Indexed keywords
CORTICOSTEROID;
SULFADIAZINE SILVER;
ARTICLE;
CASE REPORT;
CONSERVATIVE TREATMENT;
EPIDERMOLYSIS BULLOSA;
FEMALE;
HUMAN;
NEWBORN;
PRIORITY JOURNAL;
SKIN APLASIA;
SPLIT THICKNESS SKIN GRAFT;
TREATMENT FAILURE;
WOUND DRESSING;
ANTI-INFECTIVE AGENTS, LOCAL;
ECTODERMAL DYSPLASIA;
EPIDERMOLYSIS BULLOSA ACQUISITA;
FEMALE;
FOOT DERMATOSES;
HUMANS;
INFANT, NEWBORN;
SILVER SULFADIAZINE;
THIGH;
2
0013887060
Congenital absence of skin and associated abnormalities resembling epidermolysis bullosa
Bart BJ, Gorlin RJ, Anderson VE, et al. Congenital absence of skin and associated abnormalities resembling epidermolysis bullosa. Arch Dermatol 1966;93:296-304
(1966)
Arch Dermatol
, vol.93
, pp. 296-304
Bart, B.J.1
Gorlin, R.J.2
Anderson, V.E.3
3
0014095405
Hereditary epidermolysis bullosa
Lowe LB. Hereditary epidermolysis bullosa. Arch Dermatol 1967;95:587-595
(1967)
Arch Dermatol
, vol.95
, pp. 587-595
Lowe, L.B.1
4
0014709377
Epidermolysis bullosa and congenital localized absence of skin
Bart BJ. Epidermolysis bullosa and congenital localized absence of skin. Arch Dermatol 1970;101:78-81
(1970)
Arch Dermatol
, vol.101
, pp. 78-81
Bart, B.J.1
5
0001174831
Hereditary epidermolysis bullosa with special emphasis on newly recognized syndromes and complications
Briggaman R. Hereditary epidermolysis bullosa with special emphasis on newly recognized syndromes and complications. Dermatol Clin 1983;1(2):263-280
(1983)
Dermatol Clin
, vol.1
, Issue.2
, pp. 263-280
Briggaman, R.1
6
0018599220
Congenital localized skin defect and epidermolysis bullosa hereditaria lethalis
Skoren L, Drzewieckil K. Congenital localized skin defect and epidermolysis bullosa hereditaria lethalis. Acta Dermatol Venereol (Stockh) 1979;59:533-537
(1979)
Acta Dermatol Venereol (Stockh)
, vol.59
, pp. 533-537
Skoren, L.1
Drzewieckil, K.2
7
84980067998
Kongenitaler, nicht syphilitischer pemphigus
Herlitz C. Kongenitaler, nicht syphilitischer pemphigus. Acta Paediatr 1935;17:315-371
(1935)
Acta Paediatr
, vol.17
, pp. 315-371
Herlitz, C.1
8
0018971047
Acquired double-barrel esophagus in epidermolysis bullosa dystrophica
Warren R, Warner T, Gilbert E, et al. Acquired double-barrel esophagus in epidermolysis bullosa dystrophica. Thorax 1980;35:472-476
(1980)
Thorax
, vol.35
, pp. 472-476
Warren, R.1
Warner, T.2
Gilbert, E.3
9
0015539256
Epidermolysis bullosa dystrophica dominans in two families in the Faroe Islands
Joensen HD. Epidermolysis bullosa dystrophica dominans in two families in the Faroe Islands. Acta Dermatol Venereol (Stockh) 1973;53:53-60
(1973)
Acta Dermatol Venereol (Stockh)
, vol.53
, pp. 53-60
Joensen, H.D.1
10
0344899231
Recessive epidermolysis bullosa dystrophica with congenital localized absence of skin: Bart's syndrome
Wojnarowska F, Eady R, Wells R. Recessive epidermolysis bullosa dystrophica with congenital localized absence of skin: Bart's syndrome. Br J Dermatol 1981;105:94-95
(1981)
Br J Dermatol
, vol.105
, pp. 94-95
Wojnarowska, F.1
Eady, R.2
Wells, R.3
11
0017808183
A mechanobulbous disease of the new born. Dart's syndrome
Smith S. A mechanobulbous disease of the new born. Dart's syndrome. Arch Dermatol 1978;114:81-84
(1978)
Arch Dermatol
, vol.114
, pp. 81-84
Smith, S.1
12
0020664556
Aplasia cutis congenita of neck and shoulder requiring a skin graft: A case report
Bailie FB. Aplasia cutis congenita of neck and shoulder requiring a skin graft: a case report. Br J Plast Surg 1983;36:72-74
(1983)
Br J Plast Surg
, vol.36
, pp. 72-74
Bailie, F.B.1