• Communications of the Korean Mathematical Society
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• v.8 no.2
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• pp.239-246
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• 1993

• Journal of the korean veterinary medical association
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• v.15 no.1112
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• pp.551-558
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• 1979

• BMB Reports
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• v.31 no.1
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• pp.2-19
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• 1998

• 대한약리학회:학술대회논문집
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• 2006.10a
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• pp.118.1-118.1
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• 2006

• Clinical and Experimental Pediatrics
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• v.63 no.1
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• pp.18-19
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• 2020

• Maxillofacial Plastic and Reconstructive Surgery
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• v.11 no.1
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• pp.231-236
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• 1989

Angioneurotic edema is rarely seen in dental practice and manifested by acute attacks of swelling of the extremities, face, airway, or abdominal visera, occuring spontaneously and suddenly or secondary to trauma. Two types are recognized : hereditary and nonhereditary. Prophylatic therapy may be used by fresh frozen plasma or antifibrinolytic agents in hereditary type. Good supportive care for acute attacks, together with a knowledge of course of the disease, can prevent asphyxiation from airway obstruction. A case of acute angioneurotic edema of the facial area in a 19-year-old man is presented in conjunction with a review of the literature. Angioneurotic edema attacks him acutely after the extraction of the lower, right 3rd molar.

• Journal of Genetic Medicine
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• v.4 no.2
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• pp.115-121
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• 2007

Hereditary motor and sensory neuropathy (HMSN; Charcot-Marie-Tooth disease, CMT) was first described by Charcot and Marie in France and, independently, by Tooth in England in 1886. HMSN is the most common form of inherited motor and sensory neuropathy, and is a genetically heterogeneous disorder of the peripheral nervous system. Using positional cloning methods, the chromosomal localization (locus) of more than 40 inherited peripheral neuropathies was found in the last 15 years. However, these genetic analyses also show that many entities do not show linkage to the known loci. This issue deals with a clinical survey of inherited peripheral neuropathies regarding diagnostic approaches based on the molecular findings.

• Bulletin of the Korean Mathematical Society
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• v.47 no.4
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• pp.715-726
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• 2010

We continue the study of fully idempotent rings initiated by Courter. It is shown that a (semi)prime ring, but not fully idempotent, can be always constructed from any (semi)prime ring. It is shown that the full idempotence is both Morita invariant and a hereditary radical property, obtaining $hs(Mat_n(R))\;=\;Mat_n(hs(R))$ for any ring R where hs(-) means the sum of all fully idempotent ideals. A non-semiprimitive fully idempotent ring with identity is constructed from the Smoktunowicz's simple nil ring. It is proved that the full idempotence is preserved by the classical quotient rings. More properties of fully idempotent rings are examined and necessary examples are found or constructed in the process.

• Bulletin of the Korean Mathematical Society
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• v.46 no.5
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• pp.867-871
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• 2009

A module M over a ring R is said to satisfy (P) if every generating set of M contains an independent generating set. The following results are proved; (1) Let $\tau$ = ($\mathbb{T}_\tau,\;\mathbb{F}_\tau$) be a hereditary torsion theory such that $\mathbb{T}_\tau$ $\neq$ Mod-R. Then every $\tau$-torsionfree R-module satisfies (P) if and only if S = R/$\tau$(R) is a division ring. (2) Let $\mathcal{K}$ be a hereditary pre-torsion class of modules. Then every module in $\mathcal{K}$ satisfies (P) if and only if either $\mathcal{K}$ = {0} or S = R/$Soc_\mathcal{K}$(R) is a division ring, where $Soc_\mathcal{K}$(R) = $\cap${I 4\leq$ $R_R$ : R/I$\in\mathcal{K}$}.

• The Journal of Korean Medicine Ophthalmology and Otolaryngology and Dermatology
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• v.19 no.3 s.31
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• pp.224-231
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• 2006

Retinitis pigmentosa(RP) is characterized by night-blindness, contraction of the visual field, distinct hereditary nature, wide-spread pigmentary in the midperiphery. We have experienced a case of retinitis pigmentosa treated by oriental medicine (Herbal medicaiton, Acupuncture & Electroacupuncture therapy). In the point of Differentiation of syndrome, this subject was diagnosed deficiency of both Gi & blood and Eum deficiency of Liver and Kidney. So we was administrated with Palmultang-Gamibang. After treatment of orient medicine, symptoms of patient were improved.