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La ricerca find articoli where soggetti phrase all words 'optic neuropathy' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 900 riferimenti
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    1. Hudnell, HK; House, D; Schmid, J; Koltai, D; Stopford, W; Wilkins, J; Savitz, DA; Swinker, M; Music, S
      Human visual function in the North Carolina Clinical Study on possible estuary-associated syndrome

      JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A
    2. Murphy, MP
      Development of lipophilic cations as therapies for disorders due to mitochondrial dysfunction

      EXPERT OPINION ON BIOLOGICAL THERAPY
    3. Crispin, SM; Mould, JRB
      Systemic hypertensive disease and the feline fundus

      VETERINARY OPHTHALMOLOGY
    4. Teoh, SCB; Yap, EY; Eong, KGA
      Neuro-ophthalmological manifestations of systemic lupus erythematosus in Asian patients

      CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    5. Fuller, JR; Vote, BJT
      Upside-down orbitopathy: unilateral orbital dependent-tissue oedema causing total visual loss

      CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    6. Finnila, S; Majamaa, K
      Phylogenetic analysis of mtDNA haplogroup TJ in a Finnish population

      JOURNAL OF HUMAN GENETICS
    7. Bergstrand, IC; Heijl, A; Wollmer, P; Hansen, F; Harris, A
      Timolol increased retrobulbar flow velocities in untreated glaucoma eyes but not in ocular hypertension

      ACTA OPHTHALMOLOGICA SCANDINAVICA
    8. Hepsen, IF; Evereklioglu, C
      Defective visual field tests in chronic heavy smokers

      ACTA OPHTHALMOLOGICA SCANDINAVICA
    9. Jacobi, FK; Meyer, J; Pusch, CM; Wissinger, B
      Quantitation of heteroplasmy in mitochondrial DNA mutations by primer extension using Vent(R)(R)(exo-) DNA polymerase and RFLP analysis

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    10. Flammer, J; Pache, M; Resink, T
      Vasospasm, its role in the pathogenesis of diseases with particular reference to the eye

      PROGRESS IN RETINAL AND EYE RESEARCH
    11. Basile, C; Addabbo, G; Montanaro, A
      Anterior ischemic optic neuropathy and dialysis: role of hypotension and anemia

      JOURNAL OF NEPHROLOGY
    12. Flammer, J; Kaiser, H; Haufschild, T
      Susac syndrome: a vasospastic disorder?

      EUROPEAN JOURNAL OF OPHTHALMOLOGY
    13. Oruc, S; Sener, EC; Akman, A; Sanac, AS
      Bilateral orbital hemorrhage induced by labor

      EUROPEAN JOURNAL OF OPHTHALMOLOGY
    14. Kapran, Z; Atmaca, LS; Albayrak, Z; Uyar, M; Eltutar, K
      Bilateral glaucomatous optic neuropathy in Takayasu's disease without cervical arterial stenosis

      EUROPEAN JOURNAL OF OPHTHALMOLOGY
    15. Levin, LA
      Animal and culture models of glaucoma for studying neuroprotection

      EUROPEAN JOURNAL OF OPHTHALMOLOGY
    16. Gomez-Zaera, M; Strom, TM; Rodriguez, B; Estivill, X; Meitinger, T; Nunes, V
      Presence of a major WFS1 mutation in Spanish wolfram syndrome pedigrees

      MOLECULAR GENETICS AND METABOLISM
    17. Wallace, DC
      Mitochondrial defects in neurodegenerative disease

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    18. Shanske, AL; Shanske, S; DiMauro, S
      The other human genome

      ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE
    19. Brega, A; Narula, J; Arbustini, E
      Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases

      JOURNAL OF NUCLEAR CARDIOLOGY
    20. Siatkowski, RM; Scott, IU; Verm, AM; Warn, AA; Farris, BK; Strominger, MB; Sklar, EML
      Optic neuropathy and chiasmopathy in the diagnosis of systemic lupus erythematosus

      JOURNAL OF NEURO-OPHTHALMOLOGY
    21. Frohman, LP
      Systemic disease and neuro-ophthalmology: Annual update 2000 (Part II)

      JOURNAL OF NEURO-OPHTHALMOLOGY
    22. Warner, JEA; Ries, KM
      Optic neuropathy in a patient with AIDS

      JOURNAL OF NEURO-OPHTHALMOLOGY
    23. Fierz, AB; Sartoretti, S; Thoelen, AM
      Optic neuropathy and central retinal artery occlusion in non-Hodgkin lymphoma

      JOURNAL OF NEURO-OPHTHALMOLOGY
    24. Van Stavern, GP; Biousse, V; Lynn, MJ; Simon, DJ; Newman, NJ
      Neuro-ophthalmic manifestations of head trauma

      JOURNAL OF NEURO-OPHTHALMOLOGY
    25. Cunningham, AV; Smith, KH
      Anterior ischemic optic neuropathy associated with Viagra

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

      JOURNAL OF NEURO-OPHTHALMOLOGY
    27. Khanim, F; Kirk, J; Latif, F; Barrett, TG
      WFS1/Wolframin mutations, Wolfram syndrome, and associated diseases

      HUMAN MUTATION
    28. Rose, G; Passarino, G; Carrieri, G; Altomare, K; Greco, V; Bertolini, S; Bonafe, M; Franceschi, C; De Benedictis, G
      Paradoxes in longevity: sequence analysis of mtDNA haplogroup J in centenarians

      EUROPEAN JOURNAL OF HUMAN GENETICS
    29. Legros, F; Chatzoglou, E; Frachon, P; de Baulny, HO; Laforet, P; Jardel, C; Godinot, C; Lombes, A
      Functional characterization of novel mutations in the human cytochrome b gene

      EUROPEAN JOURNAL OF HUMAN GENETICS
    30. Ravn, K; Wibrand, F; Hansen, FJ; Horn, N; Rosenberg, T; Schwartz, M
      An mtDNA mutation, 14453G -> A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    31. Shah, P; Whittaker, K; Wells, AP; Khaw, PT
      Exercise-induced visual loss associated with advanced glaucoma in young adults

      EYE
    32. Lim, M; Kent, D; Clark, D
      An unusual case of ocular self-injury

      EYE
    33. Vorwerk, CK
      Neuroprotection of retinal diseases

      OPHTHALMOLOGE
    34. Yoles, E; Friedmann, I; Barouch, R; Shani, Y; Schwartz, M
      Self-protective mechanism awakened by glutamate in retinal ganglion cells

      JOURNAL OF NEUROTRAUMA
    35. Cohen, BH; Gold, DR
      Mitochondrial cytopathy in adults: What we know so far

      CLEVELAND CLINIC JOURNAL OF MEDICINE
    36. Miller, NR
      Visual manifestations of temporal arteritis

      RHEUMATIC DISEASE CLINICS OF NORTH AMERICA
    37. Tsao, CY; Mendell, JR; Bartholomew, D
      High mitochondrial DNA T8993G mutation (> 90%) without typical features ofLeigh's and NARP syndromes

      JOURNAL OF CHILD NEUROLOGY
    38. Kahaly, GJ
      Imaging in thyroid-associated orbitopathy

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    39. Ng, JD; Nunery, WR; Martin, RT; Ng, PA; Bonnin, JM; Elkins, AD
      Effects of hyperbaric oxygen therapy on hydroxyapatite orbital implant vascularization in rabbits

      OPHTHALMIC PLASTIC AND RECONSTRUCTIVE SURGERY
    40. Howell, N; Herrnstadt, C; Mackey, DA
      Different patterns of expansion/contraction during the evolution of an mtDNA simple repeat

      MOLECULAR BIOLOGY AND EVOLUTION
    41. Friedman, J; Standaert, DG
      Dystonia and its disorders

      NEUROLOGIC CLINICS
    42. Opial, D; Boehnke, M; Tadesse, S; Lietz-Partzsch, A; Flammer, J; Munier, F; Mermoud, A; Hirano, M; Fluckiger, F; Mojon, DS
      Leber's hereditary optic neuropathy mitochondrial DNA mutations in normal-tension glaucoma

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    43. Granata, M; Ammendolea, C; Trudu, R; Spimpolo, N; Martelletti, P
      Thrombosis of the retinal artery in a patient with Churg-Strauss syndrome

      CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
    44. Pantaleoni, C; D'Arrigo, S; Bagnasco, I; Piozzi, E; Carrara, F; Scaioli, V; Riva, D
      Papillitis as an onset sign of Leber's hereditary optic neuropathy: a casereport

      BRAIN & DEVELOPMENT
    45. Li, HF; Yuan, JM
      Miller Fisher syndrome: toward a more comprehensive understanding

      CHINESE MEDICAL JOURNAL
    46. Taylor, RW; Singh-Kler, R; Hayes, CM; Smith, PEM; Turnbull, DM
      Progressive mitochondrial disease resulting from a novel missense mutationin the mitochondrial DNA ND3 gene

      ANNALS OF NEUROLOGY
    47. Brown, MD; Zhadanov, S; Allen, JC; Hosseini, S; Newman, NJ; Atamonov, VV; Mikhailovskaya, IE; Sukernik, RI; Wallace, DC
      Novel mtDNA mutations and oxidative phosphorylation dysfunction in RussianLHON families

      HUMAN GENETICS
    48. Uimonen, S; Moilanen, JS; Sorri, M; Hassinen, IE; Majamaa, K
      Hearing impairment in patients with 3243A -> G mtDNA mutation: phenotype and rate of progression

      HUMAN GENETICS
    49. Glueck, CJ; Fontaine, RN; Wang, P
      Interaction of heritable and estrogen-induced thrombophilia: Possible etiologies for ischemic optic neuropathy and ischemic stroke

      THROMBOSIS AND HAEMOSTASIS
    50. Nesher, G; Nesher, R; Rozenman, Y; Sonnenblick, M
      Visual hallucinations in giant cell arteritis: Association with visual loss

      JOURNAL OF RHEUMATOLOGY
    51. Barnouin, J; Barrios, TV; Chassagne, M; Cristia, RP; Arnaud, J; Mestre, PF; Montoya, ME; Favier, A
      Nutritional and food protection against epidemic emerging neuropathy. Epidemiological findings in the unique disease-free urban area of Cuba

      INTERNATIONAL JOURNAL FOR VITAMIN AND NUTRITION RESEARCH
    52. Jiang, RS; Hsu, CY; Shen, BH
      Endoscopic optic nerve decompression for the treatment of traumatic optic neuropathy

      RHINOLOGY
    53. Dickinson, AJ; Perros, P
      Controversies in the clinical evaluation of active thyroid-associated orbitopathy: use of a detailed protocol with comparative photographs for objective assessment

      CLINICAL ENDOCRINOLOGY
    54. Hsu, CT; Kerrison, JB; Miller, NR; Goldberg, MF
      Choroidal infarction, anterior ischemic optic neuropathy, and central retinal artery occlusion from polyarteritis nodosa

      RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES
    55. Biousse, V; Newman, NJ
      Neuro-ophthalmology of mitochondrial diseases

      SEMINARS IN NEUROLOGY
    56. Gold, DR; Cohen, BH
      Treatment of mitochondrial cytopathies

      SEMINARS IN NEUROLOGY
    57. Al-Falki, YH
      Bilateral occipital infarcts in a hemodialysis patient

      AMERICAN JOURNAL OF NEPHROLOGY
    58. Huoponen, K; Schurr, TG; Chen, YS; Wallace, DC
      Mitochondrial DNA variation in an Aboriginal Australian population: Evidence for genetic isolation and regional differentiation

      HUMAN IMMUNOLOGY
    59. Tateishi, U; Terae, S; Ogata, A; Sawamura, Y; Suzuki, Y; Abe, S; Miyasaka, K
      MR imaging of the brain in lymphomatoid granulomatosis

      AMERICAN JOURNAL OF NEURORADIOLOGY
    60. Dot, C; Hamard, P; Metge, F; Hamard, H
      Bilateral acute ischemic optic neuropathy in 3 days in a case of Horton arteritis

      JOURNAL FRANCAIS D OPHTALMOLOGIE
    61. Krivosic, V; Vignal-Clermont, C; Blain, P; Gaudric, A
      Acute optic neuropathy in methyl alcohol intoxication: a case report

      JOURNAL FRANCAIS D OPHTALMOLOGIE
    62. Pulkes, T; Hanna, MG
      Human mitochondrial DNA diseases

      ADVANCED DRUG DELIVERY REVIEWS
    63. Pritchard, J; Anand, P; Broome, J; Davis, C; Gothard, L; Hall, E; Maher, J; McKinna, F; Millington, J; Misra, VP; Pitkin, A; Yarnold, JR
      Double-blind randomized phase II study of hyperbaric oxygen in patients with radiation-induced brachial plexopathy

      RADIOTHERAPY AND ONCOLOGY
    64. Takanashi, T; Uchida, S; Arita, M; Okada, M; Kashii, S
      Orbital inflammatory pseudotumor and ischemic vasculitis in Churg-Strauss syndrome - Report of two cases and review of the literature

      OPHTHALMOLOGY
    65. Hayreh, SS
      Risk factors in AION

      OPHTHALMOLOGY
    66. Pilitsis, JG; Rengachary, SS
      Complications of head injury

      NEUROLOGICAL RESEARCH
    67. Chinnery, PF; Andrews, RM; Turnbull, DM; Howell, N
      Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    68. Dimauro, S; Schon, EA
      Mitochondrial DNA mutations in human disease

      AMERICAN JOURNAL OF MEDICAL GENETICS
    69. Triepels, RH; Van den Heuvel, LP; Trijbels, JM; Smeitink, JA
      Respiratory chain complex I deficiency

      AMERICAN JOURNAL OF MEDICAL GENETICS
    70. Chinnery, PF; Turnbull, DM
      Epidemiology and treatment of mitochondrial disorders

      AMERICAN JOURNAL OF MEDICAL GENETICS
    71. Brown, MD; Allen, JC; Van Stavern, GP; Newman, NJ; Wallace, DC
      Clinical, genetic, and biochemical characterization of a leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations

      AMERICAN JOURNAL OF MEDICAL GENETICS
    72. Howell, N; Kubacka, I; McDonough, B; Hodess, AB; Harter, DH
      MtDNA analysis of Leber hereditary optic neuropathy associated with spondyloepiphyseal dysplasia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    73. Dufour, H; Muracciole, X; Metellus, P; Regis, J; Chinot, O; Grisoli, F
      Long-term tumor control and functional outcome in patients with cavernous sinus meningiomas treated by radiotherapy with or without previous surgery:Is there an alternative to aggressive tumor removal?

      NEUROSURGERY
    74. Seme, MT; Summerfelt, P; Neitz, J; Eells, JT; Henry, MM
      Differential recovery of retinal function after mitochondrial inhibition by methanol intoxication

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    75. Dupuis, A; Prieur, I; Lunardi, J
      Toward a characterization of the connecting module of complex I

      JOURNAL OF BIOENERGETICS AND BIOMEMBRANES
    76. Chomyn, A
      Mitochondrial genetic control, of assembly and function of complex I in mammalian cells

      JOURNAL OF BIOENERGETICS AND BIOMEMBRANES
    77. Wittig, I; Augstein, P; Brown, GK; Fujii, T; Rotig, A; Rustin, P; Munnich, A; Seibel, P; Thorburn, D; Wissinger, B; Tamboom, K; Metspalu, A; Lamantea, E; Zeviani, M; Wehnert, MS
      Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chain

      JOURNAL OF INHERITED METABOLIC DISEASE
    78. Endo, T; Numagami, Y; Jokura, H; Ikeda, H; Shirane, R; Yoshimoto, T
      Aspergillus parasellar abscess mimicking radiation-induced neuropathy - Case report

      SURGICAL NEUROLOGY
    79. Tzen, CY; Tsai, JD; Wu, TY; Chen, BF; Chen, ML; Lin, SP; Chen, SC
      Tubulointerstitial nephritis associated with a novel mitochondrial point mutation

      KIDNEY INTERNATIONAL
    80. Dinowitz, M; Leen, JS; Hameed, M; Wolansky, L; Frohman, L
      Sudden painless visual loss

      SURVEY OF OPHTHALMOLOGY
    81. Levin, LA
      Relevance of the site of injury of glaucoma to neuroprotective strategies

      SURVEY OF OPHTHALMOLOGY
    82. Solano, A; Playan, A; Lopez-Perez, MJ; Montoya, J
      Genetic diseases of the mitochondrial DNA.

      SALUD PUBLICA DE MEXICO
    83. Dimitri, D
      Diagnostic criteria and definition of the clinical course of multiple sclerosis

      REVUE NEUROLOGIQUE
    84. Durand, MC; Goulon-Goeau, C; Schweitzer, A; Cheliout-Herault, F; Raphael, JC; Gajdos, P
      Ten cases of Miller Fisher syndrome. Electrophysiological study.

      REVUE NEUROLOGIQUE
    85. Kacer, B; Hattenbach, LO; Horle, S; Scharrer, I; Kroll, P; Koch, F
      Central retinal vein occlusion and nonarteritic ischemic optic neuropathy in 2 patients with mild iron deficiency anemia

      OPHTHALMOLOGICA
    86. Haciyakupoglu, G; Isiguzel, I; Zorludemir, S; Zeren, H; Bagdatoglu, H; Menziletlioglu, S; Haciyakupoglu, S; Aksoy, K; Daglioglu, K
      Early ultrastructural findings and superoxide dismutase levels in experimental ischemic optic neuropathy: Effect of hypertension and hypotension on ischemic changes

      OPHTHALMOLOGICA
    87. Rodriguez-Hernandez, M; Hirano, M; Naini, A; Santiesteban, R
      Biochemical studies of patients with Cuban epidemic neuropathy

      OPHTHALMIC RESEARCH
    88. Riggs, JE; Ellis, BD; Hogg, JP; Al-Azzaz, A; Schochet, SS
      Acute periaqueductal syndrome associated with the G11778A mitochondrial DNA mutation

      NEUROLOGY
    89. Lubben, B; Stoll, W; Grenzebach, U
      Optic nerve decompression in the comatose and conscious patients after trauma

      LARYNGOSCOPE
    90. Flammer, J
      The glaucomatous optic neuropathy: a reperfusion damage

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    91. Buchwald, HJ; Spraul, CW; Wagner, P; Lang, GK
      Optic nerve evulsion: Metaanalysis

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    92. Wenkel, H
      Bilateral amaurosis in 11 patients with giant cell arteritis confirmed by arterial biopsy

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    93. Wilhelm, B; Ludtke, H; Peters, T; Schmid, R; Wilhelm, H; Zrenner, E
      Automated swinging flashlight test in patients with optic nerve disorders

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    94. Aguilera, I; Garcia-Lozano, JR; Munoz, A; Arenas, J; Campos, Y; Chinchon, I; Roldan, AN; Bautista, J
      Mitochondrial DNA point mutation in the COI gene in a patient with McArdle's disease

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    95. Inglese, M; Rovaris, M; Bianchi, S; Comi, G; Filippi, M
      Magnetization transfer and diffusion tensor MR imaging of the optic radiations and calcarine cortex from patients with Leber's hereditary optic neuropathy

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    96. Schmidt, RH; Rietz, LA; Patel, BCK; Osborne, AG; Pratt, D; Digre, KB
      Compressive optic neuropathy caused by renal osteodystrophy - Case report

      JOURNAL OF NEUROSURGERY
    97. Vogel, H
      Mitochondrial myopathies and the role of the pathologist in the molecular era

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    98. Inglese, M; Rovaris, M; Bianchi, S; La Mantia, L; Mancardi, GL; Ghezzi, A; Montagna, P; Salvi, F; Filippi, M
      Magnetic resonance imaging, magnetisation transfer imaging, and diffusion weighted imaging correlates of optic nerve, brain, and cervical cord damagein Leber's hereditary optic neuropathy

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    99. Klivenyi, P; Karg, E; Rozsa, C; Horvath, R; Komoly, S; Nemeth, I; Turi, S; Vecsei, L
      alpha-Tocopherol/lipid ratio in blood is decreased in patients with Leber's hereditary optic neuropathy and asymptomatic carriers of the 11778 mtDNA mutation

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    100. Finnila, S; Autere, J; Lehtovirta, M; Hartikainen, P; Mannermaa, A; Soininen, H; Majamaa, K
      Increased risk of sensorineural hearing loss and migraine in patients witha rare mitochondrial DNA variant 4336A > G in tRNA(Gln)

      JOURNAL OF MEDICAL GENETICS


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Documento generato il 16/02/20 alle ore 20:27:17