Endocrinol Metab 22:853-8. 2009
  9. doi request reprint Autoimmune Thyroiditis, Pernicious Anaemia, Vitiligo and Scleroatrophic Lichen in a boy with short-chain acylCoA dehydrogenase deficiency
    Stefano Stagi
    Paediatric Endocrinology Unit, University of Florence, A Meyer Children s Hospital, Florence, Italy
    Horm Res Paediatr 73:409-13. 2010
  10. ncbi request reprint Bone density and metabolism in subjects with microdeletion of chromosome 22q11 (del22q11)
    Stefano Stagi
    Department of Paediatrics, University of Florence, Florence, Italy
    Eur J Endocrinol 163:329-37. 2010

Collaborators

Detail Information

Publications29

  1. doi request reprint Partial growth hormone deficiency and changed bone quality and mass in type I trichorhinophalangeal syndrome
    Stefano Stagi
    Pediatric Endocrinology Unit, University of Florence, A Meyer Children s Hospital, Florence, Italy
    Am J Med Genet A 146:1598-604. 2008
    ..In this report we describe two cases of type I TRPS with partial growth hormone deficiency and significant bone mass and quality impairment, which was unresponsive to GH treatment...
  2. pmc The ever-expanding conundrum of primary osteoporosis: aetiopathogenesis, diagnosis, and treatment
    Stefano Stagi
    Health Sciences Department, University of Florence, Anna Meyer Children s University Hospital, Florence, Italy
    Ital J Pediatr 40:55. 2014
    ..Finally, some options for the treatment of PO will be briefly discussed. ..
  3. pmc Coeliac disease and risk for other autoimmune diseases in patients with Williams-Beuren syndrome
    Stefano Stagi
    Department of Health Sciences, University of Florence, Anna Meyer Children s University Hospital, Florence, Italy
    BMC Med Genet 15:61. 2014
    ..A higher prevalence of coeliac disease (CD) has been reported in patients with Williams-Beuren syndrome (WBS), though coexistence with other autoimmune diseases has not been evaluated...
  4. ncbi request reprint Vitamin D levels and effects of vitamin D replacement in children with periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome
    Stefano Stagi
    Health s Sciences Department, University of Florence, Anna Meyer Children s University Hospital, Florence, Italy Electronic address
    Int J Pediatr Otorhinolaryngol 78:964-8. 2014
    ..The periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis (PFAPA) syndrome is an autoinflammatory disease characterized by regularly recurrent fever episodes due to seemingly unprovoked inflammation...
  5. pmc Kawasaki disease in a girl with Turner syndrome: a remarkable association
    Stefano Stagi
    Department of Health Sciences, University of Florence, Anna Meyer Children s University Hospital, Florence, Italy
    Ital J Pediatr 40:24. 2014
    ..Attention should be given to this phenomenon, as patients with Turner syndrome are themselves at higher risk of cardiovascular defects. Further studies are needed to better clarify this issue...
  6. pmc Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype
    Stefano Stagi
    Health s Sciences Department, University of Florence, Anna Meyer Children s University Hospital, Florence, Italy
    BMC Med Genet 15:16. 2014
    ..In monosomy 1p36, the presence of obesity is poorly defined, and glucose metabolism deficiency is rarely reported. However, the presence of a typical Prader-Willi-like phenotype in patients with monosomy 1p36 is controversial...
  7. doi request reprint Thyroid function and morphology in subjects with microdeletion of chromosome 22q11 (del(22)(q11))
    Stefano Stagi
    Paediatric Endocrinology Unit, University of Florence, Anna Meyer Children s Hospital, Florence, Italy
    Clin Endocrinol (Oxf) 72:839-44. 2010
    ..Abnormalities of thyroid function are sporadically reported in this syndrome, but very few studies have specifically assessed this issue, and thyroid morphology has not been systematically studied...
  8. ncbi request reprint Growth hormone neurosecretory dysfunction in a boy with hypohidrotic/anhidrotic ectodermal dysplasia: definition of short stature, molecular characterization and long-term hGH replacement treatment to final height
    S Stagi
    Paediatric Endocrinology Unit, University of Florence, Anna Meyer Children s Hospital, Florence, Italy
    J Pediatr Endocrinol Metab 22:853-8. 2009
    ....
  9. doi request reprint Autoimmune Thyroiditis, Pernicious Anaemia, Vitiligo and Scleroatrophic Lichen in a boy with short-chain acylCoA dehydrogenase deficiency
    Stefano Stagi
    Paediatric Endocrinology Unit, University of Florence, A Meyer Children s Hospital, Florence, Italy
    Horm Res Paediatr 73:409-13. 2010
    ..As has been reported in other mitochondrial disorders, we hypothesised that autoimmune diseases are also present in SCAD deficiency. Furthermore, we discuss the possible pathogenetic relationship between these diseases...
  10. ncbi request reprint Bone density and metabolism in subjects with microdeletion of chromosome 22q11 (del22q11)
    Stefano Stagi
    Department of Paediatrics, University of Florence, Florence, Italy
    Eur J Endocrinol 163:329-37. 2010
    ..Although hypoparathyroidism with hypocalcaemia is one of the most frequent clinical features of monoallelic microdeletion of chromosome 22q11 (22q11DS), bone mass and metabolism have not yet been assessed in these patients...
  11. doi request reprint Final height in patients perinatally infected with the human immunodeficiency virus
    S Stagi
    Department of Paediatrics, Anna Meyer Children s University Hospital, Florence, Italy
    Horm Res Paediatr 74:165-71. 2010
    ..Data concerning final height are completely lacking in human immunodeficiency virus (HIV)-infected children...
  12. doi request reprint Increased risk of coeliac disease in patients with congenital hypothyroidism
    Stefano Stagi
    Department of Paediatrics, University of Florence, Anna Meyer Children s Hospital, Italy
    Horm Res Paediatr 76:186-92. 2011
    ..In patients with congenital hypothyroidism (CH), the presence of coeliac disease (CD) has been sporadically described...
  13. ncbi request reprint Congenital hypothyroidism in Young-Simpson syndrome
    S Stagi
    Paediatric Endocrinology Unit, Department of Paediatrics, University of Florence, A Meyer Children s Hospital, Florence, Italy
    J Pediatr Endocrinol Metab 21:1089-92. 2008
    ..It is important to underline that the association of congenital hypothyroidism, blepharophimosis and ptosis allows an exact clinical diagnosis, since the majority of other clinical aspects are common to other disorders...
  14. doi request reprint Thyroid hypoplasia as a cause of congenital hypothyroidism in Williams syndrome
    S Stagi
    Pediatric Endocrinology Unit, Department of Pediatrics, University of Florence, Florence, Italy
    Horm Res 70:316-8. 2008
    ....
  15. ncbi request reprint Thyroid function and morphology in patients affected by Williams syndrome
    Stefano Stagi
    Paediatric Endocrinology Unit, Univeristy of Florence, A Meyer Children s Hospital, Florence, Italy
    Clin Endocrinol (Oxf) 63:456-60. 2005
    ..To evaluate the prevalence of abnormalities of thyroid function and morphology in a cohort of patients with Williams syndrome (WS)...
  16. ncbi request reprint Precocious puberty in a girl with floating-harbor syndrome
    Stefano Stagi
    Paediatric Endocrinology Unit, University of Florence, Italy
    J Pediatr Endocrinol Metab 20:1333-7. 2007
    ..20 SDS). This report suggests that, in patients with FHS, precocious puberty should be taken into consideration; in these patients, a careful endocrinological followup for the possible presence of growth and pubertal disorders is needed...
  17. ncbi request reprint Bone status evaluation with calcaneal ultrasound in children with chronic rheumatic diseases. A one year followup study
    Fernanda Falcini
    Department of Pediatrics, Rheumatology Unit, University of Florence, Italy
    J Rheumatol 30:179-84. 2003
    ..To evaluate at baseline and after one year the bone status in children with chronic rheumatic diseases (CRD) using quantitative ultrasound techniques...
  18. ncbi request reprint Changed bone status in human immunodeficiency virus type 1 (HIV-1) perinatally infected children is related to low serum free IGF-I
    Stefano Stagi
    Department of Paediatrics, University of Florence, Anna Meyer Children s Hospital, Florence, Italy
    Clin Endocrinol (Oxf) 61:692-9. 2004
    ..Adults and children affected by human immunodeficiency virus type-1 (HIV-1) infection show bone demineralization. Little is known about skeletal status using a quantitative high-frequency ultrasound (QUS) technique in these patients...
  19. ncbi request reprint Thyroid function and anti-thyroid autoantibodies in untreated children with vertically acquired chronic hepatitis C virus infection
    Giuseppe Indolfi
    Department of Paediatrics, University of Florence, Anna Meyer Children s Hospital, Florence, Italy
    Clin Endocrinol (Oxf) 68:117-21. 2008
    ..We investigated thyroid function and anti-thyroid autoantibodies in a cohort of untreated children with vertically acquired, chronic, HCV infection...
  20. ncbi request reprint Osteoprotegerin serum levels in children with type 1 diabetes: a potential modulating role in bone status
    Fiorella Galluzzi
    Department of Paediatrics, A Meyer Children s Hospital, Via Luca Giordano 13, 50132 Florence, Italy
    Eur J Endocrinol 153:879-85. 2005
    ....
  21. ncbi request reprint Williams-beuren syndrome is a genetic disorder associated with impaired glucose tolerance and diabetes in childhood and adolescence: new insights from a longitudinal study
    Stefano Stagi
    Department of Health Sciences, University of Florence, Chieti, Italy
    Horm Res Paediatr 82:38-43. 2014
    ..However, few and sporadic data are available in children, adolescents, and young adults with WBS...
  22. ncbi request reprint Oral clonidine provocative test in the diagnosis of growth hormone deficiency in childhood: should we make the timing uniform?
    Fiorella Galluzzi
    Paediatrics Endocrinology Unit, Department of Paediatrics, University of Florence, Florence, Italy
    Horm Res 66:285-8. 2006
    ....
  23. ncbi request reprint Thyroid hypoplasia of the left lobe in two girls affected by Williams syndrome
    Stefano Stagi
    Paediatric Endocrinology Unit, Department of Paediatrics, University of Florence, A Meyer Children s Hospital, Florence, Italy
    Clin Dysmorphol 12:267-8. 2003
    ..However, thyroid function in these patients is rarely studied. This paper reports thyroid hypoplasia of the left lobe in two girls affected by Williams syndrome, suggesting that it may be a feature of this syndrome...
  24. ncbi request reprint Undetectable serum IgA and low IgM concentration in children with congenital hypothyroidism
    Stefano Stagi
    Pediatric Endocrinology Unit, A Meyer Children Hospital, Florence, Italy
    Clin Immunol 116:94-8. 2005
    ..IgA and IgM deficiency is correlated with the severity of congenital hypothyroidism and may help to evaluate the duration and severity of thyroid hormone deficiency during prenatal life...
  25. ncbi request reprint Diagnosis of growth hormone deficiency by using the arginine provocative test: is it possible to shorten testing time without altering validity?
    Fiorella Galluzzi
    Paediatric Endocrinolgy Unit, Department of Paediatrics, University of Florence, and Azienda Ospedaliero Universitaria Meyer, IT 50100 Florence, Italy
    Horm Res 72:142-5. 2009
    ..The arginine test is used for the diagnosis of growth hormone deficiency (GHD), but its duration is not uniform and varies from 180 to 90 min...
  26. ncbi request reprint Association of low bone mass with vitamin d receptor gene and calcitonin receptor gene polymorphisms in juvenile idiopathic arthritis
    Laura Masi
    Department of Pediatrics, University of Florence, Florence, Italy
    J Rheumatol 29:2225-31. 2002
    ..To compare bone density with polymorphisms in the calcitonin receptor (CTR) and vitamin D receptor (VDR) genes in 50 patients with juvenile idiopathic arthritis and 80 matched controls...
  27. ncbi request reprint Increased prevalence of growth hormone deficiency in patients with vernal keratoconjuntivitis; An interesting new association
    Stefano Stagi
    Department of Health s Sciences, University of Florence, Florence, Italy
    Hormones (Athens) 13:382-8. 2014
    ..The notable difference between genders and VKC's resolution with puberty have persistently suggested a role of hormonal factors in VKC development...
  28. ncbi request reprint Age-dependent association of exposure to television screen with children's urinary melatonin excretion?
    Roberto Salti
    Department of Pediatrics, University of Florence, Florence, Italy
    Neuro Endocrinol Lett 27:73-80. 2006
    ....