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La ricerca find articoli where authors phrase all words 'DEYMEER F' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 27 riferimenti
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    1. Plante-Bordeneuve, V; Parman, Y; Guiochon-Mantel, A; Alj, Y; Deymeer, F; Serdaroglu, P; Eraksoy, M; Said, G
      The range of chronic demyelinating neuropathy of infancy: a clinico-pathological and genetic study of 15 unrelated cases

      JOURNAL OF NEUROLOGY
    2. 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
    3. Deymeer, F; Serdaroglu, P; Ozdemir, C
      Juvenile and late-onset myasthenia gravis

      NEUROMUSCULAR DISEASES: FROM BASIC MECHANISMS TO CLINICAL MANAGE MENT
    4. Bissar-Tadmouri, N; Parman, Y; Boutrand, L; Deymeer, F; Serdaroglu, P; Vandenberghe, A; Battaloglu, E
      Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type I and HNPP patients

      CLINICAL GENETICS
    5. 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
    6. Deymeer, F; Serdaroglu, P; Ozdemir, C
      Familial infantile myasthenia: confusion in terminology

      NEUROMUSCULAR DISORDERS
    7. 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
    8. 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
    9. 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
    10. 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
    11. 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
    12. 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
    13. FLEISCHHAUER R; MITROVIC N; DEYMEER F; LEHMANNHORN F; LERCHE H
      EFFECTS OF TEMPERATURE AND MEXILETINE ON THE F1473S NA-CONGENITA( CHANNEL MUTATION CAUSING PARAMYOTONIA)

      Pflugers Archiv
    14. 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
    15. 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
    16. 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
    17. WAGNER S; KURZ LL; BENZ S; MAILANDER V; DEYMEER F; LEHMANNHORN F; RUDEL R
      THE DOMINANT MYOTONIA-CAUSING MUTATION G200R LEADS TO A RIGHT SHIFT OF THE ACTIVATION CURVE OF THE MUSCLE CHLORIDE CHANNEL HCLC-1

      Pflugers Archiv
    18. 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
    19. 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
    20. BISSARTADMOURI N; PARMAN YG; DEYMEER F; OZDEMIR C; BATTALOGLU E
      DETECTION OF DNA DUPLICATIONS IN TURKISH CMT1 PATIENTS

      American journal of human genetics
    21. 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
    22. 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
    23. MAILANDER V; HEINE R; DEYMEER F; LEHMANNHORN F
      NOVEL MUSCLE CHLORIDE CHANNEL MUTATIONS AND THEIR EFFECTS ON HETEROZYGOUS CARRIERS

      American journal of human genetics
    24. 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
    25. HEINE R; GEORGE AL; PIKA U; DEYMEER F; RUDEL R; LEHMANNHORN F
      PROOF OF A NONFUNCTIONAL MUSCLE CHLORIDE CHANNEL IN RECESSIVE MYOTONIA-CONGENITA (BECKER) BY DETECTION OF A 4 BASE-PAIR DELETION

      Human molecular genetics
    26. DEYMEER F; JONES HR
      PEDIATRIC MEDIAN MONONEUROPATHIES - A CLINICAL AND ELECTROMYOGRAPHIC STUDY

      Muscle & nerve
    27. 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 04/08/20 alle ore 21:27:27