-
1
-
-
0000486941
-
A propos d'une anomalie pigmentaire inédite.
-
Ichikawa T, Higara Y. A propos d'une anomalie pigmentaire inédite. Jpn J Dermatol 1933 ; 34 : 360-4.
-
(1933)
Jpn J Dermatol
, vol.34
, pp. 360-364
-
-
Ichikawa, T.1
Higara, Y.2
-
2
-
-
0002531661
-
Dyschromatosis symmetrica herediteria
-
Toyama I. Dyschromatosis symmetrica herediteria. Jpn J Dermatol 1929 ; 29 : 95-6.
-
(1929)
Jpn J Dermatol
, vol.29
, pp. 95-96
-
-
Toyama, I.1
-
3
-
-
0036413571
-
-
Sethuraman G, D'Souza M, Mohan Thappa D, Srinivas CR, Smilest L. Clin Exp Dermatol 2002 ; 27 : 477-479.
-
(2002)
Clin Exp Dermatol
, vol.27
, pp. 477-479
-
-
Sethuraman, G.1
D'Souza, M.2
Mohan Thappa, D.3
Srinivas, C.R.4
Smilest, L.5
-
4
-
-
33646033001
-
Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family
-
Bukhari IA, El-Harith EA, Stuhrmann M. Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family. J Eur Acad Dermatol Venereol. 2006; 20(5): 628-9.
-
(2006)
J Eur Acad Dermatol Venereol
, vol.20
, Issue.5
, pp. 628-629
-
-
Bukhari, I.A.1
El-Harith, E.A.2
Stuhrmann, M.3
-
5
-
-
0036862123
-
Dyschromatosis universalis hereditaria: Report of a case and review of the literature
-
Al Hawsawi K, Al Aboud K, Ramesh V, Al Aboud D. Dyschromatosis universalis hereditaria: report of a case and review of the literature. Pediatr Dermatol. 2002; 19: 523-526.
-
(2002)
Pediatr Dermatol
, vol.19
, pp. 523-526
-
-
Al Hawsawi, K.1
Al Aboud, K.2
Ramesh, V.3
Al Aboud, D.4
-
7
-
-
0042888576
-
Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria
-
Miyamura Y, Suzuki T, Kono M, Inagaki K, Ito S, Suzuki N, Tomita Y: Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria. Am J Hum Genet 2003; 73:693-699.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 693-699
-
-
Miyamura, Y.1
Suzuki, T.2
Kono, M.3
Inagaki, K.4
Ito, S.5
Suzuki, N.6
Tomita, Y.7
-
8
-
-
4644229966
-
A novel mutation of DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria
-
Li M, Jiang YX, Liu JB, et al: A novel mutation of DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria. Clin Exp Dermatol 2004; 29:533-535.
-
(2004)
Clin Exp Dermatol
, vol.29
, pp. 533-535
-
-
Li, M.1
Jiang, Y.X.2
Liu, J.B.3
-
9
-
-
2342476651
-
Novel mutations of the RNA-specific adenosine deaminase gene (DSRAD) in Chinese families with dyschromatosis symmetrica hereditaria
-
Liu Q, Liu W, Jiang L, et al: Novel mutations of the RNA-specific adenosine deaminase gene (DSRAD) in Chinese families with dyschromatosis symmetrica hereditaria. J Invest Dermatol. 2004;122:896-899.
-
(2004)
J Invest Dermatol
, vol.122
, pp. 896-899
-
-
Liu, Q.1
Liu, W.2
Jiang, L.3
-
10
-
-
20544455231
-
Mutation analysis of the ADAR1 Gene in Dyschromatosis Symmetrica Hereditaria and genetic differentiation from both Dyschromatosis Universalis Hereditaria and Acropigmentatio Reticularis
-
Suzuki N, Suzuki T, Inagaki K, Ito S, Kono M, Fukai K, Takama H, Sato K, Ishikawa O, Abe M, Shimizu H, Kawai M, Horikawa T, Yoshida K, Matsumoto K, Terui T, Tsujioka K, Tomita Y. Mutation analysis of the ADAR1 Gene in Dyschromatosis Symmetrica Hereditaria and genetic differentiation from both Dyschromatosis Universalis Hereditaria and Acropigmentatio Reticularis. J Invest Dermatol. 2005; 124 : 1186-92.
-
(2005)
J Invest Dermatol
, vol.124
, pp. 1186-1192
-
-
Suzuki, N.1
Suzuki, T.2
Inagaki, K.3
Ito, S.4
Kono, M.5
Fukai, K.6
Takama, H.7
Sato, K.8
Ishikawa, O.9
Abe, M.10
Shimizu, H.11
Kawai, M.12
Horikawa, T.13
Yoshida, K.14
Matsumoto, K.15
Terui, T.16
Tsujioka, K.17
Tomita, Y.18
-
11
-
-
1542378712
-
Dyschromatosis universalis hereditaria: Familial case and ultrastructural skin investigation
-
Nuber UA, Tinschert S, Mundlos S, Hauber I. Dyschromatosis universalis hereditaria: familial case and ultrastructural skin investigation. Am J Med Gen A. 2004; 125(3): 261-6.
-
(2004)
Am J Med Gen A
, vol.125
, Issue.3
, pp. 261-266
-
-
Nuber, U.A.1
Tinschert, S.2
Mundlos, S.3
Hauber, I.4
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