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3. [Rhabdomyolysis and myoglobinuria]. Lindner A; Zierz S Nervenarzt; 2003 Jun; 74(6):505-15. PubMed ID: 12799789 [TBL] [Abstract][Full Text] [Related]
4. Familial paroxysmal rhabdomyolysis: management of two cases of the non-exertional type. Ramesh V; Gardner-Medwin D Dev Med Child Neurol; 1992 Jan; 34(1):73-9. PubMed ID: 1544519 [TBL] [Abstract][Full Text] [Related]
5. [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]
6. Amino acid metabolism in patients with a hereditary myopathy and paroxysmal myoglobinuria. Wahren J; Linderholm H; Felig P Acta Med Scand; 1979; 206(4):309-14. PubMed ID: 506803 [No Abstract] [Full Text] [Related]
7. Strabismus as a possible sign of subclinical muscular dystrophy predisposing to rhabdomyolysis and myoglobinuria: a study of an affected family. Lewandowski KB Can Anaesth Soc J; 1982 Jul; 29(4):372-6. PubMed ID: 7104807 [TBL] [Abstract][Full Text] [Related]
8. Acute rhabdomyolysis with myoglobinuria. Miller BH; Gross JS Va Med Mon (1918); 1967 Apr; 94(4):213-9. PubMed ID: 6041747 [No Abstract] [Full Text] [Related]
10. The clinical diagnosis of McArdle's disease. Identification of another family with deficiency of muscle phosphorylase. Rowland LP; Lovelace RE; Schotland DL; Araki S; Carmel P Neurology; 1966 Jan; 16(1):93-100. PubMed ID: 5215287 [No Abstract] [Full Text] [Related]
11. [Hreditary myopathies]. Kuhn E Ergeb Inn Med Kinderheilkd; 1969; 28():188-290. PubMed ID: 4897097 [No Abstract] [Full Text] [Related]