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Servicezeiten in Frankfurt am Main ab 1. Dezember 2025: Montag bis Freitag 9–18 Uhr und Samstag 10–16 Uhr
Service hours in Frankfurt am Main from 1 December 2025: Monday to Friday 9:00-18:00 and Saturday 10:00-16:00

Wegen Wartungsarbeiten ist vom 12. bis 14. Januar 2026 der Museumslesesaal, sowie vom 14. bis 16. Januar 2026 der Musiklesesaal geschlossen. // Due to maintenance work the museum reading room will be closed from 12 to 14 January 2026 and the music reading room from 14 to 16 January 2026.

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	81	Genetic Diagnosis of Hyperoxaluria Type 3 Patients Using Haplotype Analysis Enthalten in Kidney & blood pressure research Bd. 50, 2025, Nr. 1: 189-197. 9 S.
	82	Upregulation of hsa_circ_0000745/hsa_circRNA_101996 in peripheral blood monocytes is associated with coronary heart disease Enthalten in Journal of laboratory medicine Bd. 49, 2025, Nr. 3: 129-138. 10 S.
	83	Voluntary exercise prevents high-fat diet-induced male infertility in rats by preserving blood-testis barrier integrity and sperm parameters Enthalten in Hormone molecular biology and clinical investigation Bd. 46, 2025, Nr. 3: 119-131. 13 S.
	84	CO2 Laser Irradiation Positively Affects the Surface Energy of Rough Titanium Surfaces Enthalten in The international journal of oral & maxillofacial implants Bd. 40, 2025, Nr. 5: 636-642
	85	Assessment of thiopurine S-methyltransferase allele frequencies and phenotype–genotype concordance in a Tunisian population Enthalten in Drug metabolism and personalized therapy Bd. 40, 2025, Nr. 3: 151-156. 06 S.
	86	Effectiveness of educational interventions for the prevention of lead poisoning in children: a systematic review Enthalten in Reviews on environmental health Bd. 40, 2025, Nr. 1: 115-132. 18 S.
	87	Pitfalls in the diagnosis of carnitine palmitoyltransferase 1 deficiency Enthalten in The journal of pediatric endocrinology and metabolism Bd. 38, 2025, Nr. 12: 1324-1331. 08 S.
	88	Mucolipidosis type II and III: clinical spectrum, genetic landscape, and longitudinal outcomes in a pediatric cohort with six novel mutations Enthalten in The journal of pediatric endocrinology and metabolism Bd. 38, 2025, Nr. 12: 1286-1298. 13 S.
	89	Prader-Willi syndrome gene expression profiling of obese and non-obese patients reveals transcriptional changes in CLEC4D and ANXA3 Enthalten in The journal of pediatric endocrinology and metabolism Bd. 38, 2025, Nr. 5: 514-524. 11 S.
	90	Medium-chain acyl-CoA dehydrogenase deficiency in North Macedonia – ten years experience Enthalten in The journal of pediatric endocrinology and metabolism Bd. 38, 2025, Nr. 5: 501-508. 08 S.

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