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Journal of AAPOS : the official publication of the... 36건

  1. [해외논문]   New trends in childhood vision impairment in a developed country   SCIE

    Pham, Chengde (The Royal Victorian Eye and Ear Hospital, Melbourne ) , Sheth, Shivanand J. (The Royal Victorian Eye and Ear Hospital, Melbourne ) , Keeffe, Jill E. (Melbourne School of Population Health, University of Melbourne, Melbourne ) , Carden, Susan M. (The Royal Victorian Eye and Ear Hospital, Melbourne)
    Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus v.21 no.6 ,pp. 496 - 498 , 2017 , 1091-8531 ,

    초록

    Background The Education Vision Assessment Clinic (EVAC) is a unique statewide service that reviews school children 4-18 years of age with low vision in Victoria, Australia, to determine their eligibility for educational support. The purpose of this study was to identify causes of vision impairment in students in Victoria using data from the EVAC. Methods Data collected from students who attended the EVAC at the Royal Victorian Eye and Ear Hospital, Melbourne, between the years 2003 and 2012 inclusive, were analyzed retrospectively. Participants were identified through the EVAC schedule of medical appointments. Medical records were reviewed for clinical and demographic information, including diagnosis of vision impairment and best-corrected visual acuity and/or visual fields. Results Of 543 students, 355 (65%) were eligible for educational assistance. Of those, 249 (70%) had best-corrected visual acuity between 20/60 and 20/200 and/or a field of vision of Conclusions Treatable and potentially preventable causes of vision impairment, such as retinopathy of prematurity and cataract, caused

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    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

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  2. [해외논문]   Macular morphology following unilateral bevacizumab injection for retinopathy of prematurity: an OCT study   SCIE

    Clark, Antony (Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada ) , Wright, Tom (Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada ) , Isaac, Maram (Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada ) , Westall, Carol (Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada ) , Mireskandari, Kamiar (Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada ) , Tehrani, Nasrin N. (University of Toronto, Toronto, Ontario, Canada)
    Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus v.21 no.6 ,pp. 499 - 501.e1 , 2017 , 1091-8531 ,

    초록

    This retrospective case series assessed the influence of unilateral intravitreal bevacizumab (IVB) for unilateral type 1 retinopathy of prematurity (ROP) on macular thickness and foveal development. Seven infants with unilateral type 1 ROP were treated with intravitreal bevacizumab 0.625 mg/0.025 ml in one eye only. To determine whether macular thickness and fovea structural development were affected by treatment, spectral domain optical coherence tomography was performed on both treated and untreated eyes. The mean gestational age of infants was 25.3 ± 0.3 weeks; the mean birth weight, 776 ± 17.6 g. Treatment was given at a mean postmenstrual age of 37.2 ± 0.4 weeks. Foveal development was normal in 3 (43%) treated versus 5 (71%) untreated eyes. The mean central foveal thickness for treated and untreated eyes was 270.1 μm ± 19.6 and 253.0 μm ± 27.2 respectively ( P = 0.15). There was small but nonsignificant difference in foveal development and thickness in eyes treated with intravitreal bevacizumab compared to fellow eyes. This study generates important data to test the hypothesis that foveal thickness is greater in unilateral type 1 ROP eyes treated with IVB compared to untreated fellow eyes.

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    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

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  3. [해외논문]   Malignant melanoma presenting as amelanotic caruncular lesion in a child   SCIE

    Walters, Alexander R. (Department of Ophthalmology, Palmetto Health/University of South Carolina, Richland ) , Keck, Katie M. (Department of Ophthalmology, Palmetto Health/University of South Carolina, Richland ) , Simmons, Oliver (Department of Otolaryngology, Palmetto Health/University of South Carolina, Richland ) , Williams, Sarah G. (Department of Pathology, Palmetto Health/University of South Carolina, Richland ) , Cross, Stephen (Department of Ophthalmology, Palmetto Health/University of South Carolina, Richland ) , Patel, Rakesh M. (Department of Ophthalmology, Palmetto Health/University of South Carolina, Richland)
    Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus v.21 no.6 ,pp. 501 - 503 , 2017 , 1091-8531 ,

    초록

    Conjunctival melanoma is a rare malignant neoplasm that can present in childhood in any part of the conjunctiva. The infrequency with which conjunctival melanoma is encountered in childhood caruncular lesions makes it a formidable but important aspect of the differential diagnosis. We report the case of a 10-year-old boy who presented with a left caruncular lesion. On histopathologic analysis, the lesion was determined to be BRAF-negative invasive melanoma arising in association with melanocytic nevus. The melanoma was excised using no-touch technique and double freeze thaw cryotherapy. A full systemic work-up revealed no metastasis or abnormality.

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    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

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  4. [해외논문]   Positive ice test in a patient with a lymphomatous infiltration of the levator palpebrae superioris   SCIE

    Yang, Hee Kyung (Department of Ophthalmology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea ) , Kim, Namju (Department of Ophthalmology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea ) , Kim, Jae Hyoung (Department of Radiology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea ) , Hwang, Jeong-Min (Department of Ophthalmology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea)
    Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus v.21 no.6 ,pp. 503 - 505 , 2017 , 1091-8531 ,

    초록

    The ice test is known to be specific for the diagnosis of ocular myasthenia gravis in patients with ptosis, with reported specificities of 97%-100%. We report a patient with diffuse large B-cell lymphoma who showed a positive result to the ice test. A 53-year-old woman presented with left eyelid ptosis of 3 weeks' duration. She had finished chemotherapy and radiotherapy for diffuse large B-cell lymphoma a year previously. On ophthalmological examination, her best-corrected visual acuity was 20/20 in each eye. Marginal reflex distances were +4 in the right eye and −1 in the left eye. Levator palpebrae superioris functions were 11 mm in the right eye and 8 mm in the left eye. Ptosis improved after 5 minutes' application of ice to both eyelids, after which marginal reflex distances were +4 in the right eye and +1 in the left eye. Thyroid function tests, anti-acetylcholine receptor antibody test, and the repetitive nerve stimulation test were all negative. Magnetic resonance imaging showed fusiform masslike enlargement of the left superior rectus muscle and left levator palpebrae superioris muscles, with enhancement suggesting metastatic infiltration.

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    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

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  5. [해외논문]   Cerebrotendinous xanthomatosis: early diagnosis on the basis of juvenile cataracts   SCIE

    Tibrewal, Sapna (Department of Ophthalmology, Casey Eye institute, Oregon Health and Science University, Portland ) , Duell, P. Barton (Knight Cardiovascular Institute, Oregon Health and Science University, Portland ) , DeBarber, Andrea E. (Department of Physiology and Pharmacology, Oregon Health and Science University, Portland ) , Loh, Allison R. (Department of Ophthalmology, Casey Eye institute, Oregon Health and Science University, Portland)
    Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus v.21 no.6 ,pp. 505 - 507 , 2017 , 1091-8531 ,

    초록

    Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive lipid storage disease characterized by a broad spectrum of clinical manifestations, including bilateral juvenile cataracts. Untreated CTX leads to progressive permanent neurologic decline and early death. Although symptoms begin in early childhood, diagnosis and replacement therapy with chenodeoxycholic acid is often delayed until adulthood. Frequently bilateral juvenile cataracts present in early childhood which provides ophthalmologists an opportunity to aid in early diagnosis and initiate treatment. We report the case of a child presenting with juvenile bilateral cataracts leading to the diagnosis of CTX. The morphology of cataracts and the effect of systemic treatment on its progression are described.

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    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

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  6. [해외논문]   The clinical presentation of bradyopsia in children   SCIE

    Khan, Arif O. (Eye Institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates)
    Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus v.21 no.6 ,pp. 507 - 509.e1 , 2017 , 1091-8531 ,

    초록

    Diagnosing bradyopsia can be challenging in young children because structural ophthalmic examination is typically normal and visual acuity can improve with pinhole despite no significant refractive error. This case series highlights the clinical presentations and features of 5 affected children (3 Arab families) who harbored the same homozygous RGS9 frameshift mutation, which seems to represent a founder effect for the Arabian Peninsula.

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    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

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  7. [해외논문]   Periorbital lesions misdiagnosed as dermoid cysts   SCIE

    Al-Muhaylib, Ahmed (Department of Ophthalmology, College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia ) , Alkatan, Hind M. (Department of Ophthalmology, College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia ) , Al-Faky, Yasser H. (Department of Ophthalmology, College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia ) , Alsuhaibani, Adel H. (Department of Ophthalmology, College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia)
    Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus v.21 no.6 ,pp. 509 - 511 , 2017 , 1091-8531 ,

    초록

    Several periorbital lesions can be clinically misdiagnosed as dermoid cyst. We retrospectively reviewed the histopathological findings for 97 biopsied periorbital lesions with a clinical diagnosis of dermoid cyst from January 2006 to July 2016 at a single center and identified 5 cases that were eventually found to have been misdiagnosed. The main presenting symptom was a long-standing mobile painless mass with intact overlying skin below the medial aspect of the brow in 4 patients and below the center of the brow in 1 patient. The tissue diagnoses included vascular lesions (hemangiomas and cavernous venous malformation) in 4 patients and pilomatrixoma in 1 patient. The agreement between the clinical and pathological diagnosis of a periocular dermoid cyst in our series was 94.8%.

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    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

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  8. [해외논문]   Gustatory lid retraction: an unusual congenital cranial dysinnervation disorder   SCIE

    Khan, Arif O. (Correspondence: Arif O. Khan, MD, Eye Institute, Cleveland Clinic Abu Dhabi, PO Box 112412 Abu Dhabi, United Arab Emirates) , Khan, Zabila
    Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus v.21 no.6 ,pp. 511 - 512 , 2017 , 1091-8531 ,

    초록

    Congenital cranial dysinnervation disorders are developmental abnormalities of cranial nerves that often include abnormal synkinesis. Among the most common ophthalmic congenital cranial dysinnervation disorders are Duane retraction syndrome and the Marcus-Gunn jaw-winking phenomenon. This report documents gustatory lid retraction as an unusual congenital cranial dysinnervation.▪▪

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    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

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  9. [해외논문]   Amblyopia due to intermediate uveitis as the presenting symptom of Crohn's disease in a 6-year-old boy   SCIE

    Symeonidis, Chrysanthos (Correspondence: Chrysanthos Symeonidis, MD, PhD, 2nd Department of Ophthalmology, School of Medicine, Aristotle University of Thessaloniki, “Papageorgiou” General Hospital, Thessaloniki Ring Road, 564 03 Thessaloniki, Macedonia, Greece) , Matsou, Artemis , Tzetzi, Despoina , Dermenoudi, Maria , Brazitikos, Periklis , Mataftsi, Asimina
    Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus v.21 no.6 ,pp. 512 - 514 , 2017 , 1091-8531 ,

    초록

    A 6-year-old boy presented with unexplained unilateral low visual acuity. Best-corrected visual acuity was counting fingers in the right eye and 20/20 in the left eye. Fundus examination of the right eye revealed intermediate uveitis, with moderate vitritis, snowballs, and snowbanking. Infectious and noninfectious conditions known to be associated with intermediate uveitis were excluded. Vitreous inflammation gradually resolved with oral steroids, and amblyopia treatment with left eye patching was advised. Several months later the boy suffered acute monoarthritis and episodes of mucopurulent diarrhea; a terminal ileum biopsy was consistent with Crohn's disease. This case of Crohn's disease and uveitis is unusual in that ocular inflammation preceded intestinal involvement, with the atypical feature of chronic intermediate uveitis.

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    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

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  10. [해외논문]   Ophthalmic findings in Frank-ter Haar syndrome: report of a sibling pair   SCIE

    Chang, Ta C. (Bascom Palmer Eye Institute, Miami, Florida ) , Bauer, Mislen (Nicklaus Children's Hospital, Division of Genetics and Metabolism, Miami, Florida ) , Puerta, Herminia S. (Nicklaus Children's Hospital, Division of Genetics and Metabolism, Miami, Florida ) , Greenberg, Matthew B. (University of Miami Miller School of Medicine, Miami, Florida ) , Cavuoto, Kara M. (Bascom Palmer Eye Institute, Miami, Florida)
    Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus v.21 no.6 ,pp. 514 - 516 , 2017 , 1091-8531 ,

    초록

    Frank-ter Haar syndrome (FTHS) is an autosomal recessive disorder characterized by abnormalities that affect the development of bone, heart, and eyes. We report a sibling pair with FTHS caused by a homozygous, novel mutation pLys133Glnfs*13 in the SH3PXD2B gene: one sibling had bilateral ocular hypertension and unilateral colobomas of iris, choroid and retina; the other, unilateral myelinated nerve fiber layer of the optic disk and papilledema due to idiopathic intracranial hypertension. Both children had refractive amblyopia and megalocornea.▪

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    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

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