110 related articles for article (PubMed ID: 1244534)
1. Carrier detection in Duchenne muscular dystrophy.
Roses AD; Roses MJ; Miller SE; Hull KL; Appel SH
N Engl J Med; 1976 Jan; 294(4):193-8. PubMed ID: 1244534
[TBL] [Abstract][Full Text] [Related]
2. Serum creatine kinase and pyruvate kinase in Duchenne muscular dystrophy carrier detection.
Percy ME; Chang LS; Murphy EG; Oss I; Verellen-Dumoulin C; Thompson MW
Muscle Nerve; 1979; 2(5):329-39. PubMed ID: 492209
[TBL] [Abstract][Full Text] [Related]
3. Pedigree testing in Duchenne muscular dystrophy.
Roses AD; Roses MJ; Metcalf BS; Hull KL; Nicholson GA; Hartwig GB; Roe CR
Ann Neurol; 1977 Oct; 2(4):271-8. PubMed ID: 617266
[TBL] [Abstract][Full Text] [Related]
4. Echinogenic action of L-alpha-lysophosphatidylcholine in Duchenne muscular dystrophy: a study on carrier detection.
Tangorra A; Curatola G; Milani-Comparetti M; Ferretti G
Am J Med Genet; 1989 Apr; 32(4):540-4. PubMed ID: 2774000
[TBL] [Abstract][Full Text] [Related]
5. Discriminant analysis of ribosomal protein synthesis findings in carrier detection of Duchenne muscular dystrophy.
Ionasescu V; Burmeister L; Hanson J
Am J Med Genet; 1980; 5(1):5-12. PubMed ID: 7395900
[TBL] [Abstract][Full Text] [Related]
6. [Blood myoglobin in children with progressive muscular dystrophy and in carriers].
Calandi C; Baretti S; Pacciani G; Bagni P; Borsotti M; Tozzi P; Adami Lami C
Quad Sclavo Diagn; 1984 Dec; 20(4):391-8. PubMed ID: 6537549
[TBL] [Abstract][Full Text] [Related]
7. Serum myoglobin in Duchenne muscular dystrophy carrier detection: a comparison with creatine kinase and hemopexin using logistic discrimination.
Percy ME; Pichora GA; Chang LS; Manchester KE; Andrews DF
Am J Med Genet; 1984 Jun; 18(2):279-87. PubMed ID: 6465202
[TBL] [Abstract][Full Text] [Related]
8. Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers.
Sumita DR; Vainzof M; Campiotto S; Cerqueira AM; Cánovas M; Otto PA; Passos-Bueno MR; Zatz M
Am J Med Genet; 1998 Dec; 80(4):356-61. PubMed ID: 9856563
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Duchenne muscular dystrophy. Morphological study of erythrocytes after treatment with L-alpha-lysophosphatidyl-choline in dystrophic patients and in the carrier state.
Dellantonio R; Capriotti M; Angeleri F; Curatola G; Mazzanti L; Bertoli E; Lenaz G
Acta Neurol Belg; 1981; 81(4):193-8. PubMed ID: 7293730
[TBL] [Abstract][Full Text] [Related]
11. [Estimation of the probability of heterozygosity in Duchenne-type progressive muscular dystrophy].
Guízar Vázquez J; Navarrete Cadena C; Rico R; Mora G; Zavala C
Bol Med Hosp Infant Mex; 1981; 38(1):23-33. PubMed ID: 7284070
[TBL] [Abstract][Full Text] [Related]
12. Duchenne muscular dystrophy carrier detection using logistic discrimination: serum creatine kinase, hemopexin, pyruvate kinase, and lactate dehydrogenase in combination.
Percy ME; Andrews DF; Thompson MW
Am J Med Genet; 1982 Sep; 13(1):27-38. PubMed ID: 7137219
[TBL] [Abstract][Full Text] [Related]
13. [Screening for elevated creatine kinase activities for the early diagnosis of Duchenne muscular dystrophy].
Beckmann R; Scheuerbrandt G
Fortschr Med; 1979 Oct; 97(39):1733-6. PubMed ID: 511067
[TBL] [Abstract][Full Text] [Related]
14. Clinical investigation in Duchenne dystrophy: V. Use of creatine kinase and pyruvate kinase in carrier detection.
Griggs RC; Mendell JR; Brooke MH; Fenichel GM; Miller JP; Province M; Moxley RT; Huntzinger D; Vaughn A; Cohen M
Muscle Nerve; 1985 Jan; 8(1):60-7. PubMed ID: 4058458
[TBL] [Abstract][Full Text] [Related]
15. [Ceruloplasmin in patients with Duchenne muscular dystrophy].
Reyes J; Holmgren J; Colombo M
Rev Med Chil; 1991 Mar; 119(3):258-61. PubMed ID: 1842117
[TBL] [Abstract][Full Text] [Related]
16. Duchenne muscular dystrophy carrier detection using logistic discrimination: serum creatine kinase and hemopexin in combination.
Percy ME; Andrews DF; Thompson MW
Am J Med Genet; 1981; 8(4):397-409. PubMed ID: 7246612
[TBL] [Abstract][Full Text] [Related]
17. Carrier detection in Duchenne muscular dystrophy. Evidence from a study of obligatory carriers and mothers of isolated cases.
Sibert JR; Harper PS; Thompson RJ; Newcombe RG
Arch Dis Child; 1979 Jul; 54(7):534-7. PubMed ID: 485196
[TBL] [Abstract][Full Text] [Related]
18. Use of dystrophin genomic and cDNA probes for solving difficulties in carrier detection and prenatal diagnosis of Duchenne muscular dystrophy.
Shomrat R; Driks N; Legum C; Shiloh Y
Am J Med Genet; 1992 Feb; 42(3):281-7. PubMed ID: 1536162
[TBL] [Abstract][Full Text] [Related]
19. Detection of preclinical Duchenne muscular dystrophy and its female carriers.
Beckmann R
Isr J Med Sci; 1977 Feb; 13(2):102-6. PubMed ID: 863671
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]