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JIMD Reports|February 23, 2013
Primary Carnitine (OCTN2) Deficiency Without Neonatal Carnitine DeficiencyL de Boer, L A J Kluijtmans, E MoravaMolecular Genetics and Metabolism|March 11, 2006
Association of 3-methylglutaconic aciduria with sensori-neural deafness, encephalopathy, and Leigh-like syndrome (MEGDEL association) in four patients with a disorder of the oxidative phosphorylationS Wortmann, R J T Rodenburg, M Huizing, et al.Central European Journal of Public Health|June 17, 2000
History of the Public Health Institute of Semmelweis Medical University, BudapestE Tahin, E MoravaOrvosi Hetilap|December 15, 1996
[Alpha thalassemia/metal retardation syndrome--a new X-chromosome linked recessive genetically inherited symptom complex]E Morava, G KosztolányiMitochondrion|June 25, 2010
Depressive behaviour in children diagnosed with a mitochondrial disorderE Morava, T Gardeitchik, T Kozicz, et al.Orvosi Hetilap|July 25, 2000
[Occurrence of X-linked ichthyosis along with atopy]F Harangi, E Morava, M AdonyiAmerican Journal of Medical Genetics|July 12, 1996
X-linked mental retardation syndrome: three brothers with the Brooks-Wisniewski-Brown syndromeE Morava, J Storcz, G KosztolányiAnalytical and Bioanalytical Chemistry|October 1, 1996
Empirical procedure for the reduction of mixed-matrix effects in inductively coupled plasma atomic emission spectrometry using an internal standard and proportional correctionJ L De Boer, M VelteropOrvosi Hetilap|April 3, 1998
[Extracorporeal membrane oxygenation in neonatology: review of the use of the method]E Morava, W Gill, M PierceCurrent Opinion in Chemical Biology|April 26, 2003
Recent efforts in engineering microbial cells to produce new chemical compoundsArjo L de Boer, Claudia Schmidt-DannertPageof 21