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  1. Article ; Online: Teleophthalmology for the Newborn Eye: Telemedicine for an Overlooked Patient Population.

    Capone, Antonio / Drenser, Kimberly A

    Ophthalmic surgery, lasers & imaging retina

    2021  Volume 52, Issue S2, Page(s) S4–S5

    MeSH term(s) Diabetic Retinopathy ; Eye Diseases/diagnosis ; Health Services Accessibility ; Humans ; Infant, Newborn ; Ophthalmology ; Telemedicine
    Language English
    Publishing date 2021-12-01
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2701167-7
    ISSN 2325-8179 ; 2325-8160
    ISSN (online) 2325-8179
    ISSN 2325-8160
    DOI 10.3928/23258160-20211115-01
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 756: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (1.OG)
    ab Jg. 2022: Lesesaal (EG)

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  2. Article ; Online: Retinal detachment in a pediatric patient with enhanced S-cone syndrome.

    Dass, Sabrina / Scoles, Drew / Trese, Matt G J / Drenser, Kimberly A

    Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus

    2023  Volume 27, Issue 4, Page(s) 229–231

    Abstract: Enhanced S-cone syndrome (ESCS), also known as Goldmann-Favre syndrome, is a retinal degeneration that presents in childhood and leads to progressive nyctalopia and visual field loss. In advanced cases, this degeneration can result in loss of central ... ...

    Abstract Enhanced S-cone syndrome (ESCS), also known as Goldmann-Favre syndrome, is a retinal degeneration that presents in childhood and leads to progressive nyctalopia and visual field loss. In advanced cases, this degeneration can result in loss of central visual acuity. We describe the case of a 15-year-old boy with ESCS who presented with retinal detachment, a rare complication.
    MeSH term(s) Male ; Humans ; Child ; Adolescent ; Retinal Degeneration/complications ; Retinal Degeneration/diagnosis ; Retinal Detachment/diagnosis ; Retinal Detachment/etiology ; Vision Disorders/diagnosis ; Vision Disorders/etiology ; Eye Diseases, Hereditary/complications ; Eye Diseases, Hereditary/diagnosis ; Electroretinography
    Language English
    Publishing date 2023-06-23
    Publishing country United States
    Document type Case Reports
    ZDB-ID 1412476-2
    ISSN 1528-3933 ; 1091-8531
    ISSN (online) 1528-3933
    ISSN 1091-8531
    DOI 10.1016/j.jaapos.2023.04.014
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Zs.A 5188: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
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    Jg. 1995 - 2021: Lesesall (2.OG)
    ab Jg. 2022: Lesesaal (EG)

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  3. Article ; Online: Pearls for Managing Pediatric Retinal Detachments.

    Drenser, Kimberly

    Ophthalmology

    2019  Volume 126, Issue 9, Page(s) 1271–1272

    MeSH term(s) Child ; Humans ; Retinal Detachment ; Retinal Perforations
    Language English
    Publishing date 2019-08-23
    Publishing country United States
    Document type Editorial ; Comment
    ZDB-ID 392083-5
    ISSN 1549-4713 ; 0161-6420
    ISSN (online) 1549-4713
    ISSN 0161-6420
    DOI 10.1016/j.ophtha.2019.03.022
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    Zs.MO 533: Show issues

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  4. Article: Wnt signaling pathway in retinal vascularization.

    Drenser, Kimberly A

    Eye and brain

    2016  Volume 8, Page(s) 141–146

    Abstract: Wnt-signaling, a ubiquitous pathway that directs differentiation, cell polarity, and tissue specificity, has been implicated as an important gene-expression pathway in retinal development. An increasing body of evidence supports the importance of Wnt- ... ...

    Abstract Wnt-signaling, a ubiquitous pathway that directs differentiation, cell polarity, and tissue specificity, has been implicated as an important gene-expression pathway in retinal development. An increasing body of evidence supports the importance of Wnt-signaling, and specifically, norrin-mediated Wnt-signaling in retinal development and retinal maintenance. Gene mutations affecting the Wnt-signaling pathways result in a variety of inherited vitreoretinopathies. Additionally, there is growing evidence that prematurity and associated retinopathy are associated with alterations in the Wnt-signaling pathways. Further investigations may allow for improved diagnoses, management, and therapies in the future.
    Language English
    Publishing date 2016-08-09
    Publishing country New Zealand
    Document type Journal Article ; Review
    ZDB-ID 2587460-3
    ISSN 1179-2744
    ISSN 1179-2744
    DOI 10.2147/EB.S94452
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  5. Article ; Online: Mechanisms Underlying Rare Inherited Pediatric Retinal Vascular Diseases: FEVR, Norrie Disease, Persistent Fetal Vascular Syndrome.

    Le, Vincent / Abdelmessih, Gabrielle / Dailey, Wendy A / Pinnock, Cecille / Jobczyk, Victoria / Rashingkar, Revati / Drenser, Kimberly A / Mitton, Kenneth P

    Cells

    2023  Volume 12, Issue 21

    Abstract: Familial Exudative Vitreoretinopathy (FEVR), Norrie disease, and persistent fetal vascular syndrome (PFVS) are extremely rare retinopathies that are clinically distinct but are unified by abnormal retinal endothelial cell function, and subsequent ... ...

    Abstract Familial Exudative Vitreoretinopathy (FEVR), Norrie disease, and persistent fetal vascular syndrome (PFVS) are extremely rare retinopathies that are clinically distinct but are unified by abnormal retinal endothelial cell function, and subsequent irregular retinal vascular development and/or aberrant inner blood-retinal-barrier (iBRB) function. The early angiogenesis of the retina and its iBRB is a delicate process that is mediated by the canonical Norrin Wnt-signaling pathway in retinal endothelial cells. Pathogenic variants in genes that play key roles within this pathway, such as
    MeSH term(s) Humans ; Child ; Familial Exudative Vitreoretinopathies/metabolism ; Endothelial Cells/metabolism ; Tetraspanins/metabolism ; Retinal Diseases/metabolism ; Vascular Diseases/metabolism ; Frizzled Receptors/genetics ; Frizzled Receptors/metabolism ; DNA-Binding Proteins/metabolism ; Transcription Factors/metabolism
    Chemical Substances Tetraspanins ; FZD4 protein, human ; Frizzled Receptors ; TSPAN12 protein, human ; ZNF408 protein, human ; DNA-Binding Proteins ; Transcription Factors
    Language English
    Publishing date 2023-11-05
    Publishing country Switzerland
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 2661518-6
    ISSN 2073-4409 ; 2073-4409
    ISSN (online) 2073-4409
    ISSN 2073-4409
    DOI 10.3390/cells12212579
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Diagnosis and Management of Familial Exudative Vitreoretinopathy: A Lifelong, Progressive, and Often Asymmetric Disease.

    Wood, Edward H / Drenser, Kimberly A / Capone, Antonio

    JAMA ophthalmology

    2019  Volume 137, Issue 9, Page(s) 1059–1060

    Language English
    Publishing date 2019-06-04
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2701705-9
    ISSN 2168-6173 ; 2168-6165
    ISSN (online) 2168-6173
    ISSN 2168-6165
    DOI 10.1001/jamaophthalmol.2019.1484
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  7. Article ; Online: Adult Coats' Disease, Dubin-Johnson Syndrome, and the Search for Targeted Therapies.

    Moinuddin, Omar / Wood, Edward H / Drenser, Kimberly A

    Ophthalmic surgery, lasers & imaging retina

    2019  Volume 50, Issue 5, Page(s) 318–321

    Abstract: Coats' disease is nonhereditary retinal vascular disorder characterized by telangiectatic retinal vessels with prominent aneurysmal changes and exudation. A conclusive etiology has not yet been determined. In this retrospective case report and literature ...

    Abstract Coats' disease is nonhereditary retinal vascular disorder characterized by telangiectatic retinal vessels with prominent aneurysmal changes and exudation. A conclusive etiology has not yet been determined. In this retrospective case report and literature review, a 64-year-old male with Dubin-Johnson syndrome presented with unilateral retinal vascular changes and exudation consistent with a diagnosis of adult Coats' disease. The authors conclude that patients with Dubin-Johnson syndrome carry mutations in a multidrug resistance associated protein (MRP). MRPs are also expressed in the retina, retinal pigment epithelium, and vascular endothelium, where they export toxins and metabolites, and may serve as a therapeutic target. [Ophthalmic Surg Lasers Imaging Retina. 2019;50:318-321.].
    MeSH term(s) Fluorescein Angiography ; Fundus Oculi ; Humans ; Jaundice, Chronic Idiopathic/diagnosis ; Jaundice, Chronic Idiopathic/therapy ; Laser Therapy/methods ; Male ; Middle Aged ; Retinal Pigment Epithelium/pathology ; Retinal Telangiectasis/diagnosis ; Retinal Telangiectasis/surgery ; Retinal Vessels/diagnostic imaging ; Retinal Vessels/surgery ; Tomography, Optical Coherence
    Language English
    Publishing date 2019-05-17
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 2701167-7
    ISSN 2325-8179 ; 2325-8160
    ISSN (online) 2325-8179
    ISSN 2325-8160
    DOI 10.3928/23258160-20190503-10
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Zs.A 756: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (1.OG)
    ab Jg. 2022: Lesesaal (EG)

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  8. Article ; Online: Genetic Testing for Retina Specialists.

    Wood, Edward H / Hariprasad, Seenu M / Drenser, Kimberly A

    Ophthalmic surgery, lasers & imaging retina

    2018  Volume 49, Issue 5, Page(s) 292–295

    MeSH term(s) Genetic Testing/history ; Genetic Testing/methods ; Genetic Therapy/methods ; History, 20th Century ; History, 21st Century ; Humans ; Ophthalmology/methods ; Retinal Diseases/diagnosis ; Retinal Diseases/genetics ; Retinal Diseases/therapy
    Language English
    Publishing date 2018-05-17
    Publishing country United States
    Document type Historical Article ; Journal Article
    ZDB-ID 2701167-7
    ISSN 2325-8179 ; 2325-8160
    ISSN (online) 2325-8179
    ISSN 2325-8160
    DOI 10.3928/23258160-20180501-01
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 756: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
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    Jg. 1995 - 2021: Lesesall (1.OG)
    ab Jg. 2022: Lesesaal (EG)

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  9. Article ; Online: Congenital X-Linked Retinoschisis: An Updated Clinical Review.

    Rao, Prethy / Dedania, Vaidehi S / Drenser, Kimberly A

    Asia-Pacific journal of ophthalmology (Philadelphia, Pa.)

    2018  Volume 7, Issue 3, Page(s) 169–175

    Abstract: We present an updated clinical review of the pathophysiology, progression, and current treatments in pediatric patients with congenital X-linked retinoschisis (CXLRS). CXLRS is an X-linked inherited retinal degeneration characterized by splitting of the ... ...

    Abstract We present an updated clinical review of the pathophysiology, progression, and current treatments in pediatric patients with congenital X-linked retinoschisis (CXLRS). CXLRS is an X-linked inherited retinal degeneration characterized by splitting of the superficial layers of the retina. Most recent classification divides CXLRS into 4 distinct clinical phenotypes: type 1, foveal; type 2, foveolamellar; type 3, complex; and type 4, foveoperipheral. The majority of retinoschisis cavities remain stable throughout life and may spontaneously collapse. However, a select number of patients progress to macula-involving peripheral retinoschisis, rhegmatogenous, and combined tractional-rhegmatogenous detachments that require further intervention. Although several advances have been made over the past several decades, medical therapy remains limited to case series‒based carbonic anhydrase therapy and prophylactic laser retinopexy. Recent advances in genetic-based clinical trials with the retinoschisis gene are promising. Vitreoretinal surgical approaches remain complex, case-based, and require careful planning depending on the configuration and location of the retinoschisis cavity.
    MeSH term(s) Diagnostic Imaging/methods ; Disease Management ; Genetic Testing/methods ; Genetic Therapy/methods ; Humans ; Retinoschisis/congenital ; Retinoschisis/diagnosis ; Retinoschisis/therapy
    Language English
    Publishing date 2018-04-09
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2756329-7
    ISSN 2162-0989 ; 2162-0989
    ISSN (online) 2162-0989
    ISSN 2162-0989
    DOI 10.22608/APO.201803
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: A Literary Pediatric Retina Fellowship With Michael T. Trese, MD.

    Wood, Edward H / Moshfeghi, Darius M / Capone, Antonio / Williams, George A / Blumenkranz, Mark S / Sieving, Paul A / Harper, Clio Armitage / Hartnett, M Elizabeth / Drenser, Kimberly A

    Ophthalmic surgery, lasers & imaging retina

    2023  Volume 54, Issue 12, Page(s) 701–712

    Abstract: Michael T. Trese, MD (1946-2022), a vitreoretinal surgeon, made significant contributions to the field of retina. Although most known for his work in pediatric retina surgery, he was a pioneer in areas such as medical retina, translational research, and ... ...

    Abstract Michael T. Trese, MD (1946-2022), a vitreoretinal surgeon, made significant contributions to the field of retina. Although most known for his work in pediatric retina surgery, he was a pioneer in areas such as medical retina, translational research, and telemedicine. This article reviews his major contributions to spread his knowledge more widely to vitreoretinal trainees and specialists. We discuss six areas where Trese made a lasting impact: lens-sparing vitrectomy, familial exudative vitreoretinopathy, congenital X-linked retinoschisis, autologous plasmin enzyme, regenerative medicine, and telemedicine.
    MeSH term(s) Male ; Child ; Humans ; Fellowships and Scholarships ; Retina/surgery ; Familial Exudative Vitreoretinopathies/surgery ; Vitreous Body ; Retinoschisis/surgery ; Vitrectomy/methods
    Language English
    Publishing date 2023-12-01
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2701167-7
    ISSN 2325-8179 ; 2325-8160
    ISSN (online) 2325-8179
    ISSN 2325-8160
    DOI 10.3928/23258160-20231020-01
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 756: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
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