
Internal Medicine/Neurology
Terry Hutchison, MD |
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| Professor of Medicine, UCSF
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| Medical School: | University of Texas, Galveston, Texas
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| Residency: | University of California, San Francisco, - Pediatrics |
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| Fellowship: | University of California, San Francisco – Child Neurology University of Texas, Galveston – Child Neurology |
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| Board Certified: | Internal Medicine Neurorehabilitation |
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| Awards and Recognition: |
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| Publications: | |||
Lopez-Aquado J, Greaves T, Hutchison HT, McCarty JM. Pneumonia in infants given adrenocorticotropic hormone for infantile spasms (letter). J Pediatr 1988;112:508.
Gahl WA, Dalakas MC, Charnas L, Chen KT, Pezeshkpour GH, Kuwabara T, Davis SL, Chesney RW, Fink J, Hutchison HT. Myopathy and cystine storage in muscles in a patient with nephropathic cystinosis. N Engl J Med 1998;319:1461-1464.
Opala G, Winter S, Vance C, Vance H, Hutchison HT, Linn LS. The Effect of valproic acid on plasma carnitine Levels. Am J Dis Child 1991;145:999-1001.
Hutchison HT, Wherry JN, et al. Differential diagnosis and treatment of conversion disorder and Guillain-Barre Syndrome, Clinical Pediatrics, Vol. 1991;30:578-585
Curry CJR, Tsai J, Hutchison HT, Jaspers NGJ, Wara D, Gatti RA. A Phenotype Linking Ataxia-Telangiectasia with the Nijmegen Breakage Syndrome. Am J Human Genetics 1989;45:270-5.
Roberts SD, Wells RD, Brown IS, Bryant JD, Hutchison HT, Kurushima C, Garbarino W, Dahl B, Vander Plaats S. The FRESNO: A pediatric functional outcome measurement system. J Rehabil Outcomes Meas 1999;3:11-99
Honarmand S, Glaser CA, Chow E, Sejvar JJ, Preas CP, Consentino GC, Hutchison HT, Bellini WJ. Measles SSPE in the differential diagnosis of encephalitis. Neurology. 2004;63:1489-1493.
Curry CJ, Bhullar S, Holmes J, Delozier CD, Roeder ER, Hutchison HT. Risk factors for perinatal arterial stroke: a study of 60 mother-child pairs. Pediatr Neurol. 2007;37:99-107.
Brunetti-Pierri N, Berg JS, Scaglia F, Belmont J, Bacino CA, Sahoo T, Lalani SR, Graham B, Lee B, Shinawi M, Shen J, Kang SH, Pursley A, Lotze T, Kennedy G, Lansky-Shafer S, Weaver C, Roeder ER, Grebe TA, Arnold GL, Hutchison T, Reimschisel T, Amato S, Geragthy MT, Innis JW, Obersztyn E, Nowakowska B, Rosengren SS, Bader PI, Grange DK, Naqvi S, Garnica AD, Bernes SM, Fong CT, Summers A, Walters WD, Lupski JR, Stankiewicz P, Cheung SW, Patel A. Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities. Nat Genet. 2008;40:1466-71 |
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