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Results: 1-25 | 26-26
Results: 1-25/26
CHROMOSOME-1 LOCALIZATION OF A GENE FOR AUTOSOMAL-DOMINANT MEDULLARY CYSTIC KIDNEY-DISEASE (ADMCKD)
Authors: CHRISTODOULOU K TSINGIS M STAVROU C ELEFTHERIOU A PAPAPAVLOU P PATSALIS PC IOANNOU P PIERIDES A DELTAS CC
Citation: K. Christodoulou et al., CHROMOSOME-1 LOCALIZATION OF A GENE FOR AUTOSOMAL-DOMINANT MEDULLARY CYSTIC KIDNEY-DISEASE (ADMCKD), Human molecular genetics, 7(5), 1998, pp. 905-911
SARCOGLYCAN DEFICIENCY CAUSES MUSCULAR-DYSTROPHY BY DISRUPTING THE ACTIN-BINDING FUNCTION OF DYSTROPHIN
Authors: KYRIAKIDES T MARQUEZ B CHRISTODOULOU K PANOUSOPOULOS A MIDDLETON LT
Citation: T. Kyriakides et al., SARCOGLYCAN DEFICIENCY CAUSES MUSCULAR-DYSTROPHY BY DISRUPTING THE ACTIN-BINDING FUNCTION OF DYSTROPHIN, Annals of neurology, 44(3), 1998, pp. 82-82
CLINICAL AND GENETIC-STUDIES OF A NOVEL FORM OF AUTOSOMAL RECESSIVE HEREDITARY MOTOR NEURONOPATHY
Authors: MIDDLETON LT ALQUDAH A ZAMBA E TSINGIS M HORAMI K MUBAIDIN A ABUSHEIK S ELKHATEEB M KYRIACOU K KYRIAKIDES T CHRISTODOULOU K
Citation: Lt. Middleton et al., CLINICAL AND GENETIC-STUDIES OF A NOVEL FORM OF AUTOSOMAL RECESSIVE HEREDITARY MOTOR NEURONOPATHY, Annals of neurology, 44(3), 1998, pp. 198-198
MEDULLARY CYSTIC KIDNEY-DISEASE WITH HYPERURICEMIA AND GOUT IN A LARGE CYPRIOT FAMILY - NO ALLELISM WITH NEPHRONOPHTHISIS TYPE-1
Authors: STAVROU C PIERIDES A ZOUVANI I KYRIACOU K ANTIGNAC C NEOPHYTOU P CHRISTODOULOU K DELTAS CC
Citation: C. Stavrou et al., MEDULLARY CYSTIC KIDNEY-DISEASE WITH HYPERURICEMIA AND GOUT IN A LARGE CYPRIOT FAMILY - NO ALLELISM WITH NEPHRONOPHTHISIS TYPE-1, American journal of medical genetics, 77(2), 1998, pp. 149-154
SENSITIVITY ANALYSIS OF THE BAGLEY CORRECTION TO SHEAR AND EXTENSIONAL RHEOLOGY
Authors: MITSOULIS E HATZIKIRIAKOS SG CHRISTODOULOU K VLASSOPOULOS D
Citation: E. Mitsoulis et al., SENSITIVITY ANALYSIS OF THE BAGLEY CORRECTION TO SHEAR AND EXTENSIONAL RHEOLOGY, Rheologica Acta, 37(5), 1998, pp. 438-448
CONGENITAL MYASTHENIC SYNDROMES (CMS) LINKED TO CHROMOSOME 17P ARE CAUSED BY DEFECTS IN ACETYLCHOLINE-RECEPTOR (ACHR) EPSILON-SUBUNIT GENE
Authors: MIDDLETON L OHNO K CHRISTODOULOU K BRENGMAN J NEOCLEOUS V DEYMEER F SERDAROGLU P OZDEMIR C ALSHEHAB A JORDAN A MAVROMATIS I MYLONAS I EVOLI A TSINGIS M ZAMBA E KYRIALLIS K ENGEL A
Citation: L. Middleton et al., CONGENITAL MYASTHENIC SYNDROMES (CMS) LINKED TO CHROMOSOME 17P ARE CAUSED BY DEFECTS IN ACETYLCHOLINE-RECEPTOR (ACHR) EPSILON-SUBUNIT GENE, Neurology, 50(4), 1998, pp. 67003-67003
MAPPING OF THE FAMILIAL INFANTILE MYASTHENIA (CONGENITAL MYASTHENIC SYNDROME TYPE IA) GENE TO CHROMOSOME 17P WITH EVIDENCE OF GENETIC HOMOGENEITY
Authors: CHRISTODOULOU K TSINGIS M DEYMEER F SERDAROGLU P OZDEMIR C ALSHEHAB A BAIRACTARIS C MAVROMATIS I MYLONAS I EVOLI A KYRIALLIS K MIDDLETON LT
Citation: K. Christodoulou et al., MAPPING OF THE FAMILIAL INFANTILE MYASTHENIA (CONGENITAL MYASTHENIC SYNDROME TYPE IA) GENE TO CHROMOSOME 17P WITH EVIDENCE OF GENETIC HOMOGENEITY, Human molecular genetics, 6(4), 1997, pp. 635-640
PACLITAXEL (PX) CARBOPLATIN (CBP) VERSUS CYCLOPHOSPHAMIDE (CTX)-CARBOPLATIN SUPPORTED BY G-CSF AS FIRST LINE CHEMOTHERAPY IN FIGO III-IV OVARIAN-CARCINOMA (OC)
Authors: POLYZOS A TSAVARIS N GIANNIKOS L KALAHANIS N CHRISTODOULOU K GIANNAKOPOULOS K NIKOU G TOSKAS A PAPARGYRIOU J KATSILAMBROS N
Citation: A. Polyzos et al., PACLITAXEL (PX) CARBOPLATIN (CBP) VERSUS CYCLOPHOSPHAMIDE (CTX)-CARBOPLATIN SUPPORTED BY G-CSF AS FIRST LINE CHEMOTHERAPY IN FIGO III-IV OVARIAN-CARCINOMA (OC), European journal of cancer, 33, 1997, pp. 545-545
THE ROLE OF SOMATOSTATIN ANALOGS IN COMPLETE ANTIANDROGEN TREATMENT IN PATIENTS WITH PROSTATIC-CARCINOMA
Authors: VAINAS G PASAITOU V GALAKTIDOU G MARIS K CHRISTODOULOU K CONSTANTINIDIS C KORTSARIS AH
Citation: G. Vainas et al., THE ROLE OF SOMATOSTATIN ANALOGS IN COMPLETE ANTIANDROGEN TREATMENT IN PATIENTS WITH PROSTATIC-CARCINOMA, Journal of experimental & clinical cancer research, 16(1), 1997, pp. 119-126
MOLECULAR-GENETICS OF AUTOSOMAL RECESSIVE HEREDITARY INCLUSION-BODY MYOPATHY
Authors: MIDDLETON LT CHRISTODOULOU K ASKANAS V ENGEL WK MCFERRIN J KYRIAKIDES T ZAMBA E PAPADOPOULLOU E
Citation: Lt. Middleton et al., MOLECULAR-GENETICS OF AUTOSOMAL RECESSIVE HEREDITARY INCLUSION-BODY MYOPATHY, Annals of neurology, 42(3), 1997, pp. 86-86
RHEOLOGICAL CHARACTERIZATION OF POLYETHYLENE TEREPHTHALATE RESINS USING A MULTIMODE PHAN-TIEN-TANNER CONSTITUTIVE RELATION
Authors: HATZIKIRIAKOS SG HEFFNER G VLASSOPOULOS D CHRISTODOULOU K
Citation: Sg. Hatzikiriakos et al., RHEOLOGICAL CHARACTERIZATION OF POLYETHYLENE TEREPHTHALATE RESINS USING A MULTIMODE PHAN-TIEN-TANNER CONSTITUTIVE RELATION, Rheologica Acta, 36(5), 1997, pp. 568-578
MAPPING OF THE FAMILIAL INFANTILE MYASTHENIA GENE TO CHROMOSOME 17P
Authors: CHRISTODOULOU K TSINGIS M DEYMEER F SERDAROGLU P OZDEMIR C ALSHEHAB A BAIRACTARIS C MAVROMATIS I MYLONAS I EVOLI A KYRIALLIS K MIDDLETON LT
Citation: K. Christodoulou et al., MAPPING OF THE FAMILIAL INFANTILE MYASTHENIA GENE TO CHROMOSOME 17P, Neurology, 48(6), 1997, pp. 3-3
CLASSIFICATION OF AUTOSOMAL RECESSIVE SPINOCEREBELLAR ATAXIAS (ARSCA)BASED ON RECENT GENETIC-STUDIES
Authors: MIDDLETON LT CHRISTODOULOU K
Citation: Lt. Middleton et K. Christodoulou, CLASSIFICATION OF AUTOSOMAL RECESSIVE SPINOCEREBELLAR ATAXIAS (ARSCA)BASED ON RECENT GENETIC-STUDIES, Neurology, 48(3), 1997, pp. 3080-3080
GENETIC-HETEROGENEITY IN FRIEDREICHS-ATAXIA - INDICATION FOR A 2ND LOCUS ON CHROMOSOME-9
Authors: CHRISTODOULOU K DEYMEER F SERDAROGLU P OZDEMIR C GEORGIOU DM PAPADOPOULOU E ZAMBA E MIDDLETON LT
Citation: K. Christodoulou et al., GENETIC-HETEROGENEITY IN FRIEDREICHS-ATAXIA - INDICATION FOR A 2ND LOCUS ON CHROMOSOME-9, American journal of human genetics, 61(4), 1997, pp. 1579-1579
MUTATION SCREENING IN THE SYNAPTOBREVIN-2 GENE IN PATIENTS WITH FAMILIAL INFANTILE MYASTHENIA
Authors: NEOCLEOUS V MIDDLETON LT CHRISTODOULOU K
Citation: V. Neocleous et al., MUTATION SCREENING IN THE SYNAPTOBREVIN-2 GENE IN PATIENTS WITH FAMILIAL INFANTILE MYASTHENIA, American journal of human genetics, 61(4), 1997, pp. 1997-1997
EVIDENCE OF GENETIC-HETEROGENEITY WITHIN THE FRIEDREICHS ATAXIA PHENOTYPE
Authors: CHRISTODOULOU K OZCELIK T GEORGIOU DM PODA M SERDAROGLU P DEYMEER F OZDEMIR C IOANNOU P MIDDLETON LT
Citation: K. Christodoulou et al., EVIDENCE OF GENETIC-HETEROGENEITY WITHIN THE FRIEDREICHS ATAXIA PHENOTYPE, Annals of neurology, 40(3), 1996, pp. 226-226
CLINICAL AND MOLECULAR-GENETIC INVESTIGATION OF AN ATYPICAL FRIEDREICHS ATAXIA FAMILY
Authors: CHRISTODOULOU K OZCELIK T NICOSIA DMG PODA M SERDAROGLU P DEYMEER F OZDEMIR C IOANNOU P MIDDLETON LT
Citation: K. Christodoulou et al., CLINICAL AND MOLECULAR-GENETIC INVESTIGATION OF AN ATYPICAL FRIEDREICHS ATAXIA FAMILY, Neurology, 46(2), 1996, pp. 2103-2103
SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY EXHIBITS HETEROGENEITY AT PROTEIN AND DNA LEVEL
Authors: KYRIAKIDES T CHRISTODOULOU K SODIEONO O OZAWA E ALDIN ASM VANCE J MIDDLETON L
Citation: T. Kyriakides et al., SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY EXHIBITS HETEROGENEITY AT PROTEIN AND DNA LEVEL, Neurology, 46(2), 1996, pp. 4082-4082
FAMILIAL INFANTILE MYASTHENIA IN EASTERN MEDITERRANEAN COUNTRIES
Authors: KYRIALLIS K CHRISTODOULOU K ALSHEHAB A BARBA V MYLONAS Y MAVROMATIS J SERDAROGLU P OZCELIK T DEYMMER F OZDEMIR C MIDDLETON LT
Citation: K. Kyriallis et al., FAMILIAL INFANTILE MYASTHENIA IN EASTERN MEDITERRANEAN COUNTRIES, Neurology, 46(2), 1996, pp. 4089-4089
PRESYMPTOMATIC MOLECULAR DIAGNOSIS OF AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE USING PKD1-LINKED AND PKD2-LINKED MARKERS IN CYPRIOT FAMILIES
Authors: DELTAS CC CHRISTODOULOU K TJAKOURI C PIERIDES A
Citation: Cc. Deltas et al., PRESYMPTOMATIC MOLECULAR DIAGNOSIS OF AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE USING PKD1-LINKED AND PKD2-LINKED MARKERS IN CYPRIOT FAMILIES, Clinical genetics, 50(1), 1996, pp. 10-18
MAPPING OF A DISTAL FORM OF SPINAL MUSCULAR-ATROPHY WITH UPPER-LIMB PREDOMINANCE TO CHROMOSOME 7P
Authors: CHRISTODOULOU K KYRIAKIDES T HRISTOVA AH GEORGIOU DM KALAYDJIEVA L YSHPEKOVA B IVANOVA T WEBER JL MIDDLETON LT
Citation: K. Christodoulou et al., MAPPING OF A DISTAL FORM OF SPINAL MUSCULAR-ATROPHY WITH UPPER-LIMB PREDOMINANCE TO CHROMOSOME 7P, Human molecular genetics, 4(9), 1995, pp. 1629-1632
CISPLATIN (C) PLUS IFOSFAMIDE (I) FOR PATIENTS WITH OVARIAN-CARCINOMA(OC) WITH PRIOR CARBOPLATIN (CBT) PLUS CYCLOPHOSPHAMIDE (CTX) CHEMOTHERAPY
Authors: POLYZOS A GIANNIKOS L VESLEMES M KALAHANIS N GIANOPOULOS A GIANNAKOPOULOS K CHRISTODOULOU K
Citation: A. Polyzos et al., CISPLATIN (C) PLUS IFOSFAMIDE (I) FOR PATIENTS WITH OVARIAN-CARCINOMA(OC) WITH PRIOR CARBOPLATIN (CBT) PLUS CYCLOPHOSPHAMIDE (CTX) CHEMOTHERAPY, European journal of cancer, 31A, 1995, pp. 524-524
GENETIC-HETEROGENEITY IN ADULT DOMINANT POLYCYSTIC KIDNEY-DISEASE IN CYPRIOT FAMILIES
Authors: CONSTANTINOUDELTAS CD PAPAGEORGIOU E BOTEVA K CHRISTODOULOU K BREUNING MH PETERS DJM PIERIDES A
Citation: Cd. Constantinoudeltas et al., GENETIC-HETEROGENEITY IN ADULT DOMINANT POLYCYSTIC KIDNEY-DISEASE IN CYPRIOT FAMILIES, Human genetics, 95(4), 1995, pp. 416-423
AUTOSOMAL-DOMINANT MOTOR NEURONOPATHY PREDOMINANTLY AFFECTING THE HANDS
Authors: MIDDLETON LT HRISTOVA AH KALAYDJIEVA L YSHPEKOVA B IVANOVA T CHRISTODOULOU K KYRIAKIDES T
Citation: Lt. Middleton et al., AUTOSOMAL-DOMINANT MOTOR NEURONOPATHY PREDOMINANTLY AFFECTING THE HANDS, Neurology, 45(4), 1995, pp. 448-448
MAPPING OF AN AUTOSOMAL-DOMINANT DISTAL FORM OF SPINAL MUSCULAR-ATROPHY TO CHROMOSOME 7P
Authors: CHRISTODOULOU K KYRIAKIDES T HRISTOVA AH GEORGIOU DM KALAJDJIEVA L YSHPEKOVA B IVANOVA T WEBER JL MIDDLETON LT
Citation: K. Christodoulou et al., MAPPING OF AN AUTOSOMAL-DOMINANT DISTAL FORM OF SPINAL MUSCULAR-ATROPHY TO CHROMOSOME 7P, American journal of human genetics, 57(4), 1995, pp. 1082-1082
Risultati: 1-25 | 26-26