Katalog der Deutschen Nationalbibliothek

Ihr Suchergebnis enthält zu viele Treffer. Bitte schränken Sie Ihre Suche weiter ein.

Ergebnis der Suche nach: "{{{1}}}"
im Bestand: Gesamter Bestand

100001 - 100010 von 13216921

	100001	Two families, two pathways: a case series of 46, XY DSD with 17α-hydroxylase deficiency and isolated 17,20-lyase deficiency due to novel CYB5A variant Enthalten in The journal of pediatric endocrinology and metabolism Bd. 38, 2025, Nr. 6: 649-657. 09 S.
	100002	Clinical and genetic insights into congenital lipoid adrenal hyperplasia: a case series from a tertiary care center in North India Enthalten in The journal of pediatric endocrinology and metabolism Bd. 38, 2025, Nr. 6: 644-648. 05 S.
	100003	Cardiac function in children with congenital adrenal hyperplasia Enthalten in The journal of pediatric endocrinology and metabolism Bd. 38, 2025, Nr. 6: 637-643. 07 S.
	100004	Impact of growth hormone therapy on bone and body composition in prepubertal children with idiopathic short stature Enthalten in The journal of pediatric endocrinology and metabolism Bd. 38, 2025, Nr. 6: 624-630. 07 S.
	100005	Impact of Covid-19 on children and adolescents with type 1 diabetes: lifestyle, telecommunication service, and quality of life Enthalten in The journal of pediatric endocrinology and metabolism Bd. 38, 2025, Nr. 6: 590-598. 09 S.
	100006	Cord blood metabolomic profiling in high risk newborns born to diabetic, obese, and overweight mothers: preliminary report Enthalten in The journal of pediatric endocrinology and metabolism Bd. 38, 2025, Nr. 6: 577-589. 13 S.
	100007	Hormonal therapy for impaired growth due to pediatric-onset inflammatory bowel disease: a systematic review and meta-analysis with trial sequential analysis Enthalten in The journal of pediatric endocrinology and metabolism Bd. 38, 2025, Nr. 6: 562-569. 08 S.
	100008	Expanding the genotypic spectrum of 3β-hydroxy-δ5-C27-steroid dehydrogenase (HSD3B7) deficiency: novel mutations and clinical outcomes Enthalten in The journal of pediatric endocrinology and metabolism Bd. 38, 2025, Nr. 5: 546-550. 05 S.
	100009	Clinical manifestations and molecular genetics of seven patients with Niemann–Pick type-C: a case series with a novel variant Enthalten in The journal of pediatric endocrinology and metabolism Bd. 38, 2025, Nr. 5: 539-545. 07 S.
	100010	Early-onset growth hormone treatment in Prader–Willi syndrome attenuates transition to severe obesity Enthalten in The journal of pediatric endocrinology and metabolism Bd. 38, 2025, Nr. 5: 525-532. 08 S.

100001 - 100010 von 13216921

Alle Materialarten

Alle Kataloge/Sammlungen

Alle Standorte > Leipzig (13216921)

Aktionen