Inborn errors of metabolism and anesthesia; so far, yet so close

  • Juan Carlos Ibla Children's Heart Institute, Children's National Medical Center, George Washington University, Washington, DC, United States

References

1. Fernandes J. The history of the glycogen storage diseases. Eur J Pediatr. 1995;154:423-4.
2. Cori GT. Glycogen structure and enzyme deficiencies in glycogen storage disease. Harvey Lect. 1952;48:145-71.
3. Cox JM. Anesthesia and glycogen-storage disease. Anesthesiology. 1968;29:1221-5.
4. Veiga-da-Cunha M, Gerin I, van Schaftingen E. How many forms of glycogen storage disease type I? Eur J Pediatr. 2000;159:314-8.
5. Wang LY, Ross AK, Li JS, Dearmey SM, Mackey JF, Worden M, et al. Cardiac arrhythmias following anesthesia induction in infantile-onset Pompe disease: A case series. Paediatr Anaesth. 2007;17:738-48.
6. Berrío Valencia MI Martínez Ochoa CM, Durango Gómez HC. Complicaciones anestésicas en pacientes con errores innatos del metabolismo sometidos a cirugía no cardiaca. Rev Colomb Anestesiol.2013;41:257-60.
How to Cite
1.
Ibla JC. Inborn errors of metabolism and anesthesia; so far, yet so close. Colomb. J. Anesthesiol. [Internet]. 2013 Oct. 1 [cited 2024 May 3];41(4):243-4. Available from: https://www.revcolanest.com.co/index.php/rca/article/view/635

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Published
2013-10-01
How to Cite
1.
Ibla JC. Inborn errors of metabolism and anesthesia; so far, yet so close. Colomb. J. Anesthesiol. [Internet]. 2013 Oct. 1 [cited 2024 May 3];41(4):243-4. Available from: https://www.revcolanest.com.co/index.php/rca/article/view/635
Section
Editorial

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