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Results: 1-8 |
Results: 8
G8363A MUTATION IN THE MITOCHONDRIAL-DNA TRNA(LYS) GENE - ANOTHER CAUSE OF LEIGH-SYNDROME
Authors: SHTILBANS A BRUNO C ANDREU AL HADJIGEORGIOU GM SHANSKE S WILT F RIDDICK L THYAGARAJAN D DIMAURO S
Citation: A. Shtilbans et al., G8363A MUTATION IN THE MITOCHONDRIAL-DNA TRNA(LYS) GENE - ANOTHER CAUSE OF LEIGH-SYNDROME, Annals of neurology, 44(3), 1998, pp. 59-59
A NONSENSE MUTATION (A15059G) IN THE CYTOCHROME-B GENE IN A PATIENT WITH EXERCISE INTOLERANCE AND MYOGLOBINURIA
Authors: ANDREU AL BRUNO C SUE CM TANJI K SHANSKE S KRISHNA S HADJIGEORGIOU GM SHTILBANS A DUNNE TC DIMAURO S
Citation: Al. Andreu et al., A NONSENSE MUTATION (A15059G) IN THE CYTOCHROME-B GENE IN A PATIENT WITH EXERCISE INTOLERANCE AND MYOGLOBINURIA, Annals of neurology, 44(3), 1998, pp. 139-139
A NOVEL MITOCHONDRIAL TRNA(ILE) POINT MUTATION IN CHRONIC PROGRESSIVEEXTERNAL OPHTHALMOPLEGIA
Authors: FRANCESCHINA L SALANI S BORDONI A SCIACCO M NAPOLI L COMI GP PRELLE A FORTUNATO F HADJIGEORGIOU GM FARINA E BRESOLIN N DANGELO MG SCARLATO G
Citation: L. Franceschina et al., A NOVEL MITOCHONDRIAL TRNA(ILE) POINT MUTATION IN CHRONIC PROGRESSIVEEXTERNAL OPHTHALMOPLEGIA, Journal of neurology, 245(11), 1998, pp. 755-758
PARTIAL DEPLETION AND MULTIPLE DELETIONS OF MUSCLE MTDNA IN FAMILIAL MNGIE SYNDROME
Authors: PAPADIMITRIOU A COMI GP HADJIGEORGIOU GM BORDONI A SCIACCO M NAPOLI L PRELLE A MOGGIO M FAGIOLARI G BRESOLIN N SALANI S ANASTASOPOULOS I GIASSAKIS G DIVARI R SCARLATO G
Citation: A. Papadimitriou et al., PARTIAL DEPLETION AND MULTIPLE DELETIONS OF MUSCLE MTDNA IN FAMILIAL MNGIE SYNDROME, Neurology, 51(4), 1998, pp. 1086-1092
ALPHA-SYNUCLEIN GENE MUTATION (G209A) IN GREEK KINDREDS WITH FAMILIALPARKINSONS-DISEASE
Authors: PAPADIMITRIOU A VELETZA V ANASTASOPOULOS I PATRIKIOU A HADJIGEORGIOU GM
Citation: A. Papadimitriou et al., ALPHA-SYNUCLEIN GENE MUTATION (G209A) IN GREEK KINDREDS WITH FAMILIALPARKINSONS-DISEASE, Neurology, 50(4), 1998, pp. 53005-53005
THE INFLUENCE OF COENZYME Q(10) ON TOTAL SERUM-CALCIUM CONCENTRATION IN 2 PATIENTS WITH KEARNS-SAYRE-SYNDROME AND HYPOPARATHYROIDISM
Authors: PAPADIMITRIOU A HADJIGEORGIOU GM DIVARI R PAPAGALANIS N COMI G BRESOLIN N
Citation: A. Papadimitriou et al., THE INFLUENCE OF COENZYME Q(10) ON TOTAL SERUM-CALCIUM CONCENTRATION IN 2 PATIENTS WITH KEARNS-SAYRE-SYNDROME AND HYPOPARATHYROIDISM, Neuromuscular disorders, 6(1), 1996, pp. 49-53
MYOGLOBINURIA DUE TO QUAIL POISONING
Authors: PAPADIMITRIOU A HADJIGEORGIOU GM TSAIRIS P PAPADIMITRIOU E OUZOUNELLI C OUZOUNELLIS T
Citation: A. Papadimitriou et al., MYOGLOBINURIA DUE TO QUAIL POISONING, European neurology, 36(3), 1996, pp. 142-145
INVOLVEMENT OF SULFHYDRYL-GROUPS IN TIME-DEPENDENT CHANGES OF DIAPHRAGM ACETYLCHOLINESTERASE ACTIVITY BY MONOVALENT (NA+, LI+) CATIONS
Authors: KOUNINIOTOUKRONTIRI P TSAKIRIS S HADJIGEORGIOU GM
Citation: P. Kouniniotoukrontiri et al., INVOLVEMENT OF SULFHYDRYL-GROUPS IN TIME-DEPENDENT CHANGES OF DIAPHRAGM ACETYLCHOLINESTERASE ACTIVITY BY MONOVALENT (NA+, LI+) CATIONS, Biochemistry and molecular biology international, 33(3), 1994, pp. 485-496
Risultati: 1-8 |