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Molecular Human Reproduction|June 8, 2004
Endogenous retroviral syncytin: compilation of experimental research on syncytin and its possible role in normal and disturbed human placentogenesisI Knerr, B Huppertz, C Weigel, et al.European Journal of Endocrinology|September 23, 2006
Metabolic decompensation in children with type 1 diabetes mellitus associated with increased serum levels of the soluble leptin receptorJ Kratzsch, I Knerr, A Galler, et al.European Journal of Pediatrics|November 14, 2022
An approach to recognising and identifying metabolic presentations in the paediatric Irish Traveller populationE B Forman, S A Lynch, I Knerr, et al.Diabetic Medicine : a Journal of the British Diabetic Association|November 1, 2007
Prevailing therapeutic regimes and predictive factors for prandial insulin substitution in 26 687 children and adolescents with Type 1 diabetes in Germany and AustriaI Knerr, S E Hofer, P M Holterhus, et al.European Journal of Pediatrics|November 26, 2016
A review of anaesthetic outcomes in patients with genetically confirmed mitochondrial disordersA Smith, E Dunne, M Mannion, et al.Molecular Genetics and Metabolism|September 2, 2014
Systemic gene dysregulation in classical Galactosaemia: Is there a central mechanism?K P Coss, E P Treacy, E J Cotter, et al.Frontiers in Genetics|October 3, 2022
Uniparental disomy screen of Irish rare disorder cohort unmasks homozygous variants of clinical significance in the TMCO1 and PRKRA genesB Molloy, E R Jones, N D Linhares, et al.Journal of Inherited Metabolic Disease|August 9, 2012
Classical Galactosaemia in Ireland: incidence, complications and outcomes of treatmentK P Coss, P P Doran, C Owoeye, et al.Journal of Inherited Metabolic Disease|January 28, 2009
Succinic semialdehyde dehydrogenase deficiency: lessons from mice and menP L Pearl, K M Gibson, M A Cortez, et al.Journal of Inherited Metabolic Disease|January 31, 2003
Glutaric aciduria type III: a distinctive non-disease?I Knerr, J Zschocke, U Trautmann, et al.Pageof 5