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 *

151 related articles for article (PubMed ID: 9850762)

  • 1. [X-linked recessive bulbospinal muscular atrophy (Kennedy's disease). A family study].
    Kaimen-Maciel DR; Medeiros M; Clímaco V; Kelian GR; da Silva LS; de Souza MM; Raskin S
    Arq Neuropsiquiatr; 1998 Sep; 56(3B):639-45. PubMed ID: 9850762
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The DNA diagnosis for bulbospinal muscular atrophy.
    Ohno M; Yamada T; Kobayashi T; Goto I
    Clin Neurol Neurosurg; 1994 Feb; 96(1):20-3. PubMed ID: 8187377
    [TBL] [Abstract][Full Text] [Related]  

  • 3. X-linked spinal muscular atrophy (Kennedy's syndrome). A kindred with hypobetalipoproteinemia.
    Warner CL; Servidei S; Lange DJ; Miller E; Lovelace RE; Rowland LP
    Arch Neurol; 1990 Oct; 47(10):1117-20. PubMed ID: 2222245
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. [A familial case of Kennedy's X-linked bulbospinal amyotrophy].
    Muradian GT; Tunian IuS; Khachunts AS; Samvelian KG
    Zh Nevrol Psikhiatr Im S S Korsakova; 1993; 93(2):84-6. PubMed ID: 8048316
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Kennedy's disease: a clinicopathologic correlation with mutations in the androgen receptor gene.
    Amato AA; Prior TW; Barohn RJ; Snyder P; Papp A; Mendell JR
    Neurology; 1993 Apr; 43(4):791-4. PubMed ID: 8469342
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Kennedy's disease: genetic diagnosis of an inherited form of motor neuron disease.
    Choi WT; MacLean HE; Chu S; Warne GL; Zajac JD
    Aust N Z J Med; 1993 Apr; 23(2):187-92. PubMed ID: 8517843
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [DNA-diagnosis of bulbospinal muscular atrophy (Kennedy's disease)].
    Malygina NA; Kazakov AE; Dubchak LV
    Zh Nevrol Psikhiatr Im S S Korsakova; 1997; 97(12):35-8. PubMed ID: 9591063
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Kennedy's disease: expansion of the CAG trinucleotide].
    Domitrz I; Jedrzejowska M; Lipowska M; Siddique T; Kwieciński H
    Neurol Neurochir Pol; 2001; 35(1 Suppl):107-14. PubMed ID: 11732276
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [X-chromosomal bulbospinal muscular atrophy (Kennedy syndrome)].
    Berkhoff M; Sturzenegger M; Spiegel R; Rösler KM; Hess CW
    Schweiz Med Wochenschr; 1998 May; 128(21):817-23. PubMed ID: 9642748
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Chromosome X-linked recessive bulbospinal neuronopathy (Kennedy's syndrome)].
    Mauri Llerda JA; Jiménez Escrig A; del Villar Sordo V
    An Med Interna; 1989 Nov; 6(11):608-9. PubMed ID: 2562713
    [No Abstract]   [Full Text] [Related]  

  • 12. [Kennedy disease: report of 2 cases].
    Seefeld M; Cunha FM; Ferraz LE; Scola RH; Werneck LC
    Arq Neuropsiquiatr; 1995 Sep; 53(3-A):471-4. PubMed ID: 8540824
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [X-linked recessive bulbospinal neuronopathy--Kennedy's syndrome].
    Andersen KV; Michler RP; Nilssen O; Tranebjaerg L; Aasly J
    Tidsskr Nor Laegeforen; 1999 Apr; 119(11):1591-4. PubMed ID: 10385801
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. [The DNA diagnosis of a familial case of Kennedy's spinal and bulbar amyotrophy].
    Petrukhin AS; Zavadenko NN; Petrukhin AA; Evgrafov OV
    Zh Nevrol Psikhiatr Im S S Korsakova; 1997; 97(3):45-8. PubMed ID: 9157759
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy.
    Belsham DD; Yee WC; Greenberg CR; Wrogemann K
    J Neurol Sci; 1992 Oct; 112(1-2):133-8. PubMed ID: 1469423
    [TBL] [Abstract][Full Text] [Related]  

  • 17. X-linked spinal and bulbar muscular atrophy (Kennedy's disease) with long-term electrophysiological evaluation: case report.
    Kouyoumdjian JA; Morita Mda P; Araújo RG
    Arq Neuropsiquiatr; 2005 Mar; 63(1):154-9. PubMed ID: 15830083
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical manifestations and AR gene mutations in Kennedy's disease.
    Liu X; Zhu M; Li X; Tang J
    Funct Integr Genomics; 2019 May; 19(3):533-539. PubMed ID: 30612224
    [TBL] [Abstract][Full Text] [Related]  

  • 19. X-linked bulbospinal muscular atrophy (Kennedy's syndrome): a report of three cases.
    Ertekin C; Sirin H
    Acta Neurol Scand; 1993 Jan; 87(1):56-61. PubMed ID: 8424313
    [TBL] [Abstract][Full Text] [Related]  

  • 20. X-linked spinal and bulbar muscular atrophy (Kennedy's disease): the first case described in the Brazilian Amazon.
    Alves CN; Braga TKK; Somensi DN; Nascimento BSVD; Lima JAS; Fujihara S
    Einstein (Sao Paulo); 2018 Jun; 16(2):eRC4011. PubMed ID: 29898093
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.