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Additional Comments on 'Clinical Trial to Evaluate the Efficacy and Safety of a Home-use Intense Pulsed Light Device for Hair Removal, Treatment of Acne and Pigmentation Disorders, and Fine Wrinkle Reduction'

Min S, Kwon HH, Park SY, Yoon JY, Suh DH

  • KMID: 2246265
  • Korean J Dermatol.
  • 2015 Jan;53(1):88-88.
No abstract available.
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Intra-Articular Pigmentation of Synovium: An Unusual Cause

Verma S, Hamilton S, Liew SM

An unusual grayish brown discoloration of the synovium was found during a knee arthroscopy of a 72-year-old man. He also had similar pigmentation affecting the skin on the legs, arms,...
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Acquired Brachial Cutaneous Dyschromatosis in a Middle Aged Male

Choi MJ, Byun JY, Choi HY, Choi YW

Acquired brachial cutaneous dyschromatosis (ABCD) is an acquired disorder of pigmentary change that presents as chronic, asymptomatic, geographic-shaped, gray-brown patches, consisting of mixed hyper and hypopigmented macules on the dorsal...
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A Case of Reticulate Acropigmentation of Dohi Presented on the Trunk

In SI, Kim YC

  • KMID: 1771556
  • Korean J Dermatol.
  • 2008 Aug;46(8):1108-1111.
Reticulate acropigmentation of Dohi is a rare dyschromic disorder that has an autosomal dominant pattern of inheritance. It presents generally during infancy or early childhood as symmetrical pinpoint to pea-sized...
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A Case of Incontinentia igmenti Achromians ( Ito )

Lee JB, Kim WJ, Kim JY

  • KMID: 1664488
  • Korean J Dermatol.
  • 1975 Mar;13(1):41-43.
Incontinentia pigmenti achromians (Ito) begins during childhood and is characterized by progressive appearance of bizarre patchy or whorl-like hypopigmentation without any preceeding or associated inflammatory changes in a fashion that...
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Hypomelanosis of Ito with Multiple Congenital Anomalies

Yu DA, Kwon O, Kim KH

Hypomelanosis of Ito (HI) is a neurocutaneous disorder, also known as incontinentia pigmenti achromians. HI has been associated with chromosomal abnormalities, especially mosaicism. Herein, we report a case of HI...
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A Case of Dyschromatosis Universalis Hereditaria Treated with a Q-switched Nd:YAG Laser

Kim DH, Kwon H, Park YL, Lee S, Whang KU, Cho MK, Lee JS, Lee SY

  • KMID: 2301946
  • Korean J Dermatol.
  • 2009 Oct;47(10):1166-1171.
Dyschromatosis universalis hereditaria is a rare pigmentary disorder that's characterized by the presence of both small and irregular sized hyperpigmented and hypopigmented macules in a generalized distribution. The pattern of...
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Carney Complex with Multiple Intracranial Aneurysms

Gwak YJ, Kim HJ, Baik SK, Kang DS

Carney complex is an autosomal dominant disease that displays such characteristic features as cardiac and cutaneous myxomas and spotty pigmentation of the skin. We report here on a case of...
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Generalized Schamberg Disease in a Child

Park JH, Kang HY

No abstract available.
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A Case of Dohi Presenting with Diffuse Pigmented Patch on Both Dorsum of Hands

Kim SM, Oh BH, Lee YW, Choe YB, Ahn KJ, Song KY

  • KMID: 2248298
  • Korean J Dermatol.
  • 2008 May;46(5):652-655.
Reticulated acropigmentation of Dohi (RAD), dyschromatosis symmetrica hereditaria, is the localized acral form of dyschromatosis universalis hereditaria that has an autosomal dominant pattern of inheritance. RAD is characterized by the...
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A Case of Post-Herpetic Nevoid Comedones

Seo JK, Jeong KH, Shin MK

No abstract available.
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A Case of Post-Herpetic Nevoid Comedones

Seo JK, Jeong KH, Shin MK

No abstract available.
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Congenital Dermal Melanocytosis on the Foot: A Case Report and Review of the Literature

Cho SI, Moon J, Jo G, Lee C, Mun JH

Dermal melanocytosis is a common pigmented skin disease, characterized by an increased number of ectopic melanocytes in the dermis. Rare variants of dermal melanocytosis that do not belong to these...
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Clinical Trial to Evaluate the Efficacy and Safety of a Home-use Intense Pulsed Light Device for Hair Removal, Treatment of Acne and Pigmentation Disorders, and Fine Wrinkle Reduction

Min S, Kwon HH, Park SY, Yoon JY, Suh DH

  • KMID: 2301531
  • Korean J Dermatol.
  • 2014 Dec;52(12):880-891.
BACKGROUND: Home-use devices designed for cosmetic purposes have recently gained popularity. Small, low-energy, low-cost intense pulsed light (IPL) systems provide safe, convenient, and private treatment for several medical conditions. OBJECTIVE: In...
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A Case of Acquired Dermal Melanocytosis showing the Manifestations of Bilateral Variant of Nevus of Ito

Lee JH, Kim MY, Park YM, Kim HO

  • KMID: 2302863
  • Korean J Dermatol.
  • 2004 Aug;42(8):1042-1044.
There are a number of pigmentation disorders due to dermal melanocytes, including Mongolian spot, nevus of Ota, nevus of Ito and blue nevus, which usually appear at birth or in...
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A quantitative evaluation of pigmented skin lesions using the L*a*b* color coordinates

Kim SC, Kim DW, Hong JP, Rah DK

The evaluation of pigmentary skin lesions by clinical doctors has been based on subjective and qualitative judgements. Observations have mostly relied on visual inspection, making the effects of treatment difficult...
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Clinical and Laboratory Findings of Pigmented Purpuric Dermatoses

Gonul M, Kulcu Cakmak S, Ozcan N, Oguz ID, Gul U, Biyikli Z

BACKGROUND: Pigmented purpuric dermatoses (PPD) are chronic, recurrent group of disorders characterized by petechial and pigmentary macules usually localized on the lower limbs. Its etiopathogenesis is unknown. There are very...
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Proposal of the New Term 'Leukoderma Nuchae' to Describe the Whitish Patch in the Spared Zone of Poikiloderma of Civatte to Differentiate It from Vitiligo

Moon KR, Yun SJ, Lee JB, Kim SJ, Won YH, Lee SC

  • KMID: 2350773
  • Korean J Dermatol.
  • 2016 Aug;54(7):566-570.
Poikiloderma of Civatte (PC) is a common, acquired condition that affects the face, neck, and upper chest of elderly persons due to life-long sun exposure. Poikiloderma describes skin manifestations of...
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A case of generalized argyria presenting with muscle weakness

Jung I, Joo EJ, Suh BS, Ham CB, Han JM, Kim YG, Yeom JS, Choi JY, Park JH

BACKGROUND: Argyria is a rare irreversible cutaneous pigmentation disorder caused by prolonged exposure to silver. Herein, we report a case of generalized argyria that developed after chronic ingestion of soluble...
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Incontinentia Pigmenti Achromians ( Ito ): Report of two cases

Kim SU, Cho CK

  • KMID: 2231795
  • Korean J Dermatol.
  • 1976 Mar;14(1):81-85.
Incontinentia pigmenti acb.romians(Ito) is characterized by progressive bizarre or whorl-like hypopigmentation on trunk and extrementies during childhood. It is similar to a negative picture of incontinentia pigmenti(Blocb-Sulzberger) and not infrequently...
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