F S WRIGHT
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Explore the profile of F S WRIGHT including associated specialties, affiliations and a list of published articles.
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109
Citations
1299
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Recent Articles
1.
Hawkins J, Moorman A, Hoffbrand A, Martineau M, WRIGHT F, Mehta A, et al.
Cancer Genet Cytogenet
. 1994 Oct;
77(2):134-43.
PMID: 7954324
Twenty-five patients with loss of part or all of 17p were selected from 701 patients with hematologic malignancies karyotyped either at diagnosis and/or at relapse and/or in refractory disease. Loss...
2.
Pledger G, Sackellares J, Treiman D, Pellock J, WRIGHT F, Mikati M, et al.
Neurology
. 1994 Oct;
44(10):1830-6.
PMID: 7936231
The National Institutes of Health sponsored a randomized, double-blind, multicenter, placebo-controlled trial of flunarizine (FNR) in epileptic patients receiving concomitant phenytoin (PHT) or carbamazepine (CBZ). Because of FNR's long half-life...
3.
Tsao C, WRIGHT F, Boesel C, Luquette M
Brain Dev
. 1994 Sep;
16(5):393-5.
PMID: 7892959
Mitochondrial myopathies are heterogeneous disorders. They may present at any age with a variable clinical course. We report a 6-year-old boy presenting as spastic cerebral palsy for 4 years, then...
4.
Williams L, Vieth R, WRIGHT F
Arch Phys Med Rehabil
. 1994 Jul;
75(7):787-91.
PMID: 8024426
In Charcot-Marie-Tooth syndrome (CMT, Hereditary Motor Sensory Neuropathy), patient complaints of cold intolerance are common but their peripheral responses to cold have not been documented. Using digital plethysmography, a simple...
5.
Tsao C, Romshe C, Lo W, WRIGHT F, Sommer A
J Child Neurol
. 1994 Apr;
9(2):135-8.
PMID: 8006362
Adrenal insufficiency has been associated with adrenoleukodystrophy and adrenomyeloneuropathy. In these diseases, plasma very long chain fatty acids are elevated. Peripheral neuropathy is frequently seen in adults with adrenomyeloneuropathy. We...
6.
Tsao C, Boesel C, WRIGHT F
J Child Neurol
. 1994 Jan;
9(1):90-1.
PMID: 8151092
Infantile acid maltase deficiency is an autosomal recessive disease that invariably leads to death in the first 2 years of life. Debrancher deficiency, also an autosomal recessive disease, however, carriers...
7.
Williams L, WRIGHT F
J Neurol Sci
. 1993 Dec;
120(2):195-200.
PMID: 8138809
Altered proportions of long-chain unsaturated n - 6 fatty acids (FA) in plasma and myelin of the heredodegenerative peripheral neuropathy, Charcot-Marie-Tooth syndrome (CMT), may implicate FA metabolism in the pathogenesis...
8.
Williams L, Shannon B, WRIGHT F
J Clin Immunol
. 1993 Nov;
13(6):389-96.
PMID: 7507126
Activated T cells, measured repeatedly in the demyelinating peripheral neuropathy, Charcot-Marie-Tooth syndrome (CMT; hereditary motor sensory neuropathy), might participate in myelin loss by a destructive inflammatory autoimmune process. To explore...
9.
Velazquez H, Perazella M, WRIGHT F, Ellison D
Ann Intern Med
. 1993 Aug;
119(4):296-301.
PMID: 8328738
Objectives: 1) To determine the incidence and severity of hyperkalemia during trimethoprim therapy. 2) To test the hypothesis that trimethoprim inhibits renal potassium excretion by blocking sodium channels in the...
10.
Morsing P, Velazquez H, Ellison D, WRIGHT F
Acta Physiol Scand
. 1993 May;
148(1):63-8.
PMID: 8333296
Cell-cell contact between the macula densa and the glomerular arterioles is is thought to provide the information pathway for the tubuloglomerular feedback (TGF) mechanism. When concentrations of sodium and chloride...