 Connection
Ronald Sokol to Nervous System Diseases
This is a "connection" page, showing publications Ronald Sokol has written about Nervous System Diseases.
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0.507 |
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Holve S, Hu D, Shub M, Tyson RW, Sokol RJ. Liver disease in Navajo neuropathy. J Pediatr. 1999 Oct; 135(4):482-93.
Score: 0.142
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Sokol RJ. Vitamin E deficiency and neurologic disease. Annu Rev Nutr. 1988; 8:351-73.
Score: 0.063
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Sokol RJ, Butler-Simon NA, Bettis D, Smith DJ, Silverman A. Tocopheryl polyethylene glycol 1000 succinate therapy for vitamin E deficiency during chronic childhood cholestasis: neurologic outcome. J Pediatr. 1987 Dec; 111(6 Pt 1):830-6.
Score: 0.063
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Sokol RJ, Guggenheim MA, Iannaccone ST, Barkhaus PE, Miller C, Silverman A, Balistreri WF, Heubi JE. Improved neurologic function after long-term correction of vitamin E deficiency in children with chronic cholestasis. N Engl J Med. 1985 Dec 19; 313(25):1580-6.
Score: 0.055
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Sokol RJ, Guggenheim MA, Heubi JE, Iannaccone ST, Butler-Simon N, Jackson V, Miller C, Cheney M, Balistreri WF, Silverman A. Frequency and clinical progression of the vitamin E deficiency neurologic disorder in children with prolonged neonatal cholestasis. Am J Dis Child. 1985 Dec; 139(12):1211-5.
Score: 0.055
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Sokol RJ. Vitamin E deficiency in adults. Ann Intern Med. 1984 May; 100(5):769-70.
Score: 0.049
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Vu TH, Tanji K, Holve SA, Bonilla E, Sokol RJ, Snyder RD, Fiore S, Deutsch GH, Dimauro S, De Vivo D. Navajo neurohepatopathy: a mitochondrial DNA depletion syndrome? Hepatology. 2001 Jul; 34(1):116-20.
Score: 0.040
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Sokol RJ. Vitamin E and neurologic function in man. Free Radic Biol Med. 1989; 6(2):189-207.
Score: 0.017
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Sokol RJ, Kayden HJ, Bettis DB, Traber MG, Neville H, Ringel S, Wilson WB, Stumpf DA. Isolated vitamin E deficiency in the absence of fat malabsorption--familial and sporadic cases: characterization and investigation of causes. J Lab Clin Med. 1988 May; 111(5):548-59.
Score: 0.016
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Burwinkel B, Amat L, Gray RG, Matsuo N, Muroya K, Narisawa K, Sokol RJ, Vilaseca MA, Kilimann MW. Variability of biochemical and clinical phenotype in X-linked liver glycogenosis with mutations in the phosphorylase kinase PHKA2 gene. Hum Genet. 1998 Apr; 102(4):423-9.
Score: 0.008
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Connection Strength
The connection strength for concepts is the sum of the scores for each matching publication.
Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
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