182 related articles for article (PubMed ID: 33087645)
1. Severe metabolic disorders coexisting with Werner syndrome: a case report.
Li H; Yang M; Shen H; Wang S; Cai H
Endocr J; 2021 Mar; 68(3):261-267. PubMed ID: 33087645
[TBL] [Abstract][Full Text] [Related]
2. The identification of a novel mutation (p.I223fs) in WRN associated with Werner syndrome.
Wu J; Pan S; Lin W; Wen J; Lu R; Chen G
Endocrine; 2024 Apr; 84(1):92-96. PubMed ID: 37856055
[TBL] [Abstract][Full Text] [Related]
3. Werner syndrome in a Lebanese family.
Jaafar B; Nasrallah M; Sievers B; Oshima J; Lessel D
Am J Med Genet A; 2022 May; 188(5):1630-1634. PubMed ID: 35037378
[TBL] [Abstract][Full Text] [Related]
4. A case of Werner syndrome without metabolic abnormality: implications for the early pathophysiology.
Takada-Watanabe A; Yokote K; Takemoto M; Fujimoto M; Irisuna H; Honjo S; Futami K; Furuichi Y; Saito Y
Geriatr Gerontol Int; 2012 Jan; 12(1):140-6. PubMed ID: 22188495
[TBL] [Abstract][Full Text] [Related]
5. Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions.
Oshima J; Sidorova JM; Monnat RJ
Ageing Res Rev; 2017 Jan; 33():105-114. PubMed ID: 26993153
[TBL] [Abstract][Full Text] [Related]
6. Werner syndrome presenting as early-onset diabetes: A case report.
Wang X; Liu S; Qin F; Liu Q; Wang Q
J Diabetes Investig; 2022 Mar; 13(3):592-598. PubMed ID: 34564935
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Adult progeria: a new mutation in the WRN gene.
Rocha ML; Chicharo AT; Sequeira G; Teixeira V
BMJ Case Rep; 2022 Nov; 15(11):. PubMed ID: 36396328
[TBL] [Abstract][Full Text] [Related]
9. Case Report: A novel
Peng H; Wang J; Liu Y; Yang H; Li L; Ma Y; Zhuo H; Jiang H
Front Endocrinol (Lausanne); 2022; 13():918979. PubMed ID: 35909544
[TBL] [Abstract][Full Text] [Related]
10. Werner syndrome and mutations of the WRN and LMNA genes in France.
Uhrhammer NA; Lafarge L; Dos Santos L; Domaszewska A; Lange M; Yang Y; Aractingi S; Bessis D; Bignon YJ
Hum Mutat; 2006 Jul; 27(7):718-9. PubMed ID: 16786514
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. [Atypical Werner syndrome: Atypical progeroid syndrome: A case report].
Barrios Sanjuanelo A; Muñoz Otero C
An Pediatr (Barc); 2010 Aug; 73(2):94-7. PubMed ID: 20452840
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Diabetes mellitus coexisted with progeria: a case report of atypical Werner syndrome with novel LMNA mutations and literature review.
He G; Yan Z; Sun L; Lv Y; Guo W; Gang X; Wang G
Endocr J; 2019 Nov; 66(11):961-969. PubMed ID: 31270292
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Werner syndrome associated with acroosteolysis.
Khalid T; Inam F; Iqbal MA
Dermatol Online J; 2022 Aug; 28(4):. PubMed ID: 36259858
[TBL] [Abstract][Full Text] [Related]
18. Werner syndrome (WRN) gene variants and their association with altered function and age-associated diseases.
Lebel M; Monnat RJ
Ageing Res Rev; 2018 Jan; 41():82-97. PubMed ID: 29146545
[TBL] [Abstract][Full Text] [Related]
19. Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndrome.
Donadille B; D'Anella P; Auclair M; Uhrhammer N; Sorel M; Grigorescu R; Ouzounian S; Cambonie G; Boulot P; Laforêt P; Carbonne B; Christin-Maitre S; Bignon YJ; Vigouroux C
Orphanet J Rare Dis; 2013 Jul; 8():106. PubMed ID: 23849162
[TBL] [Abstract][Full Text] [Related]
20. A novel compound heterozygous mutation in Werner syndrome results in WRN transcript decay.
Müller FB; Tsianakas A; Kuwert C; Korge BP; Hunzelmann N
Br J Dermatol; 2005 May; 152(5):1030-2. PubMed ID: 15888165
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
