Published in J Clin Endocrinol Metab on October 16, 2009
Evaluation of the hypothalamic-pituitary-adrenal axis and its relationship with central respiratory dysfunction in children with Prader-Willi syndrome. Orphanet J Rare Dis (2015) 0.75
Does priming with sex steroids improve the diagnosis of normal growth hormone secretion in short children? Indian J Endocrinol Metab (2014) 0.75
Adrenal function: A gold standard test for adrenal insufficiency in children? Nat Rev Endocrinol (2010) 0.75
Comprehensive geriatric assessment adds information to Eastern Cooperative Oncology Group performance status in elderly cancer patients: an Italian Group for Geriatric Oncology Study. J Clin Oncol (2002) 3.53
Renal outcome in patients with congenital anomalies of the kidney and urinary tract. Kidney Int (2009) 3.13
The natural history of euthyroid Hashimoto's thyroiditis in children. J Pediatr (2006) 1.95
Growth hormone-releasing hormone resistance in pseudohypoparathyroidism type ia: new evidence for imprinting of the Gs alpha gene. J Clin Endocrinol Metab (2003) 1.67
Corticotropin tests for hypothalamic-pituitary- adrenal insufficiency: a metaanalysis. J Clin Endocrinol Metab (2008) 1.58
Antimicrobial use and Pseudomonas aeruginosa susceptibility profile in a cystic fibrosis centre. Int J Antimicrob Agents (2005) 1.49
KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes. Hum Mutat (2005) 1.47
The 148M allele of the PNPLA3 gene is associated with indices of liver damage early in life. J Hepatol (2010) 1.45
Growth hormone secretory pattern and response to treatment in children with short stature followed to adult height. Clin Endocrinol (Oxf) (2003) 1.45
Outcome of children with neuroblastoma after progression or relapse. A retrospective study of the Italian neuroblastoma registry. Eur J Cancer (2009) 1.44
May T1 diabetes mellitus protect from asthma? Allergol Immunopathol (Madr) (2012) 1.40
Diabetes insipidus--diagnosis and management. Horm Res Paediatr (2012) 1.26
Fungal infections in children with cancer: a prospective, multicenter surveillance study. Pediatr Infect Dis J (2006) 1.25
Neuroblastoma in adolescents: the Italian experience. Cancer (2006) 1.19
Improved survival of children with neuroblastoma between 1979 and 2005: a report of the Italian Neuroblastoma Registry. J Clin Oncol (2010) 1.18
Assessment of adiponectin and leptin as biomarkers of positive metabolic outcomes after lifestyle intervention in overweight and obese children. J Clin Endocrinol Metab (2008) 1.15
The natural history of the normal/mild elevated TSH serum levels in children and adolescents with Hashimoto's thyroiditis and isolated hyperthyrotropinaemia: a 3-year follow-up. Clin Endocrinol (Oxf) (2012) 1.11
Insights into the structure and regulation of glucokinase from a novel mutation (V62M), which causes maturity-onset diabetes of the young. J Biol Chem (2005) 1.11
Seasonal changes in mortality rates from main causes of death in Japan (1970--1999). Eur J Epidemiol (2004) 1.11
Younger age at onset and sex predict celiac disease in children and adolescents with type 1 diabetes: an Italian multicenter study. Diabetes Care (2004) 1.09
Wolfram syndrome: new mutations, different phenotype. PLoS One (2012) 1.08
Other complications and associated conditions with diabetes in children and adolescents. Pediatr Diabetes (2009) 1.07
Results of early reevaluation of growth hormone secretion in short children with apparent growth hormone deficiency. J Pediatr (2002) 1.07
Effect of 2 years of cortisol normalization on the impaired bone mass and turnover in adolescent and adult patients with Cushing's disease: a prospective study. Clin Endocrinol (Oxf) (2003) 1.06
Insulin resistance and secretion indexes in healthy Italian children and adolescents: a multicentre study. Acta Biomed (2009) 1.06
Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutation. Eur J Paediatr Neurol (2007) 1.04
Wolfram syndrome (diabetes insipidus, diabetes, optic atrophy, and deafness): clinical and genetic study. Diabetes Care (2008) 1.03
The diagnosis of children with central diabetes insipidus. J Pediatr Endocrinol Metab (2007) 1.02
Genetic analysis and evaluation of resistance to thyrotropin and growth hormone-releasing hormone in pseudohypoparathyroidism type Ib. J Clin Endocrinol Metab (2007) 1.01
Novel HESX1 mutations associated with a life-threatening neonatal phenotype, pituitary aplasia, but normally located posterior pituitary and no optic nerve abnormalities. J Clin Endocrinol Metab (2006) 1.01
Endocrine aspects of coeliac disease. J Pediatr Endocrinol Metab (2003) 1.01
Evaluation of insulin resistance in a cohort of HIV-infected youth. Eur J Endocrinol (2007) 1.01
19q13.11 cryptic deletion: description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadias. Eur J Hum Genet (2012) 1.00
Non-Hodgkin's lymphoma and type of tobacco smoke. Cancer Epidemiol Biomarkers Prev (2004) 0.98
Vasopressin and desmopressin in central diabetes insipidus: adverse effects and clinical considerations. Pediatr Endocrinol Rev (2004) 0.98
Validation and ease of use of a new pen device for self-administration of recombinant human growth hormone: results from a two-center usability study. Med Devices (Auckl) (2013) 0.98
Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism. Pediatr Res (2003) 0.98
Thyroid morphology and subclinical hypothyroidism in children and adolescents with Williams syndrome. J Pediatr (2007) 0.97
Epidemiology and clinical course of Burkholderia cepacia complex infections, particularly those caused by different Burkholderia cenocepacia strains, among patients attending an Italian Cystic Fibrosis Center. J Clin Microbiol (2004) 0.96
Mutations at the same residue (R50) of Kir6.2 (KCNJ11) that cause neonatal diabetes produce different functional effects. Diabetes (2006) 0.96
Diabetes incidence in 0- to 14-year age-group in Italy: a 10-year prospective study. Diabetes Care (2004) 0.96
Association of alleles at polymorphic sites in the Osteopontin encoding gene in young type 1 diabetic patients. Clin Immunol (2009) 0.95
Cut-off limits of the GH response to GHRH plus arginine test and IGF-I levels for the diagnosis of GH deficiency in late adolescents and young adults. Eur J Endocrinol (2007) 0.94
The accuracy of the glucagon test compared to the insulin tolerance test in the diagnosis of adrenal insufficiency in young children with growth hormone deficiency. J Clin Endocrinol Metab (2010) 0.94
Type 1 diabetes risk for human leukocyte antigen (HLA)-DR3 haplotypes depends on genotypic context: association of DPB1 and HLA class I loci among DR3- and DR4-matched Italian patients and controls. Hum Immunol (2008) 0.94
Peripheral blood stem cell tumor cell contamination and survival of neuroblastoma patients. Clin Cancer Res (2006) 0.93
Role of active follow-up for early diagnosis of relapse after elective end of therapies. Pediatr Blood Cancer (2005) 0.93
Thyroid function in obese children and adolescents. Horm Res Paediatr (2010) 0.92
Severe impairment of bone mass and turnover in Cushing's disease: comparison between childhood-onset and adulthood-onset disease. Clin Endocrinol (Oxf) (2002) 0.91
19q13 microdeletion syndrome: Further refining the critical region. Eur J Med Genet (2012) 0.90
Developmental abnormalities of the posterior pituitary gland. Endocr Dev (2009) 0.89
Matrix metalloproteinase 2 may be a marker of microangiopathy in children and adolescents with type 1 diabetes mellitus. Diabetes Res Clin Pract (2005) 0.89
ISPAD Clinical Practice Consensus Guidelines 2006-2007. Other complications and associated conditions. Pediatr Diabetes (2007) 0.89
Central diabetes insipidus in children and young adults: etiological diagnosis and long-term outcome of idiopathic cases. J Clin Endocrinol Metab (2013) 0.88
High incidence of childhood type 1 diabetes in Liguria, Italy, from 1989 to 1998. Diabetes Care (2003) 0.88
Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche. Eur J Endocrinol (2011) 0.88
Characterization of thyroglobulin epitopes in Sardinian adults and juveniles with Hashimoto's thyroiditis: evidence against a major effect of age and genetic background on B-cell epitopes. Clin Endocrinol (Oxf) (2009) 0.88
Recombinant human GH replacement therapy in children with pseudohypoparathyroidism type Ia: first study on the effect on growth. J Clin Endocrinol Metab (2010) 0.87
Blood ketone bodies in patients with recent-onset type 1 diabetes (a multicenter study). Pediatr Diabetes (2006) 0.87
Variations of the perforin gene in patients with type 1 diabetes. Diabetes (2008) 0.86
Telemedicine in the management of young patients with type 1 diabetes mellitus: a follow-up study. Acta Biomed (2003) 0.86
rs9939609 in the FTO gene is associated with obesity but not with several biochemical parameters in Sardinian obese children. Ann Hum Genet (2011) 0.86
Neuroblastoma in the newborn. A study of the Italian Neuroblastoma Registry. Eur J Cancer (2009) 0.85
Prevalence of type 1 diabetes autoantibodies (GADA, IA2, and IAA) in overweight and obese children. Diabetes Care (2009) 0.85
Use of Attribute Driven Incremental Discretization and Logic Learning Machine to build a prognostic classifier for neuroblastoma patients. BMC Bioinformatics (2014) 0.85
Thyroid function and structure are affected in childhood obesity. J Clin Endocrinol Metab (2008) 0.85
Oral glucose tolerance test in Italian overweight/obese children and adolescents results in a very high prevalence of impaired fasting glycaemia, but not of diabetes. Diabetes Metab Res Rev (2009) 0.84
Pitfalls in the diagnosis of central adrenal insufficiency in children. Endocr Dev (2009) 0.84
MDM2 SNP309 genotype influences survival of metastatic but not of localized neuroblastoma. Pediatr Blood Cancer (2009) 0.84
Malignant neuroblastic tumors in adolescents. Cancer Lett (2005) 0.84
Adult height in patients with permanent growth hormone deficiency with and without multiple pituitary hormone deficiencies. J Clin Endocrinol Metab (2006) 0.84
Outcome of primary endorectal pull-through for the treatment of classic Hirschsprung disease. J Laparoendosc Adv Surg Tech A (2008) 0.84
Bone marrow of neuroblastoma patients shows downregulation of CXCL12 expression and presence of IFN signature. Pediatr Blood Cancer (2011) 0.84
Hirschsprung disease: do risk factors of poor surgical outcome exist? J Pediatr Surg (2008) 0.83
New aspects of the physiology of the GH-IGF-1 axis. Endocr Dev (2013) 0.83
Gene expression profile of human bone marrow stromal cells determined by restriction fragment differential display analysis. J Cell Biochem (2004) 0.83
Effect of body mass index on the growth hormone response to clonidine stimulation testing in children with short stature. Clin Endocrinol (Oxf) (2011) 0.83
The use of neuroimaging for assessing disorders of pituitary development. Clin Endocrinol (Oxf) (2012) 0.83