These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 19623708)

  • 1. [A weak man... X chromosome associated progressive bulbospinal neuropathy (or bulbospinal amyotrophy) or Kennedy syndrome].
    Ricard D; Sallansonnet-Froment M; De Greslan T
    Rev Neurol (Paris); 2009 Feb; 165 Spec No 1():F29, F31. PubMed ID: 19623708
    [No Abstract]   [Full Text] [Related]  

  • 2. [Clinical features and genetic diagnosis of Kennedy disease].
    Xie MQ; Li XG; Cui LY; Liu MS; Li BH; Zhao YH
    Zhonghua Yi Xue Za Zhi; 2010 Sep; 90(35):2498-500. PubMed ID: 21092480
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Clinical and genetic analysis of a pedigree of Kennedy disease].
    Ou-Yang ZY; Song SJ; Liu JR; Zhang BR; Wu DW
    Zhejiang Da Xue Xue Bao Yi Xue Ban; 2011 Sep; 40(5):555-8. PubMed ID: 21984161
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A family with probable autosomal dominant bulbospinal muscular atrophy with gynecomastia].
    Matsuura E; Hokezu Y; Nakagawa M; Arimura H; Nagamatsu K
    Rinsho Shinkeigaku; 1999 Nov; 39(11):1135-7. PubMed ID: 10689936
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Molecular diagnosis for a patient with Kennedy disease].
    Tan J; Huang S; Wang H; Cai R; Zhao X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):754-6. PubMed ID: 25449082
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review.
    Valera Yepes R; Virgili Casas M; Povedano Panades M; Guerrero Gual M; Villabona Artero C
    Endocrinol Nutr; 2015 May; 62(5):224-30. PubMed ID: 25857692
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Investigation of a family with Kennedy disease by genetic analysis].
    Fan R; Zhang L; Zhang J; Shao B; Pan D; Lyu J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):750-3. PubMed ID: 25449081
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spinal and Bulbar Muscular Atrophy.
    Grunseich C; Fischbeck KH
    Neurol Clin; 2015 Nov; 33(4):847-54. PubMed ID: 26515625
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Chronic X-linked recessive bulbospinal amyotrophy (Kennedy-Stefanis type). Apropos of a case].
    Serratrice G; Guastalla P
    Sem Hop; 1984 Mar; 60(14):1003-5. PubMed ID: 6326279
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Perspectives of Kennedy's disease.
    Finsterer J
    J Neurol Sci; 2010 Nov; 298(1-2):1-10. PubMed ID: 20846673
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [X-linked recessive bulbospinal neuropathy (Kennedy syndrome)].
    Wulff CH; Sørensen SA; Trojaborg W
    Ugeskr Laeger; 1995 Nov; 157(46):6440-1. PubMed ID: 7483104
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Study on clinical manifestation, genotype and genetic characteristics of two Kennedy disease pedigrees].
    Yang J; Zhang C; Hu ZH; Zhan YX; Cao JQ; Ren H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):125-31. PubMed ID: 20376789
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A patient with Kennedy-Alter-Sung syndrome showing cardiomyopathy].
    Hattori T; Ikeda S; Yoshida K; Yanagisawa N; Furihata K; Yoshida K
    Rinsho Shinkeigaku; 1995 Nov; 35(11):1246-9. PubMed ID: 8720337
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Kennedy disease in a patient with progressive speech disorder].
    Kárteszi J; Morava E; Czakó M; Gáti I; Czopf J; Kosztolányi G; Melegh B
    Orv Hetil; 2001 Sep; 142(35):1915-7. PubMed ID: 11601179
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Kennedy disease in two sisters with biallelic CAG expansions of the androgen receptor gene.
    Müller KI; Nilssen Ø; Nebuchenykh M; Løseth S; Jonsrud C; Hoem G; Van Ghelue M; Arntzen KA
    Neuromuscul Disord; 2022 Jan; 32(1):75-79. PubMed ID: 34922802
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Kennedy disease misdiagnosed as polymyositis: a case report.
    Harutunian GM; Beydoun SR; Rison RA
    BMC Res Notes; 2013 Sep; 6():389. PubMed ID: 24073646
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genotype and clinical phenotype analysis of a Family with Kennedy disease.
    Cai BC; Zhong LF; Liu YH; Sui ZY; Yang Q; Zeng DT; Li X; Xu WD; Chen T
    Medicine (Baltimore); 2023 Apr; 102(15):e33502. PubMed ID: 37058074
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [X-chromosomal recessive spinobulbar muscular atrophy (Kennedy type). Description of a family, clinical aspects, molecular genetics, differential diagnosis and therapy].
    Kuhlenbäumer G; Bocchicchio M; Kress W; Young P; Oberwittler C; Stögbauer F
    Nervenarzt; 1998 Aug; 69(8):660-5. PubMed ID: 9757416
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Goserelin cannot improve the weakness of a patient with kennedy disease after 40-week administration.
    Shi ZG; Jiang DK; Zhao M; Zhang SQ
    CNS Neurosci Ther; 2012 Dec; 18(12):1021-3. PubMed ID: 23121864
    [No Abstract]   [Full Text] [Related]  

  • 20. [Molecular genetic study of a family with Kennedy syndrome including a symptomatic heterozygote].
    De Ferron E; Le Roux MG; Pascal O; Moisan JP; Fève JR
    Rev Neurol (Paris); 1994 Dec; 150(12):854-7. PubMed ID: 7676123
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.