Zobrazeno 1 - 10
of 26
pro vyhledávání: '"R J, Barohn"'
Autor:
R G, Miller, D H, Moore, D A, Forshew, J S, Katz, R J, Barohn, M, Valan, M B, Bromberg, K L, Goslin, M C, Graves, L F, McCluskey, A L, McVey, T, Mozaffar, J M, Florence, A, Pestronk, M, Ross, E P, Simpson, S H, Appel, Lauren, Elman
Publikováno v:
Neurology. 77:973-979
Objective: To use a historical placebo control design to determine whether lithium carbonate slows progression of amyotrophic lateral sclerosis (ALS). Methods: A phase II trial was conducted at 10 sites in the Western ALS Study Group using similar do
Autor:
R J, Barohn, A A, Amato
Publikováno v:
Seminars in Neurology. 19:45-58
Although muscle disease classically presents with proximal extremity weakness, some myopathic disorders, including several types of muscular dystrophy, result in predominantly, or exclusively, distal muscle involvement. Accurate diagnosis of these re
Publikováno v:
Journal of clinical neuromuscular disease. 2(2)
Publikováno v:
Journal of clinical neuromuscular disease. 2(2)
Publikováno v:
Musclenerve. 37(4)
We developed a disease-specific, 10-point functional rating scale for patients with inclusion body myositis (IBMFRS). The IBMFRS was utilized as a secondary outcome measure in a multicenter pilot trial of the clinical safety and tolerability of high-
Publikováno v:
Musclenerve. 24(3)
A number of presentations of chronic demyelinating polyneuropathy have been identified, each distinguished by its phenotypic pattern. In addition to classic chronic inflammatory demyelinating polyneuropathy (CIDP), which is characterized clinically b
Autor:
J, Katz, R J, Barohn
Publikováno v:
Physical medicine and rehabilitation clinics of North America. 12(2)
Many recent strides have increased our understanding of the immune-mediated diseases of neuromuscular junction transmission. Nevertheless, patients with myasthenia gravis and the Lambert-Eaton myasthenic syndrome often present diagnostic and therapeu
Publikováno v:
The Annals of thoracic surgery. 70(1)
Publikováno v:
Musclenerve. 23(4)
McArdle's disease or myophosphorylase deficiency is one of the most common muscle glycogenoses and typically presents in childhood or adolescence with exercise intolerance, myalgia, myoglobinuria, and cramps in exercising muscle. We describe an elder
Autor:
M A, Ross, R G, Miller, L, Berchert, G, Parry, R J, Barohn, C, Armon, W W, Bryan, J, Petajan, S, Stromatt, J, Goodpasture, D, McGuire
Publikováno v:
Neurology. 50(3)
We modified the World Federation of Neurology (WFN) diagnostic criteria for ALS to facilitate early diagnosis and used these criteria for enrollment of ALS patients in a clinical trial. The criteria developed required lower motor neuron (LMN) involve