-
1
-
-
38849204872
-
Dyskeratosis congenita: A historical perspective
-
10.1016/j.mad.2007.10.006. 18054794
-
Dyskeratosis congenita: a historical perspective. AJ Walne I Dokal, Mech Ageing Dev 2008 129 48 59 10.1016/j.mad.2007.10.006 18054794
-
(2008)
Mech Ageing Dev
, vol.129
, pp. 48-59
-
-
Walne, A.J.1
Dokal, I.2
-
2
-
-
0033754823
-
Dyskeratosis congenita in all its forms
-
10.1046/j.1365-2141.2000.02109.x. 11054058
-
Dyskeratosis congenita in all its forms. I Dokal, Br J Haematol 2000 110 768 779 10.1046/j.1365-2141.2000.02109.x 11054058
-
(2000)
Br J Haematol
, vol.110
, pp. 768-779
-
-
Dokal, I.1
-
3
-
-
17144380033
-
Peripheral neuropathy - A novel finding in dyskeratosis congenita
-
10.1016/j.ejpn.2005.01.007. 15843075
-
Peripheral neuropathy - a novel finding in dyskeratosis congenita. P Ip R Knight I Dokal AY Manzur F Muntoni, Eur J Paediatr Neurol 2005 9 85 89 10.1016/j.ejpn.2005.01.007 15843075
-
(2005)
Eur J Paediatr Neurol
, vol.9
, pp. 85-89
-
-
Ip, P.1
Knight, R.2
Dokal, I.3
Manzur, A.Y.4
Muntoni, F.5
-
4
-
-
38049019132
-
Human diseases of telomerase dysfunction: Insights into tissue aging
-
10.1093/nar/gkm644. 17913752
-
Human diseases of telomerase dysfunction: insights into tissue aging. CK Garcia WE Wright JW Shay, Nucleic Acids Res 2007 35 7406 7416 10.1093/nar/gkm644 17913752
-
(2007)
Nucleic Acids Res
, vol.35
, pp. 7406-7416
-
-
Garcia, C.K.1
Wright, W.E.2
Shay, J.W.3
-
5
-
-
0032424906
-
Dyskeratosis Congenita (DC) Registry: Identification of new features of DC
-
10.1046/j.1365-2141.1998.01103.x. 9886310
-
Dyskeratosis Congenita (DC) Registry: identification of new features of DC. S Knight T Vulliamy A Copplestone E Gluckman P Mason I Dokal, Br J Haematol 1998 103 990 996 10.1046/j.1365-2141.1998.01103.x 9886310
-
(1998)
Br J Haematol
, vol.103
, pp. 990-996
-
-
Knight, S.1
Vulliamy, T.2
Copplestone, A.3
Gluckman, E.4
Mason, P.5
Dokal, I.6
-
6
-
-
0026509150
-
Dyskeratosis congenita associated with elevated fetal hemoglobin, X-linked ocular albinism, and juvenile-onset diabetes mellitus
-
10.1111/j.1525-1470.1992.tb01223.x. 1376473
-
Dyskeratosis congenita associated with elevated fetal hemoglobin, X-linked ocular albinism, and juvenile-onset diabetes mellitus. M Reichel AC Grix RR Isseroff, Pediatr Dermatol 1992 9 103 106 10.1111/j.1525-1470.1992. tb01223.x 1376473
-
(1992)
Pediatr Dermatol
, vol.9
, pp. 103-106
-
-
Reichel, M.1
Grix, A.C.2
Isseroff, R.R.3
-
8
-
-
0033848842
-
Multiple intrapulmonary arteriovenous fistulas in childhood
-
10.1007/s002460010120. 10982718
-
Multiple intrapulmonary arteriovenous fistulas in childhood. A Sands E Dalzell B Craig M Shields, Pediatr Cardiol 2000 21 493 496 10.1007/s002460010120 10982718
-
(2000)
Pediatr Cardiol
, vol.21
, pp. 493-496
-
-
Sands, A.1
Dalzell, E.2
Craig, B.3
Shields, M.4
-
9
-
-
0021331420
-
Progressive immune failure in dyskeratosis congenita. Report of an adult in whom Pneumocystis carinii and fatal disseminated candidiasis developed
-
10.1001/archinte.144.2.397. 6607716
-
Progressive immune failure in dyskeratosis congenita. Report of an adult in whom Pneumocystis carinii and fatal disseminated candidiasis developed. HP Wiedemann J McGuire JM Dwyer J Sabetta JB Gee GJ Smith J Loke, Arch Intern Med 1984 144 397 399 10.1001/archinte.144.2.397 6607716
-
(1984)
Arch Intern Med
, vol.144
, pp. 397-399
-
-
Wiedemann, H.P.1
McGuire, J.2
Dwyer, J.M.3
Sabetta, J.4
Gee, J.B.5
Smith, G.J.6
Loke, J.7
-
10
-
-
0034772743
-
X-linked dyskeratosis congenita: Restrictive pulmonary disease and a novel mutation
-
10.1136/thorax.56.11.891. 11641517
-
X-linked dyskeratosis congenita: restrictive pulmonary disease and a novel mutation. WF Safa GG Lestringant PM Frossard, Thorax 2001 56 891 894 10.1136/thorax.56.11.891 11641517
-
(2001)
Thorax
, vol.56
, pp. 891-894
-
-
Safa, W.F.1
Lestringant, G.G.2
Frossard, P.M.3
-
11
-
-
38349144367
-
Dyskeratosis congenita: A genetic disorder of many faces
-
10.1111/j.1399-0004.2007.00923.x. 18005359
-
Dyskeratosis congenita: a genetic disorder of many faces. M Kirwan I Dokal, Clin Genet 2008 73 103 112 10.1111/j.1399-0004.2007.00923.x 18005359
-
(2008)
Clin Genet
, vol.73
, pp. 103-112
-
-
Kirwan, M.1
Dokal, I.2
-
12
-
-
0015667466
-
Dyskeratosis congenita with pancytopenia. Another constitutional anemia
-
4746551
-
Dyskeratosis congenita with pancytopenia. Another constitutional anemia. S Inoue G Mekanik M Mahallati WW Zuelzer, Am J Dis Child 1973 126 389 396 4746551
-
(1973)
Am J Dis Child
, vol.126
, pp. 389-396
-
-
Inoue, S.1
Mekanik, G.2
Mahallati, M.3
Zuelzer, W.W.4
-
13
-
-
20044379963
-
Usual interstitial pneumonia complicating dyskeratosis congenita
-
10.4065/80.6.817. 15945534
-
Usual interstitial pneumonia complicating dyskeratosis congenita. JP Utz JH Ryu JL Myers VV Michels, Mayo Clin Proc 2005 80 817 821 10.4065/80.6.817 15945534
-
(2005)
Mayo Clin Proc
, vol.80
, pp. 817-821
-
-
Utz, J.P.1
Ryu, J.H.2
Myers, J.L.3
Michels, V.V.4
-
14
-
-
0037396165
-
Treatment of dyskeratosis congenita with granulocyte-macrophage colony-stimulating factor and erythropoietin
-
10.1097/00043426-200304000-00015. 12679652
-
Treatment of dyskeratosis congenita with granulocyte-macrophage colony-stimulating factor and erythropoietin. E Erduran S Hacisalihoglu Y Ozoran, J Pediatr Hematol Oncol 2003 25 333 335 10.1097/00043426-200304000-00015 12679652
-
(2003)
J Pediatr Hematol Oncol
, vol.25
, pp. 333-335
-
-
Erduran, E.1
Hacisalihoglu, S.2
Ozoran, Y.3
-
15
-
-
34548153469
-
Splenic peliosis and rupture in patients with dyskeratosis congenita on androgens and granulocyte colony-stimulating factor
-
10.1111/j.1365-2141.2007.06718.x. 17760812
-
Splenic peliosis and rupture in patients with dyskeratosis congenita on androgens and granulocyte colony-stimulating factor. N Giri PA Pitel D Green BP Alter, Br J Haematol 2007 138 815 817 10.1111/j.1365-2141.2007.06718.x 17760812
-
(2007)
Br J Haematol
, vol.138
, pp. 815-817
-
-
Giri, N.1
Pitel, P.A.2
Green, D.3
Alter, B.P.4
|