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Results: 1-25 | 26-43
Results: 1-25/43
THE EFFECT OF MATRIX MICROSTRUCTURE AND REINFORCEMENT SHAPE ON THE CREEP DEFORMATION OF NEAR-GAMMA TITANIUM ALUMINIDE COMPOSITES
Authors: KAMPE SL CHRISTODOULOU J FENG CR CHRISTODOULOU L MICHEL DJ
Citation: Sl. Kampe et al., THE EFFECT OF MATRIX MICROSTRUCTURE AND REINFORCEMENT SHAPE ON THE CREEP DEFORMATION OF NEAR-GAMMA TITANIUM ALUMINIDE COMPOSITES, Acta materialia, 46(8), 1998, pp. 2881-2894
NOVEL MITOCHONDRIAL-DNA VARIANT THAT MAY GIVE A FALSE-POSITIVE DIAGNOSIS FOR THE T8993C MUTATION
Authors: WHITE SL THORBURN DR CHRISTODOULOU J DAHL HHM
Citation: Sl. White et al., NOVEL MITOCHONDRIAL-DNA VARIANT THAT MAY GIVE A FALSE-POSITIVE DIAGNOSIS FOR THE T8993C MUTATION, Molecular diagnosis, 3(2), 1998, pp. 113-117
RETT-SYNDROME - SIGNIFICANT CLINICAL OVERLAP WITH ANGELMAN-SYNDROME BUT NOT WITH METHYLATION STATUS
Authors: ELLAWAY C BUCHHOLZ T SMITH A LEONARD H CHRISTODOULOU J
Citation: C. Ellaway et al., RETT-SYNDROME - SIGNIFICANT CLINICAL OVERLAP WITH ANGELMAN-SYNDROME BUT NOT WITH METHYLATION STATUS, Journal of child neurology, 13(9), 1998, pp. 448-451
HIGH PREVALENCE OF LUNG DIFFUSION IMPAIRMENT IN NORMOXAEMIC PATIENTS WITH EARLY LIVER-CIRRHOSIS
Authors: MIMIDIS K SPIROPOULOS K CHAROKOPOS N KARATZA C CHRISTODOULOU J THOMOPOULOS K MARGARITIS V NIKOLOPOULOU V
Citation: K. Mimidis et al., HIGH PREVALENCE OF LUNG DIFFUSION IMPAIRMENT IN NORMOXAEMIC PATIENTS WITH EARLY LIVER-CIRRHOSIS, Medical science research, 26(2), 1998, pp. 101-103
COMBINATION OF NONINVASIVE METHODS TO DIAGNOSE PULMONARY ARTERIAL-HYPERTENSION IN CHRONIC OBSTRUCTIVE PULMONARY-DISEASE
Authors: SPIROPOULOS K CHAROKOPOS N PETSAS T TRAKADA G MAZARAKIS A CHRISTODOULOU J ALEXOPOULOS D
Citation: K. Spiropoulos et al., COMBINATION OF NONINVASIVE METHODS TO DIAGNOSE PULMONARY ARTERIAL-HYPERTENSION IN CHRONIC OBSTRUCTIVE PULMONARY-DISEASE, Medical science research, 26(1), 1998, pp. 67-70
MULTI-METAL BINDING-SITE OF SERUM-ALBUMIN
Authors: BAL W CHRISTODOULOU J SADLER PJ TUCKER A
Citation: W. Bal et al., MULTI-METAL BINDING-SITE OF SERUM-ALBUMIN, Journal of inorganic biochemistry, 70(1), 1998, pp. 33-39
EARLY TREATMENT OF MENKES DISEASE WITH PARENTERAL COOPER-HISTIDINE - LONG-TERM FOLLOW-UP OF 4 TREATED PATIENTS
Authors: CHRISTODOULOU J DANKS DM SARKAR B BAERLOCHER KE CASEY R HORN N TUMER Z CLARKE JTR
Citation: J. Christodoulou et al., EARLY TREATMENT OF MENKES DISEASE WITH PARENTERAL COOPER-HISTIDINE - LONG-TERM FOLLOW-UP OF 4 TREATED PATIENTS, American journal of medical genetics, 76(2), 1998, pp. 154-164
THE ASSOCIATION OF PROTEIN-LOSING ENTEROPATHY WITH COBALAMIN-C DEFECT
Authors: ELLAWAY C CHRISTODOULOU J KAMATH R CARPENTER K WILCKEN B
Citation: C. Ellaway et al., THE ASSOCIATION OF PROTEIN-LOSING ENTEROPATHY WITH COBALAMIN-C DEFECT, Journal of inherited metabolic disease, 21(1), 1998, pp. 17-22
COMPLEX-I DEFICIENCY IN ASSOCIATION WITH STRUCTURAL ABNORMALITIES OF THE DIAPHRAGM AND BRAIN
Authors: ELLAWAY C NORTH K ARBUCKLE S CHRISTODOULOU J
Citation: C. Ellaway et al., COMPLEX-I DEFICIENCY IN ASSOCIATION WITH STRUCTURAL ABNORMALITIES OF THE DIAPHRAGM AND BRAIN, Journal of inherited metabolic disease, 21(1), 1998, pp. 72-73
INTRAGENIC COMPLEMENTATION AT THE ARGININOSUCCINATE LYASE LOCUS - RECONSTRUCTION OF THE ACTIVE-SITE
Authors: HOWELL PL TURNER MA CHRISTODOULOU J WALKER DC CRAIG HJ SIMARD LR PLODER L MCINNES RR
Citation: Pl. Howell et al., INTRAGENIC COMPLEMENTATION AT THE ARGININOSUCCINATE LYASE LOCUS - RECONSTRUCTION OF THE ACTIVE-SITE, Journal of inherited metabolic disease, 21, 1998, pp. 72-85
CISPLATIN BINDING-SITES ON HUMAN ALBUMIN
Authors: IVANOV AI CHRISTODOULOU J PARKINSON JA BARNHAM KJ TUCKER A WOODROW J SADLER PJ
Citation: Ai. Ivanov et al., CISPLATIN BINDING-SITES ON HUMAN ALBUMIN, The Journal of biological chemistry, 273(24), 1998, pp. 14721-14730
AUTOMATED-ANALYSIS OF MITOCHONDRIAL-ENZYMES IN CULTURED SKIN FIBROBLASTS
Authors: WILLIAMS AJ COAKLEY J CHRISTODOULOU J
Citation: Aj. Williams et al., AUTOMATED-ANALYSIS OF MITOCHONDRIAL-ENZYMES IN CULTURED SKIN FIBROBLASTS, Analytical biochemistry, 259(2), 1998, pp. 176-180
PROGRESSIVE MYOCLONIC EPILEPSIES - RECENT GENETIC ADVANCES
Authors: ELLAWAY CJ ELLIOTT EJ CHRISTODOULOU J
Citation: Cj. Ellaway et al., PROGRESSIVE MYOCLONIC EPILEPSIES - RECENT GENETIC ADVANCES, Journal of paediatrics and child health, 33(2), 1997, pp. 91-95
MITOCHONDRIAL ELECTRON-TRANSPORT CHAIN DEFECT PRESENTING AS HYPOGLYCEMIA
Authors: FRECKMANN ML THORBURN DR KIRBY DM KAMATH KR HAMMOND J DENNETT X CHRISTODOULOU J
Citation: Ml. Freckmann et al., MITOCHONDRIAL ELECTRON-TRANSPORT CHAIN DEFECT PRESENTING AS HYPOGLYCEMIA, The Journal of pediatrics, 130(3), 1997, pp. 431-436
MITOCHONDRIAL MYOPATHY WITH TRNA(LEU(UUR)) MUTATION AND COMPLEX-I DEFICIENCY RESPONSIVE TO RIBOFLAVIN
Authors: OGLE RF CHRISTODOULOU J FAGAN E BLOK RB KIRBY DM SELLER KL DAHL HHM THORBURN DR
Citation: Rf. Ogle et al., MITOCHONDRIAL MYOPATHY WITH TRNA(LEU(UUR)) MUTATION AND COMPLEX-I DEFICIENCY RESPONSIVE TO RIBOFLAVIN, The Journal of pediatrics, 130(1), 1997, pp. 138-145
INTRAGENIC COMPLEMENTATION AT THE HUMAN ARGININOSUCCINATE LYASE FOCUS- IDENTIFICATION OF THE MAJOR COMPLEMENTING ALLELES
Authors: WALKER DC CHRISTODOULOU J CRAIG HJ SIMARD LR PLODER L HOWELL PL MCINNES RR
Citation: Dc. Walker et al., INTRAGENIC COMPLEMENTATION AT THE HUMAN ARGININOSUCCINATE LYASE FOCUS- IDENTIFICATION OF THE MAJOR COMPLEMENTING ALLELES, The Journal of biological chemistry, 272(10), 1997, pp. 6777-6783
PULMONARY VASCULAR DILATATION IN NORMOXAEMIC PATIENTS WITH EARLY LIVER-CIRRHOSIS
Authors: MIMIDIS K TOULGARIDIS T CHRISTODOULOU J KARATZA C SPIROPOULOS K THOMOPOULOS K CHAROKOPOS N MARGARITIS V NIKOLOPOULOU V
Citation: K. Mimidis et al., PULMONARY VASCULAR DILATATION IN NORMOXAEMIC PATIENTS WITH EARLY LIVER-CIRRHOSIS, Gut, 41, 1997, pp. 232-232
AUTOMATED QUANTITATION OF TOTAL PROTEIN IN CULTURED SKIN FIBROBLASTS
Authors: WILLIAMS AJ COAKLEY JC CHRISTODOULOU J
Citation: Aj. Williams et al., AUTOMATED QUANTITATION OF TOTAL PROTEIN IN CULTURED SKIN FIBROBLASTS, Clinica chimica acta, 259(1-2), 1997, pp. 129-136
CHARACTERIZATION OF AN FBN1 GENE MUTATION, G1013R, IN A CHILD WITH NEONATAL MARFAN-SYNDROME (NMFS) AND MITOCHONDRIAL COMPLEX (CI) DEFICIENCY
Authors: ADES LC HOLMAN KJ WATSON KC MURRELL M CLARKE JTR CHRISTODOULOU J
Citation: Lc. Ades et al., CHARACTERIZATION OF AN FBN1 GENE MUTATION, G1013R, IN A CHILD WITH NEONATAL MARFAN-SYNDROME (NMFS) AND MITOCHONDRIAL COMPLEX (CI) DEFICIENCY, American journal of human genetics, 61(4), 1997, pp. 2367-2367
EARLY COPPER-HISTIDINE TREATMENT FOR MENKES DISEASE
Authors: TUMER Z HORN N TONNESEN T CHRISTODOULOU J CLARKE JTR SARKAR B
Citation: Z. Tumer et al., EARLY COPPER-HISTIDINE TREATMENT FOR MENKES DISEASE, Nature genetics, 12(1), 1996, pp. 11-13
LEIGH-SYNDROME - CLINICAL-FEATURES AND BIOCHEMICAL AND DNA ABNORMALITIES
Authors: RAHMAN S BLOK RB DAHL HHM DANKS DM KIRBY DM CHOW CW CHRISTODOULOU J THORBURN DR
Citation: S. Rahman et al., LEIGH-SYNDROME - CLINICAL-FEATURES AND BIOCHEMICAL AND DNA ABNORMALITIES, Annals of neurology, 39(3), 1996, pp. 343-351
DETERMINATION OF GOLD AND PLATINUM IN THE PRESENCE OF BLOOD-PLASMA PROTEINS USING INDUCTIVELY-COUPLED PLASMA-MASS SPECTROMETRY WITH DIRECT-INJECTION NEBULIZATION
Authors: CHRISTODOULOU J KASHANI M KEOHANE BM SADLER PJ
Citation: J. Christodoulou et al., DETERMINATION OF GOLD AND PLATINUM IN THE PRESENCE OF BLOOD-PLASMA PROTEINS USING INDUCTIVELY-COUPLED PLASMA-MASS SPECTROMETRY WITH DIRECT-INJECTION NEBULIZATION, Journal of analytical atomic spectrometry, 11(11), 1996, pp. 1031-1035
REPOLARIZATION ABNORMALITIES WITH PROLONGED HYPERVENTILATION IN APPARENTLY HEALTHY-SUBJECTS - INCIDENCE, MECHANISMS AND AFFECTING FACTORS
Authors: ALEXOPOULOS D CHRISTODOULOU J TOULGARIDIS T SITAFIDIS G MANIAS O HAHALIS G VAGENAKIS AG
Citation: D. Alexopoulos et al., REPOLARIZATION ABNORMALITIES WITH PROLONGED HYPERVENTILATION IN APPARENTLY HEALTHY-SUBJECTS - INCIDENCE, MECHANISMS AND AFFECTING FACTORS, European heart journal, 17(9), 1996, pp. 1432-1437
FIRST PRENATAL-DIAGNOSIS OF THE CARNITINE TRANSPORTER DEFECT
Authors: CHRISTODOULOU J TEO SH HAMMOND J SIM KG HSU BYL STANLEY CA WATSON B LAU KC WILCKEN B
Citation: J. Christodoulou et al., FIRST PRENATAL-DIAGNOSIS OF THE CARNITINE TRANSPORTER DEFECT, American journal of medical genetics, 66(1), 1996, pp. 21-24
PREGNANCY AND ARGININOSUCCINIC ACIDURIA
Authors: WORTHINGTON S CHRISTODOULOU J WILCKEN B PEAT B
Citation: S. Worthington et al., PREGNANCY AND ARGININOSUCCINIC ACIDURIA, Journal of inherited metabolic disease, 19(5), 1996, pp. 621-623
Risultati: 1-25 | 26-43