-
1
-
-
84980115073
-
Congenital poikiloderma with traumatic bullae formation and progressive cutaneous atrophy
-
Kindler T. Congenital poikiloderma with traumatic bullae formation and progressive cutaneous atrophy. Br J Dermatol 1954; 66: 104.
-
(1954)
Br J Dermatol
, vol.66
, pp. 104
-
-
Kindler, T.1
-
2
-
-
0024334916
-
Kindler's syndrome: Report of two cases and review of the literature
-
Forman AB, Prendiville JS, Esterly NB, et al. Kindler's syndrome: Report of two cases and review of the literature. Pediatr Dermatol 1989; 6: 91.
-
(1989)
Pediatr Dermatol
, vol.6
, pp. 91
-
-
Forman, A.B.1
Prendiville, J.S.2
Esterly, N.B.3
-
4
-
-
0014581206
-
Hereditary sclerosing poikiloderma: Report of two families with an unusual and distinctive genodermatosis
-
Weary PE, Hsu YT, Richardson DR, et al. Hereditary sclerosing poikiloderma: report of two families with an unusual and distinctive genodermatosis. Arch Dermatol 1969; 100: 413.
-
(1969)
Arch Dermatol
, vol.100
, pp. 413
-
-
Weary, P.E.1
Hsu, Y.T.2
Richardson, D.R.3
-
5
-
-
51249195723
-
Über Katarakten in Verbindung mit einer eigentümlichen Hautdegeneration
-
Rothmund A. Über Katarakten in Verbindung mit einer eigentümlichen Hautdegeneration. Albrecht Von Graefes Arch Ophth 1868; 14: 159.
-
(1868)
Albrecht Von Graefes Arch Ophth
, vol.14
, pp. 159
-
-
Rothmund, A.1
-
6
-
-
0001743196
-
A hitherto undescribed familial disease
-
Thomson MS. A hitherto undescribed familial disease. Br J Dermatol Suppl. 1923; 35: 455.
-
(1923)
Br J Dermatol Suppl.
, vol.35
, pp. 455
-
-
Thomson, M.S.1
-
8
-
-
0000605996
-
Atrophia cutis reticularis cum pigmentatione, dystrophia ungium et leukoplakia oris
-
Zinsser F. Atrophia cutis reticularis cum pigmentatione, dystrophia ungium et leukoplakia oris. Ikonogr Dermatol 1906; 5: 219.
-
(1906)
Ikonogr Dermatol
, vol.5
, pp. 219
-
-
Zinsser, F.1
-
9
-
-
0002924576
-
Dyskeratosis congenita with pigmentation, dystrophia unguis and leukokeratosis oris
-
Cole HN, Rauschkolb JC, Toomey J. Dyskeratosis congenita with pigmentation, dystrophia unguis and leukokeratosis oris. Arch Dermatol Syphiligr 1930; 21: 71.
-
(1930)
Arch Dermatol Syphiligr
, vol.21
, pp. 71
-
-
Cole, H.N.1
Rauschkolb, J.C.2
Toomey, J.3
-
10
-
-
0000757535
-
A unique case of reticular pigmentation of the skin with atrophy
-
Engman EF. A unique case of reticular pigmentation of the skin with atrophy. Arch Dermatol Syphiligr 1926; 13: 685.
-
(1926)
Arch Dermatol Syphiligr
, vol.13
, pp. 685
-
-
Engman, E.F.1
-
11
-
-
12444321655
-
Typus maculatus der bullösen hereditären dystrophie
-
Da Costa M, Valk J. Typus maculatus der bullösen hereditären dystrophie. Arch Dermatol Syphiligr 1908; 91: 3.
-
(1908)
Arch Dermatol Syphiligr
, vol.91
, pp. 3
-
-
Da Costa, M.1
Valk, J.2
-
12
-
-
0141881146
-
Dermatopathia pigmentosa reticularis hypohidrotica et atrophica
-
Gahlen W. Dermatopathia pigmentosa reticularis hypohidrotica et atrophica. Dermatol Wochenschr 1964; 150: 193.
-
(1964)
Dermatol Wochenschr
, vol.150
, pp. 193
-
-
Gahlen, W.1
-
13
-
-
0002665724
-
A propos de l'incontinentia pigmenti, delimitation de deux syndromes differents figurant sous le meme terme
-
Franceschetti A, Jadassohn W. A propos de l'incontinentia pigmenti, delimitation de deux syndromes differents figurant sous le meme terme. Dermatologica 1954; 108: 1.
-
(1954)
Dermatologica
, vol.108
, pp. 1
-
-
Franceschetti, A.1
Jadassohn, W.2
-
14
-
-
0141915722
-
Incontinentia pigmenti avec etat poikilodermique
-
Degos R, Touraine R. Incontinentia pigmenti avec etat poikilodermique. Bull Soc Fr Dermatol Syph 1961; 68: 6.
-
(1961)
Bull Soc Fr Dermatol Syph
, vol.68
, pp. 6
-
-
Degos, R.1
Touraine, R.2
-
15
-
-
76549186135
-
Über die kongenitalen Poikilodermien. Ein analytischer Versuch
-
Marghescu S, Braun-Falco O. Über die kongenitalen Poikilodermien. Ein analytischer Versuch. Dermat Wschr 1965; 151: 9.
-
(1965)
Dermat Wschr
, vol.151
, pp. 9
-
-
Marghescu, S.1
Braun-Falco, O.2
-
16
-
-
0036938591
-
Kongenitale bullöse Poikilodermie (Kindler-Syndrom)
-
Binder B, Metze D, Smolle J. Kongenitale bullöse Poikilodermie (Kindler-Syndrom). Hautarzt 2002; 53: 546.
-
(2002)
Hautarzt
, vol.53
, pp. 546
-
-
Binder, B.1
Metze, D.2
Smolle, J.3
-
17
-
-
0024309209
-
Poikiloderma of Theresa Kindler: Report of a case with ultrastructural study, and review of the literature
-
Hovnanian A, Blanchet-Bardon C, de Prost Y. Poikiloderma of Theresa Kindler: report of a case with ultrastructural study, and review of the literature. Pediatr Dermatol 1989; 6: 82.
-
(1989)
Pediatr Dermatol
, vol.6
, pp. 82
-
-
Hovnanian, A.1
Blanchet-Bardon, C.2
De Prost, Y.3
-
18
-
-
0018188218
-
Congenital poikiloderma with features of hereditary acrokeratotic poikiloderma
-
Draznin MB, Esterly NB, Fretzin DF. Congenital poikiloderma with features of hereditary acrokeratotic poikiloderma. Arch Dermatol 1978; 114: 1207.
-
(1978)
Arch Dermatol
, vol.114
, pp. 1207
-
-
Draznin, M.B.1
Esterly, N.B.2
Fretzin, D.F.3
-
22
-
-
0021946090
-
Kindler's syndrome in two related Kurdish families
-
Hacham Zadeh S, Garfunkel AA. Kindler's syndrome in two related Kurdish families. Am J Med Genet 1985; 20: 43.
-
(1985)
Am J Med Genet
, vol.20
, pp. 43
-
-
Hacham Zadeh, S.1
Garfunkel, A.A.2
-
25
-
-
0019460693
-
Immunofluorescence mapping of antigenic determinants within the dermal-epidermal junction in the mechanobullous diseases
-
Hintner H, Stingl G, Schuler G, et al. Immunofluorescence mapping of antigenic determinants within the dermal-epidermal junction in the mechanobullous diseases. J Invest Dermatol 1981; 76: 113.
-
(1981)
J Invest Dermatol
, vol.76
, pp. 113
-
-
Hintner, H.1
Stingl, G.2
Schuler, G.3
-
26
-
-
15144354119
-
Immunohistochemical, ultrastructural, and molecular features of Kindler's syndrome distinguish it from dystrophic epidermolysis bullosa
-
Shimizu H, Sato M, Ban M, et al. Immunohistochemical, ultrastructural, and molecular features of Kindler's syndrome distinguish it from dystrophic epidermolysis bullosa. Arch Dermatol 1997; 133: 1111.
-
(1997)
Arch Dermatol
, vol.133
, pp. 1111
-
-
Shimizu, H.1
Sato, M.2
Ban, M.3
-
28
-
-
0031788823
-
Detection of antigens by immunofluorescence on ultrathin cryosections on skin
-
Ishiko A, Shimizu H, Masunaga T, et al. Detection of antigens by immunofluorescence on ultrathin cryosections on skin. J Histochem Cytochem 1998; 46: 1455.
-
(1998)
J Histochem Cytochem
, vol.46
, pp. 1455
-
-
Ishiko, A.1
Shimizu, H.2
Masunaga, T.3
-
29
-
-
0022365197
-
Poikilodermie congenitale avec formation de bulles traumatiques et atrophie cutanée progressive. Poikilodermie de Theresa Kindler
-
Blanchet-Bardon C, Nazzaro V, Mimoz C, Puissant A. Poikilodermie congenitale avec formation de bulles traumatiques et atrophie cutanée progressive. poikilodermie de Theresa Kindler. Ann Dermatol Venereol 1985; 112: 703.
-
(1985)
Ann Dermatol Venereol
, vol.112
, pp. 703
-
-
Blanchet-Bardon, C.1
Nazzaro, V.2
Mimoz, C.3
Puissant, A.4
-
30
-
-
0020375481
-
Poikilodermie diffuse avec acrokeratose et precession de lesions bulleuses: Maladie de Weary-Kindler
-
Maleville J, Cavaroc Y, Boiron G, et al. Poikilodermie diffuse avec acrokeratose et precession de lesions bulleuses: maladie de Weary-Kindler. Ann Dermatol Venereol 1982; 109: 949.
-
(1982)
Ann Dermatol Venereol
, vol.109
, pp. 949
-
-
Maleville, J.1
Cavaroc, Y.2
Boiron, G.3
-
31
-
-
0000206883
-
4 solutions in fixation
-
4 solutions in fixation. J Appl Physiol 1961; 32: 1637.
-
(1961)
J Appl Physiol
, vol.32
, pp. 1637
-
-
Millonig, G.1
-
32
-
-
78651181230
-
A simplified lead citrate stain for use in electron microscopy
-
Venable JM, Coggeshall R. A simplified lead citrate stain for use in electron microscopy. J Cell Biol 1965; 25: 407.
-
(1965)
J Cell Biol
, vol.25
, pp. 407
-
-
Venable, J.M.1
Coggeshall, R.2
-
34
-
-
0029793189
-
Kindler's syndrome: Report of a case with ultrastructural study and review of the literature
-
Patrizi A, Pauluzzi P, Neri I, et al. Kindler's syndrome: report of a case with ultrastructural study and review of the literature. Pediatr Dermatol 1996; 13: 397.
-
(1996)
Pediatr Dermatol
, vol.13
, pp. 397
-
-
Patrizi, A.1
Pauluzzi, P.2
Neri, I.3
-
35
-
-
85046113818
-
Kindler's syndrome with recurrence of bullae in the fifth decade
-
Ban M, Hosoe H, Yamada T, et al. Kindler's syndrome with recurrence of bullae in the fifth decade. Br J Dermatol 1996; 135: 489.
-
(1996)
Br J Dermatol
, vol.135
, pp. 489
-
-
Ban, M.1
Hosoe, H.2
Yamada, T.3
-
36
-
-
0032948619
-
Abnormal deposition of type VII collagen in Kindler's syndrome
-
Wiebe CB, Larjava HS. Abnormal deposition of type VII collagen in Kindler's syndrome. Arch Dermatol Res 1999; 291: 6.
-
(1999)
Arch Dermatol Res
, vol.291
, pp. 6
-
-
Wiebe, C.B.1
Larjava, H.S.2
-
39
-
-
0033856761
-
Vascular changes in erythropoietic protoporphyria: Histopathologic and immunohistochemical study
-
Timonen K, Kariniemi AL, Niemi KM, et al. Vascular changes in erythropoietic protoporphyria: Histopathologic and immunohistochemical study. J Am Acad Dermatol 2000; 43: 489.
-
(2000)
J Am Acad Dermatol
, vol.43
, pp. 489
-
-
Timonen, K.1
Kariniemi, A.L.2
Niemi, K.M.3
-
40
-
-
0026558997
-
Histologic and immunofluorescence study of cutaneous porphyrias
-
Maynard B, Peters MS. Histologic and immunofluorescence study of cutaneous porphyrias. J Cutan Pathol 1992; 19: 40.
-
(1992)
J Cutan Pathol
, vol.19
, pp. 40
-
-
Maynard, B.1
Peters, M.S.2
-
41
-
-
0029395844
-
Chronic discoid lupus erythematosus: An immunopathological and electron microscopic study
-
Shahidullah M, Lee YS, Khor CJ, Ratnam KV. Chronic discoid lupus erythematosus: an immunopathological and electron microscopic study. Ann Acad Med Singapore 1995; 24: 789.
-
(1995)
Ann Acad Med Singapore
, vol.24
, pp. 789
-
-
Shahidullah, M.1
Lee, Y.S.2
Khor, C.J.3
Ratnam, K.V.4
-
42
-
-
0020639669
-
Verrucous lupus erythematosus: Ultrastructural studies on a distinct variant of chronic discoid lupus erythematosus
-
Santa Cruz DJ, Uitto J, Eisen AZ, Prioleau PG. Verrucous lupus erythematosus: ultrastructural studies on a distinct variant of chronic discoid lupus erythematosus. J Am Acad Dermatol 1983; 9: 82.
-
(1983)
J Am Acad Dermatol
, vol.9
, pp. 82
-
-
Santa Cruz, D.J.1
Uitto, J.2
Eisen, A.Z.3
Prioleau, P.G.4
-
43
-
-
0031874011
-
Dyskeratosis congenita: A light microscopic and ultrastructural study
-
Kagoura M, Morohashi M. Dyskeratosis congenita: a light microscopic and ultrastructural study. Eur J Dermatol 1998; 8: 307.
-
(1998)
Eur J Dermatol
, vol.8
, pp. 307
-
-
Kagoura, M.1
Morohashi, M.2
-
44
-
-
0032980582
-
Kindler's syndrome: Absence of definite ultrastructural feature
-
Sentürk N, Usubutun A, Sahin S, et al. Kindler's syndrome: Absence of definite ultrastructural feature. J Am Acad Dermatol 1999; 40: 335.
-
(1999)
J Am Acad Dermatol
, vol.40
, pp. 335
-
-
Sentürk, N.1
Usubutun, A.2
Sahin, S.3
-
45
-
-
0033883496
-
Death receptors in cutaneous biology and disease
-
Wehrli P, Viard I, Bullani R, et al. Death receptors in cutaneous biology and disease. J Invest Dermatol 2000; 115: 141.
-
(2000)
J Invest Dermatol
, vol.115
, pp. 141
-
-
Wehrli, P.1
Viard, I.2
Bullani, R.3
-
46
-
-
12944293136
-
Revised classification system for inherited epidermolysis bullosa: Report on the second international consensus meeting on diagnosis and classification of epidermolysis bullosa
-
Fine JD, Eady RA, Bauer EA, et al. Revised classification system for inherited epidermolysis bullosa: Report on the second international consensus meeting on diagnosis and classification of epidermolysis bullosa. J Am Acad Dermatol 2000; 42: 1051.
-
(2000)
J Am Acad Dermatol
, vol.42
, pp. 1051
-
-
Fine, J.D.1
Eady, R.A.2
Bauer, E.A.3
-
47
-
-
0036251498
-
Mechanisms of UV-induced signal transduction
-
Kulms D, Schwarz T. Mechanisms of UV-induced signal transduction. J Dermatol 2002; 29: 180.
-
(2002)
J Dermatol
, vol.29
, pp. 180
-
-
Kulms, D.1
Schwarz, T.2
-
48
-
-
0028212937
-
Apoptosis and its role in human disease
-
Barr PJ, Tomei LD. Apoptosis and its role in human disease. Biotechnology 1994; 12: 487.
-
(1994)
Biotechnology
, vol.12
, pp. 487
-
-
Barr, P.J.1
Tomei, L.D.2
-
49
-
-
12444341588
-
Kindler's syndrome: A simultaneous occurrence of hereditary epidermolysis bullosa and poikiloderma congenitale or a distinct clinical entity?
-
Angelova I, Dourmishev A, Kazandjieva J, Vassileva S. Kindler's syndrome: a simultaneous occurrence of hereditary epidermolysis bullosa and poikiloderma congenitale or a distinct clinical entity? CEEDVA Bull 2001; 3: 62.
-
(2001)
CEEDVA Bull
, vol.3
, pp. 62
-
-
Angelova, I.1
Dourmishev, A.2
Kazandjieva, J.3
Vassileva, S.4
-
50
-
-
0035724198
-
Kindler's syndrome complicated by squamous cell carcinoma of the hard palate: Successful treatment with high-dose radiation therapy and granulocyte-macrophage colony-stimulating factor
-
Lotem M, Raben M, Zeltser R, et al. Kindler's syndrome complicated by squamous cell carcinoma of the hard palate: successful treatment with high-dose radiation therapy and granulocyte-macrophage colony-stimulating factor. Br J Dermatol 2001; 144: 1262.
-
(2001)
Br J Dermatol
, vol.144
, pp. 1262
-
-
Lotem, M.1
Raben, M.2
Zeltser, R.3
-
51
-
-
0035034884
-
Premature aging and predisposition to cancers caused by mutations in the RecQ family helicases
-
Furuichi Y. Premature aging and predisposition to cancers caused by mutations in the RecQ family helicases. Ann N Y Acad Sci 2001; 928: 121.
-
(2001)
Ann N Y Acad Sci
, vol.928
, pp. 121
-
-
Furuichi, Y.1
-
52
-
-
0002224507
-
Heritable diseases with increased sensitivity to cellular injury
-
Fitzpatrick TB, Eisen AZ, Wolff K, Freedberg IM, Austen K, eds. New York: McGraw-Hill
-
Kramer KH. Heritable diseases with increased sensitivity to cellular injury. In Fitzpatrick TB, Eisen AZ, Wolff K, Freedberg IM, Austen K, eds. Dermatology in general medicine, 4th edn. New York: McGraw-Hill, 1993; 1974.
-
(1993)
Dermatology in General Medicine, 4th Edn.
, pp. 1974
-
-
Kramer, K.H.1
-
53
-
-
0035891464
-
Diseases associated with photosensitivity
-
Murphy GM. Diseases associated with photosensitivity. J Photochem Photobiol B 2001; 64: 93.
-
(2001)
J Photochem Photobiol B
, vol.64
, pp. 93
-
-
Murphy, G.M.1
-
54
-
-
0035960043
-
The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita
-
Vulliamy TJ, Marrone A, Goldman F, et al. The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita. Nature 2001; 413: 432.
-
(2001)
Nature
, vol.413
, pp. 432
-
-
Vulliamy, T.J.1
Marrone, A.2
Goldman, F.3
-
55
-
-
0031799895
-
X-Linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nuclear functions
-
Heiss NS, Knight SW, Vulliamy TJ, et al. X-Linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nuclear functions. Nat Genet 1998; 19: 32.
-
(1998)
Nat Genet
, vol.19
, pp. 32
-
-
Heiss, N.S.1
Knight, S.W.2
Vulliamy, T.J.3
-
56
-
-
0242515916
-
Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome
-
Jobard F, Bouadjar B, Caux F, et al. Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome. Hum Mol Genet 2003; 12: 925.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 925
-
-
Jobard, F.1
Bouadjar, B.2
Caux, F.3
-
57
-
-
0038389789
-
Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome
-
Siegel DH, Ashton GH, Penagos HG, et al. Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome. Am J Hum Genet 2003; 73: 174.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 174
-
-
Siegel, D.H.1
Ashton, G.H.2
Penagos, H.G.3
|