152 related articles for article (PubMed ID: 33118681)
1. Preface to Management guideline for Werner syndrome 2020.
Takemoto M; Yokote K
Geriatr Gerontol Int; 2021 Feb; 21(2):131-132. PubMed ID: 33118681
[No Abstract] [Full Text] [Related]
2. Management guideline for Werner syndrome 2020. 4. Osteoporosis associated with Werner syndrome.
Mori S; Takemoto M; Kubota Y; Taniguchi T; Motegi SI; Taniguchi A; Nakagami H; Maezawa Y; Koshizaka M; Kato H; Tsukamoto K; Kuzuya M; Yokote K
Geriatr Gerontol Int; 2021 Feb; 21(2):146-149. PubMed ID: 33155383
[No Abstract] [Full Text] [Related]
3. Updated understanding of WRN variants using the Japanese whole-genome reference panel 3.5KJPNv2.
Fukunaga H; Prise KM; Taki Y
Geriatr Gerontol Int; 2019 Sep; 19(9):961-962. PubMed ID: 31490004
[No Abstract] [Full Text] [Related]
4. WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects.
Yokote K; Chanprasert S; Lee L; Eirich K; Takemoto M; Watanabe A; Koizumi N; Lessel D; Mori T; Hisama FM; Ladd PD; Angle B; Baris H; Cefle K; Palanduz S; Ozturk S; Chateau A; Deguchi K; Easwar TK; Federico A; Fox A; Grebe TA; Hay B; Nampoothiri S; Seiter K; Streeten E; Piña-Aguilar RE; Poke G; Poot M; Posmyk R; Martin GM; Kubisch C; Schindler D; Oshima J
Hum Mutat; 2017 Jan; 38(1):7-15. PubMed ID: 27667302
[TBL] [Abstract][Full Text] [Related]
5. Recent Trends in WRN Gene Mutation Patterns in Individuals with Werner Syndrome.
Yamaga M; Takemoto M; Takada-Watanabe A; Koizumi N; Kitamoto T; Sakamoto K; Ishikawa T; Koshizaka M; Maezawa Y; Yokote K
J Am Geriatr Soc; 2017 Aug; 65(8):1853-1856. PubMed ID: 28394436
[TBL] [Abstract][Full Text] [Related]
6. Uncommon cause of cirrhosis-A case of Werner syndrome with a novel WRN mutation.
Amalnath SD; Sargolzaeiaval F; Oshima J; Baskar D
Indian J Gastroenterol; 2017 Jul; 36(4):323-325. PubMed ID: 28795391
[TBL] [Abstract][Full Text] [Related]
7. A novel WRN mutation identified in a patient with Werner syndrome and acute generalized exanthematous pustulosis.
Kawai T; Hayashi R; Hama N; Shinkuma S; Fujimoto A; Shimomura Y; Abe R
Eur J Dermatol; 2018 Aug; 28(4):553-554. PubMed ID: 29952303
[No Abstract] [Full Text] [Related]
8. Nailfold scleroderma-like capillary abnormalities in Werner syndrome (adult progeria).
Ingegnoli F; Crotti C
Vasc Med; 2017 Jun; 22(3):246-247. PubMed ID: 28466674
[No Abstract] [Full Text] [Related]
9. Characteristic Clinical Features of Werner Syndrome with a Novel Compound Heterozygous WRN Mutation c.1720+1G>A Plus c.3139-1G>C.
Matsumoto N; Ohta Y; Deguchi K; Kishida M; Sato K; Shang J; Takemoto M; Hishikawa N; Yamashita T; Watanabe A; Yokote K; Takemoto M; Oshima J; Abe K
Intern Med; 2019 Apr; 58(7):1033-1036. PubMed ID: 30568144
[TBL] [Abstract][Full Text] [Related]
10. Werner syndrome: a changing pattern of clinical manifestations in Japan (1917~2008).
Goto M; Ishikawa Y; Sugimoto M; Furuichi Y
Biosci Trends; 2013 Feb; 7(1):13-22. PubMed ID: 23524889
[TBL] [Abstract][Full Text] [Related]
11. The progerias.
Fossel M
J Anti Aging Med; 2003; 6(2):123-38. PubMed ID: 14614801
[No Abstract] [Full Text] [Related]
12. Management guideline for Werner syndrome 2020. 5. Infection associated with Werner syndrome.
Taniguchi T; Takemoto M; Kubota Y; Motegi SI; Taniguchi A; Nakagami H; Maezawa Y; Koshizaka M; Kato H; Mori S; Tsukamoto K; Kuzuya M; Yokote K
Geriatr Gerontol Int; 2021 Feb; 21(2):150-152. PubMed ID: 33135262
[No Abstract] [Full Text] [Related]
13. The ophthalmic diagnosis and management of four siblings with Werner syndrome.
Lyons C; Gallagher D; McSwiney T; McElnea E; Kinsella F
Int Ophthalmol; 2019 Jun; 39(6):1371-1378. PubMed ID: 29705892
[TBL] [Abstract][Full Text] [Related]
14. A novel splice-site mutation of WRN (c.IVS28+2T>C) identified in a consanguineous family with Werner Syndrome.
Wu PF; Jin JY; Li JJ; He JQ; Fan LL; Jin M; Huang H; Xia K; Tang JY; Xiang R
Mol Med Rep; 2017 Jun; 15(6):3735-3738. PubMed ID: 28440507
[TBL] [Abstract][Full Text] [Related]
15. Management guideline for Werner syndrome 2020 1. Dyslipidemia and fatty liver associated with Werner syndrome.
Tsukamoto K; Takemoto M; Kubota Y; Taniguchi T; Motegi SI; Taniguchi A; Nakagami H; Maezawa Y; Koshizaka M; Kato H; Mori S; Kuzuya M; Yokote K
Geriatr Gerontol Int; 2021 Feb; 21(2):133-138. PubMed ID: 33258561
[TBL] [Abstract][Full Text] [Related]
16. WRN, the Werner Syndrome Gene, Exhibits Frameshift Mutations in Gastric and Colorectal Cancers.
Lee JH; Kim SS; Kim MS; Yoo NJ; Lee SH
Pathol Oncol Res; 2017 Apr; 23(2):451-452. PubMed ID: 28012115
[No Abstract] [Full Text] [Related]
17. The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis.
Muftuoglu M; Oshima J; von Kobbe C; Cheng WH; Leistritz DF; Bohr VA
Hum Genet; 2008 Nov; 124(4):369-77. PubMed ID: 18810497
[TBL] [Abstract][Full Text] [Related]
18. Werner syndrome: entering the helicase era.
Epstein CJ; Motulsky AG
Bioessays; 1996 Dec; 18(12):1025-7. PubMed ID: 8976161
[TBL] [Abstract][Full Text] [Related]
19. [Werner's syndrome].
Suzuki K; Hattori Y; Kasai K
Nihon Rinsho; 2006 Sep; Suppl 3():134-7. PubMed ID: 17022517
[No Abstract] [Full Text] [Related]
20. [Werner syndrome].
Kato Y
Ryoikibetsu Shokogun Shirizu; 2000; (32):454-7. PubMed ID: 11212773
[No Abstract] [Full Text] [Related]
[Next] [New Search]