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    1. Abbruzzese, G; Agid, Y; Albanese, A; Alf, C; Allen, R; Amar, K; de Andrade, LA; Ang, LC; Angelini, C; Archer, RL; Arunodaya, GR; Baltzan, M; Baral, K; Barnett, H; Bergamasco, B; Berger, M; Bernard, J; Bharucha, NE; Bhatia, K; Blary, N; Black, S; Bodis-Wollner, I; Boyson, SJ; Bral-Kulaksizoglu, I; Brooks, DJ; Brown, JD; Burke, RE; Calne, DOC; Calne, SM; Cardoso, F; Cardozo-Pelaez, F; Chang, YJ; Chen, CC; Chen, RS; Chen, R; Chowdhury, A; Christie, S; Chu, CC; Chu, NS; Clarida, L; Collette, EM; Comella, C; Conneally, PM; Crossman, AR; Csanda, E; Dalmau, J; Dalvi, A; De Feijter, A; Deecke, L; Desai, H; De Ybenes, J; Dihenia, B; Direnfeld, L; Dodel, R; Donat, J; Doudet, D; Duane, DD; Duff, J; Duvoisin, R; Eggert, K; Elble, RJ; Elmer, LW; Emre, M; Fariello, R; Fernendy, HH; Findley, LJ; Fink, S; Freissmuth, M; Friedman, JH; de la Fuente-Fernandez, R; Furtado, S; Furukawa, Y; Galvez-Jimenez, N; Gauthier, S; Gawel, MJ; Gilman, S; Gladstone, RM; Goetz, CG; Gomori, A; Gopinathan, G; Gordin, A; Gorell, JM; Greenamyre, JT; Grimes, DA; Gurvit, H; Guttman, M; Guzman, DA; Hachinski, V; Hanagasi, H; Hardy, J; Harik, SJ; Hassan, MN; Hattori, N; Hauser, RA; Hayashi, H; Heller, GL; Hobson, D; Hochschorner, G; Hortnagel, H; Horowski, R; Howse, DC; Huang, CC; Huk, II; Hurtig, H; Hutton, JT; Jaffe, ME; Jankovic, J; Jardine, M; Jog, M; Johnson, B; Kagamihara, Y; Karagoz, N; Kasper, S; Kato, S; Kebabian, JW; Kertsz, A; Khadilkar, SV; Kirk, A; Kish, S; Kitaguchi, T; Kofman, OS; Koide, R; Komori, T; Kostyuk, PG; Kumar, R; Kuo, HC; Kurlan, R; Kurland, L; Kurtuncu, M; Lalkaka, JA; Lambert, M; Landau, W; Lang, AE; Lassmann, H; Lee, CS; Lees, AJ; Lieberman, A; Litvan, I; Loeb, C; Logan, WJ; Lozano, AM; Lu, CS; Lucy, D; Lynch, T; Manyam, BV; Maraganore, D; Marshall, FT; Martin, WRW; Martin, WE; Mathias, C; Matsubera, S; Mendis, T; Menkes, JH; Metz, LN; Miyazaki, Y; Mizuno, Y; Mohr, E; Moodley, LG; Moore, R; Morris, JL; Muthane, U; Nagaraja, D; Nair, CPV; Narabayashi, H; Nomura, Y; Norris, JW; Obeso, JA; O'Brien, C; Oertel, W; Ohtake, T; Okiyama, R; Ozdemir, C; Pal, PK; Panisset, M; Paty, DW; Paulson, GW; Perlmutter, J; Pfeiffer, RF; Pifl, C; Pincus, JH; Poewe, W; Quinn, N; Rajput, AH; Rajput, A; Ransmayr, G; Rascol, O; Robinson, R; Rocca, WA; Roos, RAC; Rosenfeld, MR; Russell, D; Ruth, TJ; Ryu, SJ; Sachdev, H; Safoschnik, G; Sahin, H; Sanchez-Ramos, J; Satishchandra, P; Schapira, A; Scheltens; Schmidley, JW; Schnaberth, G; Schneider, E; Schneider, JS; Schutz, W; Seeberger, LC; Segawa, M; Sethi, KD; Shah, A; Shannon, K; Shelton, P; Shihabuddin, B; Shimizu, T; Shinotoh, H; Siddique, T; Siderowf, A; Sieghart, W; Simard, A; Simmonds, DC; Singhal, BS; Sluga, E; Snow, BJ; Soukop, W; Sperk, G; Spieker, S; Steele, JC; Stewart, S; Stoessl, AJ; Subramony, SH; Sundaram, M; Sung, CY; Surya, N; Sweet, RD; Tabbal, SD; Takahashi, H; Taniguchi, M; Tarsy, D; Teravainen, H; Tetrud, JW; Tolosa, E; Tourtellotte, WW; Troupin, AS; Tsui, JKC; Tuite, P; Uc, EY; Ueki, Y; Uitti, R; Uyu, C; van Hilten, JJ; Veerendrakumar, M; Veloso, F; Viallet, F; Voll, C; Vrooman, M; Wang, X; Ward, I; Ward, A; Waters, C; Weng, YH; Wenning, GK; Williams, BJ; Wilson, TW; Wolters, EC; Wooten, FG; Wszolek, Z; Yahr, MD; Yanagisawa, N; Yokochi, F; Young, RR; Yu, CM; Zifko, U
      An open letter to the Committee on the Nobel Prize in Medicine

      PARKINSONISM & RELATED DISORDERS
    2. Van Oosterom, FJT; Brete, GJV; Ozdemir, C; Hovius, SER
      Treatment of phalangeal fractures injured hands

      JOURNAL OF HAND SURGERY-BRITISH AND EUROPEAN VOLUME
    3. Plaster, NM; Tawil, R; Tristani-Firouzi, M; Canun, S; Bendahhou, S; Tsunoda, A; Donaldson, MR; Iannaccone, ST; Brunt, E; Barohn, R; Clark, J; Deymeer, F; George, AL; Fish, FA; Hahn, A; Nitu, A; Ozdemir, C; Serdaroglu, P; Subramony, SH; Wolfe, G; Fu, YH; Ptacek, LJ
      Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

      CELL
    4. Iskit, SH; Alpay, H; Tugtepe, H; Ozdemir, C; Ayyildiz, SH; Ozel, K; Bayramicli, M; Tetik, C; Dagli, TE
      Analysis of 33 pediatric trauma victims in the 1999 Marmara, Turkey earthquake

      JOURNAL OF PEDIATRIC SURGERY
    5. Deymeer, F; Serdaroglu, P; Ozdemir, C
      Juvenile and late-onset myasthenia gravis

      NEUROMUSCULAR DISEASES: FROM BASIC MECHANISMS TO CLINICAL MANAGE MENT
    6. Su, T; Ozdemir, C; Ling, H
      On extracting the radiation center representation of antenna radiation patterns on a complex platform

      MICROWAVE AND OPTICAL TECHNOLOGY LETTERS
    7. Ozdemir, C; Bhalla, R; Ling, H
      A radiation center representation of antenna radiation patterns on a complex platform

      IEEE TRANSACTIONS ON ANTENNAS AND PROPAGATION
    8. Onengut, S; Kavaslar, GN; Battaloglu, E; Serdaroglu, P; Deymeer, F; Ozdemir, C; Calafell, F; Tolun, A
      Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and Indians

      ANNALS OF HUMAN GENETICS
    9. Ozdemir, C
      The beginning is over - The overdue modernization of legislation on Germancitizenship

      INTERNATIONALE POLITIK
    10. Deymeer, F; Serdaroglu, P; Ozdemir, C
      Familial infantile myasthenia: confusion in terminology

      NEUROMUSCULAR DISORDERS
    11. Ozdemir, C; Ling, H
      ACSAR-antenna coupling synthetic aperture radar imaging algorithm

      JOURNAL OF ELECTROMAGNETIC WAVES AND APPLICATIONS
    12. Ozata, M; Odabasi, Z; Caglayan, S; Beyhan, Z; Vural, O; Ozdemir, C
      Event-related brain potentials in male hypogonadism

      JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
    13. Deymeer, F; Lehmann-Horn, F; Serdaroglu, P; Cakirkaya, S; Benz, S; Rudel, R; Ozdemir, C
      Electrical myotonia in heterozygous carriers of recessive myotonia congenita

      MUSCLE & NERVE
    14. 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
    15. Ozdemir, S; Zorba, O; Bodur, AE; Ozdemir, C
      Some selected analytical and sensory data of frozen stored yoghurt

      NAHRUNG-FOOD
    16. BISSARTADMOURI N; PARMAN YG; DEYMEER F; OZDEMIR C; VANDENBERGHE A; BATTALOGLU E
      DETECTION OF JUNCTION FRAGMENTS IN TURKISH CMT1A HNPP PATIENTS/

      European journal of human genetics
    17. WAGNER S; DEYMEER F; KURZ LL; BENZ S; SCHLEITHOFF L; LEHMANNHORN F; SERDAROGLU P; OZDEMIR C; RUDEL R
      THE DOMINANT CHLORIDE CHANNEL MUTANT G200R CAUSING FLUCTUATING MYOTONIA - CLINICAL FINDINGS, ELECTROPHYSIOLOGY, AND CHANNEL PATHOLOGY

      Muscle & nerve
    18. DEYMEER F; OGE AE; SERDAROGLU P; YAZICI J; OZDEMIR C; BASLO A
      THE USE OF BOTULINUM TOXIN IN LOCALIZING NEUROMYOTONIA TO THE TERMINAL BRANCHES OF THE PERIPHERAL-NERVE

      Muscle & nerve
    19. DEYMEER F; CAKIRKAYA S; SERDAROGLU P; SCHLEITHOFF L; LEHMANNHORN F; RUDEL R; OZDEMIR C
      TRANSIENT WEAKNESS AND COMPOUND MUSCLE ACTION-POTENTIAL DECREMENT IN MYOTONIA-CONGENITA

      Muscle & nerve
    20. 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
    21. Ozdemir, C; Bhalla, R; Trintinalia, LC; Ling, H
      ASAR - Antenna synthetic aperture radar imaging

      IEEE TRANSACTIONS ON ANTENNAS AND PROPAGATION
    22. 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
    23. DEYMEER F; SERDAROGLU P; PODA M; GULSENPARMAN Y; OZCELIK T; OZDEMIR C
      SEGMENTAL DISTRIBUTION OF MUSCLE WEAKNESS IN SMA-III - IMPLICATIONS FOR DETERIORATION IN MUSCLE STRENGTH WITH TIME

      Neuromuscular disorders
    24. SENYUVA C; YUCEL A; ERDAMAR S; CETINKALE O; SERADJMIR M; OZDEMIR C
      THE FATE OF ALLOPLASTIC MATERIALS PLACED UNDER A BURN SCAR - AN EXPERIMENTAL-STUDY

      Burns
    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 GENE TO CHROMOSOME 17P

      Neurology
    26. OZDEMIR C; LING H
      JOINT TIME-FREQUENCY INTERPRETATION OF SCATTERING PHENOMENOLOGY IN DIELECTRIC-COATED WIRES

      IEEE transactions on antennas and propagation
    27. 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
    28. BISSARTADMOURI N; PARMAN YG; DEYMEER F; OZDEMIR C; BATTALOGLU E
      DETECTION OF DNA DUPLICATIONS IN TURKISH CMT1 PATIENTS

      American journal of human genetics
    29. 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
    30. 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
    31. 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
    32. KAVASLAR GN; TELATAR M; SERDAROGLU P; DEYMEER F; OZDEMIR C; TOLUN A
      IDENTIFICATION OF A ONE-BASEPAIR DELETION IN EXON-6 OF THE DYSTROPHINGENE

      Human mutation
    33. TAWIL R; PTACEK LJ; PAVLAKIS SG; DEVIVO DC; PENN AS; OZDEMIR C; GRIGGS RC
      ANDERSENS-SYNDROME - OR KLEIN-LISAK-ANDERSEN SYNDROME - REPLY

      Annals of neurology
    34. TAWIL R; PTACEK LJ; PAVLAKIS SG; DEVIVO DC; PENN AS; OZDEMIR C; GRIGGS RC
      ANDERSENS-SYNDROME - POTASSIUM-SENSITIVE PERIODIC PARALYSIS, VENTRICULAR ECTOPY, AND DYSMORPHIC FEATURES

      Annals of neurology
    35. DEYMEER F; OGE AE; BAYINDIR C; KAYMAZ C; NISANCI Y; ADALET K; YATES JRW; OZDEMIR C
      EMERY-DREIFUSS MUSCULAR-DYSTROPHY WITH UNUSUAL FEATURES

      Muscle & nerve


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 05/08/20 alle ore 18:37:41