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 *

141 related articles for article (PubMed ID: 8048316)

  • 1. [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]  

  • 2. [Familial case of late recessive X-linked Kennedy's spinal and bulbar amyotrophy].
    Badalian LO; Temin PA; Arkhipov BA; Zavadenko NN; Bulaeva NV; Lysov VL
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1989; 89(12):39-44. PubMed ID: 2633568
    [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. [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]  

  • 5. [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]  

  • 6. [Neuroendocrine syndrome: pseudomyopathic spinal amyotrophy with gynecomastia related to the X chromosome. Kennedy's syndrome. 3 cases].
    Serratrice G; Pellissier JF; Pouget J; Saint-Jean JC
    Presse Med; 1987 Feb; 16(6):299-302. PubMed ID: 2950466
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Kennedy's syndrome. A differential diagnosis of amyotrophic lateral sclerosis with slow progress and good prognosis].
    Lindvall B; Dahle L
    Lakartidningen; 1994 Oct; 91(43):3913-7. PubMed ID: 7967961
    [No 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. [Sensory nerve involvement in X-linked bulbospinal amyotrophy (Kennedy syndrome). Contributions of electrophysiologic and histologic data].
    Penisson-Besnier I; Dubas F; Delestre F; Emile J
    Neurophysiol Clin; 1989 May; 19(2):163-70. PubMed ID: 2542754
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. [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]  

  • 13. [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]  

  • 14. 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]  

  • 15. The expanded trinucleotide repeat in Kennedy's disease.
    Fischbeck KH
    Proc Assoc Am Physicians; 1995 Jul; 107(2):228-30. PubMed ID: 8624856
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. [X chromosome-linked bulbospinal neuronopathy in adults].
    Mozolevskiĭ IuV
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1989; 89(3):121-3. PubMed ID: 2728735
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Familial distal progressive spinal amyotrophy with asymmetry of the lower limbs].
    Nedelec C; Dubas F; Truelle JL; Pouplard F; Delestre F; Penisson-Besnier I
    Rev Neurol (Paris); 1987; 143(11):765-7. PubMed ID: 3432850
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. [X-linked bulbo-spinal neuronopathy. Kennedy's syndrome].
    Serratrice G; Pellissier JF; Pouget J
    Rev Neurol (Paris); 1988; 144(11):756-8. PubMed ID: 3231965
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.