-
1
-
-
0029165277
-
DNA damage, mutation and fine structure DNA repair in aging
-
1 Bohr VA, Anson RM. DNA damage, mutation and fine structure DNA repair in aging. Mutat Res 1995; 338: 25-34
-
(1995)
Mutat Res
, vol.338
, pp. 25-34
-
-
Bohr, V.A.1
Anson, R.M.2
-
2
-
-
0024380089
-
MRI in Cockayne syndrome type I
-
2 Boltshauser E, Yalcinkaya C, Reutter F, Prader A, Valavanis A. MRI in Cockayne syndrome type I. Neuroradiology 1989; 31: 276-277
-
(1989)
Neuroradiology
, vol.31
, pp. 276-277
-
-
Boltshauser, E.1
Yalcinkaya, C.2
Reutter, F.3
Prader, A.4
Valavanis, A.5
-
3
-
-
0031690075
-
The evolution of aging: A new approach to an old problem of biology
-
3 Bowles JT. The evolution of aging: a new approach to an old problem of biology. Med-Hypotheses 1998; 51: 179-221
-
(1998)
Med-Hypotheses
, vol.51
, pp. 179-221
-
-
Bowles, J.T.1
-
4
-
-
0002362694
-
Dwarfism with retinal atrophy and deafness
-
4 Cockayne EA. Dwarfism with retinal atrophy and deafness. Arch Dis Child 1936; 11: 1-8
-
(1936)
Arch Dis Child
, vol.11
, pp. 1-8
-
-
Cockayne, E.A.1
-
5
-
-
0023553037
-
A clinical and radiological study of two brothers affected by Cockayne syndrome type II
-
5 Colabucci F, Rossodivita A, Parigi A, Colavita N. A clinical and radiological study of two brothers affected by Cockayne syndrome Type II. Rays 1987; 12: 57-63
-
(1987)
Rays
, vol.12
, pp. 57-63
-
-
Colabucci, F.1
Rossodivita, A.2
Parigi, A.3
Colavita, N.4
-
7
-
-
0031982758
-
The premature aging Syndroms: Insights into the aging process
-
7 Dyer CAE, Sinclair AJ. The premature aging Syndroms: insights into the aging process. Age and Aging 1998; 27: 73-80
-
(1998)
Age and Aging
, vol.27
, pp. 73-80
-
-
Dyer, C.A.E.1
Sinclair, A.J.2
-
9
-
-
0024428765
-
Clinical an biochemical studies in three patients with severe early infantile Cockayne syndrome
-
9 Jaeken J, Klocker H, Schwaiger H, Bellmann R, Hirsch-Kauffmann M, Schweiger M. Clinical an biochemical studies in three patients with severe early infantile Cockayne syndrome. Hum Genet 1989; 83: 339-346
-
(1989)
Hum Genet
, vol.83
, pp. 339-346
-
-
Jaeken, J.1
Klocker, H.2
Schwaiger, H.3
Bellmann, R.4
Hirsch-Kauffmann, M.5
Schweiger, M.6
-
10
-
-
0020265071
-
Invited editorial comment: Early onset of Cockayne syndrome
-
10 Lowry RB. Invited editorial comment: early onset of Cockayne syndrome. Am J Med Genet 1982; 13: 209-210
-
(1982)
Am J Med Genet
, vol.13
, pp. 209-210
-
-
Lowry, R.B.1
-
11
-
-
84924051784
-
Cockayne's syndrome. An heredo-familial disorder of growth and development
-
11 Macdonald WB, Fitch KD, Lewis IC. Cockayne's syndrome. An heredo-familial disorder of growth and development. Pediatrics 1960; 25: 997-1007
-
(1960)
Pediatrics
, vol.25
, pp. 997-1007
-
-
Macdonald, W.B.1
Fitch, K.D.2
Lewis, I.C.3
-
12
-
-
0031891880
-
Molecular analysis of mutations in the CSB (ERCC 6) gene in patients with Cockayne syndrome
-
12 Mallery DL, Tanganelli B, Colella S, Steingrimsdottir H, van Gool AJ, Troelstra C, Stefanini M, Lehmann AR. Molecular analysis of mutations in the CSB (ERCC 6) gene in patients with Cockayne syndrome. Am J Hum Genet 1998; 62(1): 77
-
(1998)
Am J Hum Genet
, vol.62
, Issue.1
, pp. 77
-
-
Mallery, D.L.1
Tanganelli, B.2
Colella, S.3
Steingrimsdottir, H.4
Van Gool, A.J.5
Troelstra, C.6
Stefanini, M.7
Lehmann, A.R.8
-
13
-
-
0019902444
-
Brief clinical report: Cockayne syndrome with early onset of manifestations
-
13 Moyer DB, Marquis P, Shertzer ME, Burton BK. Brief clinical report: Cockayne syndrome with early onset of manifestations. Am J Med Genet 1982; 13: 225-230
-
(1982)
Am J Med Genet
, vol.13
, pp. 225-230
-
-
Moyer, D.B.1
Marquis, P.2
Shertzer, M.E.3
Burton, B.K.4
-
14
-
-
0026508774
-
Cockayne syndrome: Review of 140 cases
-
14 Nance MA, Berry SA. Cockayne syndrome: review of 140 Cases. Am J Med Genet 1992; 42: 68-84
-
(1992)
Am J Med Genet
, vol.42
, pp. 68-84
-
-
Nance, M.A.1
Berry, S.A.2
-
15
-
-
0023901408
-
Cockayne syndrome: Magnetic Resonance Images of the brain in a severe form with early onset
-
15 Nishio H, Kodama S, Matsuo T, Ichihashi M, Ito H, Fujiwara Y. Cockayne syndrome: Magnetic Resonance Images of the brain in a severe form with early onset. J Inher Metab Dis 1988; 11: 88-102
-
(1988)
J Inher Metab Dis
, vol.11
, pp. 88-102
-
-
Nishio, H.1
Kodama, S.2
Matsuo, T.3
Ichihashi, M.4
Ito, H.5
Fujiwara, Y.6
-
16
-
-
0022922411
-
Cockayne's syndrome presenting cerebral ishemic attack: Case report
-
Abstract
-
16 Shirasaki N, Hayashi M, Handa Y, Kabuto M, Tsuji T, Kawano H, Kabayashi H. Cockayne's syndrome presenting cerebral ishemic attack: case report. No-To-Shinkei 1986; 38 (9): 871-875 (Abstract!)
-
(1986)
No-To-Shinkei
, vol.38
, Issue.9
, pp. 871-875
-
-
Shirasaki, N.1
Hayashi, M.2
Handa, Y.3
Kabuto, M.4
Tsuji, T.5
Kawano, H.6
Kabayashi, H.7
-
17
-
-
0018732978
-
Cockayne syndrome: Unusual neuropathological findings and review of the literature
-
17 Soffer D, Grotsky HW, Rapin I, Suzuki K. Cockayne syndrome: Unusual neuropathological findings and review of the literature. Ann Neurol 1979; 6: 340-348
-
(1979)
Ann Neurol
, vol.6
, pp. 340-348
-
-
Soffer, D.1
Grotsky, H.W.2
Rapin, I.3
Suzuki, K.4
-
18
-
-
0030826732
-
The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex
-
18 Van Gool AJ, Citterio E, Rademakers S, van Os R, Vermeulen W, Constantnou A, Egly JM, Bootsma D, Hoeijmakers JH. The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex. EMBO J 1997; 16/19: 5955-5965
-
(1997)
EMBO J
, vol.16
, Issue.19
, pp. 5955-5965
-
-
Van Gool, A.J.1
Citterio, E.2
Rademakers, S.3
Van Os, R.4
Vermeulen, W.5
Constantnou, A.6
Egly, J.M.7
Bootsma, D.8
Hoeijmakers, J.H.9
|