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European Journal of Endocrinology|July 5, 2005
Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasiaV Dolzan, J Sólyom, G Fekete, et al.International Immunology|September 22, 2006
The 8.1 ancestral MHC haplotype is associated with delayed onset of colonization in cystic fibrosisJudit Laki, István Laki, Krisztina Németh, et al.Lung Cancer (Amsterdam, Netherlands)|June 4, 2023
Comparative expression analysis of immune-related markers in surgically resected lung neuroendocrine neoplasmsBence Ferencz, Zsolt Megyesfalvi, Kristóf Csende, et al.Brain : a Journal of Neurology|December 18, 2007
Properties of in vivo interictal spike generation in the human subiculumDániel Fabó, Zsófia Maglóczky, Lucia Wittner, et al.Orvosi Hetilap|January 11, 2007
[Nucleotide sequence variants of the glucocorticoid receptor gene and their significance in determining glucocorticoid sensitivity]Judit Majnik, Attila Patócs, Katalin Balogh, et al.American Journal of Human Genetics|February 27, 2018
Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX ChildrenAnu Bashamboo, Caroline Eozenou, Anne Jorgensen, et al.Brain : a Journal of Neurology|July 27, 2010
Laminar analysis of slow wave activity in humansRichárd Csercsa, Balázs Dombovári, Dániel Fabó, et al.Journal of Pediatric Gastroenterology and Nutrition|July 4, 2013
Incidence, Paris classification, and follow-up in a nationwide incident cohort of pediatric patients with inflammatory bowel diseaseKatalin E Müller, Péter L Lakatos, András Arató, et al.BMC Pulmonary Medicine|July 21, 2026
Development of experimental isolated lung perfusion model using surgically resected tumorous human lobesÁron Bertram Gellért, Katalin Dezső, Melinda Rezeli, et al.Pageof 16