-
1
-
-
84888705039
-
Disorders of keratinization
-
In Burns T. Breathnach S. Cox N. Griffiths C. eds. 8th edn. Wiley-Blackwell, West Sussex.
-
Judge MR, McLean WHI, Munro CS,. Disorders of keratinization. In, Burns T, Breathnach S, Cox N, Griffiths C, eds. Rook's Textbook of Dermatology, 8th edn. Wiley-Blackwell, West Sussex, 2010: 19.66-19.69.
-
(2010)
Rook's Textbook of Dermatology
, pp. 1966-1969
-
-
Judge, M.R.1
McLean, W.H.I.2
Munro, C.S.3
-
3
-
-
0023271916
-
Peeling skin syndrome: A clinical, ultrastructural and biochemical study
-
DOI 10.1111/j.1365-2133.1987.tb05799.x
-
Mevorah B, Frenk E, Saurat JH, Siegenthaler G,. Peeling skin syndrome: a clinical, ultrastructural and biochemical study. Br J Dermatol 1987; 116: 117-125. (Pubitemid 17216813)
-
(1987)
British Journal of Dermatology
, vol.116
, Issue.1
, pp. 117-125
-
-
Mevorah, B.1
Frenk, E.2
Saurat, J.H.3
Siegenthaler, G.4
-
4
-
-
0028347941
-
Skin peeling syndrome
-
Tolat SN, Gharpuray MB,. Skin peeling syndrome. Cutis 1994; 53: 255-257. (Pubitemid 24146818)
-
(1994)
Cutis
, vol.53
, Issue.5
, pp. 255-257
-
-
Tolat, S.N.1
Gharpuray, M.B.2
-
6
-
-
0033674338
-
Acral peeling skin syndrome
-
Hashimoto K, Hamzavi I, Tanaka K, Shwayder T,. Acral peeling skin syndrome. J Am Acad Dermatol 2000; 43: 1112-1119.
-
(2000)
J Am Acad Dermatol
, vol.43
, pp. 1112-1119
-
-
Hashimoto, K.1
Hamzavi, I.2
Tanaka, K.3
Shwayder, T.4
-
7
-
-
33847770555
-
Facial peeling skin syndrome: A case report and a brief review
-
DOI 10.1111/j.1365-4632.2006.03074.x
-
Janjua SA, Hussain I, Khachemoune A,. Facial peeling skin syndrome: a case report and brief review. Int J Dermatol 2007; 46: 287-289. (Pubitemid 46390288)
-
(2007)
International Journal of Dermatology
, vol.46
, Issue.3
, pp. 287-289
-
-
Janjua, S.A.1
Hussain, I.2
Khachemoune, A.3
-
8
-
-
0031716252
-
Localized peeling skin syndrome: Case report with ultrastructural study
-
DOI 10.1046/j.1365-2133.1998.02416.x
-
Brusasco A, Veraldi S, Tadini G, Caputo R,. Localized peeling skin syndrome: case report with ultrastructural study. Br J Dermatol 1998; 139: 492-495. (Pubitemid 28430469)
-
(1998)
British Journal of Dermatology
, vol.139
, Issue.3
, pp. 492-495
-
-
Brusasco, A.1
Veraldi, S.2
Tadini, G.3
Caputo, R.4
-
9
-
-
77952700774
-
Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Soreze 2009
-
Oji V, Tadini G, Akiyama M, et al. Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Soreze 2009. J Am Acad Dermatol 2010; 63: 607-641.
-
(2010)
J Am Acad Dermatol
, vol.63
, pp. 607-641
-
-
Oji, V.1
Tadini, G.2
Akiyama, M.3
-
10
-
-
79952285443
-
Clinical presentation and etiology of ichthyoses. Overwiew of the new nomenclature and classification
-
Oji V,. Clinical presentation and etiology of ichthyoses. Overwiew of the new nomenclature and classification. Hautarzt 2010; 61: 891-902.
-
(2010)
Hautarzt
, vol.61
, pp. 891-902
-
-
Oji, V.1
-
11
-
-
79951482804
-
Peeling skin syndrome: Genetic defects in late terminal differentiation of the epidermis
-
Bowden PE,. Peeling skin syndrome: genetic defects in late terminal differentiation of the epidermis. J Invest dermatol 2011; 131: 561-564.
-
(2011)
J Invest Dermatol
, vol.131
, pp. 561-564
-
-
Bowden, P.E.1
-
12
-
-
77955577355
-
Loss of the corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: Unraveling the peeling skin disease
-
Oji V, Ecki KM, Aufenvenne K, et al. Loss of the corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease. Am J Hum Genet 2010; 87: 274-281.
-
(2010)
Am J Hum Genet
, vol.87
, pp. 274-281
-
-
Oji, V.1
Ecki, K.M.2
Aufenvenne, K.3
-
13
-
-
79951497066
-
Inflammatory peeling skin syndrome caused by a mutation in CDSN encoding corneodesmosin
-
Israeli S, Zamir H, Sarig O, et al. Inflammatory peeling skin syndrome caused by a mutation in CDSN encoding corneodesmosin. J Invest Dermatol 2011; 131: 779-781.
-
(2011)
J Invest Dermatol
, vol.131
, pp. 779-781
-
-
Israeli, S.1
Zamir, H.2
Sarig, O.3
-
14
-
-
77952425665
-
Acral peeling skin syndrome with TGM5 gene mutations may resemble epidermolysis bullosa simplex in young individuals
-
Kiritsi D, Cosgarea I, Franzke CW, et al. Acral peeling skin syndrome with TGM5 gene mutations may resemble epidermolysis bullosa simplex in young individuals. J Invest Dermatol 2010; 130: 1741-1746.
-
(2010)
J Invest Dermatol
, vol.130
, pp. 1741-1746
-
-
Kiritsi, D.1
Cosgarea, I.2
Franzke, C.W.3
-
15
-
-
0001302921
-
Skin shedding (Keratolysis exfoliativa congenita): Report of a case
-
Fox H,. Skin shedding (Keratolysis exfoliativa congenita): report of a case. Arch Dermatol 1921; 3: 202.
-
(1921)
Arch Dermatol
, vol.3
, pp. 202
-
-
Fox, H.1
-
16
-
-
0007894691
-
Familial study of three unusual cases of congenital ichthyosiform erythroderma
-
Wile UJ,. Familial study of three unusual cases of congenital ichthyosiform erythroderma. Arch Dermatol 1924; 9: 487-498.
-
(1924)
Arch Dermatol
, vol.9
, pp. 487-498
-
-
Wile, U.J.1
-
17
-
-
0014480387
-
Familial contunial skin peeling
-
Kurban AK, Azar HA,. Familial contunial skin peeling. Br J Dermatol 1969; 81: 191-195.
-
(1969)
Br J Dermatol
, vol.81
, pp. 191-195
-
-
Kurban, A.K.1
Azar, H.A.2
-
19
-
-
0028057582
-
Peeling skin syndrome
-
Aras N, Sutman K, Tastan HB, Baykal K,. Peeling skin syndrome. J Am Acad Dermatol 1994; 30: 135-136. (Pubitemid 24033834)
-
(1994)
Journal of the American Academy of Dermatology
, vol.30
, Issue.1
, pp. 135-136
-
-
Aras, N.1
Sutman, K.2
Tastan, H.B.3
Baykal, K.4
Can, C.5
-
20
-
-
0032943675
-
Peeling skin syndrome
-
Tastan HB, Akar A, Gur AR, Deveci S,. Peeling skin syndrome. Int J Dermatol 1999; 38: 208-210. (Pubitemid 29155360)
-
(1999)
International Journal of Dermatology
, vol.38
, Issue.3
, pp. 208-210
-
-
Tastan, H.B.1
Akar, A.2
Gur, A.R.3
Deveci, S.4
-
21
-
-
77950686707
-
Generalized peeling skin syndrome: Case report and review of the literature
-
Kharfi M, Khaled A, Ammar D, et al. Generalized peeling skin syndrome: case report and review of the literature. Dermatol Online J 2010; 16: 1-6.
-
(2010)
Dermatol Online J
, vol.16
, pp. 1-6
-
-
Kharfi, M.1
Khaled, A.2
Ammar, D.3
-
24
-
-
33646671465
-
Peeling skin syndrome
-
Ilknur T, Demirtaşoǧlu M, Akarsu S, et al. Peeling skin syndrome. Eur J Dermatol. 2006; 16: 287-289. (Pubitemid 43736152)
-
(2006)
European Journal of Dermatology
, vol.16
, Issue.3
, pp. 287-289
-
-
Ilknur, T.1
Demirtasoglu, M.2
Akarsu, S.3
Lebe, B.4
Gunes, A.T.5
Ozkan, S.6
-
25
-
-
28144445201
-
A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome
-
DOI 10.1086/497707
-
Cassidy AJ, van Steensel MAM, Steijlen PM, et al. A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome. Am J Hum Genet 2005; 77: 909-917. (Pubitemid 41698513)
-
(2005)
American Journal of Human Genetics
, vol.77
, Issue.6
, pp. 909-917
-
-
Cassidy, A.J.1
Van Steensel, M.A.M.2
Steijlen, P.M.3
Van Geel, M.4
Van Der Velden, J.5
Morley, S.M.6
Terrinoni, A.7
Melino, G.8
Candi, E.9
McLean, W.H.I.10
-
26
-
-
27744572193
-
Peeling skin syndrome with aminoaciduria
-
DOI 10.1111/j.1525-1470.2005.22406.x
-
Inamadar AC, Palit A,. Peeling skin syndrome with aminoaciduria. Ped Dermatol 2005; 22: 314-316. (Pubitemid 41583308)
-
(2005)
Pediatric Dermatology
, vol.22
, Issue.4
, pp. 314-316
-
-
Inamadar, A.C.1
Palit, A.2
-
27
-
-
33646700787
-
A case of peeling skin syndrome successfully treated with topical calcipotriol [1]
-
DOI 10.1111/j.1346-8138.2006.00102.x
-
Mizuno Y, Suga Y, Hasegawa T, et al. A case of peeling skin syndrome successfully treated with topical calcipotriol. J Dermatol 2006; 33: 430-432. (Pubitemid 43736335)
-
(2006)
Journal of Dermatology
, vol.33
, Issue.6
, pp. 430-432
-
-
Mizuno, Y.1
Suga, Y.2
Hasegawa, T.3
Haruna, K.4
Kohroh, K.5
Ogawa, H.6
Ikeda, S.7
Shimizu, T.8
Komatsu, N.9
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