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30. Enigmatic conflict of clinical and molecular diagnosis in Duchenne/Becker muscular dystrophy. Dubowitz V Neuromuscul Disord; 2006 Dec; 16(12):865-6. PubMed ID: 17118656 [No Abstract] [Full Text] [Related]
31. [Critical evaluation of changes of serum CK after exertion in the identification of carriers of Duchenne's muscular dystrophy]. Cordone G; Venzano V; Rossi G; Cavallero G; Minetti C Pediatr Med Chir; 1984; 6(6):819-22. PubMed ID: 6545595 [TBL] [Abstract][Full Text] [Related]
32. Subclinical Becker's muscular dystrophy presenting with severe heart failure. Yokota R; Shirotani M; Kouchi I; Hirai T; Uemori N; Ohta Y; Mitsui Y; Hattori R Intern Med; 2004 Mar; 43(3):204-8. PubMed ID: 15098601 [TBL] [Abstract][Full Text] [Related]
33. Duchenne muscular dystrophy: issues in expanding newborn screening. Kemper AR; Wake MA Curr Opin Pediatr; 2007 Dec; 19(6):700-4. PubMed ID: 18025940 [TBL] [Abstract][Full Text] [Related]
34. Genetic and environmental components of serum creatine kinase (CK) and pyruvate kinase (PK) in normal twins: implication for genetic risks estimates in Duchenne muscular dystrophy carriers. Rapaport D; Colletto GM; Zatz M Am J Med Genet; 1988 Oct; 31(2):291-8. PubMed ID: 3232697 [TBL] [Abstract][Full Text] [Related]
35. Early symptoms of Duchenne muscular dystrophy--description of cases of an 18-month-old and an 8-year-old patient. Iwańczak F; Stawarski A; Potyrała M; Siedlecka-Dawidko J; Agrawal GS Med Sci Monit; 2000; 6(3):592-5. PubMed ID: 11208376 [TBL] [Abstract][Full Text] [Related]
36. Review of Duchenne muscular dystrophy (DMD) for the pediatricians in the community. Verma S; Anziska Y; Cracco J Clin Pediatr (Phila); 2010 Nov; 49(11):1011-7. PubMed ID: 20724320 [No Abstract] [Full Text] [Related]
37. Biomarkers and surrogate endpoints in Duchenne: meeting report. Aartsma-Rus A; Ferlini A; Vroom E Neuromuscul Disord; 2014 Aug; 24(8):743-5. PubMed ID: 24951452 [No Abstract] [Full Text] [Related]
38. Evaluation of early second trimester maternal serum creatine kinase isoenzyme BB as a marker of poor pregnancy outcome. Jenkins CB; Ghidini A; Spong CY; Eglinton GS; Pezzullo JC; Michejda M Fetal Diagn Ther; 1997; 12(6):356-9. PubMed ID: 9475367 [TBL] [Abstract][Full Text] [Related]
39. Evaluation of carrier detection of Duchenne muscular dystrophy using carbonic anhydrase III and creatine kinase. Heath R; Carter ND; Jeffery S; Edwards RJ; Watts DC; Watts RL Am J Med Genet; 1985 Jun; 21(2):291-6. PubMed ID: 3925781 [TBL] [Abstract][Full Text] [Related]
40. Creatine-kinase and pyruvate-kinase activities in normal children: implications in Duchenne muscular dystrophy carrier detection. Passos MR; Gonzalez CH; Zatz M Am J Med Genet; 1985 Oct; 22(2):255-62. PubMed ID: 4050856 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]