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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. Urganci, N; Erkan, T; Serdaroglu, P; Ozcelik, G; Dogan, S; Kayaalp, N
      A rare cause of high transaminasemia: Autosomal muscle dystrophy with gamma sarcoglycan

      JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
    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. Deymeer, F; Serdaroglu, P; Ozdemir, C
      Juvenile and late-onset myasthenia gravis

      NEUROMUSCULAR DISEASES: FROM BASIC MECHANISMS TO CLINICAL MANAGE MENT
    5. Celet, B; Akman-Demir, G; Serdaroglu, P; Yentur, SP; Tasci, B; van Noort, JM; Eraksoy, M; Saruhan-Direskeneli, G
      Anti-a alpha B-crystallin immunoreactivity in inflammatory nervous system diseases

      JOURNAL OF NEUROLOGY
    6. 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
    7. 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
    8. Deymeer, F; Serdaroglu, P; Ozdemir, C
      Familial infantile myasthenia: confusion in terminology

      NEUROMUSCULAR DISORDERS
    9. Oktem-Tanor, O; Baykan-Kurt, B; Gurvit, IH; Akman-Demir, G; Serdaroglu, P
      Neuropsychological follow-up of 12 patients with neuro-Behcet disease

      JOURNAL OF NEUROLOGY
    10. 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
    11. Coban, O; Bahar, S; Akman-Demir, G; Tasci, B; Yurdakul, S; Yazici, H; Serdaroglu, P
      Masked assessment of MRI findings: is it possible to differentiate neuro-Behcet's disease from other central nervous system diseases? (vol 41, pg 255, 1999)

      NEURORADIOLOGY
    12. Coban, O; Bahar, S; Akman-Demir, G; Tasci, B; Yurdakul, S; Yazici, H; Serdaroglu, P
      Masked assessment of MRI findings: is it possible to differentiate neuro-Behcet's disease from other central nervous system

      NEURORADIOLOGY
    13. 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
    14. Erdogru, T; Kocak, T; Serdaroglu, P; Kadioglu, A; Tellaloglu, S
      Evaluation and therapeutic approaches of voiding and erectile dysfunction in neurological Behcet's syndrome

      JOURNAL OF UROLOGY
    15. Akman-Demir, G; Serdaroglu, P; Tasci, B
      Clinical patterns of neurological involvement in Behcet's disease: evaluation of 200 patients

      BRAIN
    16. SERDAROGLU P
      BEHCETS-DISEASE AND THE NERVOUS-SYSTEM

      Journal of neurology
    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. TASCI B; DIRESKENELI H; SERDAROGLU P; AKMANDEMIR G; ERAKSOY M; SARUHANDIRESKENELI G
      HUMORAL IMMUNE-RESPONSE TO MYCOBACTERIAL HEAT-SHOCK-PROTEIN (HSP)65 IN THE CEREBROSPINAL-FLUID OF NEURO-BEHCET PATIENTS

      Clinical and experimental immunology
    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. 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
    25. 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
    26. AKMANDEMIR G; BAHAR S; BAYKANKURT B; GURVIT IH; SERDAROGLU P
      INTRACRANIAL HYPERTENSION IN BEHCETS-DISEASE

      European journal of neurology
    27. 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
    28. COBAN O; BAHAR S; AKMANDEMIR G; SERDAROGLU P; BAYKANKURT B; TOLUN R; YURDAKUL S; YAZICI H
      A CONTROLLED-STUDY OF RELIABILITY AND VALIDITY OF MRI FINDINGS IN NEURO-BEHCETS DISEASE

      Neuroradiology
    29. 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
    30. 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
    31. AKMANDEMIR G; BAYKANKURT B; SERDAROGLU P; GURVIT H; YURDAKUL S; YAZICI H; BAHAR S; AKTIN E
      7-YEAR FOLLOW-UP OF NEUROLOGIC INVOLVEMENT IN BEHCET-SYNDROME

      Archives of 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


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 05/08/20 alle ore 18:18:27