Results 211 to 220 of about 61,421 (256)
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Clinical & Experimental Ophthalmology, 2000
ABSTRACT Purpose: To determine the causes, and relative incidence of the common causes, of optic nerve atrophy in children under 10 years old and to compare prevalent aetiologies with those given in previous studies. Methods: The Wilmer Information System database was searched to identify all children, diagnosed between 1987 and 1997 with optic atrophy,
A V, Mudgil, M X, Repka
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ABSTRACT Purpose: To determine the causes, and relative incidence of the common causes, of optic nerve atrophy in children under 10 years old and to compare prevalent aetiologies with those given in previous studies. Methods: The Wilmer Information System database was searched to identify all children, diagnosed between 1987 and 1997 with optic atrophy,
A V, Mudgil, M X, Repka
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Journal of Clinical Neuroscience, 2012
Thallium poisoning is rare and its exposure is usually suicidal, homicidal or by accidental entry into the food chain. It involves multiple systems. Alopecia and painful neuropathy are its cardinal features, others being gastrointestinal disturbances, encephalopathy, tachycardia, ataxia, hepatorenal and cardiac damage.
Sanjeev, Jha, M K, Ansari
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Thallium poisoning is rare and its exposure is usually suicidal, homicidal or by accidental entry into the food chain. It involves multiple systems. Alopecia and painful neuropathy are its cardinal features, others being gastrointestinal disturbances, encephalopathy, tachycardia, ataxia, hepatorenal and cardiac damage.
Sanjeev, Jha, M K, Ansari
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Neurologic Clinics, 2010
Optic atrophy is a clinical term used to describe an optic disc thought to be paler than normal. Optic atrophy is not a diagnosis but an ophthalmoscopic sign. Evidence of visual loss (acuity, color vision, peripheral vision) should be present.
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Optic atrophy is a clinical term used to describe an optic disc thought to be paler than normal. Optic atrophy is not a diagnosis but an ophthalmoscopic sign. Evidence of visual loss (acuity, color vision, peripheral vision) should be present.
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Archives of Ophthalmology, 1958
Congenital hereditary optic atrophy is a rare but important specific entity, which is seldom recognized by most ophthalmologists. It is distinct from Leber's hereditary optic atrophy, particularly as to its age of onset, course, relative absence of associated physical abnormalities, and pattern of hereditary transmission.
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Congenital hereditary optic atrophy is a rare but important specific entity, which is seldom recognized by most ophthalmologists. It is distinct from Leber's hereditary optic atrophy, particularly as to its age of onset, course, relative absence of associated physical abnormalities, and pattern of hereditary transmission.
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American Journal of Ophthalmology, 1921
The author was able to observe nine cases of this disease affecting two generations of a family. He also reviews some of the more recent literature regarding it and inclines to the view that a low grade toxic retinitis may be the essential lesion. Read before the American Ophthalmological Society, June, 1920.
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The author was able to observe nine cases of this disease affecting two generations of a family. He also reviews some of the more recent literature regarding it and inclines to the view that a low grade toxic retinitis may be the essential lesion. Read before the American Ophthalmological Society, June, 1920.
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Pediatrics, 1964
An attempt has been made to determine the significance and outcome of optic atrophy as an apparently isolated entity in the pediatric age group. A follow-up study was made of 48 children who presented in early childhood with optic atrophy with no known cause and no obvious systemic or neurological disease. It was found that the prognosis
J F, SCHWARTZ +3 more
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An attempt has been made to determine the significance and outcome of optic atrophy as an apparently isolated entity in the pediatric age group. A follow-up study was made of 48 children who presented in early childhood with optic atrophy with no known cause and no obvious systemic or neurological disease. It was found that the prognosis
J F, SCHWARTZ +3 more
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American Journal of Ophthalmology, 1985
A 32-year-old fumigation assistant developed systemic and neuro-ophthalmic manifestations of methyl bromide poisoning, including increased serum bromide level (6.6 mg/100 ml), paresthesias and burning dysesthesia on his hands and feet, and visual impairment.
C T, Chavez, R S, Hepler, B R, Straatsma
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A 32-year-old fumigation assistant developed systemic and neuro-ophthalmic manifestations of methyl bromide poisoning, including increased serum bromide level (6.6 mg/100 ml), paresthesias and burning dysesthesia on his hands and feet, and visual impairment.
C T, Chavez, R S, Hepler, B R, Straatsma
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Dominant juvenile optic atrophy
Ophthalmic Paediatrics and Genetics, 1985Optic atrophy beginning in early childhood and accompanied by tritan-type dyschromatopsia, but normal ERG and abnormal VCEP, is described in a family. Differential diagnosis of hereditary optic atrophy is discussed.
A, Neetens, M C, Rubbens
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Optic Atrophy and Neurosyphilis
Annual Review of Medicine, 1971Two major recent advances in late syphilis of interest to every clinician have occurred in the past decade. These are: 1. the frequency of clinically progressive late seronegative syphilis; and 2. the presence of treponemes in patients with late syphilis despite penicillin therapy. The presence of trepo nemes in lymph nodes, despite penicillin therapy
J L, Smith, C W, Israel
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Leber's hereditary optic atrophy
Ophthalmic Paediatrics and Genetics, 1989Leber described a particular type of hereditary optic atrophy in 1871. The clinical features of all cases since reported are reviewed. There is characteristically acute visual loss, circumpapillary teleangiectatic micropathy, tortuosity of the retinal vessels and oedema in the retinal nerve fibres.
T A, Berninger, A C, Bird, G B, Arden
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