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  1. AU="Abramowicz, Stéphane"
  2. AU=Howatt Deborah A.
  3. AU="Basir, Seemi Farhat"
  4. AU="Luc Girard"
  5. AU="Sujay Ray"
  6. AU="Raziel J Davison"
  7. AU="O'Connor, Andrew"
  8. AU="Mendoza, Luis Alfonso"
  9. AU="Shadyro, Oleg I"
  10. AU="Duce, James A"
  11. AU="Jiménez‐Yuste, Victor"
  12. AU=Jang Jinah
  13. AU="Ullman, Natalie L"
  14. AU="Ding, Xiao-Qiang"
  15. AU="Goyal, Madhav"
  16. AU="Schwarz, E Bimla"
  17. AU="Yamamoto, Naoyuki"
  18. AU="Mansi, Ruaa Abdullah"
  19. AU="Feng, Ruifang"
  20. AU="Rzaigui, Mohamed"
  21. AU="Kuznetsova, Iren"
  22. AU="Töreki, Josefin"
  23. AU="Simon Hatcher" AU="Simon Hatcher"
  24. AU="Gui, Wenwu"
  25. AU="Komdeur, Annemarijn"
  26. AU="Stange, E. F."
  27. AU="McKenzie, Jodi A"
  28. AU="Chung, Mei"
  29. AU="Cezmi A Akdis"
  30. AU="Schlechter, Chelsey R"
  31. AU=Hedayati Manouchehr Ahmadi AU=Hedayati Manouchehr Ahmadi
  32. AU="Gould, Sven B"
  33. AU="Ko, Kyung Dae"
  34. AU="Elaheh Mahmoodi-Khaledi"
  35. AU=Jenkins Kathy J
  36. AU="Joseph Burgess"
  37. AU="Barbosa da Costa, Alana Vitor"
  38. AU="François Lebargy"
  39. AU=Serag Eman AU=Serag Eman
  40. AU="Yang, Guichun"
  41. AU="Amory, Jonathan R"
  42. AU="Reformat, Marek"

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  1. Artikel ; Online: ACUTE EXACERBATION OF CHRONIC CENTRAL SEROUS CHORIORETINOPATHY AT THE SITE OF A RETINAL PIGMENT EPITHELIUM APERTURE.

    Abramowicz, Stéphane / Pasteels, Brigitte / Postelmans, Laurence

    Retinal cases & brief reports

    2023  Band 18, Heft 2, Seite(n) 206–210

    Abstract: Purpose: To describe an atypical case of chronic central serous chorioretinopathy with acute exacerbation consisting of severe exudation at the site of a retinal pigment epithelium aperture.: Methods: Case report.: Results: A 39-year-old man ... ...

    Abstract Purpose: To describe an atypical case of chronic central serous chorioretinopathy with acute exacerbation consisting of severe exudation at the site of a retinal pigment epithelium aperture.
    Methods: Case report.
    Results: A 39-year-old man presented with a recurrence of central serous chorioretinopathy in the right eye. Initial evaluation was notable for a retinal pigment epithelium aperture overlying a chronic avascular pigment epithelial detachment. He was initially treated with topical dorzolamide and indomethacin. During the follow-up, application of topical dermal steroid for a case of athlete's foot led to severe fibrinous exudation originating from the site of the retinal pigment epithelium aperture. Half-fluence verteporfin photodynamic therapy induced rapid and complete resolution of the retinal findings.
    Conclusion: Photodynamic therapy allowed for excellent resolution of an atypical exudative and fibrinous form of central serous chorioretinopathy associated with a retinal pigment epithelium aperture.
    Mesh-Begriff(e) Male ; Humans ; Adult ; Central Serous Chorioretinopathy/chemically induced ; Central Serous Chorioretinopathy/diagnosis ; Central Serous Chorioretinopathy/drug therapy ; Retinal Pigment Epithelium ; Photosensitizing Agents/therapeutic use ; Tomography, Optical Coherence ; Visual Acuity ; Fluorescein Angiography ; Photochemotherapy ; Chronic Disease ; Retrospective Studies
    Chemische Substanzen Photosensitizing Agents
    Sprache Englisch
    Erscheinungsdatum 2023-08-01
    Erscheinungsland United States
    Dokumenttyp Case Reports ; Journal Article
    ISSN 1937-1578
    ISSN (online) 1937-1578
    DOI 10.1097/ICB.0000000000001340
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Choroidal Nodules in Ocular Sarcoidosis.

    Abramowicz, Stéphane / Wassef, Michel / Touhami, Sara

    Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG

    2023  Band 40, Heft 4, Seite(n) e2023039

    Abstract: Background and aim: Ocular sarcoidosis is present in 30-60% of all sarcoidosis patients. Our purpose is to increase awareness of the various presentations of ocular sarcoidosis.: Methods: Short image-based clinical case report.: Results: We report ...

    Abstract Background and aim: Ocular sarcoidosis is present in 30-60% of all sarcoidosis patients. Our purpose is to increase awareness of the various presentations of ocular sarcoidosis.
    Methods: Short image-based clinical case report.
    Results: We report on a case of ocular sarcoidosis presenting with unilateral choroidal nodules in a middle-aged man. Sarcoid uveitis is generally bilateral and rather symmetrical. However, choroidal nodules are an exception to this rule, as they generally arise unilaterally. Choroidal nodules are highly responsive to oral corticosteroids. When left untreated, they may evolve to chorioretinal atrophy and secondary choroidal neovascularization.
    Conclusions: Knowledge of this presentation of ocular sarcoidosis can help clinicians optimize treatment outcomes for patients.
    Sprache Englisch
    Erscheinungsdatum 2023-12-20
    Erscheinungsland Italy
    Dokumenttyp Journal Article
    ZDB-ID 1339192-6
    ISSN 2532-179X ; 1124-0490
    ISSN (online) 2532-179X
    ISSN 1124-0490
    DOI 10.36141/svdld.v40i4.15122
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Atypical retinopathy in ataxia with vitamin E deficiency: report of a sibship.

    Abramowicz, Stéphane / Dentel, Alexandre / Chouraqui, Maxime / Bodaghi, Bahram / Touhami, Sara

    Neurogenetics

    2023  Band 25, Heft 1, Seite(n) 33–38

    Abstract: Typical retinitis pigmentosa (RP) may not be the only retinal phenotype encountered in ataxia with vitamin E deficiency (AVED). The following short case series describes a novel form of retinopathy in AVED. We describe two patients with AVED belonging to ...

    Abstract Typical retinitis pigmentosa (RP) may not be the only retinal phenotype encountered in ataxia with vitamin E deficiency (AVED). The following short case series describes a novel form of retinopathy in AVED. We describe two patients with AVED belonging to the same consanguineous sibship. Both presented an unusual retinopathy consisting of scattered, multifocal, nummular, hyperautofluorescent atrophic retinal patches. The retinopathy remained stable under vitamin E supplementation. We hypothesize these changes to be the result of arrested AVED-related RP following early supplementation with α-tocopherol acetate.
    Mesh-Begriff(e) Humans ; Carrier Proteins/genetics ; Ataxia/complications ; Ataxia/genetics ; Vitamin E Deficiency/complications ; Vitamin E Deficiency/genetics ; Retinitis Pigmentosa/complications ; Retinitis Pigmentosa/genetics ; Pedigree ; Mutation
    Chemische Substanzen Carrier Proteins
    Sprache Englisch
    Erscheinungsdatum 2023-12-18
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 1339887-8
    ISSN 1364-6753 ; 1364-6745
    ISSN (online) 1364-6753
    ISSN 1364-6745
    DOI 10.1007/s10048-023-00741-9
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

    Volltext online

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    Verfügbar in ZB MED Köln/Königswinter

    Zs.A 5295: Hefte anzeigen Standort:
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    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (2.OG)
    ab Jg. 2022: Lesesaal (EG)

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  4. Artikel: Immune recovery uveitis in Whipple's disease: an unusual ocular presentation.

    Lequain, Hippolyte / Abramowicz, Stéphane / Seiller, Julien / Abukhashbah, Amro / Burillon, Carole / Vignot, Emmanuelle / Brunet, Olivier / Sève, Pascal

    Journal of ophthalmic inflammation and infection

    2024  Band 14, Heft 1, Seite(n) 10

    Abstract: Purpose: To describe an unusual case of Whipple's disease (WD) complicated by uveitis, and subsequent paradoxical worsening after effective antibiotic treatment targeting Tropheryma whipplei (TW).: Methods: Case report.: Results: A 53-year-old ... ...

    Abstract Purpose: To describe an unusual case of Whipple's disease (WD) complicated by uveitis, and subsequent paradoxical worsening after effective antibiotic treatment targeting Tropheryma whipplei (TW).
    Methods: Case report.
    Results: A 53-year-old male presented with bilateral knee arthritis, weight loss, chronic low-grade fever, and cognitive disorders. He was under treatment with tumor necrosis factor α inhibitors (TNFi) for seronegative spondyloarthritis. Given this unusual clinical presentation, further investigations were performed and revealed blood, saliva, stool, synovial fluid and cerebrospinal fluid positivity for TW, confirming the diagnosis of systemic WD. Ophthalmologic examination revealed bilateral posterior uveitis and an aqueous humor sample confirmed the presence of intraocular TW. TNFi were stopped, and the patient was subsequently treated with adequate antibiotics (ceftriaxone, followed by doxycycline and hydroxychloroquine), and subconjunctival corticosteroid injections. After a transient improvement of the ocular symptoms, he presented a recurrence of posterior segment inflammation, leading to repeated PCR testing for TW which were negative. Therefore, paradoxical worsening of the inflammation in the context of immune recovery uveitis (IRU) was thought to be the culprit. The patient was treated with systemic corticosteroid therapy, allowing for rapid improvement of the ocular findings.
    Conclusions: This case underlines the possibility of IRU complicating WD. Ophthalmologists, rheumatologists, and internists should be aware of this rare complication, particularly in the context of previous immunosuppressive therapy.
    Sprache Englisch
    Erscheinungsdatum 2024-02-13
    Erscheinungsland Germany
    Dokumenttyp Journal Article
    ZDB-ID 2592309-2
    ISSN 1869-5760
    ISSN 1869-5760
    DOI 10.1186/s12348-024-00390-5
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel: Subtle Combined Hamartoma of the Retina and Retinal Pigment Epithelium Causing Recurrent Exodeviation.

    Abramowicz, Stéphane / Delvaulx, Philippine / Delle Fave, Martina Maria / Le Roux, Pauline / Buisseret, Déborah / Postolache, Lavinia

    Case reports in ophthalmology

    2022  Band 13, Heft 1, Seite(n) 305–312

    Abstract: A 3-year-old girl presented with recurrent exotropia following primary strabismus surgery. Careful fundus examination of the left eye revealed loss of the foveal reflex and presence of a subtle grayish mass with overlying white fluff. Optical coherence ... ...

    Abstract A 3-year-old girl presented with recurrent exotropia following primary strabismus surgery. Careful fundus examination of the left eye revealed loss of the foveal reflex and presence of a subtle grayish mass with overlying white fluff. Optical coherence tomography through the lesion revealed disorganization of inner and outer retinal layers with accompanying epiretinal gliosis. Together, these findings were suggestive of combined hamartoma of the retina and retinal pigment epithelium (CHRRPE). No syndromic association was found. CHRRPE is a rare retinal tumor that usually presents with visual loss, strabismus, or follows an asymptomatic course. Retinal tumors must be kept in mind whenever loss of foveal reflex occurs concurrently with strabismus.
    Sprache Englisch
    Erscheinungsdatum 2022-04-22
    Erscheinungsland Switzerland
    Dokumenttyp Case Reports
    ZDB-ID 2577666-6
    ISSN 1663-2699
    ISSN 1663-2699
    DOI 10.1159/000524074
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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