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100001 - 100010 von 1050611

	100001	Heterozygous CDC73 mutation causing hyperparathyroidism in children and adolescents: a report of 2 cases Enthalten in The journal of pediatric endocrinology and metabolism Bd. 35, 2022, Nr. 12: 1547-1551. 05 S.
	100002	Cathelicidin as a marker for subclinical cardiac changes and microvascular complications in children and adolescents with type 1 diabetes Enthalten in The journal of pediatric endocrinology and metabolism Bd. 35, 2022, Nr. 12: 1509-1517. 09 S.
	100003	The association between plasma carnitines and duration of diabetic ketoacidosis treatment in children with type 1 diabetes Enthalten in The journal of pediatric endocrinology and metabolism Bd. 35, 2022, Nr. 12: 1505-1508. 04 S.
	100004	Insights into the implication of obesity in hypogonadism among adolescent boys Enthalten in The journal of pediatric endocrinology and metabolism Bd. 35, 2022, Nr. 12: 1497-1504. 08 S.
	100005	Effect of obesity and excessive body fat on glycaemic control in paediatric type 1 diabetes Enthalten in The journal of pediatric endocrinology and metabolism Bd. 35, 2022, Nr. 12: 1474-1480. 07 S.
	100006	Triple burden of malnutrition and role of anaemia in the development of complications associated with type 1 diabetes in Indian children and youth Enthalten in The journal of pediatric endocrinology and metabolism Bd. 35, 2022, Nr. 12: 1464-1473. 10 S.
	100007	The efficacy and safety of dipeptidyl peptidase-4 inhibitors and glucagon-like peptide-1 agonists in pediatric patients with type 2 diabetes: a systematic review Enthalten in The journal of pediatric endocrinology and metabolism Bd. 35, 2022, Nr. 12: 1457-1463. 07 S.
	100008	Advantages of monitoring rT3 and dividing LT3 dose in the treatment of consumptive hypothyroidism associated with infantile hepatic hemangioma Enthalten in The journal of pediatric endocrinology and metabolism Bd. 35, 2022, Nr. 11: 1453-1456. 04 S.
	100009	A case of severe systemic type 1 pseudohypoaldosteronism with 10 years of evolution Enthalten in The journal of pediatric endocrinology and metabolism Bd. 35, 2022, Nr. 11: 1448-1452. 05 S.
	100010	Acromicric dysplasia due to a novel missense mutation in the fibrillin 1 gene in a three-generation family Enthalten in The journal of pediatric endocrinology and metabolism Bd. 35, 2022, Nr. 11: 1443-1447. 05 S.

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