hushu-doctor-oh

Dr. Sewoong Oh

About Dr. Sewoong Oh

Director of Cheonho Branch

  • Licensed Dermatologist 
  • Former Director of Leaders Skin Group, Dogok Branch
  • Chief of Dermatology Dept., Daejeon Army Hospital
  • Completed Internship & Residency at Yonsei Severance Hospital
  • M.Med at School of Medicine, Yonsei University
  • Member, Korean Dermatological Association
  • Member, the Association of Korean Dermatologists
  • Member, the Korean Hair Research Society
  • Member, the Korean Society of Hair Restoration Surgery
  • Member, Korean Acne Care Association
  • Member, the Korean Atopic Dermatitis Association
  • Member, Korean Association of Stemcell Therapy
  • Member, Korean Society of Aesthetic Surgery
  • Director of Research, Best Stemcell Research Association
  • Completed the whole course of Pacific Health Education Center
  • Research fellow, Gene Therapy Div., Dermatology Dept., Osaka University

Days

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  2012 Korean Medical Society for Cosmetics

– Roles of cosmetics in pigmentation treatment and Management

 

 2012 International Society of Aesthetic Plastic Surgery, Geneva, Swiss

– SCAFFOLD THREAD LIFITING WITH CELLUAR MATERIALS

 2007 the 21st World Congress of Dermatology, Buenos Aires, Argentina

– Novel keratin 5 mutations in epidermolysis bullosa simplex

– COL7A1 Mutational Analysis in Korean Patients with Dystrophic Epidermolysis Bullosa

 2007 the 15th Korea-Japan Joint Meeting of Dermatology, Jeju, Korea

– Polypoid eccrine nevus

– Dilated cardiomyopathy in dystrophic epidermolysis bullosa: a case of a novel mutation

 2007 the 59th Spring Seminar, Korean Dermatological Association

– A clinical case of milia en plaque

– A clinical case of papillomavirus

 2007 the 17th Conference of Dermatology Research Association

– Novel keratin 5 mutation in epidermolysis bullosa simplex

 2006 the 5th Korea-China International Conference of Dermatology and Mycology, Seoul, Korea

– Dilated cardiomyopathy in dystrophic epidermolysisbullosa: a case of a novel mutation

 2006 the 58th Spring Seminar, Korean Dermatological Association

– A clinical case of indeterminate cell histiocytosis

– A clinical case of dilated cardiomyopathy in a child patient with dystrophic epidermolysis bullosa 

 2006 the 16th Conference of Dermatology Research Association

– Schematic representation of type VII collagen domain orgazination

– COL7A1 mutation analysis in Korean patients with dystrophic epidermolysis bullosa

 2005 14th EADV Annual Congress, London, UK

– Keratin 17 mutation in pachyonychia congenita type 2 with early onset steatocystoma multiplex and Hutchinson-like tooth deformity

 2005 the 14th Korea-Japan Joint Meeting of Dermatology, Kumamoto, Kyushu, Japan

– Keratin 17 mutation in pachyonychia congenita type 2 with early onset steatocystoma multiplex and Hutchinson-like tooth deformity

 2005 the 57th Spring Seminar, Korean Dermatological Association

– A case of hypotrichosis simplex of the scalp

– A case of basal cell carcinoma of the vulva

– A case of psoriasis improved by Etanercept

– A case of actinic granuloma

– A case of Wegener’s granulomatosis with severe skin necrosis

– A case of psoriasis improved by Infliximab

 2004 the 56th Fall Seminar, Korean Dermatological Association

– New Keratin 5 mutation in Koebner type epidermolysis bullosa simplex 

– A clinical study of Eruptive pseudoangiomatosis

– A statistical study of dermatosis in Gangnam area of Seoul (1996~2003)

 2004 the 22nd Contact Dermatitis and Allergy Symposium

– Skin irritation caused by friction of melamine foam

– Erythema multiforme caused by Acetaminophen patch test

 New Keratin 5 mutation in Koebner type epidermolysis bullosa simplex. 
  The Korean Society for Investigative Dermatology Journal 2004;11(4) 97-100
 Erythema multiforme induced by acetaminophen: a recurrence at distant sites following patch testing 
  Contact Dermatitis 53:56-7, 2005
 Genotype-phenotype correlation in recessive dystrophic epidermolysis bullosa
  : when missense doesn’t make sense.
  J. Invest Dermatol. 124:863-6, 2005
 Two cases of Eruptive pseudoangiomatosis 
  The Korean Society for Investigative Dermatology Journal 2006;44(1):91-93
 Wegener’s granulomatosis with severe skin necrosis 
  The Korean Society for Investigative Dermatology Journal 2006;44(7):892-895
 A case of hypotrichosis simplex of the scalp 
  The Korean Society for Investigative Dermatology Journal 2006;44(2):212-215
 Keratin 17 mutation in Pachyonychiacongenita type 2 with early onset steatocystoma multiplex 
  and Hutchinson-like tooth deformity 
   J. Dermatol. 2006;3:161-164
 Recessive dystrophic epidermolysisbullosa associated with dilated cardiomyopathy
  Br J Dermatol. 2007;157:610-2.
 Coccygeal polypoideccrinenaevus 
  Br J Dermatol 2007;157(3):614-5 / Br J Dermatol 2007;157:610-2.
 Novel keratin 5 mutations in epidermolysisbullosa simplex: Cases with unusual genotype –phenotype
  correlation. 
  J Dermatol Sci 48(3):229-32
 COL7A1 mutational analysis in Korean patients with dystrophic epidermolysisbullosa
  Br J Dermatol. 2007;157(6):1260-4
 A case of milla en plaque treated with modified Rhomboid transposition flap milla en plaque
  The Korean Society for Investigative Dermatology Journal 2007:45(11) 1227~1229
 Miliary Osteoma Cutis on the Jaw 
  The Korean Society for Investigative Dermatology Journal  2008;46(2)289-291
 A novel homozygous keratin 14 mutation in a patient with autosomal recessive epidermolysis bullosa
  simplex and squamous cell carcinoma of the tongue. 
  Br J Dermatol. 2010 Apr;162(4):880-2 
 Novel and recurrent mutations in Keratin 5 & 14 in Korean patients with Epidermolysis bullosa simplex 
   J Dermatol Sci. 2010 Feb;57(2):90-4.
 Filaggrin mutation c.3321delA in a Korean patient with ichthyosis vulgaris and atopic dermatitis
  Dermatology 2009;218(2):186-7
 Compound heterozygosity for a premature termination codon and missense mutation in the exon 10
  of the uroporphyrinogen III cosynthase gene causes a severe phenotype of congenital erythropoietic
  porphyria
  J Eur Acad Dermatol Venereol. 2009 Apr;23(4):470-1
 
  Novel deletion mutation (c.3717del5) in COL7A1 in a patient with recessive dystrophic epidermolysis bullosa.
  The Journal of Dermatology 2012;39:1-2
  Mild phenotype of epidermolytic hyperkeratosis mimicking ichthyosis bullosa of Siemens is related to specific

   mutation in 2B domain of KRT1.

  Journal of Dermatological Science 2013, 70 : 220–225
 
•  Cosmeceuticals: A Treatment tool of Hyperpigmentation
   Journal of Korean Medical Society for Cosmetics 2013;2(1):1~4