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European Journal of Pediatrics|February 1, 1982
A familial progressive neurodegenerative disease with 2-oxoglutaric aciduriaA Kohlschütter, A Behbehani, U Langenbeck, et al.Scandinavian Journal of Gastroenterology|August 28, 2003
Glutathione S-transferase genotype and p53 mutations in adenocarcinoma of the small intestineL Nørum Pedersen, L Kaerlev, P Stubbe Teglbjaerg, et al.Hormone Research|January 1, 1992
Growth response to recombinant human growth hormone of mammalian cell origin in prepubertal growth hormone-deficient children during the first two years of treatmentP Stubbe, S D Frasier, N Stahnke, et al.Journal of Reproduction and Fertility. Supplement|January 1, 1987
Consequence of excess iodine supply in a Thoroughbred stud in southern BrazilC A Silva, H Merkt, P N Bergamo, et al.Clinical Endocrinology|March 5, 2002
Complete virilization in congenital adrenal hyperplasia: clinical course, medical management and disease-related complicationsJ Woelfle, W Hoepffner, W G Sippell, et al.BMC Genomics|May 19, 2026
Genomic signatures of population isolation in an endangered European rodentPaige A Byerly, Alina von Thaden, Gregor Rolshausen, et al.Clinical Research in Cardiology : Official Journal of the German Cardiac Society|July 24, 2014
Characteristics, management modalities and outcome in chronic systolic heart failure patients treated in tertiary care centers: results from the EVIdence based TreAtment in Heart Failure (EVITA-HF) registryW von Scheidt, C Zugck, M Pauschinger, et al.Genome Research|November 14, 2024
Haplotype-resolved genome and population genomics of the threatened garden dormouse in EuropePaige A Byerly, Alina von Thaden, Evgeny Leushkin, et al.Pageof 6