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127 results on '"Jameson, Elisabeth"'

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1. Impact of elosulfase alfa in patients with morquio A syndrome who have limited ambulation: An open‐label, phase 2 study

2. Characterising a homozygous two‐exon deletion in UQCRH: comparing human and mouse phenotypes

5. Emotional and behavioral problems, quality of life and metabolic control in NTBC-treated Tyrosinemia type 1 patients

6. Efficacy and safety of cyclic pyranopterin monophosphate substitution in severe molybdenum cofactor deficiency type A: a prospective cohort study

8. Expanding the phenotype in argininosuccinic aciduria: need for new therapies

9. Neurocognitive outcome and mental health in children with tyrosinemia type 1 and phenylketonuria:A comparison between two genetic disorders affecting the same metabolic pathway

10. Neurocognitive outcome and mental health in children with tyrosinemia type 1 and phenylketonuria: A comparison between two genetic disorders affecting the same metabolic pathway

11. Diagnosing childhood-onset inborn errors of metabolism by next-generation sequencing

12. Neurocognitive outcome and mental health in children with tyrosinemia type 1 and phenylketonuria: A comparison between two genetic disorders affecting the same metabolic pathway

19. Dietary Management, Clinical Status and Outcome of Patients with Citrin Deficiency in the UK

21. Molecular genetic investigations identify new clinical phenotypes associated with BCS1L-related mitochondrial disease

22. MOESM3 of Emotional and behavioral problems, quality of life and metabolic control in NTBC-treated Tyrosinemia type 1 patients

23. Emotional and behavioral problems, quality of life and metabolic control in NTBC-treated Tyrosinemia type 1 patients

24. List of Contributors

25. Contributors

26. Molecular genetic investigations identify new clinical phenotypes associated with BCS1L-related mitochondrial disease

30. 10 years of galsulfase in a tertiary treatment center

31. Impaired antibacterial autophagy links granulomatous intestinal inflammation in Niemann-Pick disease type C1 and XIAP deficiency with NOD2 variants in Crohn's disease

32. Improvement in pulmonary function and serum immunoglobulin G in long-term enzyme replacement therapy with velmanase alfa(human recombinant alpha-mannosidase) in alpha-mannosidosis patients

33. Long-term enzyme replacement therapy with velmanase alfa (human recombinant alpha-mannosidase) improves mobility in alpha-mannosidosis patients

34. Improvement in fine and gross motor proficiency after long-term enzyme replacement therapy with velmanase alfa (human recombinant alpha mannosidase) in alpha-mannosidosis patients

35. Impact of elosulfase alfa in patients with morquio A syndrome who have limited ambulation: An open-label, phase 2 study

37. Impaired antibacterial autophagy links granulomatous intestinal inflammation in Niemann–Pick disease type C1 and XIAP deficiency with NOD2 variants in Crohn's disease

38. Haemophagocytic lymphohistiocytosis and other immunological anomalies in infantile onset lysosomal acid lipase deficiency

40. Efficacy and safety of cyclic pyranopterin monophosphate substitution in severe molybdenum cofactor deficiency type A: a prospective cohort study

42. List of Contributors

45. I-cell disease: The experience of six centres

48. Optic neuropathy in methylmalonic acidemia and propionic acidemia.

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