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Pubblicazioni
HORMONE RESEARCH IN PAEDIATRICS
Rivista
Codice:
E203043
ISSN:
1663-2818
Dati Generali
Dati Generali
Pubblicazioni (29)
Pulisci
Ordina Pubblicazioni:
crescente
decrescente
A new compound heterozygous MRAP-alfa gene mutation in a case of familiar glucocorticoid deficiency due to a mutation of the MC2R
Abstract
Clinical Case of Cushing Syndrome in Secreting NET
Abstract
Clinical and MRI imaging follow-up in a girl with POU1F-1 gene mutation.
Abstract
Congenital hyperinsulinism of infancy: a case of atypical form?
Abstract
Congenital hyperinsulinism of infancy: peculiar characteristics of patients in the italian registry
Abstract
Congenital hyperinsulinism of infancy: the italian National Registry
Abstract
Corticotropin tests for assessment of the hypothalamus-pituitary-adrenal axis in patients with Prader-Willi syndrome
Abstract
De novo IGF1R gene deletion in an IUGR-SGA boy with high IGF1 levels and without catch-up growth
Abstract
GH Stimulated Levels in Prader-Willi Syndrome During the Transition Period between Childhood and Adult
Abstract
GH THERAPY IN A NON-GHD SHORT CHILD WITH SYRINGOMYELIA AND CHIARI I MALFORMATION
Abstract
Genetic analysis of italian patients with congenital hyperinsulinism of infancy.
Articolo
Genotype and Phenotype Characterization of a Series of Italian Patients Affected with Idiopatic Central Hypothyroidism
Abstract
Hyperthyrotropinemia of the Preterm Newborn: Treat or Not to Treat?
Abstract
IGRO A NEW MEDICAL SOFTWARE TO IMPROVE GH TREATMENT IN CHILDREN WITH GH DEFICIENCY: A STUDY BASED ON ITS DAILY USE IN CLINICAL PRACTICE
Abstract
Influence of the Application of the POI Score on the Results of GH Therapy in Prader-Willi
Abstract
Molecular and clinical analysis of Italian patients with congenital hyperinsulinism of infancy.
Abstract
N323K mutation of HSD3B2 gene in two siblings: sexual ambiguity limited to male gender
Abstract
Non dipping phenomenon and nocturnal hypoglicemia in T1DM
Abstract
POI: a score to modulate GH treatment in children with Prader-Willi Syndrome.
Articolo
Prevalence of central adrenal insufficiency in patients with Prader-Willi syndrome
Abstract
Retinal thinning in young patients with type 1 diabetes mellitus: is it the first sign of diabetic retinopathy?
Abstract
SHOX region mutation in Leri-Weil dischondrosteosis (LWS)
Abstract
Screening for diabetic retinopathy by nonmidriatic retinal imaging
Abstract
The effect of prolonged GH treatment on upper airways and sleep-disordered breathing of 50 non-severely obese children with Prader-Willi syndrome
Abstract
Therapeutic Troubles of Cushing's Disease in Adolescence: Report of a Case
Abstract
Thyroid Function Anomalies in Children with Down Syndrome: Early TSH Alteration can Predict Future Hypothyroidism Development?
Abstract
Thyroid disorders in children and adolescents with Prader-Willi syndrome: data from 299 Italian patiens
Abstract
Treg function as a marker to define the susceptibility to T1DM clinical onset in a healthy subject with antibodies positivity?
Abstract
Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism
Abstract
No Results Found
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