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Journal Abstract Search

285 related items for PubMed ID: 7726386

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  • 5. Methylmalonic Acidemia.
    Mahmud S, Awais Ul Hassan Shah S, Ali S.
    J Coll Physicians Surg Pak; 2015 Jun; 25(6):462-4. PubMed ID: 26101005
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  • 7. Methylmalonic acidemia with the unusual complication of severe hyperglycemia.
    Boeckx RL, Hicks JM.
    Clin Chem; 1982 Aug; 28(8):1801-3. PubMed ID: 7046992
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  • 8. [Diagnosis and treatment of methylmalonic acidemia in 14 cases].
    Jin H, Zou LP, Zhang CH, Fang F, Xiao J, Wu HS, Zhu C, Guo W, Jin Z.
    Zhonghua Er Ke Za Zhi; 2004 Aug; 42(8):581-4. PubMed ID: 15347443
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  • 9. Parenteral nutrition in propionic and methylmalonic acidemia.
    Kahler SG, Millington DS, Cederbaum SD, Vargas J, Bond LD, Maltby DA, Gale DS, Roe CR.
    J Pediatr; 1989 Aug; 115(2):235-41. PubMed ID: 2502611
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  • 10. Development of a signs and symptoms outcome measure for caregivers of patients with methylmalonic acidemia and propionic acidemia (MMAPAQ).
    Sikirica V, Schwartz EJ, Vockley J, Stagni K, Bellenger MA, Banerjee G, Durgam N, Moshkovich O.
    Mol Genet Metab; 2024 Aug; 143(1-2):108577. PubMed ID: 39303317
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  • 11. Liver and/or kidney transplantation in amino and organic acid-related inborn errors of metabolism: An overview on European data.
    Molema F, Martinelli D, Hörster F, Kölker S, Tangeraas T, de Koning B, Dionisi-Vici C, Williams M, additional individual contributors of MetabERN.
    J Inherit Metab Dis; 2021 May; 44(3):593-605. PubMed ID: 32996606
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  • 12. The Relationship between Dietary Intake, Growth, and Body Composition in Inborn Errors of Intermediary Protein Metabolism.
    Evans M, Truby H, Boneh A.
    J Pediatr; 2017 Sep; 188():163-172. PubMed ID: 28629683
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  • 15. Methylmalonic and propionic acidemia among hospitalized pediatric patients: a nationwide report.
    Jiang YZ, Shi Y, Shi Y, Gan LX, Kong YY, Zhu ZJ, Wang HB, Sun LY.
    Orphanet J Rare Dis; 2019 Dec 16; 14(1):292. PubMed ID: 31842933
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  • 16. Decreased plasma l-arginine levels in organic acidurias (MMA and PA) and decreased plasma branched-chain amino acid levels in urea cycle disorders as a potential cause of growth retardation: Options for treatment.
    Molema F, Gleich F, Burgard P, van der Ploeg AT, Summar ML, Chapman KA, Lund AM, Rizopoulos D, Kölker S, Williams M, Additional individual contributors from E-IMD.
    Mol Genet Metab; 2019 Apr 16; 126(4):397-405. PubMed ID: 30827756
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  • 18. Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia.
    Baumgartner MR, Hörster F, Dionisi-Vici C, Haliloglu G, Karall D, Chapman KA, Huemer M, Hochuli M, Assoun M, Ballhausen D, Burlina A, Fowler B, Grünert SC, Grünewald S, Honzik T, Merinero B, Pérez-Cerdá C, Scholl-Bürgi S, Skovby F, Wijburg F, MacDonald A, Martinelli D, Sass JO, Valayannopoulos V, Chakrapani A.
    Orphanet J Rare Dis; 2014 Sep 02; 9():130. PubMed ID: 25205257
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  • 19. Understanding acute metabolic decompensation in propionic and methylmalonic acidemias: a deep metabolic phenotyping approach.
    Haijes HA, Jans JJM, van der Ham M, van Hasselt PM, Verhoeven-Duif NM.
    Orphanet J Rare Dis; 2020 Mar 06; 15(1):68. PubMed ID: 32143654
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  • 20. [Outcomes of patients with combined methylmalonic acidemia and homocystinuria after treatment].
    Huang Z, Han LS, Ye J, Qiu WJ, Zhang HW, Gao XL, Wang Y, Ji WJ, Li XY, Gu XF.
    Zhonghua Er Ke Za Zhi; 2013 Mar 06; 51(3):194-8. PubMed ID: 23751581
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