-
1
-
-
0000605996
-
Atrophia cutis reticularis cum pigmentione, dystrophia unguium et leukokeratosis oris
-
Zinsser F. Atrophia cutis reticularis cum pigmentione, dystrophia unguium et leukokeratosis oris. Ikonogr Dermatol 1906; 5: 219-23.
-
(1906)
Ikonogr Dermatol
, vol.5
, pp. 219-223
-
-
Zinsser, F.1
-
2
-
-
0000757535
-
A unique case of reticular pigmentation of the skin with atrophy
-
Engmann MF. A unique case of reticular pigmentation of the skin with atrophy. Arch Dermatol Syphilol. 1926; 13: 685-7.
-
(1926)
Arch Dermatol Syphilol.
, vol.13
, pp. 685-687
-
-
Engmann, M.F.1
-
3
-
-
0002924576
-
Dyskeratosis congenita with pigmentatia, dystrophia unguis and leukokeratosis oris
-
Cole HN, Rauschkolb JC, Toomer J. Dyskeratosis congenita with pigmentatia, dystrophia unguis and leukokeratosis oris. Arch Dermatol Syphilol. 1930; 21: 71-95.
-
(1930)
Arch Dermatol Syphilol.
, vol.21
, pp. 71-95
-
-
Cole, H.N.1
Rauschkolb, J.C.2
Toomer, J.3
-
4
-
-
0016238775
-
Dyskeratosis congenita with associated periodontal disease
-
Wald C, Diner H. Dyskeratosis congenita with associated periodontal disease. Oral Surg Med Pathol. 1974; 37: 736-44.
-
(1974)
Oral Surg Med Pathol.
, vol.37
, pp. 736-744
-
-
Wald, C.1
Diner, H.2
-
5
-
-
0015319556
-
Dyskeratosis congenita: Relationship to Fanconi anemia
-
Steier W, Van Voolen A, Selmanowitz V. Dyskeratosis congenita: relationship to Fanconi anemia. Blood. 1972; 39: 510-21.
-
(1972)
Blood
, vol.39
, pp. 510-521
-
-
Steier, W.1
Van Voolen, A.2
Selmanowitz, V.3
-
6
-
-
0026733377
-
Dyskeratosis congenita: Clinical and genetic heterogeneity
-
Drachtman R, Alter B. Dyskeratosis congenita: clinical and genetic heterogeneity. Am J Pediatr Hematol Oncol. 1922; 14: 297-304.
-
(1922)
Am J Pediatr Hematol Oncol.
, vol.14
, pp. 297-304
-
-
Drachtman, R.1
Alter, B.2
-
8
-
-
7344266233
-
Dyskeratosis congenita, report of a large kindred
-
Connor JM, Teague RH. Dyskeratosis congenita, report of a large kindred. Br J Dermatol. 1958; 77: 704-12.
-
(1958)
Br J Dermatol.
, vol.77
, pp. 704-712
-
-
Connor, J.M.1
Teague, R.H.2
-
9
-
-
0029884355
-
Gastrointestinal problems in a child with dyskeratosis congenita
-
Berezin S, Schwarz S, Slim M. Gastrointestinal problems in a child with dyskeratosis congenita. AJG. 1996; 91: 1271-2.
-
(1996)
AJG
, vol.91
, pp. 1271-1272
-
-
Berezin, S.1
Schwarz, S.2
Slim, M.3
-
10
-
-
0026605562
-
Bronchoalveolar disease in dyskeratosis congenita
-
Verra F, Kouzon S, Saiag P, Bignon J, De Cremoux H. Bronchoalveolar disease in dyskeratosis congenita. Eur Respir J. 1992; 5: 497-9.
-
(1992)
Eur Respir J.
, vol.5
, pp. 497-499
-
-
Verra, F.1
Kouzon, S.2
Saiag, P.3
Bignon, J.4
De Cremoux, H.5
-
12
-
-
0028412593
-
Dyskeratosis congenita showing usual interstitial pneumonia
-
Imokawa S, Sato A, Toyoshima M, Yoshitomi A. Dyskeratosis congenita showing usual interstitial pneumonia. Intern Med. 1994; 33: 226-30.
-
(1994)
Intern Med.
, vol.33
, pp. 226-230
-
-
Imokawa, S.1
Sato, A.2
Toyoshima, M.3
Yoshitomi, A.4
-
13
-
-
0029967609
-
Allogeneic marrow transplantation for aplastic anaemia associated with dyskeratosis congenita
-
Langston AA, Sanders JE, Deeg HJ et al. Allogeneic marrow transplantation for aplastic anaemia associated with dyskeratosis congenita. Br J Haemat. 1996; 92: 758-65.
-
(1996)
Br J Haemat.
, vol.92
, pp. 758-765
-
-
Langston, A.A.1
Sanders, J.E.2
Deeg, H.J.3
-
14
-
-
0031045320
-
Fatal interstitial pulmonary disease in a patient with dyskeratosis congenita after allogeneic bone marrow transplantation
-
Yabe M, Yabe H, Hattori K et al. Fatal interstitial pulmonary disease in a patient with dyskeratosis congenita after allogeneic bone marrow transplantation. Bone Marrow Transplant. 1997; 19: 389-92.
-
(1997)
Bone Marrow Transplant
, vol.19
, pp. 389-392
-
-
Yabe, M.1
Yabe, H.2
Hattori, K.3
-
15
-
-
0031035442
-
Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita
-
Devriendt K, Matthijs G, Legius E et al. Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita. Am J Hum Genet. 1997; 60: 581-7.
-
(1997)
Am J Hum Genet.
, vol.60
, pp. 581-587
-
-
Devriendt, K.1
Matthijs, G.2
Legius, E.3
-
16
-
-
0026729432
-
"Stem cell" origin of the hematopoietic defect in dyskeratosis congenita
-
Marsh JCW, Will AJ, Hows JM et al. "Stem cell" origin of the hematopoietic defect in dyskeratosis congenita. Blood. 1992; 79; 3138-44.
-
(1992)
Blood
, vol.79
, pp. 3138-3144
-
-
Marsh, J.C.W.1
Will, A.J.2
Hows, J.M.3
-
17
-
-
0015667466
-
Dyskeratosis congenita with pancytopenia, another constitutional anemia
-
Inoue S, Mekanik G, Mahallati M, Zuelzer WW. Dyskeratosis congenita with pancytopenia, another constitutional anemia. Am J Dis Child. 1973; 126: 389-96.
-
(1973)
Am J Dis Child.
, vol.126
, pp. 389-396
-
-
Inoue, S.1
Mekanik, G.2
Mahallati, M.3
Zuelzer, W.W.4
-
18
-
-
0026507198
-
T-cell immunodeficiency in dyskeratosis congenita
-
Lee BW, Yap HK, Quah TC, Chong A, Seah CC. T-cell immunodeficiency in dyskeratosis congenita. Arch Dis Child. 1992; 67: 524-6.
-
(1992)
Arch Dis Child.
, vol.67
, pp. 524-526
-
-
Lee, B.W.1
Yap, H.K.2
Quah, T.C.3
Chong, A.4
Seah, C.C.5
-
19
-
-
0016727683
-
Dyskeratosis congenita: Clinical features and genetic aspects
-
Sirinavan C, Trowbridge AA. Dyskeratosis congenita: clinical features and genetic aspects. J Med Genet. 1975; 12: 339-54.
-
(1975)
J Med Genet.
, vol.12
, pp. 339-354
-
-
Sirinavan, C.1
Trowbridge, A.A.2
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