WordNet

a pattern of symptoms indicative of some disease
a complex of concurrent things; "every word has a syndrome of meanings"
German electrical engineer (1816-1892) (同)Ernst Werner von Siemens
engineer who was a brother of Ernst Werner von Siemens and who moved to England (1823-1883) (同)Karl Wilhelm Siemens, Sir Charles William Siemens

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1. 表皮水疱症のマネージメントの概要 overview of the management of epidermolysis bullosa
2. 表皮水疱症の疫学、病因、分類、および臨床的特徴 epidemiology pathogenesis classification and clinical features of epidermolysis bullosa
3. 新生児における小水疱性および膿疱性の病変 vesiculobullous and pustular lesions in the newborn
4. 表皮水疱症の診断 diagnosis of epidermolysis bullosa
5. 皮膚扁平上皮癌の治療および予後 treatment and prognosis of cutaneous squamous cell carcinoma

Medenica L1, Lens M.
Dermatology online journal.Dermatol Online J.2008 Mar 15;14(3):2.
Dystrophic epidermolysis bullosa (DEB) and aplasia cutis congenita (ACC), also known as congenital localized absence of skin (CLAS) are rare clinical entities. Aplasia cutis congenita presented in conjunction with simplex, junctional, or dystrophic types of epidermolysis bullosa (EB) is classified a
PMID 18627704

[Epidermolysis bullosa dystrophica (Hallopeau-Siemens syndrome) of the hand -- surgical strategy and results].

Diedrichson J1, Talanow D, Safi A.
Handchirurgie, Mikrochirurgie, plastische Chirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft für Handchirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft für Mikrochirurgie der Peripheren Nerven und Gefässe : Organ der Vereinigung der Deutschen Plastischen Chirurgen.Handchir Mikrochir Plast Chir.2005 Oct;37(5):316-22.
Dystrophic epidermolysis bullosa is an inherited, blister-forming skin disease. The Hallopeau-Siemens syndrome type is one of the most severe forms. Even minimal trauma to the skin leads to excessive blister formation that always heals with scars because the defect is located in the dermis at the de
PMID 16287016

[Recessive dystrophic epidermolysis bullosa (Hallopeau-Siemens) with IgA nephropathy: 4 cases].

Farhi D1, Ingen-Housz-Oro S, Ducret F, Rioux-Leclercq N, Cam G, Simon P, Martinez F, Fumeron C, Dubertret L, Blanchet-Bardon C.
Annales de dermatologie et de vénéréologie.Ann Dermatol Venereol.2004 Nov;131(11):963-7.
BACKGROUND: The Hallopeau-Siemens type of recessive dystrophic epidermolysis bullosa (HS-RDEB) is a severe hereditary dermatosis, associated with a collagen VII deficiency. A chronic inflammatory syndrome, secondary to recurrent cutaneous infections, may be the cause of AA amyloidosis, with chronic
PMID 15602383