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Results:
1-13
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Results: 13
Authors:
ISAACS JD
SIMS HF
POWELL CK
BENNETT MJ
HALE DE
TREEM WR
STRAUSS AW
Citation: Jd. Isaacs et al., MATERNAL ACUTE FATTY LIVER OF PREGNANCY-ASSOCIATED WITH FETAL TRIFUNCTIONAL PROTEIN-DEFICIENCY - MOLECULAR CHARACTERIZATION OF A NOVEL MATERNAL MUTANT ALLELE, Pediatric research, 40(3), 1996, pp. 393-398
Authors:
MATHUR A
POWELL CK
SIMS HF
ALLA VL
BENNETT M
STRAUSS AW
Citation: A. Mathur et al., MOLECULAR-BASIS OF VERY LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY - SCREENING AND MUTATIONAL ANALYSIS OF 17 PATIENTS, Pediatric research, 39(4), 1996, pp. 866-866
Authors:
MATHUR A
SIMS HF
POWELL CK
STRAUSS AW
Citation: A. Mathur et al., INFANTILE CARDIOMYOPATHY - A COMMON CLINICAL MANIFESTATION OF VERY LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY, Circulation, 94(8), 1996, pp. 315-315
Authors:
POWELL CK
SIMS HF
AHUJA A
STRAUSS AW
Citation: Ck. Powell et al., THE MOLECULAR-BASIS OF VERY LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY CAUSING INFANTILE CARDIOMYOPATHY, Pediatric research, 37(4), 1995, pp. 32-32
Authors:
POWELL CK
ISAACS JD
SIMS HF
STRAUSS AW
Citation: Ck. Powell et al., MOLECULAR CHARACTERIZATION OF FETAL LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY ASSOCIATED WITH ACUTE FATTY LIVER OF PREGNANCY, Pediatric research, 37(4), 1995, pp. 151-151
Authors:
SIMS HF
BRACKETT JC
POWELL CK
TREEM WR
HALE DE
BENNETT MJ
GIBSON B
SHAPIRO S
STRAUSS AW
Citation: Hf. Sims et al., THE MOLECULAR-BASIS OF PEDIATRIC LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY ASSOCIATED WITH MATERNAL ACUTE FATTY LIVER OF PREGNANCY, Proceedings of the National Academy of Sciences of the United Statesof America, 92(3), 1995, pp. 841-845
Authors:
STRAUSS AW
POWELL CK
HALE DE
ANDERSON MM
AHUJA A
BRACKETT JC
SIMS HF
Citation: Aw. Strauss et al., MOLECULAR-BASIS OF HUMAN MITOCHONDRIAL VERY-LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY CAUSING CARDIOMYOPATHY AND SUDDEN-DEATH IN CHILDHOOD, Proceedings of the National Academy of Sciences of the United Statesof America, 92(23), 1995, pp. 10496-10500
Authors:
BRACKETT JC
SIMS HF
RINALDO P
SHAPIRO S
POWELL CK
BENNETT MJ
STRAUSS AW
Citation: Jc. Brackett et al., 2 ALPHA-SUBUNIT DONOR SPLICE-SITE MUTATIONS CAUSE HUMAN TRIFUNCTIONALPROTEIN-DEFICIENCY, The Journal of clinical investigation, 95(5), 1995, pp. 2076-2082
Authors:
HOLLAND MP
POWELL CK
Citation: Mp. Holland et Ck. Powell, A LONGITUDINAL SURVEY OF THE INFORMATION-SEEKING AND USE HABITS OF SOME ENGINEERS, College & research libraries, 56(1), 1995, pp. 7-15
Authors:
BRACKETT JC
SIMS HF
POWELL CK
RINALDO P
STRAUSS AW
Citation: Jc. Brackett et al., MOLECULAR CHARACTERIZATION OF LONG-CHAIN 3-HYDROXYACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY, Circulation, 90(4), 1994, pp. 159-159
Authors:
BRACKETT JC
SIMS HF
POWELL CK
RINALDO P
STRAUSS AW
Citation: Jc. Brackett et al., MOLECULAR CHARACTERIZATION OF LONG-CHAIN 3-HYDROXYACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY, Circulation, 90(4), 1994, pp. 159-159
Authors:
POWELL CK
SIMS HF
BRACKETT JC
STRAUSS AW
Citation: Ck. Powell et al., COMPLETE CHARACTERIZATION OF THE HUMAN CARDIAC LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE CDNA AND GENE, Circulation, 90(4), 1994, pp. 245-245
Authors:
POWELL CK
SIMS HF
BRACKETT JC
STRAUSS AW
Citation: Ck. Powell et al., COMPLETE CHARACTERIZATION OF THE HUMAN CARDIAC LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE CDNA AND GENE, Circulation, 90(4), 1994, pp. 245-245
Risultati:
1-13
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