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Medical treatment of hyperammonemia

Bibliographic reference Nassogne, Marie-Cécile ; Vincent, Marie. Medical treatment of hyperammonemia. In: Current Approach to Hyperammonemia,  2014
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  1. Häberle Johannes, Boddaert Nathalie, Burlina Alberto, Chakrapani Anupam, Dixon Marjorie, Huemer Martina, Karall Daniela, Martinelli Diego, Crespo Pablo, Santer René, Servais Aude, Valayannopoulos Vassili, Lindner Martin, Rubio Vicente, Dionisi-Vici Carlo, Suggested guidelines for the diagnosis and management of urea cycle disorders, 10.1186/1750-1172-7-32
  2. Wijburg Frits A., Nassogne Marie-Cécile, Disorders of the Urea Cycle and Related Enzymes, Inborn Metabolic Diseases (2012) ISBN:9783642157196 p.297-310, 10.1007/978-3-642-15720-2_20
  3. Leonard J.V., Morris A.A.M., Urea cycle disorders, 10.1053/siny.2001.0085
  4. Dionisi-Vici Carlo, Ogier de Baulny Hélène, Emergency Treatments, Inborn Metabolic Diseases (2012) ISBN:9783642157196 p.103-111, 10.1007/978-3-642-15720-2_5
  5. Nyhan William L., Metabolic Emergencies, Inherited Metabolic Diseases (2010) ISBN:9783540747222 p.44-47, 10.1007/978-3-540-74723-9_9
  6. Bachmann C, Eur. J. Pediatr., 162, 410 (2003)
  7. Nassogne M. C., Héron B., Touati G., Rabier D., Saudubray J. M., Urea cycle defects: Management and outcome, 10.1007/s10545-005-0303-7
  8. Leonard James, Morris Andrew, Diagnosis and early management of inborn errors of metabolism presenting around the time of birth1, 10.1080/08035250500349413
  9. Enns Gregory M., Berry Susan A., Berry Gerard T., Rhead William J., Brusilow Saul W., Hamosh Ada, Survival after Treatment with Phenylacetate and Benzoate for Urea-Cycle Disorders, 10.1056/nejmoa066596
  10. Praphanproj V., Boyadjiev S. A., Waber L. J., Brusilow S. W., Geraghty M. T., 10.1023/a:1005661631281
  11. Gessler Peter, Buchal Peter, Schwenk Hans U., Wermuth Bendicht, Favourable long-term outcome after immediate treatment of neonatal hyperammonemia due to N-acetylglutamate synthase deficiency, 10.1007/s00431-009-1006-0
  12. Singh R. H., Nutritional management of patients with urea cycle disorders, 10.1007/s10545-007-0718-4
  13. Summar Marshall, Current strategies for the management of neonatal urea cycle disorders, 10.1067/mpd.2001.111834
  14. WHO Technical Report Series: Protein and amino acid requirement in human nutrition . Report of a joint WHO/FAO/UNU expert consultation Series 935 ( 2007 ).
  15. Leonard James V., The nutritional management of urea cycle disorders, 10.1067/mpd.2001.111835
  16. Huner G., Baykal T., Demir F., Demirkol M., Breastfeeding experience in inborn errors of metabolism other than phenylketonuria, 10.1007/s10545-005-0457-3
  17. Åvitsland Tone Lise, Kristensen Charlotte, Emblem Ragnhild, Veenstra Marijke, Mala Tom, Bjørnland Kristin, Percutaneous Endoscopic Gastrostomy in Children: A Safe Technique with Major Symptom Relief and High Parental Satisfaction : , 10.1097/01.mpg.0000229550.54455.63
  18. Nagasaka Hironori, Yorifuji Tohru, Murayama Kei, Kubota Mitsuru, Kurokawa Keiji, Murakami Tomoko, Kanazawa Masaki, Takatani Tomozumi, Ogawa Atsushi, Ogawa Emi, Yamamoto Shigenori, Adachi Masanori, Kobayashi Kunihiko, Takayanagi Masaki, Effects of arginine treatment on nutrition, growth and urea cycle function in seven Japanese boys with late-onset ornithine transcarbamylase deficiency, 10.1007/s00431-006-0143-y
  19. Scaglia Fernando, New insights in nutritional management and amino acid supplementation in urea cycle disorders, 10.1016/j.ymgme.2010.02.019
  20. Burlina Alberto B., Ogier Helen, Korall Herbert, Trefz Friedrich K., Long-Term Treatment with Sodium Phenylbutyrate in Ornithine Transcarbamylase-Deficient Patients, 10.1006/mgme.2001.3156
  21. Williams M, J. Inherit. Metab. Dis., 33, S118 (2010)
  22. Wilcken Bridget, Problems in the management of urea cycle disorders, 10.1016/j.ymgme.2003.10.016
  23. Berry Gerard T., Steiner Robert D., Long-term management of patients with urea cycle disorders, 10.1067/mpd.2001.111837
  24. Maestri Nancy E., McGowan Kathryn D., Brusilow Saul W., Plasma glutamine concentration: A guide in the management of urea cycle disorders, 10.1016/s0022-3476(05)81200-4
  25. Bachmann Claude, Interpretation of plasma amino acids in the follow-up of patients: The impact of compartmentation, 10.1007/s10545-007-0772-y
  26. Morgan T. M., Schlegel C., Edwards K. M., Welch-Burke T., Zhu Y., Sparks R., Summar M., , Vaccines Are Not Associated With Metabolic Events in Children With Urea Cycle Disorders, 10.1542/peds.2010-1628
  27. DUTOIT ANDREA P., FLICK RANDALL R., SPRUNG JURAJ, BABOVIC-VUKSANOVIC DUSICA, WEINGARTEN TOBY N., Anesthetic implications of ornithine transcarbamylase deficiency : ANESTHESIA AND ORNITHINE TRANSCARBAMYLASE DEFICIENCY, 10.1111/j.1460-9592.2010.03322.x
  28. Krivitzky Lauren, Babikian Talin, Lee Hye-Seung, Thomas Nina Hattiangadi, Burk-Paull Karen L, Batshaw Mark L, Intellectual, Adaptive, and Behavioral Functioning in Children With Urea Cycle Disorders, 10.1203/pdr.0b013e3181a27a16
  29. Cederbaum Julie A., LeMons Cynthia, Rosen Mindy, Ahrens Mary, Vonachen Sharon, Cederbaum Stephen D., Psychosocial issues and coping strategies in families affected by urea cycle disorders, 10.1067/mpd.2001.111839
  30. Oechsner M, Steen C, Sturenburg H J, Kohlschutter A, Hyperammonaemic encephalopathy after initiation of valproate therapy in unrecognised ornithine transcarbamylase deficiency, 10.1136/jnnp.64.5.680
  31. Mercimek-Mahmutoglu S., Moeslinger D., Häberle J., Engel K., Herle M., Strobl M.W., Scheibenreiter S., Muehl A., Stöckler-Ipsiroglu S., Long-term outcome of patients with argininosuccinate lyase deficiency diagnosed by newborn screening in Austria, 10.1016/j.ymgme.2010.01.013
  32. Sander J, Eur. J. Pediatr., 162, 417 (2003)
  33. Bachmann Claude, Long-term outcome of patients with urea cycle disorders and the question of neonatal screening, 10.1007/s00431-003-1347-z
  34. Levrat Virginie, Forest Isabelle, Fouilhoux Alain, Acquaviva Cécile, Vianey-Saban Christine, Guffon Nathalie, Carglumic acid: an additional therapy in the treatment of organic acidurias with hyperammonemia?, 10.1186/1750-1172-3-2
  35. Crombez Eric A., Cederbaum Stephen D., Hyperargininemia due to liver arginase deficiency, 10.1016/j.ymgme.2004.11.004
  36. Palladino Andrew A., Stanley Charles A., The hyperinsulinism/hyperammonemia syndrome, 10.1007/s11154-010-9146-0
  37. Heitink-Pollé Katja M J, Prinsen Berthil H. C. M. T., de Koning Tom J, van Hasselt Peter M, Bierings Marc B, High Incidence of Symptomatic Hyperammonemia in Children with Acute Lymphoblastic Leukemia Receiving Pegylated Asparaginase, JIMD Reports (2012) ISBN:9783642324413 p.103-108, 10.1007/8904_2012_156