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La ricerca find articoli where soggetti phrase all words 'OPHTHALMOPLEGIA' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 532 riferimenti
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    1. Teoh, SCB; Yap, EY; Eong, KGA
      Neuro-ophthalmological manifestations of systemic lupus erythematosus in Asian patients

      CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    2. Mika-Gruttner, A; Marx, J; Thomke, F; Fitzek, S; Fitzek, C; Urban, PP; Stoeter, P; Hopf, HC
      Significance of electrophysiology in brainstem ischemia and normal diffusion weighted and high resolution MRI

      KLINISCHE NEUROPHYSIOLOGIE
    3. Hsu, HC; Chen, HJ; Lu, K; Liang, CL
      Reversible bilateral internuclear ophthalmoplegia following head injury

      ACTA OPHTHALMOLOGICA SCANDINAVICA
    4. Marx, JJ; Thoemke, F; Fitzek, S; Vucurevic, G; Fitzek, C; Mika-Gruettner, A; Urban, PP; Stoeter, P; Hopf, HC
      A new method to investigate brain stem structural-functional correlations using digital post-processing MRI - reliability in ischemic internuclear ophthalmoplegia

      EUROPEAN JOURNAL OF NEUROLOGY
    5. Wong, LJC
      Recognition of mitochondrial DNA deletion syndrome with non-neuromuscular multisystemic manifestation

      GENETICS IN MEDICINE
    6. Bandini, F; Faga, D; Simonetti, S
      Ocular myasthenia mimicking a one-and-a-half syndrome

      JOURNAL OF NEURO-OPHTHALMOLOGY
    7. Chan, JW
      Isolated unilateral post-traumatic internuclear ophthalmoplegia

      JOURNAL OF NEURO-OPHTHALMOLOGY
    8. Arsava, EM; Uluc, K; Kansu, T; Dogulu, CF; Soylemezoglu, F; Selekler, K
      Granulomatous hypophysitis and bilateral optic neuropathy

      JOURNAL OF NEURO-OPHTHALMOLOGY
    9. Spelbrink, JN; Li, FY; Tiranti, V; Nikali, K; Yuan, QP; Tariq, M; Wanrooij, S; Garrido, N; Comi, G; Morandi, L; Santoro, L; Toscano, A; Fabrizi, GM; Somer, H; Croxen, R; Beeson, D; Poulton, L; Suomalainen, A; Jacobs, HT; Zeviani, M; Larsson, C
      Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene LF-like protein localized in mitochondria

      NATURE GENETICS
    10. Krespi, Y; Aykutlu, E; Coban, U; Tuncay, R; Bahar, S
      Internuclear ophthalmoplegia and cerebellar ataxia: Report of one case

      CEREBROVASCULAR DISEASES
    11. Shoubridge, EA
      Nuclear genetic defects of oxidative phosphorylation

      HUMAN MOLECULAR GENETICS
    12. Nagashima, T; Kato, H; Maguchi, S; Chuma, T; Mano, Y; Goto, Y; Nonaka, I; Nagashima, K
      A mitochondrial encephalo-myo-neuropathy with a nucleotide position 3271 (T-C) point mutation in the mitochondrial DNA

      NEUROMUSCULAR DISORDERS
    13. Spagnolo, M; Tomelleri, G; Vattemi, G; Filosto, M; Rizzuto, N; Tonin, P
      A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia

      NEUROMUSCULAR DISORDERS
    14. Todd, L; King, J; Darlington, CL; Smith, PF
      Optokinetic reflex dysfunction in multiple sclerosis

      NEUROREPORT
    15. Craighero, L; Carta, A; Fadiga, L
      Peripheral oculomotor palsy affects orienting of visuospatial attention

      NEUROREPORT
    16. Miller, NR
      Visual manifestations of temporal arteritis

      RHEUMATIC DISEASE CLINICS OF NORTH AMERICA
    17. Masson, C
      Le syndrome anti-GQ1b

      PRESSE MEDICALE
    18. Li, HF; Yuan, JM
      Miller Fisher syndrome: toward a more comprehensive understanding

      CHINESE MEDICAL JOURNAL
    19. Barthelemy, C; de Baulny, HO; Diaz, J; Cheval, MA; Frachon, P; Romero, N; Goutieres, F; Fardeau, M; Lombes, A
      Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation

      ANNALS OF NEUROLOGY
    20. Sciacco, M; Prelle, A; Comi, GP; Napoli, L; Battistel, A; Bresolin, N; Tancredi, L; Lamperti, C; Bordoni, A; Fagiolari, G; Ciscato, P; Chiveri, L; Perini, MP; Fortunato, F; Adobbati, L; Messina, S; Toscano, A; Martinelli-Boneschi, F; Papadimitriou, A; Scarlato, G; Moggio, M
      Retrospective study of patients affected of a large population with mitochondrial disorders: clinical, morphological and molecular genetic evaluation

      JOURNAL OF NEUROLOGY
    21. Mandava, P; Chaljub, G; Patterson, K; Hollingsworth, JW
      MR imaging of cavernous sinus invasion by mucormycosis: a case study

      CLINICAL NEUROLOGY AND NEUROSURGERY
    22. Shoffner, JM
      An introduction: Oxidative phosphorylation diseases

      SEMINARS IN NEUROLOGY
    23. Biousse, V; Newman, NJ
      Neuro-ophthalmology of mitochondrial diseases

      SEMINARS IN NEUROLOGY
    24. Sladky, JT
      Histopathological features of peripheral nerve and muscle in mitochondrialdisease

      SEMINARS IN NEUROLOGY
    25. Gray, OM; Forbes, RB; Morrow, JI
      Primary isolated brainstem injury producing internuclear ophthalmoplegia

      BRITISH JOURNAL OF NEUROSURGERY
    26. Hirano, M; Davidson, M; DiMauro, S
      Mitochondria and the heart

      CURRENT OPINION IN CARDIOLOGY
    27. Muthukumar, N; Veerarajkumar, N; Madeswaran, K
      Bilateral internuclear ophthalmoplegia following mild head injury

      CHILDS NERVOUS SYSTEM
    28. Pulkes, T; Hanna, MG
      Human mitochondrial DNA diseases

      ADVANCED DRUG DELIVERY REVIEWS
    29. Finsterer, J; Milvay, E
      Diagnostic yield of the lactate stress test in respiratory chain disordersunder absolute and relative workload

      JOURNAL OF NEUROSCIENCE METHODS
    30. Flaherty, MP; Grattan-Smith, P; Steinberg, A; Jamieson, R; Engle, EC
      Congenital fibrosis of the extraocular muscles associated with cortical dysplasia and maldevelopment of the basal ganglia

      OPHTHALMOLOGY
    31. Yuki, N; Odaka, M; Hirata, K
      Acute ophthalmoparesis (without ataxia) associated with anti-GQ1b IgG antibody - Clinical features

      OPHTHALMOLOGY
    32. Suomalainen, A; Kaukonen, J
      Diseases caused by nuclear genes affecting mtDNA stability

      AMERICAN JOURNAL OF MEDICAL GENETICS
    33. Wallace, DC
      Mouse models for mitochondrial disease

      AMERICAN JOURNAL OF MEDICAL GENETICS
    34. Thorburn, DR; Dahl, HHM
      Mitochondrial disorders: Genetics, counseling, prenatal diagnosis and reproductive options

      AMERICAN JOURNAL OF MEDICAL GENETICS
    35. Nardin, RA; Johns, DR
      Mitochondrial dysfunction and neuromuscular disease

      MUSCLE & NERVE
    36. Tanji, K; Bonilla, E
      Optical imaging techniques (Histochemical, immunohistochemical, and in situ hybridization staining methods) to visualize mitochondria

      METHODS IN CELL BIOLOGY, VOL 65
    37. Hamideh, F; Prete, PE
      Ophthalmologic manifestations of rheumatic diseases

      SEMINARS IN ARTHRITIS AND RHEUMATISM
    38. Solano, A; Playan, A; Lopez-Perez, MJ; Montoya, J
      Genetic diseases of the mitochondrial DNA.

      SALUD PUBLICA DE MEXICO
    39. Durand, MC; Goulon-Goeau, C; Schweitzer, A; Cheliout-Herault, F; Raphael, JC; Gajdos, P
      Ten cases of Miller Fisher syndrome. Electrophysiological study.

      REVUE NEUROLOGIQUE
    40. Ahmed, MAS; Powell, A; Borgstein, R; Alsford, L
      Unusual cause of an abduction deficit in a 14 year old girl

      POSTGRADUATE MEDICAL JOURNAL
    41. Hosoya, T; Adachi, M; Yamaguchi, K; Yamaguchi, K; Kato, T; Sugai, Y
      Abducens nerve enhancement demonstrated by multiplanar reconstruction of contrast-enhanced three-dimensional MRI

      NEURORADIOLOGY
    42. Frohman, EM; Zhang, H; Kramer, PD; Fleckenstein, J; Hawker, K; Racke, MK; Frohman, TC
      MRI characteristics of the MLF in MS patients with chronic internuclear ophthalmoparesis

      NEUROLOGY
    43. Casali, C; Bonifati, V; Santorelli, FM; Casari, G; Fortini, D; Patrignani, A; Fabbrini, G; Carrozzo, R; D'Amati, G; Locuratolo, N; Vanacore, N; Damiano, M; Pierallini, A; Pierelli, F; Amabile, GA; Meco, G
      Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a sephardic Jewish family

      NEUROLOGY
    44. Deschauer, M; Muller, T; Dreha, S; Zierz, S
      Familial mitochondrial chronic progressive external ophthalmoplegia. Five families with different genetics

      NERVENARZT
    45. Rojas-Garcia, R; Gallardo, E; Serrano-Munuera, C; de Luna, N; Ortiz, E; Roig, C; Grau-Veciana, JM; Illa, I
      Anti-GQ1b antibodies: usefulness of its detection for the diagnosis of Miller-Fisher syndrome

      MEDICINA CLINICA
    46. Wong, AMF; Musallam, S; Tomlinson, RD; Shannon, P; Sharpe, JA
      Opsoclonus in three dimensions: oculographic, neuropathologic and modelling correlates

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    47. Susuki, K; Yuki, N; Hirata, K
      Fine specificity of anti-GQ1b IgG and clinical features

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    48. Wanke, I; Doerfler, A; Stolke, D; Forsting, M
      Carotid cavernous fistula due to a ruptured intracavernous aneurysm of theinternal carotid artery: treatment with selective endovascular occlusion of the aneurysm

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    49. Kline, LB; Hoyt, WF
      The Tolosa-Hunt syndrome

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    50. Winer, JB
      Bickerstaff's encephalitis and the Miller Fisher syndrome

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    51. Milea, D; Napolitano, M; Dechy, H; Le Hoang, P; Delattre, JY; Pierrot-Deseilligny, C
      Complete bilateral horizontal gaze paralysis disclosing multiple sclerosis

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    52. Odaka, M; Yuki, N; Hirata, K
      Anti-GQ1b IgG antibody syndrome: clinical and immunological range

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    53. 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
    54. Kelley, SO; Steinberg, SV; Schimmel, P
      Fragile T-stem in disease-associated human mitochondrial tRNA sensitizes structure to local and distant mutations

      JOURNAL OF BIOLOGICAL CHEMISTRY
    55. Lewis, S; Hutchison, W; Di Nezza, L; Thyagarajan, D; Marotta, R; Dahl, H
      Refinement of the adPEO linked locus on Chr10 and analysis of MRS4 and three other candidate genes

      FEBS LETTERS
    56. Clay, AS; Behnia, M; Brown, KK
      Mitochondrial disease - A pulmonary and critical-care medicine perspective

      CHEST
    57. McMullan, TFW; Tyers, AG
      X linked dominant congenital isolated bilateral ptosis: the definition andcharacterisation of a new condition

      BRITISH JOURNAL OF OPHTHALMOLOGY
    58. Seneca, S; Verhelst, H; De Meirleir, L; Meire, F; Groote, CCD; Lissens, W; Van Coster, R
      A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome

      ARCHIVES OF NEUROLOGY
    59. Sato, K; Yoshikawa, H
      Bilateral abducens nerve paresis associated with anti-GQ1b IgG antibody

      AMERICAN JOURNAL OF OPHTHALMOLOGY
    60. Larsson, NG; Oldfors, A
      Mitochondrial myopathies

      ACTA PHYSIOLOGICA SCANDINAVICA
    61. Thomke, F; Strothjohann, M; Mike-Gruttner, A
      Adaptive phenomena in internuclear ophthalmoplegia: Introduction

      KLINISCHE NEUROPHYSIOLOGIE
    62. Lopez, ME; Van Zeeland, NL; Dahl, DB; Weindruch, R; Aiken, JM
      Cellular phenotypes of age-associated skeletal muscle mitochondrial abnormalities in rhesus monkeys

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    63. Saiwaki, T; Shiga, K; Fukuyama, R; Tsutsumi, Y; Fushiki, S
      A unique junctional palindromic sequence in mitochondrial DNA from a patient with progressive external ophthalmoplegia

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    64. Alpini, D; Caputo, D; Hahan, A; Pugnetti, L; Monti, B; Razzari, S; Cesarani, A
      Grading brainstem involvement in multiple sclerosis - by means of electro-oculography

      JOURNAL OF NEUROVIROLOGY
    65. Fernandez-Moreno, MA; Bornstein, B; Petit, N; Garesse, R
      The pathophysiology of mitochondrial biogenesis: Towards four decades of mitochondrial DNA research

      MOLECULAR GENETICS AND METABOLISM
    66. Barshop, BA; Nyhan, WL; Naviaux, RK; McGowan, KA; Friedlander, M; Haas, RH
      Kearns-Sayre syndrome presenting as 2-oxoadipic aciduria

      MOLECULAR GENETICS AND METABOLISM
    67. Kelley, SO; Steinberg, SV; Schimmel, P
      Functional defects of pathogenic human mitochondrial tRNAs related to structural fragility

      NATURE STRUCTURAL BIOLOGY
    68. Quigley, AF; Kapsa, RMI; Esmore, D; Hale, G; Byrne, E
      Mitochondrial respiratory chain activity in idiopathic dilated cardiomyopathy

      JOURNAL OF CARDIAC FAILURE
    69. Hahn, CD; Nicolle, DA; Lownie, SP; Drake, CG
      Giant cavernous carotid aneurysms: Clinical presentation in fifty-seven cases

      JOURNAL OF NEURO-OPHTHALMOLOGY
    70. Eggenberger, ER; Kaufman, DI
      Ocular Motility Review for 1997-1998: Part II

      JOURNAL OF NEURO-OPHTHALMOLOGY
    71. Leavitt, JA
      Myasthenia gravis with a paraneoplastic marker

      JOURNAL OF NEURO-OPHTHALMOLOGY
    72. Eggenberger, ER; Desai, NP; Kaufman, DI; Pless, M
      Internuclear ophthalmoplegia after coronary artery catheterization and percutaneous transluminal coronary balloon angioplasty

      JOURNAL OF NEURO-OPHTHALMOLOGY
    73. Caccavale, A; Mignemi, L
      Acute onset of a bilateral areflexical mydriasis in Miller-Fisher syndrome: A rare neuro-ophthalmologic disease

      JOURNAL OF NEURO-OPHTHALMOLOGY
    74. Paul, R; Desnuelle, C; Pouget, J; Pellissier, JF; Richelme, C; Monfort, MF; Butori, C; Saunieres, A; Paquis-Flucklinger, V
      Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletions

      EUROPEAN JOURNAL OF HUMAN GENETICS
    75. Hirano, M; Vu, TH
      Defects of intergenomic communication: Where do we stand?

      BRAIN PATHOLOGY
    76. Kajander, OA; Rovio, AT; Majamaa, K; Poulton, J; Spelbrink, JN; Holt, IJ; Karhunen, PJ; Jacobs, HT
      Human mtDNA sublimons resemble rearranged mitochondrial genoms found in pathological states

      HUMAN MOLECULAR GENETICS
    77. Nagashima, T; Kato, H; Kase, M; Maguchi, S; Mizutani, Y; Matsuda, K; Chuma, T; Mano, Y; Goto, Y; Minami, N; Nonaka, I; Nagashima, K
      Oculopharyngeal muscular dystrophy in a Japanese family with a short GCG expansion (GCG)(11) in PABP2 gene

      NEUROMUSCULAR DISORDERS
    78. Finsterer, J; Eichberger, H; Jarius, C
      Lactate-stress testing in 54 patients with mitochondriopathy

      EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE
    79. Marin-Garcia, J; Goldenthal, MJ
      Mitochondrial biogenesis defects and neuromuscular disorders

      PEDIATRIC NEUROLOGY
    80. Uc, EY; Wenger, DA; Jankovic, J
      Niemann-Pick disease type C: Two cases and an update

      MOVEMENT DISORDERS
    81. Haftel, LT; Lev, D; Barash, V; Gutman, A; Bujanover, Y; Lerman-Sagie, T
      Familial mitochondrial intestinal pseudo-obstruction and neurogenic bladder

      JOURNAL OF CHILD NEUROLOGY
    82. Ishikawa, Y; Goto, Y; Ishikawa, Y; Minami, R
      Progression in a case of Kearns-Sayre syndrome

      JOURNAL OF CHILD NEUROLOGY
    83. Shoffner, JM
      Mitochondrial myopathy diagnosis

      NEUROLOGIC CLINICS
    84. Ferreiro, A; Estournet, B; Chateau, D; Romero, NB; Laroche, C; Odent, S; Toutain, A; Cabello, A; Fontan, D; dos Santos, HG; Haenggeli, CA; Bertini, E; Urtizberea, JA; Guicheney, P; Fardeau, M
      Multi-minicore disease - Searching for boundaries: Phenotype analysis of 38 cases

      ANNALS OF NEUROLOGY
    85. Nishino, I; Spinazzola, A; Papadimitriou, A; Hammans, S; Steiner, I; Hahn, CD; Connolly, AM; Verloes, A; Guimaraes, J; Maillard, I; Hamano, H; Donati, MA; Semrad, CE; Russell, JA; Andreu, AL; Hadjigeorgiou, GM; Vu, TH; Tadesse, S; Nygaard, TG; Nonaka, I; Hirano, I; Bonilla, E; Rowland, LP; DiMauro, S; Hirano, M
      Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations

      ANNALS OF NEUROLOGY
    86. Echaniz-Laguna, A; Battaglia, F; Heymann, R; Tranchant, C; Warter, JM
      The Miller Fisher syndrome: neurophysiological and MRI evidence of both peripheral and central origin in one case

      JOURNAL OF NEUROLOGY
    87. Vielhaber, S; Kudin, A; Schroder, R; Elger, CE; Kunz, WS
      Muscle fibres: applications for the study of the metabolic consequences ofenzyme deficiencies in skeletal muscle

      BIOCHEMICAL SOCIETY TRANSACTIONS
    88. St John, JC; Sakkas, D; Barratt, CLR
      A role for mitochondrial DNA and sperm survival

      JOURNAL OF ANDROLOGY
    89. Bursztyn, J; Mikaeloff, Y; Kaminska, A; Plouin, P; Soufflet, C; Dulac, O; Chaix, Y
      Alternating hemiplegia of childhoood and oculomotor anomalies

      JOURNAL FRANCAIS D OPHTALMOLOGIE
    90. El Mansouri, Y; Zaghloul, K; Amraoui, A
      Oculomotor paralyses in the course of diabetes - About 12 cases

      JOURNAL FRANCAIS D OPHTALMOLOGIE
    91. Spanggord, HM; Lee, AG
      Intracranial inflammatory pseudotumor: a case report and review of the literature

      NEURO-OPHTHALMOLOGY
    92. Yoshino, H; Harukawa, H; Asano, A
      IgG antiganglioside antibodies in Guillain-Barre syndrome with bulbar palsy

      JOURNAL OF NEUROIMMUNOLOGY
    93. Vu, TH; Tanji, K; Pallotti, F; Golzi, V; Hirano, M; DiMauro, S; Bonilla, E
      Analysis of mtDNA deletions in muscle by in situ hybridization

      MUSCLE & NERVE
    94. Malik, S; Sudoyo, H; Marzuki, S
      Microphotometric analysis of NADH-tetrazolium reductase deficiency in fibroblasts of patients with Leber hereditary optic neuropathy

      JOURNAL OF INHERITED METABOLIC DISEASE
    95. Santorelli, FM; De Joanna, G; Casali, C; Tessa, A; Siciliano, G; Amabile, GA; Pierelli, F; Vilarinho, L; Santoro, L
      Multiple mtDNA deletions: Clinical and molecular correlations

      JOURNAL OF INHERITED METABOLIC DISEASE
    96. Parker, JC
      Commentary: Human mitochondrial cytopathies

      ANNALS OF CLINICAL AND LABORATORY SCIENCE
    97. Spence, CA; Duong, DH; Monsein, L; Dennis, MW
      Ophthalmoplegia resulting from an intraorbital hematoma

      SURGICAL NEUROLOGY
    98. Deramo, VA; Jayamanne, DGR; Auerbach, DB; Danesh-Meyer, H; Purvin, VA
      Acute bilateral ophthalmoplegia in a young woman

      SURVEY OF OPHTHALMOLOGY
    99. Kaukonen, J; Juselius, JK; Tiranti, V; Kyttala, A; Zeviani, M; Comi, GP; Keranen, S; Peltonen, L; Suomalainen, A
      Role of adenine nucleotide translocator 1 in mtDNA maintenance

      SCIENCE
    100. Gaultier, C; Angibaud, G; Laille, M; Lacassin, F
      A probable Miller Fisher syndrome during dengue fever.

      REVUE NEUROLOGIQUE


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Documento generato il 07/08/20 alle ore 18:10:27