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    1. Walter, MC; Lochmuller, H
      Novel approaches to treat muscular dystrophies

      EXPERT OPINION ON INVESTIGATIONAL DRUGS
    2. Karpati, G; Lochmuller, H
      When running a stop sign may be a good thing

      ANNALS OF NEUROLOGY
    3. Jahn, K; Mohammadi, B; Krampfl, K; Abicht, A; Lochmuller, H; Bufler, J
      Deactivation and desensitization of mouse embryonic- and adult-type nicotinic receptor channel currents

      NEUROSCIENCE LETTERS
    4. O'Hara, AJ; Howell, JM; Taplin, RH; Fletcher, S; Lloyd, F; Kakulas, B; Lochmuller, H; Karpati, G
      The spread of transgene expression at the site of gene construct injection

      MUSCLE & NERVE
    5. Jaksch, M; Horvath, R; Horn, N; Auer, DP; Macmillan, C; Peters, J; Gerbitz, KD; Kraegeloh-Mann, I; Muntau, A; Karcagi, V; Kalmanchey, R; Lochmuller, H; Shoubridge, EA; Freisinger, P
      Homozygosity (E140K) in SCO2 causes delayed infantile onset of cardiomyopathy and neuropathy

      NEUROLOGY
    6. Lampe, J; Gossrau, G; Reichmann, H; Walter, MC; Mendel, B; Lochmuller, H
      Prion codon 129 homozygosity and sporadic inclusion body myositis

      NEUROLOGY
    7. Lampe, J; Gossrau, G; Reichmann, H; Koch, R; Walter, MC; Mendel, B; Lochmuller, H
      Prion codon 129 homozygosity and sporadic inclusion body myositis

      NEUROLOGY
    8. Jaksch, M; Lochmuller, H; Schmitt, F; Volpel, B; Obermaier-Kusser, B; Horvath, R
      A mutation in mt tRNALeu ((UUR)) causing a neuropsychiatric syndrome with depression and cataract

      NEUROLOGY
    9. Walter, MC; Lochmuller, H; Schlotter, B; Reilich, P; Muller-Felber, W; Pongratz, D
      New insights in pathogenesis and therapy of sporadic inclusion body myositis (s-IBM)

      NERVENARZT
    10. Moll, J; Barzaghi, P; Lin, S; Bezakova, G; Lochmuller, H; Engvall, E; Muller, U; Ruegg, MA
      An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy

      NATURE
    11. Nalbantoglu, J; Larochelle, N; Wolf, E; Karpati, G; Lochmuller, H; Holland, PC
      Muscle-specific overexpression of the adenovirus primary receptor CAR overcomes low efficiency of gene transfer to mature skeletal muscle

      JOURNAL OF VIROLOGY
    12. Jaksch, M; Kleinle, S; Scharfe, C; Klopstock, T; Pongratz, D; Muller-Hocker, J; Gerbitz, KD; Liechti-Gallati, S; Lochmuller, H; Horvath, R
      Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies

      JOURNAL OF MEDICAL GENETICS
    13. Thirion, C; Stucka, R; Mendel, B; Gruhler, A; Jaksch, M; Nowak, KJ; Binz, N; Laing, NG; Lochmuller, H
      Characterization of human muscle type cofilin (CFL2) in normal and regenerating muscle

      EUROPEAN JOURNAL OF BIOCHEMISTRY
    14. Borner, GV; Zeviani, M; Tiranti, V; Carrara, F; Hoffmann, S; Gerbitz, KD; Lochmuller, H; Pongratz, D; Klopstock, T; Melberg, A; Holme, E; Paabo, S
      Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patients

      HUMAN MOLECULAR GENETICS
    15. Stucka, R; Abicht, A; Song, IH; Bonsch, D; Deufel, T; Lochmuller, H
      A modified alignment of human and rodent 5 ' untranslated sequences of theacetylcholine receptor epsilon subunit gene reveals additional regions of high homology

      NEUROMUSCULAR DISORDERS
    16. Walter, MC; Lochmuller, H; Toepfer, M; Schlotter, B; Reilich, P; Schroder, M; Muller-Felber, W; Pongratz, D
      High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study

      JOURNAL OF NEUROLOGY
    17. Horvath, R; Abicht, A; Shoubridge, EA; Karcagi, V; Rozsa, C; Komoly, S; Lochmuller, H
      Leber's hereditary optic neuropathy presenting as multiple sclerosis-like disease of the CNS

      JOURNAL OF NEUROLOGY
    18. Toepfer, M; Schroeder, M; Muller-Felber, W; Lochmuller, H; Sitter, T; Pongratz, D; Schiffl, H
      Successful management of polyneuropathy associated with IgM gammopathy of undetermined significance with antibody-based immunoadsorption

      CLINICAL NEPHROLOGY
    19. Muller-Hocker, J; Schafer, S; Mendel, B; Lochmuller, H; Pongratz, D
      Nemaline cardiomyopathy in a young adult: An ultraimmunohistochemical study and review of the literature

      ULTRASTRUCTURAL PATHOLOGY
    20. Walter, MC; Lochmuller, H; Reilich, P; Klopstock, T; Huber, R; Hartard, M; Hennig, M; Pongratz, D; Muller-Felber, W
      Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study

      NEUROLOGY
    21. Horvath, R; Lochmuller, H; Stucka, R; Yao, JB; Shoubridge, EA; Kim, SH; Gerbitz, KD; Jaksch, M
      Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiency

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    22. Li, HW; Alonso-Vanegas, M; Colicos, MA; Jung, SS; Lochmuller, H; Sadikot, AF; Snipes, GJ; Seth, P; Karpati, G; Nalbantoglu, J
      Intracerebral adenovirus-mediated p53 tumor suppressor gene therapy for experimental human glioma

      CLINICAL CANCER RESEARCH
    23. Weller, B; Carpenter, S; Lochmuller, H; Karpati, G
      Myopathy with trabecular muscle fibers

      NEUROMUSCULAR DISORDERS
    24. Lochmuller, H
      Prospects of gene therapy for muscular dystrophy

      NERVENHEILKUNDE
    25. Toepfer, M; Schroeder, M; Unger, JW; Lochmuller, H; Pongratz, D; Muller-Felber, W
      Neuromyotonia, myocloni, sensory neuropathy and cerebellar symptoms in a patient with antibodies to neuronal nucleoproteins (anti-Hu-antibodies)

      CLINICAL NEUROLOGY AND NEUROSURGERY
    26. Toepfer, M; Fischer, P; Abicht, A; Lochmuller, H; Pongratz, D; Muller-Felber, W
      Localization of transforming growth factor beta in association with neuromuscular junctions in adult human muscle

      CELLULAR AND MOLECULAR NEUROBIOLOGY
    27. Lampe, J; Kitzler, H; Walter, MC; Lochmuller, H; Reichmann, H
      Methionine homozygosity at prion gene codon 129 may predispose to sporadicinclusion-body myositis

      LANCET
    28. Abicht, A; Stucka, R; Karcagi, V; Herczegfalvi, A; Horvath, R; Mortier, W; Schara, U; Ramaekers, V; Jost, W; Brunner, J; Janssen, G; Seidel, U; Schlotter, B; Muller-Felber, W; Pongratz, D; Rudel, R; Lochmuller, H
      A common mutation (epsilon 1267delG) in congenital myasthenic patients of Gypsy ethnic origin

      NEUROLOGY
    29. Munz, B; Wiedmann, M; Lochmuller, H; Werner, S
      Cloning of novel injury-regulated genes - Implications for an important role of the muscle-specific protein skNAC in muscle repair

      JOURNAL OF BIOLOGICAL CHEMISTRY
    30. Lochmuller, H; Johns, T; Shoubridge, EA
      Expression of the E6 and E7 genes of human papillomavirus (HPV16) extends the life span of human myoblasts

      EXPERIMENTAL CELL RESEARCH
    31. Toepfer, M; Folwaczny, C; Lochmuller, H; Schroeder, M; Riepl, RL; Pongratz, D; Muller-Felber, W
      Noninvasive C-13-octanoic acid breath test shows delayed gastric emptying in patients with amyotrophic lateral sclerosis

      DIGESTION
    32. HOWELL JM; LOCHMULLER H; OHARA A; FLETCHER S; KAKULAS BA; MASSIE B; NALBANTOGLU J; KARPATI G
      HIGH-LEVEL DYSTROPHIN EXPRESSION AFTER ADENOVIRUS-MEDIATED DYSTROPHINMINIGENE TRANSFER TO SKELETAL-MUSCLE OF DYSTROPHIC DOGS - PROLONGATION OF EXPRESSION WITH IMMUNOSUPPRESSION

      Human gene therapy
    33. YANG L; LOCHMULLER H; LUO J; MASSIE B; NALBANTOGLU J; KARPATI G; PETROF BJ
      ADENOVIRUS-MEDIATED DYSTROPHIN MINIGENE TRANSFER IMPROVES MUSCLE STRENGTH IN ADULT DYSTROPHIC (MDX) MICE

      Gene therapy
    34. Kramer, R; Lochmuller, H; Abicht, A; Rudel, R; Brinkmeier, H
      Myotonic ADR-MDX mutant mice show less severe muscular dystrophy than MDX mice

      NEUROMUSCULAR DISORDERS
    35. ACSADI G; OHAGAN D; LOCHMULLER H; PRESCOTT S; LAROCHELLE N; NALBANTOGLU J; JANI A; KARPATI G
      INTERFERONS IMPAIR EARLY TRANSGENE EXPRESSION BY ADENOVIRUS-MEDIATED GENE-TRANSFER IN MUSCLE-CELLS

      Journal of molecular medicine
    36. TOEPFER M; SCHIFFL H; FRICKE H; LOCHMULLER H; HELD E; PONGRATZ D; MULLERFELBER W
      INFLAMMATORY DEMYELINATING NEUROPATHY IN PATIENTS WITH END-STAGE RENAL-DISEASE RECEIVING CONTINUOUS AMBULATORY PERITONEAL-DIALYSIS (CAPD)

      Peritoneal dialysis international
    37. TOEPFER M; SITTER T; LOCHMULLER H; PONGRATZ D; MULLERFELBER W
      DRUG-INDUCED SYSTEMIC LUPUS-ERYTHEMATOSUS AFTER 8 YEARS OF TREATMENT WITH CARBAMAZEPINE

      European Journal of Clinical Pharmacology
    38. HORVATH R; LOCHMULLER H; SHOUBRIDGE E; KARCAGI V; KOMOLY S
      LEHERS HEREDITARY OPTIC NEUROPATHY PRESENTING AS DEMYELINATING (MS-LIKE) DISEASE OF THE CENTRAL-NERVOUS-SYSTEM

      Neurology
    39. NALBANTOGLU J; LI HW; LOCHMULLER H; ALONSOVANEGAS M; SADIKOT A; BARTUS RT; KARPATI G
      INTRACAROTID INFUSION OF BRADYKININ ANALOG RMP-7 COMBINED WITH INHALATION OF CO2 ENHANCES THE DELIVERY OF ADENOVIRAL RECOMBINANT TO RAT INTRACEREBRAL GLIOMAS

      Neurology
    40. LOCHMULLER H; KRAMER R; ABICHT A; RUDEL R; BRINKMEIER H
      MYOTONIC ADR-MDX MUTANT MICE SHOW LESS SIGNS OF MUSCULAR-DYSTROPHY THAN MDX MICE

      Neurology
    41. TOEPFER M; LOCHMULLER H; HIRSCHMANN M; FISCHER P; OLMA M; PONGRATZ D; MULLERFELBER W
      EXPRESSION OF CHEMOKINES IN NORMAL MUSCLE AND INFLAMMATORY MYOPATHIES

      Neurology
    42. KARPATI G; LOCHMULLER H; LI G; MASSIE B; NALBANTOGLU J
      CONTROLLED TRANSGENE EXPRESSION IN SKELETAL-MUSCLES AFTER ADENOVIRUS-MEDIATED GENE-TRANSFER

      Neurology
    43. PETROF BJ; LOCHMULLER H; GUIBINGA GH; MASSIE B; NALBANTOGLU J; KARPATI G
      COMBINATORIAL BLOCKADE OF T-CELL SIGNALING FACILITATES PRIMARY AND SECONDARY ADENOVIRUS-MEDIATED DYSTROPHIN GENE-TRANSFER IN MDX MICE

      Neurology
    44. HIRSCHMANN M; LOCHMULLER H; TOEPFER M; SCHLOTTER B; SCHRODER M; MULLERFELBER W; NAUMANN M; SCHNEIDER C; TOYKA KV; PONGRATZ DE
      HIGH-DOSE INTRAVENOUS IMMUNOGLOBULIN (IVIG) IN THE TREATMENT OF INCLUSION-BODY MYOSITIS - A DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY

      Neurology
    45. GUIBINGA GH; LOCHMULLER H; MASSIE B; NALBANTOGLU J; KARPATI G; PETROF BJ
      COMBINATORIAL BLOCKADE OF CALCINEURIN AND CD28 SIGNALING FACILITATES PRIMARY AND SECONDARY THERAPEUTIC GENE-TRANSFER BY ADENOVIRUS VECTORS IN DYSTROPHIC (MDX) MOUSE MUSCLES

      Journal of virology
    46. ZHAO JE; LOCHMULLER H; NALBANTOGLU J; ALLEN C; PRESCOTT S; MASSIE B; KARPATI G
      STUDY OF ADENOVIRUS-MEDIATED DYSTROPHIN MINIGENE TRANSFER TO SKELETAL-MUSCLE BY COMBINED MICROSCOPIC DISPLAY OF ADENOVIRAL DNA AND DYSTROPHIN

      Human gene therapy
    47. LAROCHELLE N; LOCHMULLER H; ZHAO J; JANI A; HALLAUER P; HASTINGS KEM; MASSIE B; PRESCOTT S; PETROF BJ; KARPATI G; NALBANTOGLU J
      EFFICIENT MUSCLE-SPECIFIC TRANSGENE EXPRESSION AFTER ADENOVIRUS-MEDIATED GENE-TRANSFER IN MICE USING A 1.35 KB MUSCLE CREATINE-KINASE PROMOTER ENHANCER/

      Gene therapy
    48. KARPATI G; LOCHMULLER H
      THE SCOPE OF GENE-THERAPY IN HUMANS - SCIENTIFIC, SAFETY AND ETHICAL CONSIDERATIONS

      Neuromuscular disorders
    49. HOWELL JM; FLETCHER S; KAKULAS BA; OHARA M; LOCHMULLER H; KARPATI G
      USE OF THE DOG-MODEL FOR DUCHENNE MUSCULAR-DYSTROPHY IN GENE-THERAPY TRIALS

      Neuromuscular disorders
    50. DURHAM HD; ALONSOVANEGAS MA; SADIKOT AF; ZHU LX; LOCHMULLER H; MASSIE B; NALBANTOGLU J; KARPATI G
      THE IMMUNOSUPPRESSANT FK506 PROLONGS TRANSGENE EXPRESSION IN BRAIN FOLLOWING ADENOVIRUS-MEDIATED GENE-TRANSFER

      NeuroReport
    51. JANI A; LOCHMULLER H; ACSADI G; SIMONEAU M; HUARD J; GARNIER A; KARPATI G; MASSIE B
      GENERATION, VALIDATION, AND LARGE-SCALE PRODUCTION OF ADENOVIRAL RECOMBINANTS WITH LARGE-SIZE INSERTS SUCH AS A 6.3 KB HUMAN DYSTROPHIN CDNA

      Journal of virological methods
    52. LI HW; LOCHMULLER H; SETH P; KARPATI G; NALBANTOGLU J
      GENE-THERAPY OF MALIGNANT GLIOMAS - ADENOVIRUS-MEDIATED WILD-TYPE P53EXPRESSION INDUCES WIDESPREAD APOPTOSIS OF HUMAN GLIOMA-CELLS INDEPENDENTLY OF ENDOGENOUS P53 STATUS

      Neurology
    53. DURHAM HD; ALONSOVANEGAS MA; SADIKOT AF; LOCHMULLER H; MASSIE B; NALBANTOGLU J; KARPATI G
      IMMUNOSUPPRESSION BY FK506 PROLONGS EXPRESSION OF A TRANSGENE DELIVERED TO MOUSE STRIATUM BY REPLICATION-DEFECTIVE ADENOVIRUS

      Neurology
    54. HORVATH R; LOCHMULLER H; KARPATI G; SHOUBRIDGE E
      EXPRESSION OF NITRIC-OXIDE SYNTHASE (NOS) ISOFORMS IN SKELETAL-MUSCLEOF PATIENTS WITH MITOCHONDRIAL DISEASE

      Neurology
    55. PETROF BJ; LOCHMULLER H; YANG LY; NALBANTOGLU J; MASSIE B; KARPATI G
      ADENOVIRUS-MEDIATED (MINI)DYSTROPHIN GENE-TRANSFER HELPS PRESERVE MUSCLE STRENGTH IN SKELETAL-MUSCLES OF MDX MICE

      Neurology
    56. MACHOWELL J; LOCHMULLER H; FLETCHER S; OHARA A; MASSIE B; KAKULAS B; KARPATI G
      EFFICIENT HIGH-LEVEL DYSTROPHIN (DYS) EXPRESSION AFTER ADENOVIRUS (AV)-MEDIATED GENE-TRANSFER (GT) INTO SKELETAL-MUSCLE OF GOLDEN RETRIEVERDYSTROPHIC DOGS

      Neurology
    57. ZHAO JE; LOCHMULLER H; MASSIE B; NALBANTOGLU J; KARPATI G
      IN-SITU POLYMERASE CHAIN-REACTION (PCR) FOR THE MICROSCOPIC DISPLAY OF ADENOVIRAL RECOMBINANTS IS A POWERFUL TOOL IN ASSESSING AVR-MEDIATEDDYSTROPHIN GENE-TRANSFER TO MUSCLE

      Neurology
    58. LOCHMULLER H; PETROF B; NALBANTOGLU J; MASSIE B; KARPATI G
      ANTIVIRAL ANTIBODIES PREVENT EFFICIENT DYSTROPHIN EXPRESSION AFTER ADENOVIRUS-MEDIATED GENE-TRANSFER TO SKELETAL-MUSCLE OF MDX MICE

      Neurology
    59. WELLER B; LOCHMULLER H; CARPENTER S; SHOUBRIDGE E; ALLEN C; KARPATI G
      TRABECULAR MYOPATHY - A DISTINCTIVE CLINICOPATHOLOGICAL ENTITY WITH MARKED OVEREXPRESSION OF VIMENTIN IN MUSCLE

      Neurology
    60. LI HW; LOCHMULLER H; YONG VW; KARPATI G; NALBANTOGLU J
      ADENOVIRUS-MEDIATED WILD-TYPE P53 GENE-TRANSFER AND OVEREXPRESSION INDUCES APOPTOSIS OF HUMAN GLIOMA-CELLS INDEPENDENT OF ENDOGENOUS P53 STATUS

      Journal of neuropathology and experimental neurology
    61. ACSADI G; LOCHMULLER H; JANI A; HUARD J; MASSIE B; PRESCOTT S; SIMONEAU M; PETROF BJ; KARPATI G
      DYSTROPHIN EXPRESSION IN MUSCLES OF MDX MICE AFTER ADENOVIRUS-MEDIATED IN-VIVO GENE-TRANSFER

      Human gene therapy
    62. PETROF BJ; LOCHMULLER H; MASSIE B; YANG LY; MACMILLAN C; ZHAO JE; NALBANTOGLU J; KARPATI G
      IMPAIRMENT OF FORCE GENERATION AFTER ADENOVIRUS-MEDIATED GENE-TRANSFER TO MUSCLE IS ALLEVIATED BY ADENOVIRAL GENE INACTIVATION AND HOST CD8(-CELL DEFICIENCY() T)

      Human gene therapy
    63. LOCHMULLER H; PETROF BJ; PARI G; LAROCHELLE N; DODELET V; WANG Q; ALLEN C; PRESCOTT S; MASSIE B; NALBANTOGLU J; KARPATI G
      TRANSIENT IMMUNOSUPPRESSION BY FK506 PERMITS A SUSTAINED HIGH-LEVEL DYSTROPHIN EXPRESSION AFTER ADENOVIRUS-MEDIATED DYSTROPHIN MINIGENE TRANSFER TO SKELETAL-MUSCLES OF ADULT DYSTROPHIC (MDX) MICE

      Gene therapy
    64. ACSADI G; OHAGAN D; LOCHMULLER H; NIGRO M; KARPATI G; JANI A
      INTERFERONS ARE MAJOR DETERMINANTS IN EFFICACY OF GENE-THERAPY IN THENEUROMUSCULAR SYSTEM BY ADENOVIRAL VECTORS

      Annals of neurology
    65. KARPATI G; LOCHMULLER H; NALBANTOGLU J; DURHAM H
      THE PRINCIPLES OF GENE-THERAPY FOR THE NERVOUS-SYSTEM

      Trends in neurosciences
    66. PARI G; LOCHMULLER H; DURHAM H; SHAW I; CASHMAN N; MASSIE B; KARPATI G; NALBANTOGLU J; ROY N; MACKENZIE A
      FUNCTIONAL-ANALYSIS OF THE NEURONAL APOPTOSIS INHIBITORY PROTEIN USING ADENOVIRAL RECOMBINANTS CONTAINING NEURONAL APOPTOSIS INHIBITORY PROTEIN EXPRESSION CASSETTE

      Neurology
    67. LAROCHELLE N; LOCHMULLER H; NALBANTOGLU J; JANI A; MASSIE B; KARPATI G
      MUSCLE-SPECIFIC GENE-EXPRESSION AFTER ADENOVIRUS-MEDIATED GENE-TRANSFER

      Neurology
    68. LOCHMULLER H; PETROF B; NALBANTOGLU J; MASSIE B; KARPATI G
      IMMUNOSUPPRESSION COUNTERACTS THE IMMUNOLOGICAL ELIMINATION OF MUSCLE-FIBERS TRANSDUCED BY REPLICATION-DEFECTIVE ADENOVIRAL RECOMBINANTS

      Neurology
    69. SLACK RS; BELLIVEAU DJ; ROSENBERG M; ATWAL J; LOCHMULLER H; ALOYZ R; HAGHIGHI A; LACH B; SETH P; COOPER E; MILLER FD
      ADENOVIRUS-MEDIATED GENE-TRANSFER OF THE TUMOR-SUPPRESSOR, P53, INDUCES APOPTOSIS IN POSTMITOTIC NEURONS

      The Journal of cell biology
    70. DURHAM HD; LOCHMULLER H; JANI A; ACSADI G; MASSIE B; KARPATI G
      TOXICITY OF REPLICATION-DEFECTIVE ADENOVIRAL RECOMBINANTS IN DISSOCIATED CULTURES OF NERVOUS-TISSUE

      Experimental neurology
    71. PETROF BJ; ACSADI G; JANI A; MASSIE B; BOURDON J; MATUSIEWICZ N; YANG LY; LOCHMULLER H; KARPATI G
      EFFICIENCY AND FUNCTIONAL CONSEQUENCES OF ADENOVIRUS-MEDIATED IN-VIVOGENE-TRANSFER TO NORMAL AND DYSTROPHIC (MDX) MOUSE DIAPHRAGM

      American journal of respiratory cell and molecular biology
    72. HUARD J; LOCHMULLER H; ACSADI G; JANI A; MASSIE B; KARPATI G
      THE ROUTE OF ADMINISTRATION IS A MAJOR DETERMINANT OF THE TRANSDUCTION EFFICIENCY OF RAT-TISSUES BY ADENOVIRAL RECOMBINANTS

      Gene therapy
    73. REIMERS CD; LOCHMULLER H; GOEBELS N; SCHLOTTER B; STEMPFLE C
      THE INFLUENCE OF EXERCISE ON THE SONOGRAM OF SKELETAL-MUSCLES

      Ultraschall in der Medizin
    74. LOCHMULLER H; JANI A; ACSADI G; HUARD J; MASSIE B; KARPATI G
      SAFETY ISSUES IN ADENOVIRUS (AV)-MEDIATED DYSTROPHIN GENE-TRANSFER - VALIDATION OF ADENOVIRAL RECOMBINANTS (AVR) AND PURITY OF AVR STOCKS

      Neurology
    75. ACSADI G; JANI A; LOCHMULLER H; HUARD J; MASSIE B; KARPATI G
      EFFICIENT ADENOVIRUS (AV)-MEDIATED DYSTROPHIN (DYS) GENE-TRANSFER INTO SKELETAL-MUSCLES AND HEARTS OF MDX MICE

      Neurology
    76. HUARD J; LOCHMULLER H; ACSADI G; JANI A; HOLLAND P; MASSIE B; KARPATI G
      DIFFERENTIAL EFFICIENCY OF GENE-TRANSFER IN NEONATAL VERSUS MATURE SKELETAL-MUSCLE, HEART AND BRAIN WITH ADENOVIRAL RECOMBINANTS (AVR) - A LESSON FOR GENE-THERAPY (GT)

      Neurology
    77. HUARD J; LOCHMULLER H; ACSADI G; JANI A; HOLLAND P; GUERIN C; MASSIE B; KARPATI G
      DIFFERENTIAL SHORT-TERM TRANSDUCTION EFFICIENCY OF ADULT VERSUS NEWBORN MOUSE-TISSUES BY ADENOVIRAL RECOMBINANTS

      Experimental and molecular pathology
    78. LOCHMULLER H; PETROF BJ; ALLEN C; PRESCOTT S; MASSIE B; KARPATI G
      IMMUNOSUPPRESSION BY FK506 MARKEDLY PROLONGS EXPRESSION OF ADENOVIRUS-DELIVERED TRANSGENE IN SKELETAL-MUSCLES OF ADULT DYSTROPHIC-[MDX] MICE

      Biochemical and biophysical research communications
    79. LOCHMULLER H; JANI A; HUARD J; PRESCOTT S; SIMONEAU M; MASSIE B; KARPATI G; ACSADI G
      EMERGENCE OF EARLY REGION-1-CONTAINING REPLICATION-COMPETENT ADENOVIRUS IN STOCKS OF REPLICATION-DEFECTIVE ADENOVIRUS RECOMBINANTS (DELTA-E1 PLUS DELTA-E3) DURING MULTIPLE PASSAGES IN 293-CELLS

      Human gene therapy
    80. ACSADI G; JANI A; HUARD J; BLASCHUK K; MASSIE B; HOLLAND P; LOCHMULLER H; KARPATI G
      CULTURED HUMAN MYOBLASTS AND MYOTUBES SHOW MARKEDLY DIFFERENT TRANSDUCIBILITY BY REPLICATION-DETECTIVE ADENOVIRUS RECOMBINANTS

      Gene therapy
    81. HEUSS D; ENGELHARDT A; LOCHMULLER H; GOBEL H; NEUNDORFER B
      EXPRESSION OF GROWTH-ASSOCIATED PROTEIN-43 AND NEURAL CELL-ADHESION MOLECULE IN CONGENITAL FIBER-TYPE DISPROPORTION WITH INTERSTITIAL MYOSITIS

      Virchows Archiv
    82. LOCHMULLER H; REIMERS CD; FISCHER P; HEUSS D; MULLERHOCKER J; PONGRATZ DE
      EXERCISE-INDUCED MYALGIA IN HYPOTHYROIDISM

      The Clinical investigator
    83. LOCHMULLER H; HEUSS D; PONGRATZ D
      MONONEURITIS MULTIPLEX IN HLA-B27-ASSOCIA TED ARTHRITIS - CASE-REPORT

      Aktuelle Neurologie
    84. VOGL T; DRESEL S; LOCHMULLER H; BERGMAN C; REIMERS C; LISSNER J
      3RD CRANIAL NERVE PALSY CAUSED BY GUMMATOUS NEUROSYPHILIS - MR FINDINGS

      American journal of neuroradiology
    85. HEUSS D; LOCHMULLER H; HABERMEYER P; REIMERS C; PONGRATZ D
      BILATERAL ENTRAPMENT NEUROPATHY OF THE SU PRASCAPULAR NERVE - REVIEW AND CASE-REPORT

      Nervenarzt


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Documento generato il 22/10/20 alle ore 11:34:25