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Journal Abstract Search
165 related items for PubMed ID: 2553027
1. Pyruvate carboxylase deficiency: acute exacerbation after ACTH treatment of infantile spasms. Rutledge SL, Snead OC, Kelly DR, Kerr DS, Swann JW, Spink DL, Martin DL. Pediatr Neurol; 1989; 5(4):249-52. PubMed ID: 2553027 [Abstract] [Full Text] [Related]
2. Pyruvate Carboxylase Deficiency Type C: A Rare Cause of Acute Transient Flaccid Paralysis with Ketoacidosis. Almomen M, Sinclair G, Stockler-Ipsiroglu SG, Horvath GA. Neuropediatrics; 2018 Dec; 49(6):369-372. PubMed ID: 30045381 [Abstract] [Full Text] [Related]
3. [Neonatal lactic acidosis caused by severe pyruvate carboxylase deficiency]. Merinero Cortés B, del Valle Martínez J, Pérez-Cerdá Silvestre C, García Muñoz MJ, Cortés Coto MT, García Aparicio J, Sáez Pérez E, Ugarte Pérez M. An Esp Pediatr; 1988 Jul; 29(1):57-60. PubMed ID: 3142324 [Abstract] [Full Text] [Related]
4. Adrenocorticotropic hormone therapy for infantile spasms alters pyruvate metabolism in the central nervous system. Miyazaki M, Hashimoto T, Yoneda Y, Saijio T, Mori K, Ito M, Kuroda Y. Brain Dev; 1998 Aug; 20(5):312-8. PubMed ID: 9761001 [Abstract] [Full Text] [Related]
7. Congenital lactic acidosis due to pyruvate carboxylase deficiency: absence of an inhibitor of TPP-ATP phosphoryl transferase. Tada K, Takada G, Omura K, Itokawa Y. Eur J Pediatr; 1978 Jan 17; 127(2):141-7. PubMed ID: 203466 [Abstract] [Full Text] [Related]
8. Pyruvate carboxylase deficiency: a benign variant with normal development. Van Coster RN, Fernhoff PM, De Vivo DC. Pediatr Res; 1991 Jul 17; 30(1):1-4. PubMed ID: 1909777 [Abstract] [Full Text] [Related]
9. Congenital lactic acidosis associated with pyruvate carboxylase deficiency. Sagy M, Barzilay Z, Barash V, Oren M, Vardi P, Cohen BE, Gutman A. Isr J Med Sci; 1981 Dec 17; 17(12):1159-63. PubMed ID: 6799424 [Abstract] [Full Text] [Related]
10. Pyruvate-carboxylase deficiency with urea cycle impairment. Greter J, Gustafsson J, Holme E. Acta Paediatr Scand; 1985 Nov 17; 74(6):982-6. PubMed ID: 3937431 [Abstract] [Full Text] [Related]
11. Lactic acidosis in paediatrics: clinical and laboratory evaluation. Stern HJ. Ann Clin Biochem; 1994 Sep 17; 31 ( Pt 5)():410-9. PubMed ID: 7832568 [No Abstract] [Full Text] [Related]
12. Disorders of pyruvate metabolism. De Meirleir L. Handb Clin Neurol; 2013 Sep 17; 113():1667-73. PubMed ID: 23622387 [Abstract] [Full Text] [Related]
14. [Inherited metabolic diseases associated with West syndrome]. Wada K, Sakuragawa N. Ryoikibetsu Shokogun Shirizu; 2002 Apr 17; (37 Pt 6):283-7. PubMed ID: 12483882 [No Abstract] [Full Text] [Related]
15. Hyperalaninemia hyperpyruvicemia and lactic acidosis due to pyruvate carboxylase deficiency of the liver; treatment with thiamine and lipoic acid. Maesaka H, Komiya K, Misugi K, Tada K. Eur J Pediatr; 1976 May 04; 122(2):159-68. PubMed ID: 817914 [Abstract] [Full Text] [Related]
16. [An autopsy case of neonatal lactic acidosis]. Giordano G, Corradi D, D'Adda T, Melissari M. Pathologica; 2001 Feb 04; 93(1):39-43. PubMed ID: 11294018 [Abstract] [Full Text] [Related]
17. Brain amino acid abnormalities in pyruvate carboxylase deficiency. Perry TL, Haworth JC, Robinson BH. J Inherit Metab Dis; 1985 Feb 04; 8(2):63-6. PubMed ID: 2878111 [Abstract] [Full Text] [Related]
18. Pyruvate carboxylase deficiency and lactic acidosis in a retarded child without Leigh's disease. Atkin BM, Buist NR, Utter MF, Leiter AB, Banker BQ. Pediatr Res; 1979 Feb 04; 13(2):109-16. PubMed ID: 219411 [Abstract] [Full Text] [Related]
19. Lactic acidosis due to pyruvate carboxylase deficiency. Haworth JC, Robinson BH, Perry TL. J Inherit Metab Dis; 1981 Feb 04; 4(2):57-8. PubMed ID: 6790846 [Abstract] [Full Text] [Related]
20. Case Report: Prenatal neurological injury in a neonate with pyruvate carboxylase deficiency type B. Xue M. Front Endocrinol (Lausanne); 2023 Feb 04; 14():1199590. PubMed ID: 37484962 [Abstract] [Full Text] [Related] Page: [Next] [New Search]