Found: 15
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Endocrine Disrupting Chemicals and Type 1 Diabetes.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 8, p. 2937, doi. 10.3390/ijms21082937
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- Article
Low-density lipoprotein oxidizability in children with chronic renal failure.
- Published in:
- Pediatrics International, 2008, v. 50, n. 4, p. 447, doi. 10.1111/j.1442-200X.2008.02614.x
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- Publication type:
- Article
Anthropometric characteristics of newborns with Prader–Willi syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 10, p. 2067, doi. 10.1002/ajmg.a.61304
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- Article
Recurrent NF1 gene variants and their genotype/phenotype correlations in patients with Neurofibromatosis type I.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 1, p. 10, doi. 10.1002/gcc.22997
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- Publication type:
- Article
Glycemic Control Improvement in Italian Children and Adolescents With Type 1 Diabetes Followed Through Telemedicine During Lockdown Due to the COVID-19 Pandemic.
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- Frontiers in Endocrinology, 2020, v. 11, p. N.PAG, doi. 10.3389/fendo.2020.595735
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- Article
EEG Patterns in Patients with Prader–Willi Syndrome.
- Published in:
- Brain Sciences (2076-3425), 2021, v. 11, n. 8, p. 1045, doi. 10.3390/brainsci11081045
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- Publication type:
- Article
Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation.
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- Frontiers in Endocrinology, 2024, p. 1, doi. 10.3389/fendo.2024.1382583
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- Publication type:
- Article
Growth hormone deficiency in a child with benign hereditary chorea caused by a de novo mutation of the TITF1/NKX2-1 gene.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 3, p. 411, doi. 10.1515/jpem-2021-0402
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- Publication type:
- Article
Isolated hypoaldosteronism as first sign of X-linked adrenal hypoplasia congenita caused by a novel mutation in NR0B1/DAX-1 gene: a case report.
- Published in:
- 2019
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- Publication type:
- Case Study
The Approach to a Child with Dysmorphic Features: What the Pediatrician Should Know.
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- Children, 2024, v. 11, n. 5, p. 578, doi. 10.3390/children11050578
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- Publication type:
- Article
Central Precocious Puberty and Response to GnRHa Therapy in Children with Cerebral Palsy and Moderate to Severe Motor Impairment: Data from a Longitudinal, Case-Control, Multicentre, Italian Study.
- Published in:
- International Journal of Endocrinology, 2017, p. 1, doi. 10.1155/2017/4807163
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- Publication type:
- Article
Copy Number Variation Analysis Increases the Number of Candidate Loci Associated with Pediatric Obesity.
- Published in:
- Hormone Research in Paediatrics, 2021, v. 94, n. 7/8, p. 251, doi. 10.1159/000519299
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- Publication type:
- Article
Ten-Year Longitudinal Study of Thyroid Function in Children with Down's Syndrome.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 82, n. 2, p. 113, doi. 10.1159/000362450
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- Publication type:
- Article
Health‐related quality of life and metabolic control in immigrant and Italian children and adolescents with type 1 diabetes and in their parents.
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- Pediatric Diabetes, 2020, v. 21, n. 6, p. 1031, doi. 10.1111/pedi.13042
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- Publication type:
- Article
The impact of BMI on long-term anthropometric and metabolic outcomes in girls with idiopathic central precocious puberty treated with GnRHas.
- Published in:
- Frontiers in Endocrinology, 2022, v. 13, p. 1, doi. 10.3389/fendo.2022.1006680
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- Publication type:
- Article