BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 9296165)

  • 1. [Clinical study of familial forms of amyotrophic lateral sclerosis. Review of the literature].
    Moulard B; Camu W; Malafosse A; Billiard M; Baldy-Moulinier M
    Rev Neurol (Paris); 1997 Jun; 153(5):314-24. PubMed ID: 9296165
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A molecular genetic approach to amyotrophic lateral sclerosis.
    Siddique T; Hu P; Hentati A; Deng G; Hung WY; McInnis MG; Warren AC; Rimmler J; Antonarakis S; Pericak-Vance MA
    Int J Neurol; 1991-1992; 25-26():60-9. PubMed ID: 11980064
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Where is the role of the genetic investigations in amyotrophic lateral sclerosis?].
    Vandenberghe N
    Rev Neurol (Paris); 2006 Jun; 162 Spec No 2():4S96-4S101. PubMed ID: 17128095
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [What is the role of the genetic survey in amyotrophic lateral sclerosis?].
    Camu W
    Rev Neurol (Paris); 2006 Jun; 162 Spec No 2():4S91-4S95. PubMed ID: 17128094
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Methods of the announcement of amyotrophic lateral sclerosis diagnosis in familial forms].
    Corcia P
    Rev Neurol (Paris); 2006 Jun; 162 Spec No 2():4S122-4S126. PubMed ID: 17128099
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cognitive impairment in familial ALS.
    Wheaton MW; Salamone AR; Mosnik DM; McDonald RO; Appel SH; Schmolck HI; Ringholz GM; Schulz PE
    Neurology; 2007 Oct; 69(14):1411-7. PubMed ID: 17909153
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in Belgium.
    Aguirre T; Matthijs G; Robberecht W; Tilkin P; Cassiman JJ
    Eur J Hum Genet; 1999 Jul; 7(5):599-602. PubMed ID: 10439968
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Differentiation between primary lateral sclerosis and amyotrophic lateral sclerosis: examination of symptoms and signs at disease onset and during follow-up.
    Tartaglia MC; Rowe A; Findlater K; Orange JB; Grace G; Strong MJ
    Arch Neurol; 2007 Feb; 64(2):232-6. PubMed ID: 17296839
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [On intra-familial clinical diversities of a familial amyotrophic lateral sclerosis with a point mutation of Cu/Zn superoxide dismutase (Asn 86-Ser].
    Maeda T; Kurahashi K; Matsunaga M; Inoue K; Inoue M
    No To Shinkei; 1997 Sep; 49(9):847-51. PubMed ID: 9311004
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Survival in amyotrophic lateral sclerosis].
    Alcaz S; Jarebinski M; Pekmezović T; Marinković Z; Apostolski S
    Srp Arh Celok Lek; 1997; 125(1-2):19-23. PubMed ID: 17974351
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation.
    Jackson M; Al-Chalabi A; Enayat ZE; Chioza B; Leigh PN; Morrison KE
    Ann Neurol; 1997 Nov; 42(5):803-7. PubMed ID: 9392581
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genistein is neuroprotective in murine models of familial amyotrophic lateral sclerosis and stroke.
    Trieu VN; Uckun FM
    Biochem Biophys Res Commun; 1999 May; 258(3):685-8. PubMed ID: 10329446
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Amyotrophic lateral sclerosis and Alzheimer disease. Lessons from model systems.
    Price DL; Wong PC; Borchelt DR; Pardo CA; Thinakaran G; Doan AP; Lee MK; Martin LJ; Sisodia SS
    Rev Neurol (Paris); 1997 Sep; 153(8-9):484-95. PubMed ID: 9683997
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Do bulbar-onset amyotrophic lateral sclerosis patients have an earlier respiratory involvement than spinal-onset amyotrophic lateral sclerosis patients?
    Pinto S; Pinto A; De Carvalho M
    Eura Medicophys; 2007 Dec; 43(4):505-9. PubMed ID: 18084174
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Amyotrophic lateral sclerosis.
    Jackson CE; Bryan WW
    Semin Neurol; 1998; 18(1):27-39. PubMed ID: 9562665
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Thioredoxin reductase 1 haplotypes modify familial amyotrophic lateral sclerosis onset.
    Mitchell J; Morris A; de Belleroche J
    Free Radic Biol Med; 2009 Jan; 46(2):202-11. PubMed ID: 18996185
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Young-onset sporadic amyotrophic lateral sclerosis: a distinct nosological entity?
    Gouveia LO; de Carvalho M
    Amyotroph Lateral Scler; 2007 Dec; 8(6):323-7. PubMed ID: 17852021
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The changes of clinical characteristics in 100 Japanese amyotrophic lateral sclerosis patients between 1980 and 2000].
    Kimura F; Shinoda K; Fujiwara S; Fujimura C; Nakajima H; Furutama D; Sugino M; Hanafusa T
    Rinsho Shinkeigaku; 2003 Jul; 43(7):385-91. PubMed ID: 14582363
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Natural history of young-adult amyotrophic lateral sclerosis.
    Sabatelli M; Madia F; Conte A; Luigetti M; Zollino M; Mancuso I; Lo Monaco M; Lippi G; Tonali P
    Neurology; 2008 Sep; 71(12):876-81. PubMed ID: 18596241
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical and genetic heterogeneity of amyotrophic lateral sclerosis.
    Sabatelli M; Conte A; Zollino M
    Clin Genet; 2013 May; 83(5):408-16. PubMed ID: 23379621
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.