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La ricerca find articoli where authors phrase all words 'CHRISTODOULOU K' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 44 riferimenti
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    1. Katsinelos, P; Kalomenopoulou, M; Christodoulou, K; Katsiba, D; Tsolkas, P; Pilpilidis, I; Papagiannis, A; Kapitsinis, I; Vasiliadis, I; Souparis, T
      Treatment of proctalgia fugax with botulinum A toxin

      EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
    2. Zouboulis, AI; Loukidou, MX; Christodoulou, K
      Enzymatic treatment of sanitary landfill leachate

      CHEMOSPHERE
    3. Mitsoulis, E; Hatzikiriakos, SG; Christodoulou, K; Vlassopoulos, D
      Some comments on "computational analysis of techniques to determine extensional viscosity from entrance flows" [Rheol Acta 39:138-151 (2000)]

      RHEOLOGICA ACTA
    4. Katsinelos, P; Christodoulou, K; Pilpilidis, I; Papagiannis, A; Patakiouta, F; Xiarchos, P; Amperiadis, P; Eugenidis, N
      Anal leukoplakia: An unusual case of anal stenosis

      ENDOSCOPY
    5. Katsinelos, P; Christodoulou, K; Pilpilidis, L; Papagiannis, A; Xiarchos, P; Tsolkas, P; Vasiliadis, L; Eugenidis, N
      Black esophagus: An unusual finding during routine endoscopy

      ENDOSCOPY
    6. Mirabella, M; Christodoulou, K; Di Giovanni, S; Ricci, E; Tonali, P; Servidei, S
      An Italian family with autosomal recessive quadriceps-sparing inclusion-body myopathy (ARQS-IBM) linked to chromosome 9p1

      NEUROLOGICAL SCIENCES
    7. Bolino, A; Muglia, M; Conforti, FL; LeGuern, E; Salih, MAM; Georgiou, DM; Christodoulou, K; Hausmanowa-Petrusewicz, I; Mandich, P; Schenone, A; Gambardella, A; Bono, F; Quattrone, A; Devoto, M; Monaco, AP
      Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2

      NATURE GENETICS
    8. Katsinelos, P; Vasiliadis, T; Xiarchos, P; Patakiouta, F; Christodoulou, K; Pilpilidis, I; Eugenidis, N
      Ursodeoxycholic acid (UDCA) for the treatment of amoxycillin-clavulanate potassium (Augmentin (R))-induced intra-hepatic cholestasis: report of two cases

      EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
    9. Christodoulou, K; Zamba, E; Tsingis, M; Mubaidin, A; Horani, K; Abu-Sheik, S; El-Khateeb, M; Kyriacou, K; Kyriakides, T; Al-Qudah, AK; Middleton, L
      A novel form of distal hereditary motor neuronopathy maps to chromosome 9p21.1-p12

      ANNALS OF NEUROLOGY
    10. Christodoulou, K; Vlahos, K
      Variable structure modelling of dynamic industry systems

      JOURNAL OF THE OPERATIONAL RESEARCH SOCIETY
    11. Wang, HL; Ohno, K; Milone, M; Brengman, JM; Evoli, A; Batocchi, AP; Middleton, LT; Christodoulou, K; Engel, AG; Sine, SM
      Fundamental gating mechanism of nicotinic receptor channel revealed by mutation causing a congenital myasthenic syndrome

      JOURNAL OF GENERAL PHYSIOLOGY
    12. Katsinelos, P; Kalomenopoulou, M; Katsiba, D; Christopoulos, S; Dimiropoulos, S; Christodoulou, K; Eugenidis, N
      Gastric outlet obstruction due to benign dilatation of gallbladder

      ENDOSCOPY
    13. Katsinelos, P; Pilpilidis, J; Xiarchos, P; Christodoulou, K; Papagianis, A; Amperiadis, P; Eugenidis, N
      Baclofen therapy for intractable hiccups induced by ultraflex esophageal endoprosthesis

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    14. Polyzos, A; Tsavaris, N; Kosmas, C; Petrikos, G; Giannikos, L; Kalahanis, N; Papadopoulos, O; Christodoulou, K; Giannakopoulos, K; Veslemes, M; Katsilambros, N
      Second-line chemotherapy with cisplatin-ifosfamide in patients with ovarian cancer previously treated with carboplatin-cyclophosphamide

      JOURNAL OF CHEMOTHERAPY
    15. Christodoulou, K; Jensen, K; Vlahos, K
      Using object-oriented simulation to explore substitution between technologies: An application to the UK mobile telecommunications industry

      TECHNOLOGICAL FORECASTING AND SOCIAL CHANGE
    16. Polyzos, A; Tsavaris, N; Kosmas, C; Giannikos, L; Katsikas, M; Kalahanis, N; Karatzas, G; Christodoulou, K; Giannakopoulos, K; Stamatiadis, D; Katsilambros, N
      A comparative study of intraperitoneal carboplatin versus intravenous carboplatin with intravenous cyclophosphamide in both arms as initial chemotherapy for stage III ovarian cancer

      ONCOLOGY
    17. Middleton, L; Ohno, K; Christodoulou, K; Brengman, J; Milone, M; Neocleous, V; Serdaroglu, P; Deymeer, F; Ozdemir, C; Mubaidin, A; Horany, K; Al-Shehab, A; Mavromatis, I; Mylonas, I; Tsingis, M; Zamba, E; Pantzaris, M; Kyriallis, K; Engel, AG
      Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit gene

      NEUROLOGY
    18. Katsinelos, P; Stavros, D; Pirpilidis, I; Christodoulou, K; Xiarchos, P; Zisis, A; Nikos, E
      Unobstructed biliary tract dilatation in a patient with breast carcinoma and dermatomyositis: A new paraneoplastic manifestation?

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    19. CHRISTODOULOU K; TSINGIS M; STAVROU C; ELEFTHERIOU A; PAPAPAVLOU P; PATSALIS PC; IOANNOU P; PIERIDES A; DELTAS CC
      CHROMOSOME-1 LOCALIZATION OF A GENE FOR AUTOSOMAL-DOMINANT MEDULLARY CYSTIC KIDNEY-DISEASE (ADMCKD)

      Human molecular genetics
    20. KYRIAKIDES T; MARQUEZ B; CHRISTODOULOU K; PANOUSOPOULOS A; MIDDLETON LT
      SARCOGLYCAN DEFICIENCY CAUSES MUSCULAR-DYSTROPHY BY DISRUPTING THE ACTIN-BINDING FUNCTION OF DYSTROPHIN

      Annals of neurology
    21. MIDDLETON LT; ALQUDAH A; ZAMBA E; TSINGIS M; HORAMI K; MUBAIDIN A; ABUSHEIK S; ELKHATEEB M; KYRIACOU K; KYRIAKIDES T; CHRISTODOULOU K
      CLINICAL AND GENETIC-STUDIES OF A NOVEL FORM OF AUTOSOMAL RECESSIVE HEREDITARY MOTOR NEURONOPATHY

      Annals of neurology
    22. STAVROU C; PIERIDES A; ZOUVANI I; KYRIACOU K; ANTIGNAC C; NEOPHYTOU P; CHRISTODOULOU K; DELTAS CC
      MEDULLARY CYSTIC KIDNEY-DISEASE WITH HYPERURICEMIA AND GOUT IN A LARGE CYPRIOT FAMILY - NO ALLELISM WITH NEPHRONOPHTHISIS TYPE-1

      American journal of medical genetics
    23. MITSOULIS E; HATZIKIRIAKOS SG; CHRISTODOULOU K; VLASSOPOULOS D
      SENSITIVITY ANALYSIS OF THE BAGLEY CORRECTION TO SHEAR AND EXTENSIONAL RHEOLOGY

      Rheologica Acta
    24. 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
      CONGENITAL MYASTHENIC SYNDROMES (CMS) LINKED TO CHROMOSOME 17P ARE CAUSED BY DEFECTS IN ACETYLCHOLINE-RECEPTOR (ACHR) EPSILON-SUBUNIT GENE

      Neurology
    25. CHRISTODOULOU K; TSINGIS M; DEYMEER F; SERDAROGLU P; OZDEMIR C; ALSHEHAB A; BAIRACTARIS C; MAVROMATIS I; MYLONAS I; EVOLI A; KYRIALLIS K; MIDDLETON LT
      MAPPING OF THE FAMILIAL INFANTILE MYASTHENIA (CONGENITAL MYASTHENIC SYNDROME TYPE IA) GENE TO CHROMOSOME 17P WITH EVIDENCE OF GENETIC HOMOGENEITY

      Human molecular genetics
    26. POLYZOS A; TSAVARIS N; GIANNIKOS L; KALAHANIS N; CHRISTODOULOU K; GIANNAKOPOULOS K; NIKOU G; TOSKAS A; PAPARGYRIOU J; KATSILAMBROS N
      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
    27. VAINAS G; PASAITOU V; GALAKTIDOU G; MARIS K; CHRISTODOULOU K; CONSTANTINIDIS C; KORTSARIS AH
      THE ROLE OF SOMATOSTATIN ANALOGS IN COMPLETE ANTIANDROGEN TREATMENT IN PATIENTS WITH PROSTATIC-CARCINOMA

      Journal of experimental & clinical cancer research
    28. MIDDLETON LT; CHRISTODOULOU K; ASKANAS V; ENGEL WK; MCFERRIN J; KYRIAKIDES T; ZAMBA E; PAPADOPOULLOU E
      MOLECULAR-GENETICS OF AUTOSOMAL RECESSIVE HEREDITARY INCLUSION-BODY MYOPATHY

      Annals of neurology
    29. HATZIKIRIAKOS SG; HEFFNER G; VLASSOPOULOS D; CHRISTODOULOU K
      RHEOLOGICAL CHARACTERIZATION OF POLYETHYLENE TEREPHTHALATE RESINS USING A MULTIMODE PHAN-TIEN-TANNER CONSTITUTIVE RELATION

      Rheologica Acta
    30. CHRISTODOULOU K; TSINGIS M; DEYMEER F; SERDAROGLU P; OZDEMIR C; ALSHEHAB A; BAIRACTARIS C; MAVROMATIS I; MYLONAS I; EVOLI A; KYRIALLIS K; MIDDLETON LT
      MAPPING OF THE FAMILIAL INFANTILE MYASTHENIA GENE TO CHROMOSOME 17P

      Neurology
    31. MIDDLETON LT; CHRISTODOULOU K
      CLASSIFICATION OF AUTOSOMAL RECESSIVE SPINOCEREBELLAR ATAXIAS (ARSCA)BASED ON RECENT GENETIC-STUDIES

      Neurology
    32. CHRISTODOULOU K; DEYMEER F; SERDAROGLU P; OZDEMIR C; GEORGIOU DM; PAPADOPOULOU E; ZAMBA E; MIDDLETON LT
      GENETIC-HETEROGENEITY IN FRIEDREICHS-ATAXIA - INDICATION FOR A 2ND LOCUS ON CHROMOSOME-9

      American journal of human genetics
    33. NEOCLEOUS V; MIDDLETON LT; CHRISTODOULOU K
      MUTATION SCREENING IN THE SYNAPTOBREVIN-2 GENE IN PATIENTS WITH FAMILIAL INFANTILE MYASTHENIA

      American journal of human genetics
    34. CHRISTODOULOU K; OZCELIK T; GEORGIOU DM; PODA M; SERDAROGLU P; DEYMEER F; OZDEMIR C; IOANNOU P; MIDDLETON LT
      EVIDENCE OF GENETIC-HETEROGENEITY WITHIN THE FRIEDREICHS ATAXIA PHENOTYPE

      Annals of neurology
    35. CHRISTODOULOU K; OZCELIK T; NICOSIA DMG; PODA M; SERDAROGLU P; DEYMEER F; OZDEMIR C; IOANNOU P; MIDDLETON LT
      CLINICAL AND MOLECULAR-GENETIC INVESTIGATION OF AN ATYPICAL FRIEDREICHS ATAXIA FAMILY

      Neurology
    36. KYRIAKIDES T; CHRISTODOULOU K; SODIEONO O; OZAWA E; ALDIN ASM; VANCE J; MIDDLETON L
      SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY EXHIBITS HETEROGENEITY AT PROTEIN AND DNA LEVEL

      Neurology
    37. KYRIALLIS K; CHRISTODOULOU K; ALSHEHAB A; BARBA V; MYLONAS Y; MAVROMATIS J; SERDAROGLU P; OZCELIK T; DEYMMER F; OZDEMIR C; MIDDLETON LT
      FAMILIAL INFANTILE MYASTHENIA IN EASTERN MEDITERRANEAN COUNTRIES

      Neurology
    38. DELTAS CC; CHRISTODOULOU K; TJAKOURI C; PIERIDES A
      PRESYMPTOMATIC MOLECULAR DIAGNOSIS OF AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE USING PKD1-LINKED AND PKD2-LINKED MARKERS IN CYPRIOT FAMILIES

      Clinical genetics
    39. CHRISTODOULOU K; KYRIAKIDES T; HRISTOVA AH; GEORGIOU DM; KALAYDJIEVA L; YSHPEKOVA B; IVANOVA T; WEBER JL; MIDDLETON LT
      MAPPING OF A DISTAL FORM OF SPINAL MUSCULAR-ATROPHY WITH UPPER-LIMB PREDOMINANCE TO CHROMOSOME 7P

      Human molecular genetics
    40. POLYZOS A; GIANNIKOS L; VESLEMES M; KALAHANIS N; GIANOPOULOS A; GIANNAKOPOULOS K; CHRISTODOULOU K
      CISPLATIN (C) PLUS IFOSFAMIDE (I) FOR PATIENTS WITH OVARIAN-CARCINOMA(OC) WITH PRIOR CARBOPLATIN (CBT) PLUS CYCLOPHOSPHAMIDE (CTX) CHEMOTHERAPY

      European journal of cancer
    41. CONSTANTINOUDELTAS CD; PAPAGEORGIOU E; BOTEVA K; CHRISTODOULOU K; BREUNING MH; PETERS DJM; PIERIDES A
      GENETIC-HETEROGENEITY IN ADULT DOMINANT POLYCYSTIC KIDNEY-DISEASE IN CYPRIOT FAMILIES

      Human genetics
    42. MIDDLETON LT; HRISTOVA AH; KALAYDJIEVA L; YSHPEKOVA B; IVANOVA T; CHRISTODOULOU K; KYRIAKIDES T
      AUTOSOMAL-DOMINANT MOTOR NEURONOPATHY PREDOMINANTLY AFFECTING THE HANDS

      Neurology
    43. CHRISTODOULOU K; KYRIAKIDES T; HRISTOVA AH; GEORGIOU DM; KALAJDJIEVA L; YSHPEKOVA B; IVANOVA T; WEBER JL; MIDDLETON LT
      MAPPING OF AN AUTOSOMAL-DOMINANT DISTAL FORM OF SPINAL MUSCULAR-ATROPHY TO CHROMOSOME 7P

      American journal of human genetics
    44. CHRISTODOULOU K; IOANNOU P; MIDDLETON L
      MOLECULAR-GENETIC DETECTION OF XP21 MUSCULAR-DYSTROPHY CARRIERS IN CYPRUS

      Biomedicine & pharmacotherapy


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Documento generato il 06/08/20 alle ore 16:46:07