D Larizza

Summary

Affiliation: University of Pavia
Country: Italy

Publications

  1. ncbi request reprint Parental GM and HLA genotypes and reduced birth weight in patients with Turner's syndrome
    Daniela Larizza
    Department of Pediatrics, University of Pavia, Italy
    J Pediatr Endocrinol Metab 15:1183-90. 2002
  2. ncbi request reprint Unusual presentation of juvenile granulosa cell tumor of the ovary
    D Larizza
    Department of Pediatric Sciences, IRCCS Policlinico San Matteo, 27100 Pavia, Italy
    J Endocrinol Invest 29:653-6. 2006
  3. doi request reprint Thyroid ultrasound in patients with Turner syndrome: influence of clinical and auxological parameters
    V Calcaterra
    Department of Pediatrics, University of Pavia and IRCCS Policlinico San Matteo Foundation, P le Golgi 2, 27100 Pavia, Italy
    J Endocrinol Invest 34:260-4. 2011
  4. doi request reprint Common immunogenetic profile in children with multiple autoimmune diseases: the signature of HLA-DQ pleiotropic genes
    Daniela Larizza
    Department of Pediatrics, IRCCS Policlinico S Matteo Foundation, Pavia, Italy
    Autoimmunity 45:470-5. 2012
  5. doi request reprint Autoimmune stigmata in Turner syndrome: when lacks an X chromosome
    Daniela Larizza
    Department of Pediatric Sciences, University of Pavia, Foundation IRCCS Policlinico San Matteo, Pavia, Italy
    J Autoimmun 33:25-30. 2009
  6. ncbi request reprint Helicobacter pylori infection and autoimmune thyroid disease in young patients: the disadvantage of carrying the human leukocyte antigen-DRB1*0301 allele
    Daniela Larizza
    Department of Pediatric Sciences, University of Pavia and Istituto di Ricovero e Cura a Carattere Scientifico Policlinico San Matteo, 27100 Pavia, Italy
    J Clin Endocrinol Metab 91:176-9. 2006
  7. ncbi request reprint Familial occurrence of Turner syndrome: casual event or increased risk?
    Daniela Larizza
    Department of Pediatrics, University of Pavia and IRCCS Policlinico San Matteo Foundation, Pavia, Italy
    J Pediatr Endocrinol Metab 24:223-5. 2011
  8. doi request reprint Early-onset metabolic syndrome in prepubertal obese children and the possible role of alanine aminotransferase as marker of metabolic syndrome
    V Calcaterra
    Department of Pediatrics, University of Pavia, Pavia, Italy
    Ann Nutr Metab 58:307-14. 2011
  9. pmc Targeting the immunogenetic diseases with the appropriate HLA molecular typing: critical appraisal on 2666 patients typed in one single centre
    M Guarene
    Laboratorio di Immunogenetica, Servizio di Immunoematologia e Medicina Trasfusionale, Fondazione IRCCS Policlinico San Matteo, 27100 Pavia, Italy
    Biomed Res Int 2013:904247. 2013
  10. ncbi request reprint Prevalence and incidence of scoliosis in Turner syndrome: a study in 49 girls followed-up for 4 years
    S Ricotti
    Rehabilitation Unit, Department of Services and Diagnostic Medicine, Policlinico San Matteo Pavia IRCCS Foundation, University of Pavia, Pavia, Italy
    Eur J Phys Rehabil Med 47:447-53. 2011

Collaborators

Detail Information

Publications30

  1. ncbi request reprint Parental GM and HLA genotypes and reduced birth weight in patients with Turner's syndrome
    Daniela Larizza
    Department of Pediatrics, University of Pavia, Italy
    J Pediatr Endocrinol Metab 15:1183-90. 2002
    ..These data might suggest a negative effect of genetic similarity on intrauterine growth in Turner's syndrome...
  2. ncbi request reprint Unusual presentation of juvenile granulosa cell tumor of the ovary
    D Larizza
    Department of Pediatric Sciences, IRCCS Policlinico San Matteo, 27100 Pavia, Italy
    J Endocrinol Invest 29:653-6. 2006
    ..We present a case report of juvenile granulosa cell tumor of the ovary (JGCT) with an unusual clinical presentation and hormonal secretion...
  3. doi request reprint Thyroid ultrasound in patients with Turner syndrome: influence of clinical and auxological parameters
    V Calcaterra
    Department of Pediatrics, University of Pavia and IRCCS Policlinico San Matteo Foundation, P le Golgi 2, 27100 Pavia, Italy
    J Endocrinol Invest 34:260-4. 2011
    ....
  4. doi request reprint Common immunogenetic profile in children with multiple autoimmune diseases: the signature of HLA-DQ pleiotropic genes
    Daniela Larizza
    Department of Pediatrics, IRCCS Policlinico S Matteo Foundation, Pavia, Italy
    Autoimmunity 45:470-5. 2012
    ....
  5. doi request reprint Autoimmune stigmata in Turner syndrome: when lacks an X chromosome
    Daniela Larizza
    Department of Pediatric Sciences, University of Pavia, Foundation IRCCS Policlinico San Matteo, Pavia, Italy
    J Autoimmun 33:25-30. 2009
    ..Medical care for patients with TS should routinely include screening for the autoimmune disorders in order to assure early detection and appropriate treatment...
  6. ncbi request reprint Helicobacter pylori infection and autoimmune thyroid disease in young patients: the disadvantage of carrying the human leukocyte antigen-DRB1*0301 allele
    Daniela Larizza
    Department of Pediatric Sciences, University of Pavia and Istituto di Ricovero e Cura a Carattere Scientifico Policlinico San Matteo, 27100 Pavia, Italy
    J Clin Endocrinol Metab 91:176-9. 2006
    ..We evaluated the prevalence of Hp antibodies in young ATD patients and investigated the possibility that a susceptible immunogenetic profile could influence the development of ATD in subjects with Hp infection...
  7. ncbi request reprint Familial occurrence of Turner syndrome: casual event or increased risk?
    Daniela Larizza
    Department of Pediatrics, University of Pavia and IRCCS Policlinico San Matteo Foundation, Pavia, Italy
    J Pediatr Endocrinol Metab 24:223-5. 2011
    ..The prevalence of Turner syndrome (TS) at birth has been estimated as approximately 1 in 2500 live female births. An increased risk of TS in subsequent pregnancies for couples who already have a daughter with TS has not been reported...
  8. doi request reprint Early-onset metabolic syndrome in prepubertal obese children and the possible role of alanine aminotransferase as marker of metabolic syndrome
    V Calcaterra
    Department of Pediatrics, University of Pavia, Pavia, Italy
    Ann Nutr Metab 58:307-14. 2011
    ..We evaluated the prevalence of MS in prepubertal obese children and the usefulness of ALT as an MS marker...
  9. pmc Targeting the immunogenetic diseases with the appropriate HLA molecular typing: critical appraisal on 2666 patients typed in one single centre
    M Guarene
    Laboratorio di Immunogenetica, Servizio di Immunoematologia e Medicina Trasfusionale, Fondazione IRCCS Policlinico San Matteo, 27100 Pavia, Italy
    Biomed Res Int 2013:904247. 2013
    ..For this reason, we suggest the Italian Scientific Society of Immunogenetics to establish guidelines to improve the appropriateness of typing requests...
  10. ncbi request reprint Prevalence and incidence of scoliosis in Turner syndrome: a study in 49 girls followed-up for 4 years
    S Ricotti
    Rehabilitation Unit, Department of Services and Diagnostic Medicine, Policlinico San Matteo Pavia IRCCS Foundation, University of Pavia, Pavia, Italy
    Eur J Phys Rehabil Med 47:447-53. 2011
    ..Turner syndrome (TS) is a sex chromosome abnormality in females characterized by gonadal dysgenesis, short stature and skeletal malformations like kyphosis and scoliosis...
  11. doi request reprint Utility of breast ultrasonography in the diagnostic work-up of precocious puberty and proposal of a prognostic index for identifying girls with rapidly progressive central precocious puberty
    V Calcaterra
    Department of Pediatrics, University of Pavia and IRCCS Policlinico San Matteo, Pavia, Italy
    Ultrasound Obstet Gynecol 33:85-91. 2009
    ....
  12. doi request reprint Thrombophilic screening in Turner syndrome
    V Calcaterra
    Department of Pediatrics, IRCCS Policlinico S Matteo Foundation, Pavia, Italy
    J Endocrinol Invest 34:676-9. 2011
    ....
  13. ncbi request reprint Prevalence of metabolic syndrome (MS) in children and adolescents with varying degrees of obesity
    V Calcaterra
    Department of Pediatric Sciences, Fondazione IRCCS Policlinico San Matteo and University of Pavia, Pavia, Italy
    Clin Endocrinol (Oxf) 68:868-72. 2008
    ..We estimated the prevalence of MS in Caucasian children and adolescents with varying degrees of obesity...
  14. ncbi request reprint Prospective evaluation of aortic dimensions in Turner syndrome: a 2-dimensional echocardiographic study
    Luca Lanzarini
    Department of Cardiology, IRCCS Policlinico S Matteo, University of Pavia, Pavia, Italy
    J Am Soc Echocardiogr 20:307-13. 2007
    ....
  15. ncbi request reprint Aortic dimensions in Turner's syndrome: two-dimensional echocardiography versus magnetic resonance imaging
    Luca Lanzarini
    Department of Cardiology, IRCCS Policlinico S Matteo, University of Pavia, Pavia, Italy
    J Cardiovasc Med (Hagerstown) 8:428-37. 2007
    ..Patients with Turner's syndrome have an increased risk of cardiac death caused by aortic disease. Consensus has not been reached about the best method to image the aorta in this syndrome...
  16. ncbi request reprint Identification of sixty-two novel and twelve known FBN1 mutations in eighty-one unrelated probands with Marfan syndrome and other fibrillinopathies
    Eloisa Arbustini
    Cardiovascular Genetic Laboratory Transplant Research Area GISM Interdisciplinary Group for Marfan Syndrome, IRCCS Policlinico San Matteo and University of Pavia, Pavia, Italy
    Hum Mutat 26:494. 2005
    ..5%). Most mutations (67.9%) occurred in cbEGF-like modules. Genotype was clinically relevant for early diagnosis and conclusion of the diagnostic work-up in patients with incomplete or atypical phenotypes...
  17. ncbi request reprint Adiponectin, IL-10 and metabolic syndrome in obese children and adolescents
    Valeria Calcaterra
    Department of Pediatrics, Found IRCCS Policlinico San Matteo and University of Pavia, Pavia, Italy
    Acta Biomed 80:117-23. 2009
    ..Our obese children showed hypoadiponectin and hyper-IL10 values. MetS was not associated with low IL-10. We probably observe a first phase of the complex mechanism implicated in the development of the MetS in children...
  18. ncbi request reprint Pregnancy in a woman with Turner syndrome and celiac disease
    V Calcaterra
    Department of Pediatric Sciences, University of Pavia and Fondazione IRCCS Policlinico San Matteo, 27100 Pavia, Italy
    J Endocrinol Invest 30:598-600. 2007
    ..We report the case of a patient, affected by Turner syndrome and celiac disease, in whom a spontaneous pregnancy occurred...
  19. ncbi request reprint Reduced sebum production in turner syndrome: a study of twenty-two patients
    V Brazzelli
    Department of Human and Hereditary Pathology, Institute of Dermatology, University of Pavia and Foundation IRCCS Policlinico S Matteo, Pavia, Italy
    Int J Immunopathol Pharmacol 24:789-92. 2011
    ..62 UA, p<0.001) and this significant difference was found in every facial zone. The reduction of sebum secretion may explain, using a simple and non-invasive method, the absence or the low incidence of acne in TS patients...
  20. ncbi request reprint Pelvic ultrasound evaluation in patients with Turner syndrome during treatment with growth hormone
    P Sampaolo
    Department of Obstetrics and Gynecology, IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy
    Ultrasound Obstet Gynecol 22:172-7. 2003
    ..Since GH interacts with gonadotropins in the stimulation of the human ovary, the aim of our study was to evaluate the possible effects of GH administration on uterine and ovarian characteristics...
  21. ncbi request reprint Recurrence of giant juvenile breast fibroadenoma in a girl with Turner's syndrome
    V Calcaterra
    Department of Pediatric Sciences, Foundation IRCCS Policlinico San Matteo and University of Pavia, Pavia, Italy
    J Pediatr Endocrinol Metab 22:281-3. 2009
    ..Such masses are called solitary giant juvenile fibroadenomas, and local recurrence is unusual. We report here a case of recurrent juvenile giant breast fibroadenoma in a girl with Turner's syndrome...
  22. doi request reprint Agenesis of internal carotid artery and hypopituitarism: case report and review of literature
    S Savasta
    Clinica Pediatrica, Piazzale Golgi 19, Fondazione Instituto di Ricovero e Cura a Carattere Scientifico Policlinico San Matteo, 27100 Pavia, Italy
    J Clin Endocrinol Metab 97:3414-20. 2012
    ..We describe one pediatric case of agenesis of the internal carotid artery with hypopituitarism and review other known cases...
  23. doi request reprint Acquired ichthyosis in a child with autoimmune thyroiditis
    Valeria Brazzelli
    Department of Human and Hereditary Pathology, Institute of Dermatology, University of Pavia and Foundation IRCCS Policlinico S Matteo, Pavia, Italy
    Pediatr Dermatol 27:413-4. 2010
    ..We describe a child with acquired ichthyosis in whom an autoimmune hypothyroidism was detected; furthermore, replacement therapy with L-thyroxine resulted in complete remission of ichthyosis...
  24. ncbi request reprint Halo nevus, rather than vitiligo, is a typical dermatologic finding of turner's syndrome: clinical, genetic, and immunogenetic study in 72 patients
    Valeria Brazzelli
    Department of Human and Hereditary Pathology, Institute of Dermatology, University of Pavia and IRCCS Policlinico S Matteo, Italy
    J Am Acad Dermatol 51:354-8. 2004
    ..19). In conclusion, this study is the first to demonstrate an increased prevalence of HN for patients with TS. Furthermore, the data suggest that a HN putative susceptibility gene in TS is located close to the HLA-C locus...
  25. ncbi request reprint Two sisters with 45,X karyotype: influence of genomic imprinting on phenotype and cognitive profile
    Daniela Larizza
    Eur J Pediatr 161:224-5. 2002
  26. ncbi request reprint Horseshoe kidney malformation in Turner syndrome is not associated with HNF-1beta gene mutations
    Elena D'Amato
    Department of Paediatrics, University of Genoa, IRCCS G Gaslini Institute, Largo Gaslini 5, 16147 Genoa, Italy
    Pediatr Nephrol 23:137-40. 2008
    ....
  27. ncbi request reprint Delineation of the ADULT syndrome phenotype due to arginine 298 mutations of the p63 gene
    Tuula Rinne
    1Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
    Eur J Hum Genet 14:904-10. 2006
    ..In addition, we have documented a gain-of-function effect on the dNp63gamma isoform caused by this mutation. We discuss the possible relevance of oral squamous cell carcinoma in one patient, who carries this p63 germline mutation...
  28. doi request reprint Variations of the perforin gene in patients with type 1 diabetes
    Elisabetta Orilieri
    Interdisciplinary Research Center of Autoimmune Diseases and Department of Medical Sciences, A Avogadro University of Eastern Piedmont, Novara, Italy
    Diabetes 57:1078-83. 2008
    ..The aim of this work was to investigate the role of PRF1 variations in type 1 diabetes...
  29. ncbi request reprint Do reduced levels of steroid 21-hydroxylase confer a survival advantage in fetuses affected by sex chromosome aberrations?
    Vilma Mantovani
    Laboratorio Centralizzato Settore Genetica, Policlinico S Orsola Malpighi, Bologna, Italy
    Eur J Hum Genet 10:137-40. 2002
    ..It may be hypothesised that reduced levels of steroid 21-hydroxylase could confer a survival advantage, leading to a successful pregnancy...