about
Endocrine implications of neurofibromatosis 1 in childhoodLack of red hair phenotype in a North-African obese child homozygous for a novel POMC null mutation: nonsense-mediated decay RNA evaluation and hair pigment chemical analysisIntradermal skin test with diabetes specific antigens in patients with type 1 diabetesEarly retesting by GHRH + arginine test shows normal GH response in most children with idiopathic GH deficiency.Bone and body composition analyzed by Dual-energy X-ray Absorptiometry (DXA) in clinical and nutritional evaluation of young patients with Cystic Fibrosis: a cross-sectional study.Lipoid congenital adrenal hyperplasia by steroidogenic acute regulatory protein (STAR) gene mutation in an Italian infant: an uncommon cause of adrenal insufficiency.No protective effect of calcitriol on beta-cell function in recent-onset type 1 diabetes: the IMDIAB XIII trial.A mixture of oleic, erucic and conjugated linoleic acids modulates cerebrospinal fluid inflammatory markers and improve somatosensorial evoked potential in X-linked adrenoleukodystrophy female carriers.Permanent diabetes during the first year of life: multiple gene screening in 54 patientsMinimal incidence of neonatal/infancy onset diabetes in Italy is 1:90,000 live birthsEffect of calcitriol on bone turnover and osteocalcin in recent-onset type 1 diabetes.Congenital primary adrenal insufficiency and selective aldosterone defects presenting as salt-wasting in infancy: a single center 10-year experience.Adrenoleukodystrophy.Celiac disease and endocrine autoimmune disorders in children: an update.Autoimmune diseases and celiac disease which came first: genotype or gluten?Early and progressive insulin resistance in young, non-obese cancer survivors treated with hematopoietic stem cell transplantation.Family history and ethnicity influencing clinical presentation of type 1 diabetes in childhood.Triple A (Allgrove) syndrome: an unusual association with syringomyelia.Diabetes-related autoantibodies in children with acute lymphoblastic leukemiaPartially reversible hypopituitarism in an adolescent with a rathke cleft cyst.Abnormal glucose tolerance in children with cystic fibrosis: the predictive role of continuous glucose monitoring system.Children with Prader-Willi syndrome exhibit more evident meal-induced responses in plasma ghrelin and peptide YY levels than obese and lean children.Glucose tolerance affects pubertal growth and final height of children with cystic fibrosis.Results of early reevaluation of growth hormone secretion in short children with apparent growth hormone deficiency.Combined therapy with insulin and growth hormone in 17 patients with type-1 diabetes and growth disorders.Incidence of insulin-dependent diabetes mellitus among Sardinian-heritage children born in Lazio region, Italy.A novel heterozygous mutation of the AIRE gene in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED).The Gly972-->Arg IRS-1 variant is associated with type 1 diabetes in continental Italy.Maintenance of a normal meal-induced decrease in plasma ghrelin levels in children with Prader-Willi syndrome.A randomized trial of nicotinamide and vitamin E in children with recent onset type 1 diabetes (IMDIAB IX).A case of primary selective hypoaldosteronism carrying three mutations in the aldosterone synthase (Cyp11b2) gene.Plasma levels of adrenomedullin in patients with adrenoleukodystrophy/adrenomyeloneuropathy.Birth weight influences the clinical phenotype and the metabolic control of patients with type 1 diabetes (T1D).Growth hormone treatment improves final height and nutritional status of children with chronic kidney disease and growth deceleration.Ovarian hyperandrogenism in adolescents and young women with type I diabetes is primarily related to birth weight and body mass index.Effects of replacement therapy on sleep architecture in children with growth hormone deficiency.Sleep characteristics in children with growth hormone deficiency.NREM sleep architecture and relation to GH/IGF-1 axis in Laron syndrome.Blue eyes as a risk factor for type 1 diabetes.Sexual dimorphism in growth and insulin-like growth factor-I in children with type 1 diabetes mellitus.
P50
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P50
description
hulumtuese
@sq
onderzoeker
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researcher
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հետազոտող
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name
Carla Bizzarri
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Carla Bizzarri
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Carla Bizzarri
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Carla Bizzarri
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Carla Bizzarri
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Carla Bizzarri
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Carla Bizzarri
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Carla Bizzarri
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Carla Bizzarri
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Carla Bizzarri
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Carla Bizzarri
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Carla Bizzarri
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Carla Bizzarri
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Carla Bizzarri
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Carla Bizzarri
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P106
P1153
7004263074
P21
P31
P496
0000-0002-5616-9185