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European Journal of Pediatrics|February 24, 2001
Cerebral spinal fluid flow, venous drainage and spinal cord compression in achondroplastic children: impact of magnetic resonance findings for decompressive surgery at the cranio-cervical junctionK Brühl, P Stoeter, B Wietek, et al.Journal of Endocrinological Investigation|January 30, 2003
Euglycemic hyperinsulinemia, but not lipid infusion, decreases circulating ghrelin levels in humansM Möhlig, J Spranger, B Otto, et al.Human Molecular Genetics|January 1, 1995
Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one familyS Mundlos, J B Mulliken, D L Abramson, et al.Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|July 7, 2001
Retinal photocoagulation does not influence intraocular levels of IGF-I, IGF-II and IGF-BP3 in proliferative diabetic retinopathy-evidence for combined treatment of PDR with somatostatin analogues and retinal photocoagulation?J Spranger, M Möhlig, M Osterhoff, et al.Journal of Medical Genetics|July 15, 2005
A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2K W Kjaer, H Eiberg, L Hansen, et al.Translational Stroke Research|September 16, 2021
The Genetic Basis of Moyamoya DiseaseR Mertens, M Graupera, H Gerhardt, et al.International Journal of Obesity (2005)|May 27, 2005
Effects of marked weight loss on plasma levels of adiponectin, markers of chronic subclinical inflammation and insulin resistance in morbidly obese womenH-P Kopp, K Krzyzanowska, M Möhlig, et al.Journal of Structural Biology|August 23, 2011
Fetal and postnatal mouse bone tissue contains more calcium than is present in hydroxyapatiteC Lange, C Li, I Manjubala, et al.Kidney International|June 15, 2007
Microalbuminuria is a major determinant of elevated plasma retinol-binding protein 4 in type 2 diabetic patientsJ Raila, A Henze, J Spranger, et al.Journal of Medical Genetics|April 5, 2005
A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomaliesO Demirhan, S Türkmen, G C Schwabe, et al.Pageof 23