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Баранов А.А., Намазова-Баранова Л.С., Боровик Т.Э., Ладодо К.С., Бушуева Т.В., Маслова О.И., Кузенкова Л.М., Журкова Н.В., Звонкова Н.Г. и др. Диетотерапия при наследственных болезнях аминокислотного обмена Методическое письмо. Москва. 2013. 97 с.
MP 2.3.1.2432-08 "Нормы физиологических потребностей в энергии и пищевых веществах для различных групп населения Российской Федерации" (утв. Главным государственным санитарным врачом РФ 18 декабря 2008 г.).
Arbeiter AK, Kranz B, Wingen AM, Bonzel KE, Dohna-Schwake C, Hanssler L, Neudorf U, Hoyer PF, Buscher R: Continuous venovenous haemodialysis (CVVHD) and continuous peritoneal dialysis (CPD) in the acute management of 21 children with inborn errors of metabolism. Nephrol Dial Transplant 2010, 25:1257–1265.
Carrillo-Carrasco N, Venditti C: Propionic Acidemia. University of Washington: Seattle; 2012. http://www.ncbi.nlm.nih.gov/books/NBK92946/.
Chapman KA, Gropman A, MacLeod E, Stagni K, Summar ML, Ueda K, Ah Mew N, Franks J, Island E, Matern D, Pena L, Smith B, Sutton RV, Urv T, Venditti C, Chakrapani A: Acute management of propionic acidemia. Mol Genet Metab 2012, 105:16–25.
Dweikat IM, Naser EN, Abu Libdeh AI OJN, Abu Gharbieh NN, Maraga NF, Abu Libdeh BY: Propionic acidemia mimicking diabetic ketoacidosis. Brain Dev 2011, 33:428–431.
Grünert SC, Müllerleile S, de Silva L, Barth M, Walter M, Walter K, Meissner T, Lindner M, Ensenauer R, Santer R, Bodamer OA, Baumgartner MR, Brunner-Krainz M, Karall D, Haase C, Knerr I, Marquardt T, Hennermann JB, Steinfeld R, Beblo S, Koch HG, Konstantopoulou V, Scholl-Bürgi S, van Teeffelen-Heithoff A, Suormala T, Sperl W, Kraus JP, Superti-Furga A, Schwab KO, Sass JO: Propionic acidemia: neonatal versus selective metabolic screening. J Inherit Metab Dis 2012, 35:41–49.
Grünert SC, Müllerleile S, De Silva L, Barth M, Walter M, Walter K, Meissner T, Lindner M, Ensenauer R, Santer R, Bodamer OA, Baumgartner MR, Brunner-Krainz M, Karall D, Haase C, Knerr I, Marquardt T, Hennermann JB, Steinfeld R, Beblo S, Koch HG, Konstantopoulou V, Scholl-Bürgi S, van Teeffelen-Heithoff A, Suormala T, Sperl W, Kraus JP, Superti-Furga A, Schwab KO, Sass JO: Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis 2013, 8:6.
Haberlandt E, Canestrini C, Brunner-Krainz M, Moslinger D, Mussner K, Plecko B, SchollBurgi S, Sperl W, Rostasy K, Karall D: Epilepsy in patients with propionic acidemia. Neuropediatrics 2009, 40:120–125.
Matthias R Baumgartner, Friederike Hörster, Carlo Dionisi-Vici, Goknur Haliloglu, Daniela Karall et al. Proposed guidelines for the diagnosis and management of methylmalonic and propionic academia Baumgartner et al. Orphanet Journal of Rare Diseases 2014, 9:130. http://www.ojrd.com/content/9/1/130.
Picca S, Bartuli A, Dionisi-Vici C: Medical management and dialysis therapy for the infant with an inborn error of metabolism. Semin Nephrol 2008, 28:477–480. Chapman KA, Summar ML: Propionic acidemia consensus conference summary. Mol Genet Metab 2012, 105:3–4.
Sass JO, Hofmann M, Skladal D, Mayatepek E, Schwahn B, Sperl W: Propionic acidemia revisited: a workshop report. Clin Pediatr (Phila) 2004, 43:837–843.