標(biāo)題: Titlebook: Clinico-Pathological Atlas of Congenital Fundus Disorders; Juan Orellana,Alan H. Friedman Book 1993 Springer Science+Business Media New Yo [打印本頁] 作者: 人工合成 時(shí)間: 2025-3-21 19:48
書目名稱Clinico-Pathological Atlas of Congenital Fundus Disorders影響因子(影響力)
書目名稱Clinico-Pathological Atlas of Congenital Fundus Disorders影響因子(影響力)學(xué)科排名
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書目名稱Clinico-Pathological Atlas of Congenital Fundus Disorders讀者反饋
書目名稱Clinico-Pathological Atlas of Congenital Fundus Disorders讀者反饋學(xué)科排名
作者: SCORE 時(shí)間: 2025-3-21 20:40 作者: ZEST 時(shí)間: 2025-3-22 03:23
Rubella Retinopathytemically, these children may have abnormalities of the brain and heart. It is important that these lenses are removed carefully, as viruses are shed on extraction, which can produce an overwhelming uveitis. Phthisis bulbi may be the sequelae of an uneventful cataract procedure.作者: 倒轉(zhuǎn) 時(shí)間: 2025-3-22 07:38 作者: 滑稽 時(shí)間: 2025-3-22 09:35
https://doi.org/10.1007/978-3-642-61119-3, however, do not have systemic changes, whereas Stickler syndrome patients have systemic manifestations. The former patients do not suffer retinal detachments, whereas more than 50% of the Stickler syndrome patients develop a retinal detachment.作者: cogitate 時(shí)間: 2025-3-22 16:46 作者: cogitate 時(shí)間: 2025-3-22 20:34 作者: 受辱 時(shí)間: 2025-3-22 23:04 作者: Collected 時(shí)間: 2025-3-23 02:56
Book 1993ussion. This book is an invaluable reference allowing the practitioner to quickly compare the case at hand with the wealth of examples presented here. The volume will train the resident and refresh the practicing ophthalmologist in quickly recognizing the plethora of congenital diseases of the eye.作者: Diuretic 時(shí)間: 2025-3-23 06:58 作者: 丑惡 時(shí)間: 2025-3-23 09:46
Modelle mit Korrelationsstrukturch may help the associated skin lesions resolve. In young adults, keratitis, iridocyclitis or chorioretinitis can be seen. Treatment for the keratitis can be lengthy while the uveitic manifestations can be difficult to control.作者: CRAB 時(shí)間: 2025-3-23 15:18 作者: 階層 時(shí)間: 2025-3-23 18:23
tal anomalies of the vitreous, retina and choroid with their appropriate pathology. The volume is divided into clinical sections dealing with the various aspects of vitreo-retinal disorders including genetic, vascular, infectious, and neoplastic entities. Detailed, instructive illustrations are pair作者: Excitotoxin 時(shí)間: 2025-3-24 02:02
Verallgemeinerte Lineare Modelle each parent. One member of each 23 chromosomal pairs is inherited from the father and the other from the mother. Via this method the child has half the genetic material from each parent. The total of 46 chromosomes includes two that determine the sex of the child. An XX determines a female, and the XY pair denotes a male.作者: 瑪瑙 時(shí)間: 2025-3-24 02:31
Abwicklungsmuster und Schadenquotenhoroiditis. The retinitis is a progressive one with extensive necrosis and hemorrhage. The vitritis that accompanies this disease is moderate, often mild in view of the extensive amount of retinal destruction.作者: 鞏固 時(shí)間: 2025-3-24 08:21
Modelle mit Korrelationsstruktur to this diagnosis. The fundal picture is often mistaken for retinitis pigmentosa. Systemic findings include Hutchinson’s teeth (pointed incisors), a broad saddle nose, bowed tibias, osteochondritis, and hepatosplenomegaly.作者: 儀式 時(shí)間: 2025-3-24 13:05
8 Daten und Tarifierungsstatistikenof congenital toxoplasmosis include fever, jaundice, chorioretinitis, intracranial calcifications on radiographic studies, hydrocephalus, and convulsions. Infants may be born with the disease, or it may not become apparent until the infant is almost 1 year old. The immunoglobulin M (IgM) fluorescent antibody test is diagnostic for the disease.作者: diathermy 時(shí)間: 2025-3-24 17:46 作者: Intrepid 時(shí)間: 2025-3-24 20:48
Cytomegalic Inclusion Diseasehoroiditis. The retinitis is a progressive one with extensive necrosis and hemorrhage. The vitritis that accompanies this disease is moderate, often mild in view of the extensive amount of retinal destruction.作者: 使習(xí)慣于 時(shí)間: 2025-3-25 00:41
Luetic Chorioretinitis to this diagnosis. The fundal picture is often mistaken for retinitis pigmentosa. Systemic findings include Hutchinson’s teeth (pointed incisors), a broad saddle nose, bowed tibias, osteochondritis, and hepatosplenomegaly.作者: 控訴 時(shí)間: 2025-3-25 07:09 作者: Condense 時(shí)間: 2025-3-25 09:53 作者: 輕信 時(shí)間: 2025-3-25 13:12 作者: ALB 時(shí)間: 2025-3-25 17:29
Basics of Ocular Genetics do we have our father’s eyes or our mother’s nose? The answer lies in our chromosomes. Our 46 chromosomes are two sets of 23 chromosomes derived from each parent. One member of each 23 chromosomal pairs is inherited from the father and the other from the mother. Via this method the child has half t作者: 停止償付 時(shí)間: 2025-3-25 20:31 作者: outskirts 時(shí)間: 2025-3-26 01:22 作者: Hyperalgesia 時(shí)間: 2025-3-26 07:01
Cytomegalic Inclusion Diseaseis thought to result from maternal infection across the placenta or as the fetus passes through the birth canal. The infant usually has retinitis or choroiditis. The retinitis is a progressive one with extensive necrosis and hemorrhage. The vitritis that accompanies this disease is moderate, often m作者: Eosinophils 時(shí)間: 2025-3-26 11:27
Herpes Simplex retinitis, there can also be focal white infiltrates as well as heaping of the retinal pigment epithelium (RPE). Neurological disturbances are always present as a sequelae of the infection. The child may have a co-existing encephalitis. Treatment of these children is with intravenous acyclovir, whi作者: anesthesia 時(shí)間: 2025-3-26 16:32 作者: FLIT 時(shí)間: 2025-3-26 20:14
Rubella Retinopathyr signs, it is easy to determine the diagnosis. These patients have deafness and cataracts that are present at birth or develop postnatally. The lenses show persistent nucleated epithelial cells in the cortex. Other ocular signs are glaucoma (due to incomplete angle cleavage) and microphthalmos. Sys作者: CHIDE 時(shí)間: 2025-3-27 00:14
Toxocara CanisVLM) syndrome, is an important cause of blindness in children. The ocular component of VLM is called ocular larval migrans, or OLM. It is frequently mistaken for retinoblastoma. The larva is absorbed into the system from the small intestine of children who have been infected while playing with puppi作者: 來這真柔軟 時(shí)間: 2025-3-27 02:55 作者: Indebted 時(shí)間: 2025-3-27 06:36
Goldmann-Favre Syndromey the autosomal recessive modes, it is the only vitreoretinal degeneration inherited in such a fashion; the other forms of vitreoretinal degeneration are autosomal dominant and in one case X-linked. Although the condition is not seen frequently, it shares many aspects with X-linked retinoschisis (an作者: 無節(jié)奏 時(shí)間: 2025-3-27 13:09
Familial Exudative Vitreoretinopathyself. Usually the eye demonstrates temporal dragging of the retina, producing a loss of acuity over several weeks. Many cases have sub-retinal exudates, and a fluorescein angiogram can document the extensive peripheral nonperfusion present in almost 90% of the eyes. Other retinal signs are detachmen作者: 惡臭 時(shí)間: 2025-3-27 13:54 作者: intoxicate 時(shí)間: 2025-3-27 19:56 作者: NEXUS 時(shí)間: 2025-3-28 00:31
Basics of Pathologyility to fix presumes that you have an idea of how it works and what has happened to “break” it. Most residents do not appreciate the pathology laboratory until they have left their residency and usually try to take a comprehensive review course at some point in their career.作者: 尾隨 時(shí)間: 2025-3-28 02:08 作者: 新手 時(shí)間: 2025-3-28 08:59 作者: 疏遠(yuǎn)天際 時(shí)間: 2025-3-28 13:37 作者: consolidate 時(shí)間: 2025-3-28 17:42
https://doi.org/10.1007/978-1-4613-9320-7anatomy; eye; pathology; retina作者: amygdala 時(shí)間: 2025-3-28 20:19 作者: 改變立場(chǎng) 時(shí)間: 2025-3-29 02:33 作者: 性行為放縱者 時(shí)間: 2025-3-29 05:20
Verallgemeinerte Lineare Modelleatient, which takes advantage of the ophthalmologist’s full medical knowledge. There is no excuse for omitting the basics such as a good history of present illness, medical history, ocular history, review of systems, medications, and allergies. This general inquiry is then followed by a complete ocular examination.作者: 埋葬 時(shí)間: 2025-3-29 08:38 作者: STAT 時(shí)間: 2025-3-29 11:41
https://doi.org/10.1007/978-3-658-34710-9 noted within the first year of life, and the presenting problem is that the child has noted decreased central acuity. Because the gene for this anomaly is present on the X chromosome, daughters are carriers and 50% of their male siblings have the disease.作者: 是比賽 時(shí)間: 2025-3-29 16:35
,?rztliches Handeln als Straftat,commonly called the neural tube. Bilateral thickenings at the cephalic end of this tube are the beginnings of the eye. With further development the thickenings become optic pits and finally optic vesicles. The optic vesicle now harbors the cells needed to form an eye. The central portion gives rise 作者: 指令 時(shí)間: 2025-3-29 23:44 作者: 種子 時(shí)間: 2025-3-30 01:35
Verallgemeinerte Lineare Modelle do we have our father’s eyes or our mother’s nose? The answer lies in our chromosomes. Our 46 chromosomes are two sets of 23 chromosomes derived from each parent. One member of each 23 chromosomal pairs is inherited from the father and the other from the mother. Via this method the child has half t作者: 合法 時(shí)間: 2025-3-30 05:59 作者: 不能平靜 時(shí)間: 2025-3-30 09:34
Verallgemeinerte Lineare Modelleof the human who has ingested contaminated pork. Usually heat destroys the organism, but if the pork is insufficiently cooked the larvae survive and grow into adults. The infested human then discharges ova in the feces, which are again ingested by swine.作者: 是貪求 時(shí)間: 2025-3-30 14:21
Abwicklungsmuster und Schadenquotenis thought to result from maternal infection across the placenta or as the fetus passes through the birth canal. The infant usually has retinitis or choroiditis. The retinitis is a progressive one with extensive necrosis and hemorrhage. The vitritis that accompanies this disease is moderate, often m作者: Euthyroid 時(shí)間: 2025-3-30 19:24 作者: ciliary-body 時(shí)間: 2025-3-30 23:33
Modelle mit Korrelationsstrukturing the second decade of life, interstitial keratitis. Optic atrophy, vessel attenuation, and a peripheral “salt and pepper” fundus are the usual keys to this diagnosis. The fundal picture is often mistaken for retinitis pigmentosa. Systemic findings include Hutchinson’s teeth (pointed incisors), a 作者: LATHE 時(shí)間: 2025-3-31 02:28
Verallgemeinerungen des kollektiven Modellsr signs, it is easy to determine the diagnosis. These patients have deafness and cataracts that are present at birth or develop postnatally. The lenses show persistent nucleated epithelial cells in the cortex. Other ocular signs are glaucoma (due to incomplete angle cleavage) and microphthalmos. Sys作者: fibula 時(shí)間: 2025-3-31 05:12
8 Daten und TarifierungsstatistikenVLM) syndrome, is an important cause of blindness in children. The ocular component of VLM is called ocular larval migrans, or OLM. It is frequently mistaken for retinoblastoma. The larva is absorbed into the system from the small intestine of children who have been infected while playing with puppi作者: 會(huì)議 時(shí)間: 2025-3-31 12:04 作者: Corporeal 時(shí)間: 2025-3-31 14:49
8 Daten und Tarifierungsstatistikeny the autosomal recessive modes, it is the only vitreoretinal degeneration inherited in such a fashion; the other forms of vitreoretinal degeneration are autosomal dominant and in one case X-linked. Although the condition is not seen frequently, it shares many aspects with X-linked retinoschisis (an作者: FEMUR 時(shí)間: 2025-3-31 20:01
