138 related articles for article (PubMed ID: 11596365)
1. [Mitochondrial diseases with recurrent myoglobinuria].
Murakami N
Ryoikibetsu Shokogun Shirizu; 2001; (36):183-5. PubMed ID: 11596365
[No Abstract] [Full Text] [Related]
2. Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy.
Tein I; De Vivo DC; Hale DE; Clarke JT; Zinman H; Laxer R; Shore A; DiMauro S
Ann Neurol; 1991 Sep; 30(3):415-9. PubMed ID: 1835339
[TBL] [Abstract][Full Text] [Related]
3. Recurrent myoglobinuria as a presenting manifestation of very long chain acyl coenzyme A dehydrogenase deficiency.
Straussberg R; Harel L; Varsano I; Elpeleg ON; Shamir R; Amir J
Pediatrics; 1997 Jun; 99(6):894-6. PubMed ID: 9164788
[No Abstract] [Full Text] [Related]
4. [Recurrent myoglobinuria in a girl due to carnitine palmitoyltransferase deficiency].
Carrasco Marina LL; Ramos Lizana J; Vázquez López M; Garrote de Marcos JM; Arregui Sierra A; Bornstein B; Arenas J
An Esp Pediatr; 1996 Jan; 44(1):67-9. PubMed ID: 8849066
[No Abstract] [Full Text] [Related]
5. [Coenzyme Q10 deficiency].
Imataka G; Yamanouchi H
Nihon Rinsho; 2002 Apr; 60 Suppl 4():462-5. PubMed ID: 12013914
[No Abstract] [Full Text] [Related]
6. [Fatal infantile mitochondrial disease].
Murakami N
Ryoikibetsu Shokogun Shirizu; 2001; (36):173-5. PubMed ID: 11596361
[No Abstract] [Full Text] [Related]
7. [Recurrent myoglobinuria caused by carnitine-palmityl-transferase deficiency].
Pamies-Andreu E; Sánchez-Román J; Bautista J; Segura DI
Rev Clin Esp; 1987 May; 180(8):462-3. PubMed ID: 3616029
[No Abstract] [Full Text] [Related]
8. Exercise intolerance and the mitochondrial respiratory chain.
DiMauro S
Ital J Neurol Sci; 1999 Dec; 20(6):387-93. PubMed ID: 10937858
[TBL] [Abstract][Full Text] [Related]
9. [Acute recurrent renal insufficiency in a patient with atraumatic rhabdomyolysis caused by carnitine-palmitoyltransferase deficiency].
Castiglione A; Cornelio F; Vendemia F; Rimoldi M; Sinico R; Baroni M; D'Amico G
Minerva Nefrol; 1981; 28(3):229-34. PubMed ID: 7329599
[No Abstract] [Full Text] [Related]
10. [Complex I (NADH-ubiquinone oxidoreductase) deficiency].
Nonaka I
Ryoikibetsu Shokogun Shirizu; 2001; (36):129-31. PubMed ID: 11596342
[No Abstract] [Full Text] [Related]
11. [Pure mitochondrial myopathy].
Murakami N; Sakuta R
Ryoikibetsu Shokogun Shirizu; 2001; (36):186-9. PubMed ID: 11596366
[No Abstract] [Full Text] [Related]
12. Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
Enns GM; Bennett MJ; Hoppel CL; Goodman SI; Weisiger K; Ohnstad C; Golabi M; Packman S
J Pediatr; 2000 Feb; 136(2):251-4. PubMed ID: 10657835
[TBL] [Abstract][Full Text] [Related]
13. [Recurrent paroxysmal myoglobinuria with acute renal insufficiency caused by muscular carnitine (palmitoyltransferase deficiency. A case].
Meunier J; Perrot D; Bret M; Pissere-Meunier J; Bouletreau P; Pasquier J; Carrier H; Berthillier G
Nouv Presse Med; 1982 Sep; 11(37):2767-71. PubMed ID: 7145668
[TBL] [Abstract][Full Text] [Related]
14. Respiratory chain deficiency presenting as recurrent myoglobinuria in childhood.
de Lonlay-Debeney P; Edery P; Cormier-Daire V; Parfait B; Chrétien D; Rötig A; Romero N; Saudubray JM; Munnich A; Rustin P
Neuropediatrics; 1999 Feb; 30(1):42-4. PubMed ID: 10222461
[TBL] [Abstract][Full Text] [Related]
15. Determination of total fatty acids in plasma: cis-5-tetradecenoic acid (C14:1 omega-9) in the diagnosis of long-chain fatty acid oxidation defects.
Divry P; Vianey-Saban C; Mathieu M
J Inherit Metab Dis; 1999 May; 22(3):286-8. PubMed ID: 10384388
[No Abstract] [Full Text] [Related]
16. [A female case of carnitine palmitoyltransferase deficiency].
Taniwaki T; Kira J; Kitaguchi T; Goto I; Sugiyama N
Rinsho Shinkeigaku; 1989 Mar; 29(3):382-4. PubMed ID: 2752669
[TBL] [Abstract][Full Text] [Related]
17. Very-long-chain acyl-coenzyme A dehydrogenase deficiency--a new cause of myoglobinuric acute renal failure.
Cairns AP; O'Donoghue PM; Patterson VH; Brown JH
Nephrol Dial Transplant; 2000 Aug; 15(8):1232-4. PubMed ID: 10910451
[No Abstract] [Full Text] [Related]
18. Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria.
Minetti C; Garavaglia B; Bado M; Invernizzi F; Bruno C; Rimoldi M; Pons R; Taroni F; Cordone G
Neuromuscul Disord; 1998 Feb; 8(1):3-6. PubMed ID: 9565984
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. Subclinical effects of long-chain fatty acid β-oxidation deficiency on the adult heart: A case-control magnetic resonance study.
Knottnerus SJG; Bleeker JC; Ferdinandusse S; Houtkooper RH; Langeveld M; Nederveen AJ; Strijkers GJ; Visser G; Wanders RJA; Wijburg FA; Boekholdt SM; Bakermans AJ
J Inherit Metab Dis; 2020 Sep; 43(5):969-980. PubMed ID: 32463482
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
