Review Neurology of inherited glycosylation disorders Hudson H Freeze, Erik A Eklund, Bobby G Ng, Marc C Patterson Congenital disorders of glycosylation comprise most of…
The real connective tissue diseasescoronary arteritis. Am J Cardiol 1986;57: 689–90. 16 Corrao S, Salli L, Arnone S, Scaglione L, et al. Echodoppler abnormalities in
Glycosylation of human fibrinogen in vivoDiabetologia (1985) 28:87-89 Diabetologia 9 Springer-Verlag 1985 Glycosylation of human fibrinogen in vivo A. L/itjens 1, A. A. te
4-Phenylbutyric acid enhances the mineralization of osteogenesis imperfecta iPSC-derived osteoblasts4-Phenylbutyric acid enhances the mineralization of osteogenesis imperfecta
Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain diseaseContents lists available at SciVerse ScienceDirect Journal of the Neurological
Microsoft Word - 03HB43-543 todaME.docDivision of Functional Genomics, Department of Post-Genomics and Diseases, Osaka University Graduate School of Medicine, Suita, (1)
FKRP geneFKRP gene fukutin related protein Normal Function The FKRP gene provides instructions for making a protein called fukutin-related protein ( FKRP). This protein is
200883.septChintalacharuvu, et al: Therapy of CIA 2049 From the Institute of Pathology and the Department of Radiology, Case Western Reserve University, Cleveland, Ohio,