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4. Necrotizing vacuolar myopathy presenting with recurrent myoglobinuria. Nandhagopal R; Al-Asmi A; Arunodaya GR; Jacob PC; Al-Azri F; Harper C Int J Neurosci; 2010 Dec; 120(12):784-6. PubMed ID: 20942590 [TBL] [Abstract][Full Text] [Related]
5. [Differential diagnosis of paroxysmal myoglobinuric syndromes within the framework of myopathy]. Schulze HA Neurologija; 1979; 27(1-4):59-65. PubMed ID: 262020 [No Abstract] [Full Text] [Related]
8. [Idiopathic paroxysmal rhabdomyolysis or essential myoglobinuria (Meyer-Betz disease)]. Michel M Pediatrie; 1967 Sep; 22(6):743-6. PubMed ID: 5621103 [No Abstract] [Full Text] [Related]
9. An adolescent girl with Meyer-Betz syndrome. Kasap B; Soylu A; Türkmen M; Kavukcu S Clin Rheumatol; 2006 Nov; 25(6):904-6. PubMed ID: 16328090 [TBL] [Abstract][Full Text] [Related]
10. [Clinical demonstrations of hereditary disorders of metabolism]. Marti HR Schweiz Med Wochenschr; 1980 Dec; 110(49):1857-63. PubMed ID: 7455656 [TBL] [Abstract][Full Text] [Related]
11. Differential diagnosis of paroxysmal myoglobinuria. A case report. Bottacchi E; Rimoldi M; Di Donato S; Camerlingo M; Gambaro P; Mamoli A Acta Neurol (Napoli); 1987 Apr; 9(2):111-5. PubMed ID: 3508346 [No Abstract] [Full Text] [Related]
12. [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]
13. [Paroxysmal paralytic myoglobinuria. Restatement according to a personal observation (author's transl)]. Ginies G; Lamisse F; Choutet P; Gautier J; Fetissoff F; Muh JP; Breteau M; Bruneau JJ Sem Hop; 1979 Apr 8-15; 55(13-14):639-45. PubMed ID: 224479 [TBL] [Abstract][Full Text] [Related]
14. [Acute myoglobinuria accompanied by renal failure in high febril infection (author's transl)]. Kaukel E; Hagenah R; Müller-Jensen A Med Klin; 1976 Mar; 71(11):462-4. PubMed ID: 1263994 [TBL] [Abstract][Full Text] [Related]
15. [A case of paroxysmal idiopathic primary myoglobinuria: its identification with various laboratory tests]. Perosa L; Pirrelli A Boll Soc Ital Biol Sper; 1965 Apr; 41(8):418-21. PubMed ID: 5875565 [No Abstract] [Full Text] [Related]
16. Idiopathic rhabdomyolysis with myoglobinuria (Meyer-Betz disease). Alpers JH; Walker B Med J Aust; 1968 Oct; 2(17):719-20. PubMed ID: 5725963 [No Abstract] [Full Text] [Related]
18. Phosphoglycerate kinase deficiency: another cause of recurrent myoglobinuria. DiMauro S; Dalakas M; Miranda AF Ann Neurol; 1983 Jan; 13(1):11-9. PubMed ID: 6830158 [TBL] [Abstract][Full Text] [Related]
19. Sporadic distal myopathy with early adult onset. Miller RG; Blank NK; Layzer RB Ann Neurol; 1979 Mar; 5(3):220-7. PubMed ID: 443754 [TBL] [Abstract][Full Text] [Related]