| ID |
Reference |
| G.39 |
Acosta, P.B., Yannicelli, S. (2001). Maple Syrup Urine Disease (MSUD). In The Ross Metabolic Formula System: Nutrition support Protocols, 4th Edition (pp. 74-102). Columbus, OH: Ross Products Division, Division of Abbott Laboratories. |
| F.3487 |
Adam, M.P., Ardinger, H.H., Pagon, R.A., Wallace, S.E., Bean, L.J.H., Mirzaa, G., & Amemiya, A., (1993). GeneReviews. Seattle (WA): University of Washington, Seattle. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/20301495 |
| F.38 |
Barshop, B.A., & Khanna, A. (Dec 2005). Domino hepatic transplantation in maple syrup urine disease. N Engl J Med, 353, 2410-1. doi:10.1056/NEJM200512013532220 |
| G.23 |
Berry, G.T. (2008, Fall). Medical Management of MSU. MSUD Family Newsletter, 25(2). Retrieved from http://www.msud-support.org/index.php?view=category&id=46%3Avolume-25-2&option=com_content&Itemid=5 |
| F.615 |
Berry, G.T., Heidenreich, R., Kaplan, P., Levine, F., Mazur, A., Palmieri, M.J., Yudkoff, M., & Segal, S. (Jan 1991). Branched-chain amino acid-free parenteral nutrition in the treatment of acute metabolic decompensation in patients with maple syrup urine disease. N Engl J Med, 324, 175-9. doi:10.1056/NEJM199101173240307 |
| F.124 |
Biggemann, B., Zass, R., & Wendel, U. (1993). Postoperative metabolic decompensation in maple syrup urine disease is completely prevented by insulin. J Inherit Metab Dis, 16, 912-3. doi:10.1007/BF00714298 |
| G.48 |
Bodamer, O.A. (2010). Overview of Maple Syrup Urine Disease. Retrieved from UpToDate, Inc website www.uptodate.com |
| F.53 |
Bodner-Leidecker, A., Wendel, U., Saudubray, J.M., & Schadewaldt, P. (Dec 2000). Branched-chain L-amino acid metabolism in classical maple syrup urine disease after orthotopic liver transplantation. J Inherit Metab Dis, 23, 805-18. doi:10.1023/a:1026708618507 |
| F.4423 |
Brown, J., Tchan, M., & Nayyar, R. (Jun 2018). Maple syrup urine disease: tailoring a plan for pregnancy. J Matern Fetal Neonatal Med, 31, 1663-1666. doi:10.1080/14767058.2017.1323328 |
| G.44 |
Children's Hospital of Michigan Metabolic Clinic (CHMMC), Division of Genetic and Metabolic Disorders. (2008). Maple Syrup Urine Disease Emergency Care Sick Plan. Detroit, MI: University of Michigan. |
| G.49 |
Chuang, D.T., Wynn, R.M., Shih, V.E. (2008). Maple Syrup Urine Disease (Branched-Chain Ketoaciduria). In Valle et al, The Online Metabolic and Molecular Basis of Inherited Disease (Chapter 87 pp.1-42). The McGraw-Hill Companies, Inc. |
| F.114 |
Danner, D.J., Wheeler, F.B., Lemmon, S.K., & Elsas, L.J. (Mar 1978). In vivo and in vitro response of human branched chain alpha-ketoacid dehydrogenase to thiamine and thiamine pyrophosphate. Pediatr Res, 12, 235-8. doi:10.1203/00006450-197803000-00016 |
| F.83 |
Dixon, M.A., & Leonard, J.V. (Nov 1992). Intercurrent illness in inborn errors of intermediary metabolism. Arch Dis Child, 67, 1387-91. doi:10.1136/adc.67.11.1387 |
| F.127 |
Duran, M., & Wadman, S.K. (1985). Thiamine-responsive inborn errors of metabolism. J Inherit Metab Dis, 8 Suppl 1, 70-5. doi:10.1007/BF01800663 |
| F.113 |
Duran, M., Tielens, A.G., Wadman, S.K., Stigter, J.C., & Kleijer, W.J. (May 1978). Effects of thiamine in a patient with a variant form of branched-chian ketoaciduria. Acta Paediatr Scand, 67, 367-72. doi:10.1111/j.1651-2227.1978.tb16336.x |
| F.82 |
Ellerine, N.P., Herring, W.J., Elsas, L.J., McKean, M.C., Klein, P.D., & Danner, D.J. (Jun 1993). Thiamin-responsive maple syrup urine disease in a patient antigenically missing dihydrolipoamide acyltransferase. Biochem Med Metab Biol, 49, 363-74. doi:10.1006/bmmb.1993.1037 |
| F.101 |
Elsas, L.J., Ellerine, N.P., & Klein, P.D. (May 1993). Practical methods to estimate whole body leucine oxidation in maple syrup urine disease. Pediatr Res, 33, 445-51. doi:10.1203/00006450-199305000-00005 |
| F.109 |
Fernhoff, P.M., Lubitz, D., Danner, D.J., Dembure, P.P., Schwartz, H.P., Hillman, R., Bier, D.M., & Elsas, L.J. (Oct 1985). Thiamine response in maple syrup urine disease. Pediatr Res, 19, 1011-6. doi:10.1203/00006450-198510000-00012 |
| F.29 |
Fuentes-Garcia, D., & Falcon-Arana, L. (Jan 2009). Perioperative management of a patient with maple syrup urine disease. Br J Anaesth, 102, 144-5. doi:10.1093/bja/aen341 |
| F.100 |
Giacoia, G.P., & Berry, G.T. (Sep 1993). Acrodermatitis enteropathica-like syndrome secondary to isoleucine deficiency during treatment of maple syrup urine disease. Am J Dis Child, 147, 954-6. doi:10.1001/archpedi.1993.02160330044015 |
| F.78 |
Grünewald, S., Hinrichs, F., & Wendel, U. (Apr 1998). Pregnancy in a woman with maple syrup urine disease. J Inherit Metab Dis, 21, 89-94. doi:10.1023/a:1005396823030 |
| G.4 |
Hartnett, C. et al. (2003, July, 29). MSUD Infant/ Flax seed oil in MSUD/ Intermittent MSUD/ Leucine and Protein Comparison/ Ordering aminoacids. Message posted to Metabolic Dietician List, <PNO-METAB-L@LISTSERV.CC.EMORY.EDU> |
| G.7 |
Hartnett, C. et al. (2009, January, 28). MSUD low leves/ 6 months MSUD/ ILE deficiency/ MSUD protocol for pregnancy/ Leucine blood spots. Message posted to Metabolic Dietician List, <PNO-METAB-L@LISTSERV.CC.EMORY.EDU> |
| F.3483 |
Heiber, S., Zulewski, H., Zaugg, M., Kiss, C., & Baumgartner, M. (2015). Successful Pregnancy in a Woman with Maple Syrup Urine Disease: Case Report. JIMD Rep, 21, 103-7. doi:10.1007/8904_2014_401 |
| F.611 |
Heldt, K., Schwahn, B., Marquardt, I., Grotzke, M., & Wendel, U. (Apr 2005). Diagnosis of MSUD by newborn screening allows early intervention without extraneous detoxification. Mol Genet Metab, 84, 313-6. doi:10.1016/j.ymgme.2004.11.010 |
| F.80 |
Henriquez, H., el Din, A., Ozand, P.T., Subramanyam, S.B., & al Gain, S.I. (Nov 1994). Emergency presentations of patients with methylmalonic acidemia, propionic acidemia and branched chain amino acidemia (MSUD). Brain Dev, 16 Suppl, 86-93. doi:10.1016/0387-7604(94)90101-5 |
| F.612 |
Hilliges, C., Awiszus, D., & Wendel, U. (Feb 1993). Intellectual performance of children with maple syrup urine disease. Eur J Pediatr, 152, 144-7. doi:10.1007/BF02072492 |
| G.35 |
Hillman, R. (1993, Spring/Summer). Protein Malnutrition. MSUD Support Newsletter, 11(1). Retrieved from http://www.msud-support.org/index.php?option=com_content&view=article&id=33:protein-malnutrition&catid=8:volume-11-1&Itemid=5
|
| F.45 |
Hmiel, S.P., Martin, R.A., Landt, M., Levy, F.H., & Grange, D.K. (May 2004). Amino acid clearance during acute metabolic decompensation in maple syrup urine disease treated with continuous venovenous hemodialysis with filtration. Pediatr Crit Care Med, 5, 278-81. doi:10.1097/01.pcc.0000113265.92664.91 |
| F.37 |
Hoffmann, B., Helbling, C., Schadewaldt, P., & Wendel, U. (Jan 2006). Impact of longitudinal plasma leucine levels on the intellectual outcome in patients with classic MSUD. Pediatr Res, 59, 17-20. doi:10.1203/01.pdr.0000190571.60385.34 |
| F.663 |
Huner, G., Baykal, T., Demir, F., & Demirkol, M. (2005). Breastfeeding experience in inborn errors of metabolism other than phenylketonuria. J Inherit Metab Dis, 28, 457-65. doi:10.1007/s10545-005-0457-3 |
| F.63 |
Jan, D., Poggi, F., Laurent, J., Rabier, D., Jouvet, P., Lacaille, F., Beringer, A., Hubert, P., Revillon, Y., & Saudubray, J.M. (Feb 1994). Liver transplantation: new indications in metabolic disorders?. Transplant Proc, 26(1):189-90. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/8108935 |
| F.73 |
Jouvet, P., Jugie, M., Rabier, D., Desgrès, J., Hubert, P., Saudubray, J.M., & Man, N.K. (Nov 2001). Combined nutritional support and continuous extracorporeal removal therapy in the severe acute phase of maple syrup urine disease. Intensive Care Med, 27, 1798-806. doi:10.1007/s00134-001-1124-2 |
| F.79 |
Jouvet, P., Poggi, F., Rabier, D., Michel, J.L., Hubert, P., Sposito, M., Saudubray, J.M., & Man, N.K. (Aug 1997). Continuous venovenous haemodiafiltration in the acute phase of neonatal maple syrup urine disease. J Inherit Metab Dis, 20, 463-72. doi:10.1023/a:1005314025760 |
| F.69 |
Kaplan, P., Mazur, A., Field, M., Berlin, J.A., Berry, G.T., Heidenreich, R., Yudkoff, M., & Segal, S. (Jul 1991). Intellectual outcome in children with maple syrup urine disease. J Pediatr, 119, 46-50. doi:10.1016/s0022-3476(05)81037-6 |
| F.23 |
Khanna, A., Hart, M., Nyhan, W.L., Hassanein, T., Panyard-Davis, J., & Barshop, B.A. (May 2006). Domino liver transplantation in maple syrup urine disease. Liver Transpl, 12, 876-82. doi:10.1002/lt.20744 |
| F.68 |
Koch, S.E., Packman, S., Koch, T.K., & Williams, M.L. (Feb 1993). Dermatitis in treated maple syrup urine disease. J Am Acad Dermatol, 28, 289-92. doi:10.1016/0190-9622(93)70036-s |
| F.77 |
Koga, Y., Iwanaga, T., Yoshida, I., Yoshino, M., Kaneko, S., & Kato, H. (Apr 1998). Maple syrup urine disease: nutritional management by intravenous hyperalimentation and uneventful course after surgical repair of dislocation of the hip. J Inherit Metab Dis, 21, 177-8. doi:10.1023/a:1005324516186 |
| F.614 |
Korein, J., Sansaricq, C., Kalmijn, M., Honig, J., & Lange, B. (Nov 1994). Maple syrup urine disease: clinical, EEG, and plasma amino acid correlations with a theoretical mechanism of acute neurotoxicity. Int J Neurosci, 79, 21-45. doi:10.3109/00207459408986065 |
| F.24 |
le Roux, C., Murphy, E., Hallam, P., Lilburn, M., Orlowska, D., & Lee, P. (Feb 2006). Neuropsychometric outcome predictors for adults with maple syrup urine disease. J Inherit Metab Dis, 29, 201-2. doi:10.1007/s10545-006-0223-1 |
| F.26 |
le Roux, C., Murphy, E., Lilburn, M., & Lee, P.J. (Feb 2006). The longest-surviving patient with classical maple syrup urine disease. J Inherit Metab Dis, 29, 190-4. doi:10.1007/s10545-006-0204-4 |
| F.20 |
Lee, J.Y., Chiong, M.A., Estrada, S.C., Cutiongco-De la Paz, E.M., Silao, C.L., & Padilla, C.D. (Dec 2008). Maple syrup urine disease (MSUD)--clinical profile of 47 Filipino patients. J Inherit Metab Dis, 31 Suppl 2, S281-5. doi:10.1007/s10545-008-0859-0 |
| F.616 |
Lee, P.J. (2006 Apr-Jun). Pregnancy issues in inherited metabolic disorders. J Inherit Metab Dis, 29, 311-6. doi:10.1007/s10545-005-0252-1 |
| F.72 |
Levin, M.L., Scheimann, A., Lewis, R.A., & Beaudet, A.L. (Jan 1993). Cerebral edema in maple syrup urine disease. J Pediatr, 122, 167-8. doi:10.1016/s0022-3476(05)83521-8 |
| F.93 |
Lin, M.C., Chen, C.H., Fu, L.S., Jan, S.L., Shu, S.G., & Chi, C.S. (2002 Sep-Oct). Management of acute decompensation of neonatal maple syrup urine disease with continuous arteriovenous haemofiltration: report of one case. Acta Paediatr Taiwan, 43(5):281-4. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/12607485 |
| G.50 |
Marriage, B. (2010). Nutrition Management of Patients with Inherited Disorders of Branched- Chain Amino Acid Metabolism. In P.B. Acosta, Nutrition Management of Patients with Inherited Metabolic Disorders (pp. 175-236). Sudbury, MA: Jones and Bartlett Publishers. |
| F.105 |
McMahon, Y., & MacDonnell, R.C. (1990). Clearance of branched chain amino acids by peritoneal dialysis in maple syrup urine disease. Adv Perit Dial, 6:31-4. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/1982835 |
| G.31 |
Morton, D.H., Strauss, K.A. (2005, Summer). Liver transplant as treatment for maple syrup disease: our perspective as pediatricians. MSUD Support Newsletter, 22(2). Retrieved from http://www.msud-support.org/index.php?view=category&id=40%3Avolume-22-2&option=com_content&Itemid=5 |
| F.51 |
Morton, D.H., Strauss, K.A., Robinson, D.L., Puffenberger, E.G., & Kelley, R.I. (Jun 2002). Diagnosis and treatment of maple syrup disease: a study of 36 patients. Pediatrics, 109, 999-1008. doi:10.1542/peds.109.6.999 |
| G.38 |
Morton, H. (1992, Fall). MSUD news from The Clinic for Special Children. MSUD Family Newsletter, 10(2). Retrieved from http://www.msud-support.org/index.php?view=article&catid=7%3Avolume-10-2&id=28%3Amsud-news-from-the-clinic-for-special-children&option=com_content&Itemid=5 |
| G.47 |
MSUD The New England Consortium of Metabolic Programs at Children’s Hospital Boston. (2006). Acute Illness Protocol. Boston, MA: Author.
|
| G.82 |
New England Consortium. Acute Illness Protocol Organic Acidemias, Maple Syrup Urine Disease (MSUD). Retrieved from http://newenglandconsortium.org/protocols/acute_illness/organic_acid_disorders/maple-syrup-urine-disease.pdf |
| F.67 |
Northrup, H., Sigman, E.S., & Hebert, A.A. (Mar 1993). Exfoliative erythroderma resulting from inadequate intake of branched-chain amino acids in infants with maple syrup urine disease. Arch Dermatol, 129(3):384-5. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/8447687 |
| F.76 |
Nyhan, W.L., Rice-Kelts, M., Klein, J., & Barshop, B.A. (Jun 1998). Treatment of the acute crisis in maple syrup urine disease. Arch Pediatr Adolesc Med, 152, 593-8. doi:10.1001/archpedi.152.6.593 |
| F.71 |
Oztürk, Y. (2008 May-Jun). Acrodermatitis enteropathica-like syndrome secondary to branched-chain amino acid deficiency in inborn errors of metabolism. Pediatr Dermatol, 25, 415. doi:10.1111/j.1525-1470.2008.00707.x |
| F.81 |
Parini, R., Sereni, L.P., Bagozzi, D.C., Corbetta, C., Rabier, D., Narcy, C., Hubert, P., & Saudubray, J.M. (Aug 1993). Nasogastric drip feeding as the only treatment of neonatal maple syrup urine disease. Pediatrics, 92(2):280-3. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/8337030 |
| F.126 |
Parsons, H.G., Carter, R.J., Unrath, M., & Snyder, F.F. (1990). Evaluation of branched-chain amino acid intake in children with maple syrup urine disease and methylmalonic aciduria. J Inherit Metab Dis, 13, 125-36. doi:10.1007/BF01799675 |
| F.52 |
Puliyanda, D.P., Harmon, W.E., Peterschmitt, M.J., Irons, M., & Somers, M.J. (Apr 2002). Utility of hemodialysis in maple syrup urine disease. Pediatr Nephrol, 17, 239-42. doi:10.1007/s00467-001-0801-2 |
| F.47 |
Riazi, R., Rafii, M., Clarke, J.T., Wykes, L.J., Ball, R.O., & Pencharz, P.B. (Jul 2004). Total branched-chain amino acids requirement in patients with maple syrup urine disease by use of indicator amino acid oxidation with L-[1-13C]phenylalanine. Am J Physiol Endocrinol Metab, 287, E142-9. doi:10.1152/ajpendo.00431.2003 |
| F.87 |
Ring, E., Zobel, G., & Stöckler, S. (Aug 1990). Clearance of toxic metabolites during therapy for inborn errors of metabolism. J Pediatr, 117, 349-50. doi:10.1016/s0022-3476(05)80585-2 |
| F.85 |
Riviello, J.J., Rezvani, I., DiGeorge, A.M., & Foley, C.M. (Jul 1991). Cerebral edema causing death in children with maple syrup urine disease. J Pediatr, 119, 42-5. doi:10.1016/s0022-3476(05)81036-4 |
| F.89 |
Ross, L.F. (Jan 2010). An ethical and policy analysis of elective transplantation for metabolic conditions diagnosed by newborn screening. J Pediatr, 156, 139-44. doi:10.1016/j.jpeds.2009.06.067 |
| F.88 |
Rutledge, S.L., Havens, P.L., Haymond, M.W., McLean, R.H., Kan, J.S., & Brusilow, S.W. (Jan 1990). Neonatal hemodialysis: effective therapy for the encephalopathy of inborn errors of metabolism. J Pediatr, 116, 125-8. doi:10.1016/s0022-3476(05)81661-0 |
| F.75 |
Schaefer, F., Straube, E., Oh, J., Mehls, O., & Mayatepek, E. (Apr 1999). Dialysis in neonates with inborn errors of metabolism. Nephrol Dial Transplant, 14, 910-8. doi:10.1093/ndt/14.4.910 |
| F.46 |
Schönberger, S., Schweiger, B., Schwahn, B., Schwarz, M., & Wendel, U. (May 2004). Dysmyelination in the brain of adolescents and young adults with maple syrup urine disease. Mol Genet Metab, 82, 69-75. doi:10.1016/j.ymgme.2004.01.016 |
| F.119 |
Scriver, C.R., Mackenzie, S., Clow, C.L., & Delvin, E. (Feb 1971). Thiamine-responsive maple-syrup-urine disease. Lancet, 1, 310-2. doi:10.1016/s0140-6736(71)91041-5 |
| F.422 |
Shellmer, D.A., DeVito Dabbs, A., Dew, M.A., Noll, R.B., Feldman, H., Strauss, K.A., Morton, D.H., Vockley, J., & Mazariegos, G.V. (Feb 2011). Cognitive and adaptive functioning after liver transplantation for maple syrup urine disease: a case series. Pediatr Transplant, 15, 58-64. doi:10.1111/j.1399-3046.2010.01411.x |
| F.21 |
Simon, E., Flaschker, N., Schadewaldt, P., Langenbeck, U., & Wendel, U. (Dec 2006). Variant maple syrup urine disease (MSUD)--the entire spectrum. J Inherit Metab Dis, 29, 716-24. doi:10.1007/s10545-006-0276-1 |
| F.91 |
Simon, E., Wendel, U., & Schadewaldt, P. (2005 Jan-Mar). Maple syrup urine disease-treatment and outcome in patients of Turkish descent in Germany. Turk J Pediatr, 47(1):8-13. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/15884622 |
| G.33 |
Singh, R. (1994, Fall/Winter). Update of Nutrition Management of MSUD. MSUD Support Newsletter, 12(2). Retrieved from http://www.msud-support.org/index.php?option=com_content&view=article&id=64:update-of-nutrition-management-of-msud&catid=15:volume-12-2&Itemid=5 |
| G.26 |
Singh, R.H. (1999, April). Advances in Nutrition Management of Patients with MSUD [PowerPoint slides]. Paper presented at the 7th Abbott Nutrition Advances in Management of Inherited Metabolic Disorders. Washington, District of Columbia. |
| F.65 |
Skladal, D., Grissenauer, G., Konstantopoulou, V., Felber, S., & Sperl, W. (Jul 2000). Very high plasma leucine concentrations without neurological symptoms in a patient with classical maple syrup urine disease. J Inherit Metab Dis, 23, 513-4. doi:10.1023/a:1005620515996 |
| G.43 |
Strauss, K.A, Puffenberger,E.G., Morton, D.H. (2006). Maple Syrup Urine Disease. In Pagon R.A., Bird T.D., Dolan C.R., Stephens K., Adam M.P., editors, GeneReviews™. Seattle, WA: University of Washington, Seattle. |
| F.613 |
Strauss, K.A., & Morton, D.H. (Jul 2003). Branched-chain Ketoacyl Dehydrogenase Deficiency: Maple Syrup Disease. Curr Treat Options Neurol, 5, 329-341. doi:10.1007/s11940-003-0039-3 |
| F.35 |
Strauss, K.A., Mazariegos, G.V., Sindhi, R., Squires, R., Finegold, D.N., Vockley, G., Robinson, D.L., Hendrickson, C., Virji, M., Cropcho, L., Puffenberger, E.G., McGhee, W., Seward, L.M., & Morton, D.H. (Mar 2006). Elective liver transplantation for the treatment of classical maple syrup urine disease. Am J Transplant, 6, 557-64. doi:10.1111/j.1600-6143.2005.01209.x |
| F.426 |
Strauss, K.A., Wardley, B., Robinson, D., Hendrickson, C., Rider, N.L., Puffenberger, E.G., Shellmer, D., Shelmer, D., Moser, A.B., & Morton, D.H. (Apr 2010). Classical maple syrup urine disease and brain development: principles of management and formula design. Mol Genet Metab, 99, 333-45. doi:10.1016/j.ymgme.2009.12.007 |
| F.28 |
Tabanlioğlu, D., Ersoy-Evans, S., & Karaduman, A. (2009 Mar-Apr). Acrodermatitis enteropathica-like eruption in metabolic disorders: acrodermatitis dysmetabolica is proposed as a better term. Pediatr Dermatol, 26, 150-4. doi:10.1111/j.1525-1470.2008.00803.x |
| F.122 |
Tain, Y.L., Huang, S.C., Hung, F.C., Wang, H.S., & Sun, P.C. (1996 Sep-Oct). Acrodermatitis enteropathica-like eruption during treatment of maple syrup urine disease: report of one case. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi, 37(5):357-60. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/8942030 |
| F.3481 |
Tchan, M., Westbrook, M., Wilcox, G., Cutler, R., Smith, N., Penman, R., Strauss, B.J., & Wilcken, B. (2013). The management of pregnancy in maple syrup urine disease: experience with two patients. JIMD Rep, 10, 113-7. doi:10.1007/8904_2013_212 |
| F.423 |
Thimm, E., Hadzik, B., & Höhn, T. (Jul 2010). Continuous venovenous hemofiltration rapidly lowers toxic metabolites in a patient with MSUD and imminent cerebral herniation. Klin Padiatr, 222, 264-5. doi:10.1055/s-0030-1247508 |
| F.86 |
Thompson, G.N., Butt, W.W., Shann, F.A., Kirby, D.M., Henning, R.D., Howells, D.W., & Osborne, A. (Jun 1991). Continuous venovenous hemofiltration in the management of acute decompensation in inborn errors of metabolism. J Pediatr, 118, 879-84. doi:10.1016/s0022-3476(05)82198-5 |
| G.5 |
Thompson, S. et al. (2006, August, 17). Intermediate MSUD and Breast feeding/ MSUD Baby/ Calories for MSUD patient/ MSUD (new dx- for newborn). Message posted to Metabolic Dietician List, <PNO-METAB-L@LISTSERV.CC.EMORY.EDU> |
| F.96 |
Tornqvist, K., & Tornqvist, H. (1996). Corneal deepithelialization caused by acute deficiency of isoleucine during treatment of a patient with maple syrup urine disease. Acta Ophthalmol Scand Suppl. doi:10.1111/j.1600-0420.1996.tb00386.x |
| F.125 |
Treacy, E., Clow, C.L., Reade, T.R., Chitayat, D., Mamer, O.A., & Scriver, C.R. (1992). Maple syrup urine disease: interrelations between branched-chain amino-, oxo- and hydroxyacids; implications for treatment; associations with CNS dysmyelination. J Inherit Metab Dis, 15, 121-35. doi:10.1007/BF01800354 |
| G.3 |
Ueda, K. et al. (2001, August, 3). MSUD "wobblies"/ MSUD and Carnation Good Start/ BTK Deficiency or Allstrom Syndrome Diet/ E-3 Component Deficiency. Message posted to Metabolic Dietician List, <PNO-METAB-L@LISTSERV.CC.EMORY.EDU> |
| G.27 |
Van Calcar, S. (2003, MONTH). Diet Treatment for Maple Syrup Urine Disease (MSUD) [PowerPoint slides]. Paper presented at the 9th Abbott Nutrition Advances in Management of Inherited Metabolic Disorders.
|
| G.6 |
Van Calcar, S. et al. (2008, March, 21). Maternal MSUD/ Beta keto thiolase deficiency/ MSUD infant/ Mild MSUD and Protein restriction/ MSUD essential fatty acid intake . Message posted to Metabolic Dietician List, <PNO-METAB-L@LISTSERV.CC.EMORY.EDU> |
| F.102 |
Van Calcar, S.C., Harding, C.O., Davidson, S.R., Barness, L.A., & Wolff, J.A. (Nov 1992). Case reports of successful pregnancy in women with maple syrup urine disease and propionic acidemia. Am J Med Genet, 44, 641-6. doi:10.1002/ajmg.1320440523 |
| F.92 |
Wang, I.J., Chu, S.Y., Wang, C.Y., Wang, P.J., & Hwu, W.L. (2003 Jul-Aug). Maple syrup urine disease presenting with neonatal status epilepticus: report of one case. Acta Paediatr Taiwan, 44(4):246-8. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/14674232 |
| G.21 |
Wasserstein, M.P. (2006, Winter). Medical Therapy for Maple Syrup Urine Disease. MSUD Family Newsletter, 23(1). Retrieved fromhttp://www.msud-support.org/index.php?view=article&catid=41%3Avolume-23-1&id=314%3Amedical-therapy-for-maple-syrup-urine-disease&option=com_content&Itemid=5 |
| G.30 |
Wendel, U. (2004/05, Winter). Diagnostics and Treatment of MSUD in Germany. MSUD Support Newsletter, 22(1). Retrieved from http://www.msud-support.org/index.php?view=category&id=39%3Avolume-22-1&option=com_content&Itemid=5 |
| F.54 |
Wendel, U., Saudubray, J.M., Bodner, A., & Schadewaldt, P. (Dec 1999). Liver transplantation in maple syrup urine disease. Eur J Pediatr, 158 Suppl 2, S60-4. doi:10.1007/pl00014324 |
| F.3482 |
Wessel, A.E., Mogensen, K.M., Rohr, F., Erick, M., Neilan, E.G., Chopra, S., Levy, H.L., Gray, K.J., Wilkins-Haug, L., & Berry, G.T. (Sep 2015). Management of a Woman With Maple Syrup Urine Disease During Pregnancy, Delivery, and Lactation. JPEN J Parenter Enteral Nutr, 39, 875-9. doi:10.1177/0148607114526451 |
| F.49 |
Yoshida, S., & Tanaka, T. (Apr 2003). Postpartum death with maple syrup urine disease. Int J Gynaecol Obstet, 81, 57-8. doi:10.1016/s0020-7292(02)00446-0 |
| F.66 |
Yoshino, M., Aoki, K., Akeda, H., Hashimoto, K., Ikeda, T., Inoue, F., Ito, M., Kawamura, M., Kohno, Y., Koga, Y., Kuroda, Y., Maesaka, H., Murakamisoda, H., Sugiyama, N., Suzuki, Y., Yano, S., & Yoshioka, A. (Apr 1999). Management of acute metabolic decompensation in maple syrup urine disease: a multi-center study. Pediatr Int, 41, 132-7. doi:10.1046/j.1442-200x.1999.4121044.x |
