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La ricerca find articoli where authors phrase all words ' MIDDLETON LT' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 30 riferimenti
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    1. Scott, WK; Nance, MA; Watts, RL; Hubble, JP; Koller, WC; Lyons, K; Pahwa, R; Stern, MB; Colcher, A; Hiner, BC; Jankovic, J; Ondo, WG; Allen, FH; Goetz, CG; Small, GW; Masterman, D; Mastaglia, F; Laing, NG; Stajich, JM; Slotterbeck, B; Booze, MW; Ribble, RC; Rampersaud, E; West, SG; Gibson, RA; Middleton, LT; Roses, AD; Haines, JL; Scott, BL; Vance, JM; Pericak-Vance, MA
      Complete genomic screen in parkinson disease - Evidence for multiple genes

      JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
    2. Martin, ER; Scott, WK; Nance, MA; Watts, RL; Hubble, JP; Koller, WC; Lyons, K; Pahwa, R; Stern, MB; Colcher, A; Hiner, BC; Jankovic, J; Ondo, WG; Allen, FH; Goetz, CG; Small, GW; Masterman, D; Mastaglia, F; Laing, NG; Stajich, JM; Ribble, RC; Booze, MW; Rogala, A; Hauser, MA; Zhang, FY; Gibson, RA; Middleton, LT; Roses, AD; Haines, JL; Scott, BL; Pericak-Vance, MA; Vance, JM
      Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease

      JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
    3. 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
    4. Pattichis, CS; Schofield, I; Merletti, R; Parker, PA; Middleton, LT
      Introduction to this Special Issue - Intelligent data analysis in electromyography and electroneurography

      MEDICAL ENGINEERING & PHYSICS
    5. 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
    6. 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
    7. 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
    8. 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
    9. 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
    10. MIDDLETON LT; CHRISTODOULOU K
      CLASSIFICATION OF AUTOSOMAL RECESSIVE SPINOCEREBELLAR ATAXIAS (ARSCA)BASED ON RECENT GENETIC-STUDIES

      Neurology
    11. KYRIAKIDES T; KYRIAKOU K; SOEDIONO O; MIDDLETON LT
      DUCHENNE MUSCULAR-DYSTROPHY - WHEN TO COMMENCE STEROIDS

      Neurology
    12. 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
    13. LENNON F; PERICAKVANCE MA; SPEER MC; WEST SG; MENOLD MM; STAJICH JM; WOLPERT CM; SLOTTERBECK BD; SAITO M; TIM RW; ROZEAR MP; MIDDLETON LT; TSUJI S; VANCE JM
      CMT2 MAPPING PROGRESS - CONFIRMATION OF A 2ND LOCUS AND EVIDENCE FOR ADDITIONAL GENETIC-HETEROGENEITY

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

      American journal of human genetics
    15. MIDDLETON LT
      CONGENITAL MYASTHENIC SYNDROMES - 34TH ENMC INTERNATIONAL WORKSHOP, 10-11 JUNE 1995

      Neuromuscular disorders
    16. 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
    17. 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
    18. 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
    19. 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
    20. NICOLAIDES AN; BARNETT HJM; BELCARO GV; BERNSTEIN EF; CALLOW A; EASTCOTT HHG; EIKELBOOM B; EKLOF B; GEROULAKOS G; HALLIDAY A; HOBSON R; KALODIKI E; LUSBY R; MALIKIDES A; MIDDLETON LT; MOORE WS; NORRIS J; PRESCOTT L; RAMASWAMI G; RUTHERFORD R; SANDMANN W; SHANIK G; SPARTERA C; THOMAS D
      CONSENSUS STATEMENT ON THE MANAGEMENT OF PATIENTS WITH ASYMPTOMATIC ATHEROSCLEROTIC CAROTID BIFURCATION LESIONS

      International angiology
    21. PATTICHIS CS; CHARALAMBOUS C; MIDDLETON LT
      EFFICIENT TRAINING OF NEURAL-NETWORK MODELS IN CLASSIFICATION OF ELECTROMYOGRAPHIC DATA

      Medical & biological engineering & computing
    22. BENOTHMANE K; SPEER M; MIDDLETON LT; LOEB D; HENTATI F; BENHAMIDA M; PERICAKVANCE MA; VANCE JM
      LINKAGE DISEQUILIBRIUM IN THE DUCHENNE-LIKE MUSCULAR-DYSTROPHY NDLMD)REGION REFINES THE LOCALIZATION OF THE DISEASE GENE TO LESS-THAN U CM

      Neurology
    23. KYRIALLIS K; HRISTOVA AH; MIDDLETON LT
      WHAT IS THE REAL EPIDEMIOLOGY OF MYASTHENIA-GRAVIS

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

      Neurology
    25. PATTICHIS CS; SCHIZAS CN; MIDDLETON LT
      NEURAL-NETWORK MODELS IN EMG DIAGNOSIS

      IEEE transactions on biomedical engineering
    26. 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
    27. MIDDLETON LT; MOSER H
      23RD ENMC WORKSHOP ON RARE NEUROMUSCULAR DISEASES - 4-6 JUNE, BAARN, THE NETHERLANDS

      Neuromuscular disorders
    28. BOTEVA K; PAPAGEORGIOU E; GEORGIOU C; ANGASTINIOTIS M; MIDDLETON LT; CONSTANTINOUDELTAS CD
      NOVEL CYSTIC-FIBROSIS MUTATION ASSOCIATED WITH MILD DISEASE IN CYPRIOT PATIENTS

      Human genetics
    29. BENOTHMANE K; MIDDLETON LT; LOPREST LJ; WILKINSON KM; LENNON F; ROZEAR MP; STAJICH JM; GASKELL PC; ROSES AD; PERICAKVANCE MA; VANCE JM
      LOCALIZATION OF A GENE (CMT2A) FOR AUTOSOMAL-DOMINANT CHARCOT-MARIE-TOOTH DISEASE TYPE-2 TO CHROMOSOME-1P AND EVIDENCE OF GENETIC-HETEROGENEITY

      Genomics
    30. VANCE JM; BENOTHMANE K; DENG H; MIDDLETON LT; LOPREST L; WILKINSON KM; LENNON F; ROZEAR MM; STAJICH JM; GASKELL PC; ROSES AD; SIDDIQUE T; PERICAKVANCE MA
      MAPPING OF THE AUTOSOMAL-DOMINANT CMT2 (CMT2A) LOCUS IN THE REGION OFCHROMOSOME-1P35-36

      American journal of human genetics


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Documento generato il 06/08/20 alle ore 16:39:54