-
1
-
-
0034797868
-
Clinical characteristics of Werner syndrome and other premature aging syndromes: Pattern of aging in progeroid syndromes
-
Gann Monograph on Cancer Research No. 49. From, (Goto M, Miller R. W, eds. ). Karger, Tokyo
-
Goto M. Clinical characteristics of Werner syndrome and other premature aging syndromes: Pattern of aging in progeroid syndromes. In: Gann Monograph on Cancer Research No.49. From premature gray hair to helicase-Werner syndrome: Implications for aging and cancer (Goto M, Miller R.W, eds.). Karger, Tokyo, 2001; pp. 27-39.
-
(2001)
premature gray hair to helicase-Werner syndrome: Implications for aging and cancer
, pp. 27-39
-
-
Goto, M.1
-
2
-
-
0030691121
-
Hierarchical deterioration of body systems in Werner's syndrome: Implications for normal ageing
-
Goto M. Hierarchical deterioration of body systems in Werner's syndrome: Implications for normal ageing. Mech Age Dev 1997; 98:239-254.
-
(1997)
Mech Age Dev
, vol.98
, pp. 239-254
-
-
Goto, M.1
-
3
-
-
0034792391
-
Nervous system disorders in Werner syndrome
-
Gann Monograph on Cancer Research No.49. From, (Goto M, Miller R.W. eds.)., Karger, Tokyo
-
Kuroda Y. Nervous system disorders in Werner syndrome: In: Gann Monograph on Cancer Research No.49. From premature gray hair to helicase-Werner syndrome:Implications for aging and cancer (Goto M, Miller R.W. eds.). Karger, Tokyo, 2001; pp.69-75.
-
(2001)
premature gray hair to helicase-Werner syndrome:Implications for aging and cancer
, pp. 69-75
-
-
Kuroda, Y.1
-
5
-
-
0031018953
-
Analysis of helicase gene mutations in Japanese Werner's syndrome patients
-
Goto M, Imamura O, Kuromitsu J, Matsumoto T, Yamabe Y, Tokutake Y, Suzuki N, Mason B, Drayna D, Sugawara M, Sugimoto M, Furuichi Y. Analysis of helicase gene mutations in Japanese Werner's syndrome patients. Hum Gent 1997; 99:191-193.
-
(1997)
Hum Gent
, vol.99
, pp. 191-193
-
-
Goto, M.1
Imamura, O.2
Kuromitsu, J.3
Matsumoto, T.4
Yamabe, Y.5
Tokutake, Y.6
Suzuki, N.7
Mason, B.8
Drayna, D.9
Sugawara, M.10
Sugimoto, M.11
Furuichi, Y.12
-
7
-
-
0013907774
-
Werner's syndrome. A review of its symptomatology, natural history, pathologic features, genetics and relationship to natural aging process
-
Epstein CJ, Martin GM, Schultz AG, Motulsky AG. Werner's syndrome. A review of its symptomatology, natural history, pathologic features, genetics and relationship to natural aging process. Medicine (Baltimore) 1966; 45:177-221.
-
(1966)
Medicine (Baltimore)
, vol.45
, pp. 177-221
-
-
Epstein, C.J.1
Martin, G.M.2
Schultz, A.G.3
Motulsky, A.G.4
-
8
-
-
0019507754
-
Family analysis of Werner's syndrome: A survey of 42 Japanese families with a review of the literature
-
Goto M, Tanimoto K, Horiuchi Y, Sasazuki T. Family analysis of Werner's syndrome: A survey of 42 Japanese families with a review of the literature. Clin Genet 1981; 19:8-15.
-
(1981)
Clin Genet
, vol.19
, pp. 8-15
-
-
Goto, M.1
Tanimoto, K.2
Horiuchi, Y.3
Sasazuki, T.4
-
9
-
-
0344867894
-
Prevalence of Werner's syndrome heterozygotes in Japan
-
Satoh M, Imai M, Sugimoto M, Goto M, Furuichi Y. Prevalence of Werner's syndrome heterozygotes in Japan. Lancet 1999; 353:1766.
-
(1999)
Lancet
, vol.353
, pp. 1766
-
-
Satoh, M.1
Imai, M.2
Sugimoto, M.3
Goto, M.4
Furuichi, Y.5
-
10
-
-
0343347966
-
A case of cataract associated with scleroderma
-
(in Japanese)
-
Ishida R. A case of cataract associated with scleroderma. Jap J Ophthalmol 1917; 21:1025-1032. (in Japanese)
-
(1917)
Jap J Ophthalmol
, vol.21
, pp. 1025-1032
-
-
Ishida, R.1
-
11
-
-
84875966509
-
Werner's syndrome: Report of a case with post-mortem findings
-
(in Japanese)
-
Hamada Y. Werner's syndrome: Report of a case with post-mortem findings. Jap J Clin Dermatol Urol 1966; 20:61-65. (in Japanese)
-
(1966)
Jap J Clin Dermatol Urol
, vol.20
, pp. 61-65
-
-
Hamada, Y.1
-
12
-
-
0342912735
-
Werner's syndrome associated with malignant melanoma
-
(in Japanese)
-
Koga M. Werner's syndrome associated with malignant melanoma. Jap J Clin Dermatol Urol 1968; 22:1160-1161. (in Japanese)
-
(1968)
Jap J Clin Dermatol Urol
, vol.22
, pp. 1160-1161
-
-
Koga, M.1
-
13
-
-
0022317420
-
Clinical, endocrine and metabolic aspects of the Werner syndrome compared with those of normal aging
-
Werner's syndrome and human aging (Salk D, Fujiwara Y, Martin GM, eds.). Plenum Press, New York
-
Imura H, Nakao Y, Kuzuya H, Okamoto M, Yamada K. Clinical, endocrine and metabolic aspects of the Werner syndrome compared with those of normal aging. In: Advances in experimental medicine and biology Vol. 190. Werner's syndrome and human aging (Salk D, Fujiwara Y, Martin GM, eds.). Plenum Press, New York, 1985; pp.171-185.
-
(1985)
Advances in experimental medicine and biology
, vol.190
, pp. 171-185
-
-
Imura, H.1
Nakao, Y.2
Kuzuya, H.3
Okamoto, M.4
Yamada, K.5
-
14
-
-
15844409553
-
Positional cloning of the Werner syndrome gene
-
Yu CE, Oshima J, Fu YH, Wijsman EM, Hisama F, Alisch R, Matthews S, Nakura J, Miki T, Ouais S, Martin GM, Mulligan J, Schellenberg GD. Positional cloning of the Werner syndrome gene. Science 1996; 272:258-262.
-
(1996)
Science
, vol.272
, pp. 258-262
-
-
Yu, C.E.1
Oshima, J.2
Fu, Y.H.3
Wijsman, E.M.4
Hisama, F.5
Alisch, R.6
Matthews, S.7
Nakura, J.8
Miki, T.9
Ouais, S.10
Martin, G.M.11
Mulligan, J.12
Schellenberg, G.D.13
-
15
-
-
0028914663
-
Hypercoagulable state indicates an additional risk factor for atherosclerosis in Werner's syndrome
-
Goto M, Kato Y. Hypercoagulable state indicates an additional risk factor for atherosclerosis in Werner's syndrome. Thromb Haemos 1995; 73:576-578.
-
(1995)
Thromb Haemos
, vol.73
, pp. 576-578
-
-
Goto, M.1
Kato, Y.2
-
16
-
-
33744990645
-
The spectrum of WRN mutations in Werner syndrome patients
-
Huang S, Lee L, Hanson NB, et al. The spectrum of WRN mutations in Werner syndrome patients. Hum Mut 2006; 27:558-567.
-
(2006)
Hum Mut
, vol.27
, pp. 558-567
-
-
Huang, S.1
Lee, L.2
Hanson, N.B.3
-
17
-
-
0034797703
-
Prevalence of Werner syndrome gene mutations in the Japanese population: A genetic epidemiological study
-
Gann Monograph on Cancer Research No. 49. From , (Goto M, Miller RW. eds. ). Karger, Tokyo
-
Satoh M, Matsumoto T, Imai M, Sugimoto M, Tsugane S, Furuichi Y, Goto M. Prevalence of Werner syndrome gene mutations in the Japanese population: A genetic epidemiological study. In: Gann Monograph on Cancer Research No.49. From premature gray hair to helicase-Werner syndrome: Implications for aging and cancer (Goto M, Miller RW. eds.). Karger, Tokyo, 2001; pp.19-25.
-
(2001)
premature gray hair to helicase-Werner syndrome: Implications for aging and cancer
, pp. 19-25
-
-
Satoh, M.1
Matsumoto, T.2
Imai, M.3
Sugimoto, M.4
Tsugane, S.5
Furuichi, Y.6
Goto, M.7
-
19
-
-
0014941144
-
Werner Syndrome
-
(in Dutch)
-
Degreef HJ. Werner Syndrome. Ned T Geneesk 1970; 114:666-668. (in Dutch)
-
(1970)
Ned T Geneesk
, vol.114
, pp. 666-668
-
-
Degreef, H.J.1
-
20
-
-
0035177905
-
Werner's syndrome (adult progeria): An affected mother and son presenting with resistant psychosis
-
Barak Y, Sirota P, Kimhi R, Slor H. Werner's syndrome (adult progeria): An affected mother and son presenting with resistant psychosis. Comprehen Psychiat 2001; 42:508-510.
-
(2001)
Comprehen Psychiat
, vol.42
, pp. 508-510
-
-
Barak, Y.1
Sirota, P.2
Kimhi, R.3
Slor, H.4
-
22
-
-
84877889945
-
Risk factor for NIDDM in asian population
-
(Sorrano-Rios M, Lefibvre PJ, eds. ), Elsevier Sci, New York
-
Goto, Y. Risk factor for NIDDM in asian population. In: Diabetes (Sorrano-Rios M, Lefibvre PJ, eds.), Elsevier Sci, New York, 1985; pp. 399-402.
-
(1985)
Diabetes
, pp. 399-402
-
-
Goto, Y.1
-
23
-
-
0028043864
-
Prevalence of diabetes mellitus in Japan compiled from literature
-
Kuzuya T. Prevalence of diabetes mellitus in Japan compiled from literature. Diab Res Clin Pract 1994; 24: S15-S21.
-
(1994)
Diab Res Clin Pract
, vol.24
-
-
Kuzuya, T.1
-
24
-
-
0028029975
-
Prevalence and incidence of diabetes mellitus by WHO criteria
-
Akazawa Y. Prevalence and incidence of diabetes mellitus by WHO criteria. Diab Res Clin Pract 1994; 24: S23-S27.
-
(1994)
Diab Res Clin Pract
, vol.24
-
-
Akazawa, Y.1
-
27
-
-
33847790504
-
Telomere dysfunction as a cause of genomic instability in Werner syndrome
-
Crabbe L, Jauch A, Naeger CM, Holtgreve-Grez H, Karlseder, J. Telomere dysfunction as a cause of genomic instability in Werner syndrome. Proc Natl Acad Sci USA 2007; 104:2205-2210.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 2205-2210
-
-
Crabbe, L.1
Jauch, A.2
Naeger, C.M.3
Holtgreve-Grez, H.4
Karlseder, J.5
-
28
-
-
0031751941
-
vivo somatic mutations in Werner's syndrome
-
Kyoizumi S, Kusunoki Y, Seyama T, Hatamochi A, Goto M. In vivo somatic mutations in Werner's syndrome. Hum Genet 1998; 103:405-410.
-
(1998)
Hum Genet
, vol.103
, pp. 405-410
-
-
Kyoizumi, S.1
Kusunoki, Y.2
Seyama, T.3
Hatamochi, A.4
Goto, M.5
|