- Localized Epidermolysis Bullosa Acquisita Limited to the Face
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Lee MH, Yoo JY, Song YB, Suh MK, Jang TJ, Kim SC
- KMID: 2246465
- Korean J Dermatol.
- 2013 Dec;51(12):990-991.
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- Epidermolysis Bullosa Acquisita: A Complete Remissions versus Patients with Long-term Persistent Activities
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Hwang DK, Lee CW
- KMID: 2303367
- Korean J Dermatol.
- 1999 Jun;37(6):715-718.
BACKGROUND: In epidermolysis bullosa acquisita, it has been recognized that there exists heterogeneity in the clinical and serologic/immunopathologic features. OBJECTIVE: We examined patients with epidermolysis bullosa acquisita to see if... -
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- A Case of Recessive Epidermolysis Bullosa Dystrophica
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Kim YT, Kim HW, Oh SH, Moon SJ, Park CK
- KMID: 1683520
- J Korean Pediatr Soc.
- 1990 Aug;33(8):1111-1116.
No abstract available. -
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- A Case of Epidermolysis Bullosa Dystrophica
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Hwang SY, Han JS, Jung GS, Kim SW, Hyun K, Chi CH
- KMID: 1677121
- J Korean Pediatr Soc.
- 1987 Sep;30(9):1049-1054.
No abstract available. -
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- A Case of Epidermolysis Bullosa Letalis
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Lee ST, Han CH, Kim SY, Lee JK, Kwon YD, Bae HI
- KMID: 1677068
- J Korean Pediatr Soc.
- 1987 Jul;30(7):818-825.
No abstract available. -
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- A Case of Epidermolysis Bullosa Dystrophica Dominant Associated with Megacolon
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Hwang YH, Park SS, Han HK, Kook HI
- KMID: 1969496
- Ewha Med J.
- 1981 Mar;4(1):23-28.
- doi: 10.12771/emj.1981.4.1.23
No abstract available in English. -
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- Pretibial Epidermolysis Bullosa with Nail Dystrophy in a Family
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Kwon NH, Kim JE, Park HJ, Cho BK
- KMID: 2301872
- Korean J Dermatol.
- 2010 Jul;48(7):606-610.
Dominant dystrophic epidermolysis bullosa-pretibial (DDEB-Pt) is an extremely rare subtype of dominant dystrophic epidermolysis bullosa (DDEB). Clinically, DDEB-Pt is characterized by trauma-induced blistering with scarring that predominantly affects the pretibial... -
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- A Possible Case of Epidermolysis Bullosa Simplex with Mottled Pigmentation
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Juhn BJ, Lee MH
- KMID: 1863735
- Korean J Dermatol.
- 2000 Mar;38(3):413-416.
Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) is a rare subtype of EBS and characterized by blistering of the skin, mottled pigmentation, and palmoplantar hyperkeratosis. We report a 3-year-old boy with mottled... -
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- Dominant Dystrophic Epidermolysis Bullosa
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Lee HJ, Jung YJ, Kim JH, Hong H, Choi EH
- KMID: 2247681
- Korean J Dermatol.
- 2010 Oct;48(10):889-892.
Dystrophic epidermolysis bullosa is a rare, chronic non-inflammatory bullous disease with a hereditary pattern of occurrence, and this disease easily produces bullae that heal with scarring and milium formation. A... -
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- A Case of Epidermolysis Bullosa Dystrophica Dominant
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Jung MJ, Lee JS, Kim YK
- KMID: 1681242
- Korean J Dermatol.
- 1994 Jun;32(3):518-522.
Epidermolysis bullosa dystrophica is rare, chronic non-inflammtory mechanobullous disease of hereditary trait, which easily produces bullae by minor trauma or sponta neosly. A 1-day old male neonate presented wide spread... -
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- A Case of Epidermolysis Bullosa Herpetiformis
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Kim BS, Im DJ, Yoon HS, Park SJ, Kim KS, Pi SY, Koh JK, Kim EA
- KMID: 1898303
- J Korean Soc Neonatol.
- 1997 Nov;4(2):253-259.
Epidermolysis bullosa (EB) is a rare inherited disease characterized by vesiculobullous lesion that arise in response to minimal trauma or shearing force to the skin. Epiderrnolysis bullosa herpetiformis-Dowling Meara, a... -
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- A Case of Koebner Variant of Epidermolysis Bullosa Simplex
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Lim SJ, Jung SP, Lim IS, Lee DK, Yoo BH
- KMID: 1838675
- J Korean Soc Neonatol.
- 2001 May;8(1):166-170.
Epidermolysis bullosa simplex (EBS), characterized by a cleavage plane through basal keratinocytes, is caused by a mutation of the genes encoding keratin 5 and 14. It is often regarded as... -
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- A Case of Epidermolysis Bullosa Acquisita
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Lee SC, Lee JY, Kim YH, Kim CW
- KMID: 2361754
- Ann Dermatol.
- 1992 Jul;4(2):120-123.
- doi: 10.5021/ad.1992.4.2.120
We report a case of epidermolysis bullosa acqumta with characteristic clinical features, subepidermal vesicles in histopathology, and deposits of IgG in basement membrane zone at routine direct immunofluorescent test. 1M NaCl-treated... -
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- A Case of Epidermolysis Bullosa Dystrophica
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Oh S, Lim SC, Han EN, Kim NI, Haw CR
- KMID: 1679275
- Korean J Dermatol.
- 1985 Jun;23(3):387-391.
Epidermolysis bullosa dystrophica(EBD) is a rare, hereditary and chronic mechanobullous disease characterized by blistering and erosions of the skin in response to even minor trauma. A 5-year old girl visited... -
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- Dystrophic Epidermolysis Bullosa in Two Sisters
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Ahn BJ, Jang HC, Kim SW, Han CD
- KMID: 2072003
- Korean J Perinatol.
- 1999 Dec;10(4):485-489.
Dystrophic epidermolysis bullosa is a rare, chronic non-inflammatory bullous disease, which easily forms bullae by minor mechanical trauma or spontaneously, is inherited either in an autosomal dominant or autosomal recessive... -
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- A Case of Epidermolysis Bullosa Dystrophica
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Lee NH, Hyun JM, kim JT
- KMID: 2039172
- Korean J Dermatol.
- 1977 Sep;15(3):327-331.
A case of Epidermolysis Bullosa Dystrophica is reported with review of pathogenesis with literatures. Epidermolysis Bulloaa Dystrophica is a rare genetic disease which is characterized by the formation of blister... -
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- A Case of Pyloric Atresia Associated with Epidermolysis Bullosa
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Son MK, Lee TK, Choeh HJ, Choeh K
- KMID: 1747740
- J Korean Pediatr Soc.
- 1996 Jul;39(7):1015-1019.
We have experienced a case of congenital pyloric atresia associated with epidermolysis bullosa in a premature newborn who was born at the gestation period of 33+3 week. She showed a... -
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- Anesthetic Management in Patients with Epidermolysis Bullosa Dystrophica
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Ko HJ, Shin OY, Kang WJ, Hong SP
- KMID: 2237825
- Korean J Anesthesiol.
- 1996 Jan;30(1):104-107.
- doi: 10.4097/kjae.1996.30.1.104
Epidermolysis bullosa dystrophica is rare, chronic non-inflammatory disease of hereditary trait, which easily ptoduces bullae spontaneously or by heat and minor trauma such as pressure or friction. We present two... -
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- A Case of Epidermolysis Bullosa Simplex ( Dowling - Meara Type )
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Chang SN, Kim SC
- KMID: 2085755
- Korean J Dermatol.
- 1994 Aug;32(4):735-739.
The Dowling-Meara type of epidermolysis bullosa simplex(EBS) is genetic disease that is transmitted as an autosomal dominant trait and is charscterized clinically by pherpetiform clustering of blisters and palmo-plantar keratoderma.... -
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- Congenital Pyloric Atresia with Junctional Epidermolysis Bullosa: a case report
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Cho MH, Han SJ
- KMID: 2422272
- J Korean Assoc Pediatr Surg.
- 1997 Jun;3(1):77-82.
- doi: 10.13029/jkaps.1997.3.1.77
The association of pyloric atresia and epidermolysis bullosa(EB) in newborn is rare and inheritant as an autosomal recessive trait. We report a newborn girl with pyloric atresia and epidermolysis bullosa.... -
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