Search results

2823 results for All evidence

Sorted by Relevance . Sort by Date

Showing results 1 to 10. View options for downloading these results.

Displaying only ARMSPrimary for your search.
Return to full search results.

  • Canadian guidelines for postoperative surveillance of upper urinary tract urothelial carcinoma (PDF)

    Source:
    Canadian Urological Association (Remove filter)

    Published by Canadian Urological Association, 01 June 2013

    Upper urinary tract urothelial carcinoma (UTUC) is a rare malignancy, accounting for 5% of urothelial tumours.1 The gold standard management for non-metastatic UTUC is radical nephrouretectomy with...

    Read Summary

    Type:
    Guidance (Remove filter)
  • Ketotic hypoglycaemia (PDF)

    Source:
    British Inherited Metabolic Disease Group (Remove filter)

    Published by British Inherited Metabolic Disease Group (BIMDG), 22 May 2013

    Ketotic hypoglycaemia is a poorly understood condition that most commonly affects young children between the ages of one and five years.  The history is characteristic.  A toddler who is unwell...

    Read Summary

    Type:
    Guidance (Remove filter)
  • Glut 1 deficiency (PDF)

    Source:
    British Inherited Metabolic Disease Group (Remove filter)

    Published by British Inherited Metabolic Disease Group (BIMDG), 01 February 2012

    Children with GLUT1 deficiency have an impaired glucose transport into the brain and glucose  levels in CSF are low (hypoglychorrhachia). As a result, seizures and secondary microcephaly  are...

    Read Summary

    Type:
    Guidance (Remove filter)
  • Carnitine transporter deficiency (PDF)

    Source:
    British Inherited Metabolic Disease Group (Remove filter)

    Published by British Inherited Metabolic Disease Group (BIMDG), 01 January 2009

    Carnitine transporter deficiency usually presents with cardiomyopathy and muscle weakness. It responds well to carnitine supplementation and for most of the time patients are healthy.  However...

    Read Summary

    Type:
    Guidance (Remove filter)
  • Citrin deficiency protocol (PDF)

    Source:
    British Inherited Metabolic Disease Group (Remove filter)

    Published by British Inherited Metabolic Disease Group (BIMDG), 01 January 2012

    This protocol provides recommendations for the emergency assessment and treatment of citrin deficiency (also known as Citrullinaemia type 2) Last revised January 2017

    Read Summary

    Type:
    Guidance (Remove filter)
  • HMG CoA Lyase deficiency (PDF)

    Source:
    British Inherited Metabolic Disease Group (Remove filter)

    Published by British Inherited Metabolic Disease Group (BIMDG), 01 January 2008

      3-hydroxy-3-methyl Glutaryl CoA lyase deficiency is a disorder of ketone synthesis. This enzyme is also on the leucine breakdown pathway. For most of the time patients are healthy & do  not...

    Read Summary

    Type:
    Guidance (Remove filter)
  • Recurrent hypoglycaemia (PDF)

    Source:
    British Inherited Metabolic Disease Group (Remove filter)

    Published by British Inherited Metabolic Disease Group (BIMDG), 22 May 2013

    Hypoglycaemia is a feature of many conditions, including well defined inherited metabolic diseases and endocrine disorders. It can also occur, for reasons that are not completely understood, in...

    Read Summary

    Type:
    Guidance (Remove filter)

Page 1 of 283

Results per page | | |