Regional anesthetic techniques are an alternative to general anesthesia for infants with Pompe's disease
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Published in | Pediatric Anesthesia Vol. 17; no. 7; pp. 697 - 702 |
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Main Authors | , , , , |
Format | Report |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.07.2007
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Subjects | |
Online Access | Get full text |
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Author | BRUCE, JAMES FLETCHER, JOAN WALKER, ROBERT W.M. BRIGGS, GERAINT WRAITH, E.D. |
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References | Amallfitano A, Bengur AR, Morse RP et al. Recombinant human acid α glucosidase enzyme therapy for infantile glycogen storage disease type II: results of phase I/II clinical trial. Genet Med 2001; 3: 132-138. Van der Hout H, Reuser AJ, Vulto AG et al. Recombinant human α glucosidase from rabbit milk in Pompe patients. Lancet 2000; 356: 397-398. Kishnani P, Voit T, Nicolino M et al. Enzyme replacement therapy with human recombinant acid alpha glucosidase (rhGAA) in infantile Pompe disease: results from a phase II clinical study. Pediatr Res 2003; 53: 259A. Pompe JC. Over idiopathische hypertrophie von het hart. Ned Tijdschr Geneeskd 1932; 76: 304-311. Ellis FR. Inherited muscle disease. Br J Anaesth 1980; 52: 153-164. Ing R, Ryan Cook D, Bengur R et al. Anesthetic management of infant with glycogen storage disease type II: a physiological approach. Pediatr Anesth 2004; 14: 514-519. Genzyme Corporation. Investigators Brochure for Myozyme, Edition number 5 (release date Sept 2005). Data on file; access provided by Genzyme. Rosen K, Broadman L. Anaesthesia for diagnostic muscle biopsy in an infant with Pompe's disease. Can Anaesth Soc J 1986: 33: 790-794. MacFarlane HJ, Soni N. Pompe's disease and anaesthesia. Anaesthesia 1986; 41: 1219-1224. Ausems M, Verbiestm J, Hermans M et al. Frequency of glycogen storage disease type II in the Netherlands: implications for genetic counselling. Eur J Hum Genet 1999; 7: 713-716. Kaplan R. Pompe's disease presenting for anesthesia. Two case reports. Anesthesiol Rev 1980; 7: 21-28. |
References_xml | – reference: Ellis FR. Inherited muscle disease. Br J Anaesth 1980; 52: 153-164. – reference: Amallfitano A, Bengur AR, Morse RP et al. Recombinant human acid α glucosidase enzyme therapy for infantile glycogen storage disease type II: results of phase I/II clinical trial. Genet Med 2001; 3: 132-138. – reference: Kishnani P, Voit T, Nicolino M et al. Enzyme replacement therapy with human recombinant acid alpha glucosidase (rhGAA) in infantile Pompe disease: results from a phase II clinical study. Pediatr Res 2003; 53: 259A. – reference: Rosen K, Broadman L. Anaesthesia for diagnostic muscle biopsy in an infant with Pompe's disease. Can Anaesth Soc J 1986: 33: 790-794. – reference: MacFarlane HJ, Soni N. Pompe's disease and anaesthesia. Anaesthesia 1986; 41: 1219-1224. – reference: Genzyme Corporation. Investigators Brochure for Myozyme, Edition number 5 (release date Sept 2005). Data on file; access provided by Genzyme. – reference: Pompe JC. Over idiopathische hypertrophie von het hart. Ned Tijdschr Geneeskd 1932; 76: 304-311. – reference: Ausems M, Verbiestm J, Hermans M et al. Frequency of glycogen storage disease type II in the Netherlands: implications for genetic counselling. Eur J Hum Genet 1999; 7: 713-716. – reference: Ing R, Ryan Cook D, Bengur R et al. Anesthetic management of infant with glycogen storage disease type II: a physiological approach. Pediatr Anesth 2004; 14: 514-519. – reference: Van der Hout H, Reuser AJ, Vulto AG et al. Recombinant human α glucosidase from rabbit milk in Pompe patients. Lancet 2000; 356: 397-398. – reference: Kaplan R. Pompe's disease presenting for anesthesia. Two case reports. Anesthesiol Rev 1980; 7: 21-28. |
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SubjectTerms | caudal epidural block femoral nerve block glycogen storage disease type II hypertrophic cardiomyopathy Pompe's disease regional anesthesia |
Title | Regional anesthetic techniques are an alternative to general anesthesia for infants with Pompe's disease |
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