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Aktuelle Gerontologie|June 1, 1976
[Problemss of tending to chronicity of diseases in geriatrics (author's transl)]B SteinmannKidney International. Supplement|May 3, 2008
Use of new peritoneal dialysis solutions in childrenA Canepa, E Verrina, F PerfumoEuropean Journal of Pediatrics|June 1, 1995
Phenotype of the Williams-Beuren syndrome associated with hemizygosity at the elastin locusD Kotzot, F Bernasconi, L Brecevic, et al.Journal of Medical Genetics|August 19, 2008
A novel mutation in the sulfate transporter gene SLC26A2 (DTDST) specific to the Finnish population causes de la Chapelle dysplasiaL Bonafé, J Hästbacka, A de la Chapelle, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 26, 1999
Determination of bone markers in pycnodysostosis: effects of cathepsin K deficiency on bone matrix degradationY Nishi, L Atley, D E Eyre, et al.Neuromuscular Disorders : NMD|March 29, 2005
Morphological, clinical and genetic aspects in a family with a novel LAMP-2 gene mutation (Danon disease)J A Lobrinus, D F Schorderet, M Payot, et al.Minerva Medica|October 13, 1979
[The hyperaminoacidurias with special reference to cystinuria]F Perfumo, G Basile, F Ginevri, et al.Pageof 31