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Results: 1-9 |
Results: 9
DUPLICATION AND TRIPLICATION WITH STAGGERED BREAKPOINTS IN HUMAN MITOCHONDRIAL-DNA
Authors: TENGAN CH MORAES CT
Citation: Ch. Tengan et Ct. Moraes, DUPLICATION AND TRIPLICATION WITH STAGGERED BREAKPOINTS IN HUMAN MITOCHONDRIAL-DNA, Biochimica et biophysica acta. Molecular basis of disease, 1406(1), 1998, pp. 73-80
MITOCHONDRIAL ENCEPHALOMYOPATHY AND HYPOPARATHYROIDISM ASSOCIATED WITH A DUPLICATION AND A DELETION OF MITOCHONDRIAL DEOXYRIBONUCLEIC-ACID
Authors: TENGAN CH KIYOMOTO BH ROCHA MS TAVARES VLS GABBAI AA MORAES CT
Citation: Ch. Tengan et al., MITOCHONDRIAL ENCEPHALOMYOPATHY AND HYPOPARATHYROIDISM ASSOCIATED WITH A DUPLICATION AND A DELETION OF MITOCHONDRIAL DEOXYRIBONUCLEIC-ACID, The Journal of clinical endocrinology and metabolism, 83(1), 1998, pp. 125-129
HYPOPARATHYROIDISM WITH 2 TYPES OF REARRANGEMENTS OF MTDNA
Authors: KIYOMOTO BH TENGAN CH GABBAI AA ROCHA MS TAVARES VLS MORAES CT
Citation: Bh. Kiyomoto et al., HYPOPARATHYROIDISM WITH 2 TYPES OF REARRANGEMENTS OF MTDNA, Neurology, 48(3), 1997, pp. 6141-6141
OXIDATIVE-PHOSPHORYLATION DYSFUNCTION DOES NOT INCREASE THE RATE OF ACCUMULATION OF AGE-RELATED MTDNA DELETIONS IN SKELETAL-MUSCLE
Authors: TENGAN CH GABBAI AA SHANSKE S ZEVIANI M MORAES CT
Citation: Ch. Tengan et al., OXIDATIVE-PHOSPHORYLATION DYSFUNCTION DOES NOT INCREASE THE RATE OF ACCUMULATION OF AGE-RELATED MTDNA DELETIONS IN SKELETAL-MUSCLE, Mutation research, 379(1), 1997, pp. 1-11
MITOCHONDRIAL-DNA DEFECTS IN BRAZILIAN PATIENTS WITH CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA
Authors: KIYOMOTO BH TENGAN CH MORAES CT OLIVEIRA ASB GABBAI AA
Citation: Bh. Kiyomoto et al., MITOCHONDRIAL-DNA DEFECTS IN BRAZILIAN PATIENTS WITH CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, Journal of the neurological sciences, 152(2), 1997, pp. 160-165
DETECTION AND ANALYSIS OF MITOCHONDRIAL-DNA DELETIONS BY WHOLE GENOMEPCR
Authors: TENGAN CH MORAES CT
Citation: Ch. Tengan et Ct. Moraes, DETECTION AND ANALYSIS OF MITOCHONDRIAL-DNA DELETIONS BY WHOLE GENOMEPCR, Biochemical and molecular medicine, 58(1), 1996, pp. 130-134
DETECTION AND ANALYSIS OF MITOCHONDRIAL-DNA DELETIONS BY WHOLE-GENOMEPCR
Authors: TENGAN CH MORAES C
Citation: Ch. Tengan et C. Moraes, DETECTION AND ANALYSIS OF MITOCHONDRIAL-DNA DELETIONS BY WHOLE-GENOMEPCR, Neurology, 46(2), 1996, pp. 3005-3005
PHENOTYPE GENOTYPE CORRELATIONS IN SKELETAL-MUSCLE OF PATIENTS WITH MTDNA DELETIONS
Authors: MORAES CT SCIACCO M RICCI E TENGAN CH HAO H BONILLA E SCHON EA DIMAURO S
Citation: Ct. Moraes et al., PHENOTYPE GENOTYPE CORRELATIONS IN SKELETAL-MUSCLE OF PATIENTS WITH MTDNA DELETIONS, Muscle & nerve, 1995, pp. 150-153
QUANTITATIVE-ANALYSIS OF THE MESSENGER TRANSFER DNA COMMON DELETION IN PATIENTS WITH MITOCHONDRIAL ABNORMALITIES
Authors: MORAES CT TENGAN CH OLIVEIRA ASB SCHMIDT B GABBAI AA
Citation: Ct. Moraes et al., QUANTITATIVE-ANALYSIS OF THE MESSENGER TRANSFER DNA COMMON DELETION IN PATIENTS WITH MITOCHONDRIAL ABNORMALITIES, Neurology, 45(4), 1995, pp. 445-446
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