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8. [A case of Kennedy-Alter-Sung syndrome with type IIa hyperlipidemia--study on sex hormone receptor and lipid metabolism]. Matsuura T; Aimoto Y; Moriwaka F; Tashiro K; Nonomura K Rinsho Shinkeigaku; 1991 Mar; 31(3):291-5. PubMed ID: 1893668 [TBL] [Abstract][Full Text] [Related]
9. [Tissue variability of androgen receptor gene in bulbospinal muscular atrophy--comparison of the number of CAG repeats between muscles and peripheral blood leukocytes]. Nakajima H; Kimura F; Shinoda K; Ohsawa N; Nakagawa T; Shimizu A Rinsho Shinkeigaku; 1993 Oct; 33(10):1103-5. PubMed ID: 8293617 [TBL] [Abstract][Full Text] [Related]
10. Longitudinal changes of outcome measures in spinal and bulbar muscular atrophy. Hashizume A; Katsuno M; Banno H; Suzuki K; Suga N; Mano T; Atsuta N; Oe H; Watanabe H; Tanaka F; Sobue G Brain; 2012 Sep; 135(Pt 9):2838-48. PubMed ID: 22773541 [TBL] [Abstract][Full Text] [Related]
11. [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]
12. Polymorphic CAG repeat length in the androgen receptor gene and association with neurodegeneration in a heterozygous female carrier of Kennedy's disease. Greenland KJ; Beilin J; Castro J; Varghese PN; Zajac JD J Neurol; 2004 Jan; 251(1):35-41. PubMed ID: 14999487 [TBL] [Abstract][Full Text] [Related]
13. Men with Kennedy disease have a reduced risk of androgenetic alopecia. Sinclair R; Greenland KJ; Egmond Sv; Hoedemaker C; Chapman A; Zajac JD Br J Dermatol; 2007 Aug; 157(2):290-4. PubMed ID: 17596176 [TBL] [Abstract][Full Text] [Related]
14. Postural tremor in X-linked spinal and bulbar muscular atrophy. Hanajima R; Terao Y; Nakatani-Enomoto S; Hamada M; Yugeta A; Matsumoto H; Yamamoto T; Tsuji S; Ugawa Y Mov Disord; 2009 Oct; 24(14):2063-9. PubMed ID: 19746452 [TBL] [Abstract][Full Text] [Related]
15. Pure bulbar motor neuron involvement linked to an abnormal CAG repeat expansion in the androgen receptor gene. Praline J; Guennoc AM; Malinge MC; de Toffol B; Corcia P Amyotroph Lateral Scler; 2008 Feb; 9(1):40-2. PubMed ID: 17852020 [TBL] [Abstract][Full Text] [Related]
16. A phenotypic-genetic study of a group of Polish patients with spinal and bulbar muscular atrophy. Tomik B; Partyka D; Sułek A; Kurek-Gryz EA; Banach M; Ostrowska M; Zaremba J; Figlewicz DA; Szczudlik A Amyotroph Lateral Scler; 2006 Jun; 7(2):72-9. PubMed ID: 16753970 [TBL] [Abstract][Full Text] [Related]
17. [A case presenting manifestations of bulbospinal muscular atrophy with senile onset, rapid progression and marked asymmetry]. Imai T; Kaneshige Y; Sasaki K; Chiba S; Matsumoto H Rinsho Shinkeigaku; 1989 Mar; 29(3):379-81. PubMed ID: 2752668 [TBL] [Abstract][Full Text] [Related]
18. Phenotypic variability in Kennedy's disease: implication of the early diagnostic features. Lee JH; Shin JH; Park KP; Kim IJ; Kim CM; Lim JG; Choi YC; Kim DS Acta Neurol Scand; 2005 Jul; 112(1):57-63. PubMed ID: 15932358 [TBL] [Abstract][Full Text] [Related]
19. [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]
20. [Two brothers with very late onset of muscle weakness in X-linked recessive spinal and bulbar muscular atrophy]. Hemmi S; Inoue K; Kutoku Y; Rikimaru M; Murakami T; Sunada Y Rinsho Shinkeigaku; 2009 Jan; 49(1):22-6. PubMed ID: 19227892 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]