These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
106 related articles for article (PubMed ID: 19222961)
1. [A case report of carnitine palmitoyltransferase II deficiency]. Zhang LX; Gao PM Zhongguo Dang Dai Er Ke Za Zhi; 2009 Feb; 11(2):1p preceeding I. PubMed ID: 19222961 [No Abstract] [Full Text] [Related]
2. Lethal neonatal multiorgan deficiency of carnitine palmitoyltransferase II. Hug G; Bove KE; Soukup S N Engl J Med; 1991 Dec; 325(26):1862-4. PubMed ID: 1961225 [No Abstract] [Full Text] [Related]
3. Neonatal carnitine palmitoyltransferase deficiency: a case with a muscular presentation. Land JM; Mistry S; Squier W; Hope P; Orford M; Saggerson ED Prog Clin Biol Res; 1992; 375():309-15. PubMed ID: 1438376 [No Abstract] [Full Text] [Related]
4. [Myoglobinuria due to a deficiency of carnitine palmitoyltransferase II. A clinical case report]. Venturini E; Pupeschi L Recenti Prog Med; 1994 May; 85(5):282-3. PubMed ID: 8023007 [TBL] [Abstract][Full Text] [Related]
5. Lethal neonatal deficiency of carnitine palmitoyltransferase 2. Scholte HR; van Tol A N Engl J Med; 1992 Jul; 327(1):56. PubMed ID: 1598114 [No Abstract] [Full Text] [Related]
11. Reversible asphyxial status in a newborn due to neonatal form of carnitine palmitoyltransferase II deficiency. Brucknerova I; Bzduch V; Behulova D; Ferianec V; Dubovicky M; Ujhazy E; Mach M Neuro Endocrinol Lett; 2008 Oct; 29(5):627-30. PubMed ID: 18987586 [TBL] [Abstract][Full Text] [Related]
12. Severe rhabdomyolysis with hypoglycemia in an adult patient with carnitine palmitoyltransferase II deficiency. Deutsch M; Vassilopoulos D; Sevastos N; Papadimitriou A; Vasiliou K; Archimandritis AJ Eur J Intern Med; 2008 Jun; 19(4):289-91. PubMed ID: 18471680 [TBL] [Abstract][Full Text] [Related]
13. Lethal neonatal and severe late infantile forms of carnitine palmitoyltransferase II deficiency associated with compound heterozygosity for different protein truncation mutations. Vladutiu GD; Quackenbush EJ; Hainline BE; Albers S; Smail DS; Bennett MJ J Pediatr; 2002 Nov; 141(5):734-6. PubMed ID: 12410208 [TBL] [Abstract][Full Text] [Related]
14. Autopsy case of the neonatal form of carnitine palmitoyltransferase-II deficiency triggered by a novel disease-causing mutation del1737C. Semba S; Yasujima H; Takano T; Yokozaki H Pathol Int; 2008 Jul; 58(7):436-41. PubMed ID: 18577113 [TBL] [Abstract][Full Text] [Related]
15. Brief report: renal tubular acidosis in carnitine palmitoyltransferase type 1 deficiency. Falik-Borenstein ZC; Jordan SC; Saudubray JM; Brivet M; Demaugre F; Edmond J; Cederbaum SD N Engl J Med; 1992 Jul; 327(1):24-7. PubMed ID: 1598098 [No Abstract] [Full Text] [Related]