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4. [Emergency treatment of inborn amino errors of amino acid metabolism detected in the neonatal period]. Saudubray JM; Amédée-Manesme O; Lavaud J; Mselati JC; Besson-Leaud M; Ogier H; Checouri A; Leraillez J; Ferre P; Coude FX; Charpentier C Arch Fr Pediatr; 1979 Dec; 36(10):969-80. PubMed ID: 121227 [TBL] [Abstract][Full Text] [Related]
5. The management and long term outcome of organic acidaemias. Leonard JV; Daish P; Naughten ER; Bartlett K J Inherit Metab Dis; 1984; 7 Suppl 1():13-7. PubMed ID: 6434837 [TBL] [Abstract][Full Text] [Related]
6. Nutrition therapy of organic acidaemias with amino acid-based formulas: emphasis on methylmalonic and propionic acidaemia. Yannicelli S J Inherit Metab Dis; 2006; 29(2-3):281-7. PubMed ID: 16763889 [TBL] [Abstract][Full Text] [Related]
7. 'Classical' organic acidurias, propionic aciduria, methylmalonic aciduria and isovaleric aciduria: long-term outcome and effects of expanded newborn screening using tandem mass spectrometry. Dionisi-Vici C; Deodato F; Röschinger W; Rhead W; Wilcken B J Inherit Metab Dis; 2006; 29(2-3):383-9. PubMed ID: 16763906 [TBL] [Abstract][Full Text] [Related]
8. Peritoneal dialysis in the treatment of metabolic crises caused by inherited disorders of organic and amino acid metabolism. Gortner L; Leupold D; Pohlandt F; Bartmann P Acta Paediatr Scand; 1989 Sep; 78(5):706-11. PubMed ID: 2596277 [TBL] [Abstract][Full Text] [Related]
9. Use of proton nuclear magnetic resonance spectroscopy in detection and study of organic acidurias. Iles RA; Hind AJ; Chalmers RA Clin Chem; 1985 Nov; 31(11):1795-801. PubMed ID: 2996806 [TBL] [Abstract][Full Text] [Related]
10. Hyperammonemia secondary to hereditary organic acidurias: a study of 29 cases. Saudubray JM; Coudé FX; Ogier H; Cathelineau L; Briand P; Charpentier C Adv Exp Med Biol; 1982; 153():135-40. PubMed ID: 7164893 [No Abstract] [Full Text] [Related]
11. Methylmalonic and propionic acidurias: management without or with a few supplements of specific amino acid mixture. Touati G; Valayannopoulos V; Mention K; de Lonlay P; Jouvet P; Depondt E; Assoun M; Souberbielle JC; Rabier D; Ogier de Baulny H; Saudubray JM J Inherit Metab Dis; 2006; 29(2-3):288-98. PubMed ID: 16763890 [TBL] [Abstract][Full Text] [Related]
12. Breastfeeding experience in inborn errors of metabolism other than phenylketonuria. Huner G; Baykal T; Demir F; Demirkol M J Inherit Metab Dis; 2005; 28(4):457-65. PubMed ID: 15902548 [TBL] [Abstract][Full Text] [Related]
13. [Combined exchange transfusion and peritoneal dialysis treatment in a neonatal case of methylmalonic acidemia with severe hyperammonemia]. Sanjurjo P; Jaquotot C; Vallo A; Uriarte R; Prats JM; Ugarte M; Rodríguez Soriano J An Esp Pediatr; 1982 Oct; 17(4):317-20. PubMed ID: 6818879 [TBL] [Abstract][Full Text] [Related]
14. Methylmalonic and propionic acidaemias: management and outcome. de Baulny HO; Benoist JF; Rigal O; Touati G; Rabier D; Saudubray JM J Inherit Metab Dis; 2005; 28(3):415-23. PubMed ID: 15868474 [TBL] [Abstract][Full Text] [Related]
15. 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; J Inherit Metab Dis; 2021 May; 44(3):593-605. PubMed ID: 32996606 [TBL] [Abstract][Full Text] [Related]
16. Cutaneous manifestations of methylmalonic and propionic acidaemia: a description based on 38 cases. Bodemer C; De Prost Y; Bachollet B; Poggi F; Teillac-Hamel D; Fraitag S; Saudubray JM Br J Dermatol; 1994 Jul; 131(1):93-8. PubMed ID: 8043426 [TBL] [Abstract][Full Text] [Related]
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18. Inborn errors of propionate metabolism: methylmalonic and propionic acidaemias. Thompson GN J Paediatr Child Health; 1992 Apr; 28(2):134-5. PubMed ID: 1562361 [No Abstract] [Full Text] [Related]
19. Differential response to renal replacement therapy in neonatal-onset inborn errors of metabolism. Porta F; Peruzzi L; Bonaudo R; Pieretti S; Busso M; Cocchi E; Conio A; Pagliardini V; Spada M Nephrology (Carlton); 2018 Oct; 23(10):957-961. PubMed ID: 29888426 [TBL] [Abstract][Full Text] [Related]
20. Molecular and phenotypic characteristics of seven novel mutations causing branched-chain organic acidurias. Stojiljkovic M; Klaassen K; Djordjevic M; Sarajlija A; Brasil S; Kecman B; Grkovic S; Kostic J; Rodriguez-Pombo P; Desviat LR; Pavlovic S; Perez B Clin Genet; 2016 Sep; 90(3):252-7. PubMed ID: 26830710 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]