不能平静
发表于 2025-3-30 09:34:35
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.
是贪求
发表于 2025-3-30 14:21:10
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
Euthyroid
发表于 2025-3-30 19:24:13
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ciliary-body
发表于 2025-3-30 23:33:57
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
LATHE
发表于 2025-3-31 02:28:59
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
fibula
发表于 2025-3-31 05:12:24
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
会议
发表于 2025-3-31 12:04:48
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Corporeal
发表于 2025-3-31 14:49:23
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
FEMUR
发表于 2025-3-31 20:01:53
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