BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 18608095)

  • 41. [Clinical characteristics of amyotrophic lateral sclerosis subsets].
    Pradat PF; Bruneteau G
    Rev Neurol (Paris); 2006 Jun; 162 Spec No 2():4S29-4S33. PubMed ID: 17128087
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Increasing incidence of ALS in Canterbury, New Zealand: a 22-year study.
    Murphy M; Quinn S; Young J; Parkin P; Taylor B
    Neurology; 2008 Dec; 71(23):1889-95. PubMed ID: 19047561
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Clinical and prognostic features of ALS/MND in different phenotypes-data from a hospital-based registry.
    Wei QQ; Chen Y; Chen X; Cao B; Ou R; Zhang L; Hou Y; Shang H
    Brain Res Bull; 2018 Sep; 142():403-408. PubMed ID: 30232045
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Duration of amyotrophic lateral sclerosis is age dependent.
    Eisen A; Schulzer M; MacNeil M; Pant B; Mak E
    Muscle Nerve; 1993 Jan; 16(1):27-32. PubMed ID: 8423829
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Phase angle is a prognostic factor for survival in amyotrophic lateral sclerosis.
    Desport JC; Marin B; Funalot B; Preux PM; Couratier P
    Amyotroph Lateral Scler; 2008 Oct; 9(5):273-8. PubMed ID: 18720089
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Reduced angiotensin II levels in the cerebrospinal fluid of patients with amyotrophic lateral sclerosis.
    Kawajiri M; Mogi M; Higaki N; Tateishi T; Ohyagi Y; Horiuchi M; Miki T; Kira JI
    Acta Neurol Scand; 2009 May; 119(5):341-4. PubMed ID: 18798831
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Natural history and clinical features of sporadic amyotrophic lateral sclerosis in China.
    Chen L; Zhang B; Chen R; Tang L; Liu R; Yang Y; Yang Y; Liu X; Ye S; Zhan S; Fan D
    J Neurol Neurosurg Psychiatry; 2015 Oct; 86(10):1075-81. PubMed ID: 26124198
    [TBL] [Abstract][Full Text] [Related]  

  • 48. The pseudopolyneuritic form of amyotrophic lateral sclerosis (Patrikios' disease).
    Cappellari A; Ciammola A; Silani V
    Electromyogr Clin Neurophysiol; 2008 Mar; 48(2):75-81. PubMed ID: 18435211
    [TBL] [Abstract][Full Text] [Related]  

  • 49. From clues to mechanisms: understanding ALS initiation and spread.
    Armon C
    Neurology; 2008 Sep; 71(12):872-3. PubMed ID: 18794489
    [No Abstract]   [Full Text] [Related]  

  • 50. [Phenotypic variation in ALS].
    Sasaki S
    Rinsho Shinkeigaku; 2006 Nov; 46(11):825-7. PubMed ID: 17432191
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Natural history and clinical features of the flail arm and flail leg ALS variants.
    Wijesekera LC; Mathers S; Talman P; Galtrey C; Parkinson MH; Ganesalingam J; Willey E; Ampong MA; Ellis CM; Shaw CE; Al-Chalabi A; Leigh PN
    Neurology; 2009 Mar; 72(12):1087-94. PubMed ID: 19307543
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Onset and spreading patterns of lower motor neuron involvements predict survival in sporadic amyotrophic lateral sclerosis.
    Fujimura-Kiyono C; Kimura F; Ishida S; Nakajima H; Hosokawa T; Sugino M; Hanafusa T
    J Neurol Neurosurg Psychiatry; 2011 Nov; 82(11):1244-9. PubMed ID: 21921087
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Identifying who will benefit from non-invasive ventilation in amyotrophic lateral sclerosis/motor neurone disease in a clinical cohort.
    Berlowitz DJ; Howard ME; Fiore JF; Vander Hoorn S; O'Donoghue FJ; Westlake J; Smith A; Beer F; Mathers S; Talman P
    J Neurol Neurosurg Psychiatry; 2016 Mar; 87(3):280-6. PubMed ID: 25857659
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Primary lateral sclerosis.
    Singer MA; Statland JM; Wolfe GI; Barohn RJ
    Muscle Nerve; 2007 Mar; 35(3):291-302. PubMed ID: 17212349
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Amyotrophic Lateral Sclerosis Regional Variants (Brachial Amyotrophic Diplegia, Leg Amyotrophic Diplegia, and Isolated Bulbar Amyotrophic Lateral Sclerosis).
    Jawdat O; Statland JM; Barohn RJ; Katz JS; Dimachkie MM
    Neurol Clin; 2015 Nov; 33(4):775-85. PubMed ID: 26515621
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Neurophysiological index as a biomarker for ALS progression: validity of mixed effects models.
    Cheah BC; Vucic S; Krishnan AV; Boland RA; Kiernan MC
    Amyotroph Lateral Scler; 2011 Jan; 12(1):33-8. PubMed ID: 21271790
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Pronostic factors and survival in motor neuron disease].
    Larrode-Pellicer P; Alberti-González O; Iñiguez-Martínez C; Santos Lasaosa S; Pérez-Lázaro C; López del Val LJ
    Neurologia; 2007; 22(6):362-7. PubMed ID: 17610164
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Pure primary lateral sclerosis--Case reports.
    Tomik B; Zur KA; Szczudlik A
    Clin Neurol Neurosurg; 2008 Apr; 110(4):387-91. PubMed ID: 18262342
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Awaji diagnostic algorithm increases sensitivity of El Escorial criteria for ALS diagnosis.
    Carvalho MD; Swash M
    Amyotroph Lateral Scler; 2009 Feb; 10(1):53-7. PubMed ID: 18985466
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Progression rate of ALSFRS-R at time of diagnosis predicts survival time in ALS.
    Gordon PH; Cheung YK
    Neurology; 2006 Oct; 67(7):1314-5; author reply 1314-5. PubMed ID: 17030785
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.