Consensus guidelines for the design and implementation of clinical trials in ALS
暂无分享,去创建一个
[1] R. Sufit,et al. Practice parameter: The care of the patient with amyotrophic lateral sclerosis (an evidence-based review) , 1999, Neurology.
[2] R. Barohn,et al. Toward earlier diagnosis of amyotrophic lateral sclerosis , 1998, Neurology.
[3] J. Cedarbaum,et al. Prognostic indicators of survival in ALS , 1998, Neurology.
[4] M. Gaweł,et al. Effect of recombinant human insulin-like growth factor-I on progression of ALS , 1997, Neurology.
[5] J. Petajan,et al. Reliability of maximal voluntary isometric contraction testing in a multicenter study of patients with amyotrophic lateral sclerosis , 1997, Muscle & nerve.
[6] K. Schulz. The quest for unbiased research: Randomized clinical trials and the CONSORT reporting guidelines , 1997, Annals of neurology.
[7] Michelle Mendoza,et al. Guidelines for the use and performance of quantitative outcome measures in ALS clinical trials , 1997, Journal of the Neurological Sciences.
[8] G. Parry,et al. Placebo-controlled trial of gabapentin in patients with amyotrophic lateral sclerosis , 1996, Neurology.
[9] National-Isometric-Muscle-Strength-Database-Consor. Muscular weakness assessment: use of normal isometric strength data. The National Isometric Muscle Strength (NIMS) Database Consortium. , 1996, Archives of physical medicine and rehabilitation.
[10] P. Leigh,et al. Dose-ranging study of riluzole in amyotrophic lateral sclerosis , 1996, The Lancet.
[11] G. Parry,et al. A placebo‐controlled trial of recombinant human ciliary neurotrophic (rhCNTF) factor in amyotrophic lateral sclerosis , 1996 .
[12] S H Appel,et al. Natural history of amyotrophic lateral sclerosis in a database population. Validation of a scoring system and a model for survival prediction. , 1995, Brain : a journal of neurology.
[13] V. Meininger,et al. A controlled trial of riluzole in amyotrophic lateral sclerosis. ALS/Riluzole Study Group. , 1994, The New England journal of medicine.
[14] J. R. Brinkmann,et al. The natural history of amyotrophic lateral sclerosis , 1993, Neurology.
[15] T. Munsat,et al. Recombinant growth hormone treatment of amyotrophic lateral sclerosis , 1993, Muscle & nerve.
[16] P. Andres,et al. Use of composite scores (megascores) to measure deficit in amyotrophic lateral sclerosis , 1988, Neurology.
[17] J. Caroscio,et al. Amyotrophic lateral sclerosis. Its natural history. , 1987, Neurologic clinics.
[18] W. Bradley,et al. Amyotrophc Lateral Sclerosis: Part 1. Clinical Features, Pathology, and E h c d Issues in Management* , 2004 .
[19] A. Chiò,et al. Motor neuron disease in the province of Turin, Italy, 1966–1980 Survival analysis in an unselected population , 1984, Journal of the Neurological Sciences.
[20] A D Rosen,et al. Amyotrophic lateral sclerosis. Clinical features and prognosis. , 1978, Archives of neurology.
[21] P. Preux,et al. Survival prediction in sporadic amyotrophic lateral sclerosis. Age and clinical form at onset are independent risk factors. , 1996, Neuroepidemiology.
[22] I. Hemmi,et al. Clinical Statistics in 515 Fatal Cases of Motor Neuron Disease , 1984 .
[23] Olarte Mr. Therapeutic trials in amyotrophic lateral sclerosis. , 1982 .