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American Journal of Medical Genetics|March 31, 1997
Omphalocele in Miller-Dieker syndrome: expanding the phenotypeD Chitayat, A Toi, R Babul, et al.Neurosurgery|May 1, 1993
Primary leptomeningeal melanoma: an unusually aggressive tumor in childhoodD Allcutt, S Michowiz, S Weitzman, et al.AJNR. American Journal of Neuroradiology|December 6, 2001
Optic pathway glioma: correlation of imaging findings with the presence of neurofibromatosisL Kornreich, S Blaser, M Schwarz, et al.Metabolic Engineering|August 11, 2000
Glucose/citrate cometabolism in Lactococcus lactis subsp. lactis biovar diacetylactis with impaired alpha-acetolactate decarboxylaseM Curic, M de Richelieu, C M Henriksen, et al.Journal of Alzheimer'S Disease : JAD|April 16, 2016
Copeptin, a Marker of Vasopressin, Predicts Vascular Dementia but not Alzheimer's DiseaseErik D Nilsson, Olle Melander, Sölve Elmståhl, et al.American Journal of Medical Genetics. Part A|February 12, 2009
Aplasia of cochlear nerves and olfactory bulbs in association with SOX10 mutationC P Barnett, R Mendoza-Londono, S Blaser, et al.European Journal of Clinical Pharmacology|January 1, 1993
Intraduodenal infusion of a water-based levodopa dispersion for optimisation of the therapeutic effect in severe Parkinson's diseaseE Bredberg, D Nilsson, K Johansson, et al.Human Genetics|February 3, 2009
Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotypeJ M Cameron, M Maj, V Levandovskiy, et al.Clinical Genetics|October 9, 2016
Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactylyK D Kernohan, A McBride, Y Xi, et al.AJNR. American Journal of Neuroradiology|April 1, 1996
Abnormal ocular enhancement in Sturge-Weber syndrome: correlation of ocular MR and CT findings with clinical and intracranial imaging findingsP D Griffiths, M B Boodram, S Blaser, et al.Pageof 29