Robbins JH, Kraemer KH, Lutzner MA, et al: Xeroderma pigmentosum: An inherited disease with sun sensitivity, multiple cutaneous neoplasms and abnormal DNA repair. Ann Intern Med1974;80:221-248.
2.
Robbins JH: Xeroderma pigmentosum. Defective DNA repair causes skin cancer and neurodegeneration . JAMA1988;260: 384-388.
3.
Cleaver JE: Defective repair replication of DNA in xeroderma pigmentosum. Nature1968;218:652-656.
4.
Tachi N., Sasaki K., Kusano T., et al: Peripheral neuropathy in four cases of group A xeroderma pigmentosum . J Child Neurol1988;3:114-119.
5.
Neisser A.: Ueber das "Xeroderma pigmentosum" (Kaposi), liodermia essentialis cum melanosi et telangiectasia. Vrtljschr Dermatol Wien1883;10:47-62.
6.
De Sanctis C. , Cacchione A.: L'idiozia xerodermica. Riv Sper Freniatr1932;56:269-292.
7.
Yano K.: Xeroderma pigmentosa mit Storungen des Zentralnervensystems: Eine histopathologische Untersuchung. Folia Psychiatr Neurol Jpn1950 ;4:143-175.
8.
Reed WB, Landing B., Sugarman G., et al: Xeroderma pigmentosum: Clinical and laboratory investigation of its basic defect. JAMA1969;207:2073-2079.
9.
Thrush DC, Holti G., Bradley WG, et al: Neurological manifestations of xeroderma pigmentosum in two siblings. J Neurol Sci1974;22:91-104.
10.
Roytta M., Anttinen A.: Xeroderma pigmentosum with neurological abnormalities. A clinical and neuropathological study. Acta Neurol Scand1986;73:191-199.
11.
Cheesbrough MJ: Xeroderma pigmentosum: A unique variant with neurological involvement. Br J Dermatol1978 ;99:61.
12.
Handa J., Nakano Y., Akiguchi I.: Cranial computed tomography findings in xeroderma pigmentosum with neurologic manifestations (de Sanctis-Cacchione syndrome). J Comput Assist Tomogr1978;2:456-459.
13.
Arlett CF, Harcourt SA, Lehmann AR, et al: Studies on a new case of xeroderma pigmentosum (XP3BR) from complementation group G with cellular sensitivity to ionizing radiation. Carcinogenesis1980;1:745-751.
14.
Hakamada S. , Watanabe K., Sobue G., et al: Xeroderma pigmentosum: Neurological, neurophysiological and morphological studies. Eur Neurol1982;21:69-76.
15.
Kenyon GS, Booth JB, Prasher DK, et al: Neuro-otological abnormalities in xeroderma pigmentosum with particular reference to deafness. Brain1985 ;108:771-784.
16.
Robbins JH, Polinsky RJ, Moshell AN: Evidence that lack of deoxyribonucleic acid repair causes death of neurons in xeroderma pigmentosum. Ann Neurol1983;13:682-684.
17.
Mimaki T., Sato K., Kozuka T., et al: A case of group-A xeroderma pigmentosum with mild neurological symptoms. Shonika Shinryo1985;48:1304-1307.
18.
Mimaki T., Naoyuki I., Abe J., et al: Neurological manifestations in xeroderma pigmentosum. Ann Neurol1986;20:70-75.
Robbins JH, Meer J., Carl J., Sonies BC: Late development of neurologic abnormalities (NA) in xeroderma pigmentosum (XP): A primary neuronal degeneration caused by defective repair of neuronal DNA. Neurology1987;37(Suppl 1):87.
21.
Robbins JH: Progressive sensorineural deafness in xeroderma pigmentosum: Its evaluation and cause. Clin Res1987;35:795A.
22.
Robbins JH: Defective DNA repair in xeroderma pigmentosum and other neurologic diseases . Curr Opin Neurol Neurosurg1988 ;1:1077-1083.
23.
Barrett SF, Tarone RE, Moshell AN, et al: The post-UV colony-forming ability of normal fibroblast strains and of the xeroderma pigmentosum group G strain. J Invest Dermatol1981;76:59-62.
24.
Robbins JH, Brumback RA, Polinsky RG, et al: Hypersensitivity to DNA-damaging agents in abiotrophies: A new explanation for degeneration of neurons, photoreceptors, and muscle in Alzheimer, Parkinson and Huntington diseases, retinitis pigmentosa, and Duchenne muscular dystrophy, in Woodhead AD, Blackett AD, Hollaender A (eds): Molecular Biology of Aging. New York, Plenum Press, 1985, pp 315-344.
25.
Robbins JH: Incorrect priority claim for the DNA-damage hypothesis. Arch Neurol1987;44:579-583.
26.
Taylor AMR , Harnden DG, Arlett CF, et al: Ataxia telangiectasia: A human mutation with abnormal radiation sensitivity. Nature1975;258:427-429.
27.
Schmickel RD , Chu EHY , Trosko JE, et al: Cockayne syndrome: A cellular sensitivity to ultraviolet light . Pediatrics1977;60: 135-139.
28.
Chamberlain S. , Lewis PD: Studies of cellular hypersensitivity to ionizing radiation in Friedreich's ataxia. J Neurol Neurosurg Psychiatry1982;45:1136-1138.
29.
Brumback RA: Cellular hypersensitivity to ionising radiation in Friedreich's ataxia . J Neurol Neurosurg Psychiatry1983;46: 878-879.
30.
Brumback RA , Panner BJ, Kingston WJ: The heart in Fried-reich's ataxia. Arch Neurol1986;43:189-192.
31.
Scudiero DA , Meyer SA, Clatterbuck BE, et al: Hypersensitivity to N-methyl-N'-nitro-N-nitrosoguanidine in fibroblasts from patients with Huntington disease, familial dysautonomia, and other primary neuronal degenerations . Proc Natl Acad Sci USA1981;78:6451-6455.
32.
Nove J., Tarone RE, Little JB, Robbins JH: Radiation sensitivity of fibroblast strains from patients with Usher's svndrome, Duchenne muscular dystrophy, and Huntington's disease. Mutat Res1987;184:29-38.
33.
Robbins JH, Otsuka F., Tarone RE, et al: Parkinson's disease and Alzheimer's disease: Hypersensitivity to X rays in cultured cell lines. J Neurol Neurosurg Psychiatry1985;48:916-923.
34.
Scudiero DA , Polinsky RJ, Brumback RA, et al: Alzheimer disease fibroblasts are hypersensitive to the lethal effects of a DNA-damaging chemical . Mutat Res1986;159:125-131.
35.
Brumback RA , Yoder FW, Andrews AD, et al: Normal pressure hydrocephalus: Recognition and relationship to neurological abnormalities in Cockayne's syndrome. Arch Neurol1978;35:337-345.
36.
Leech RW, Brumback RA, Miller RH, et al: Cockayne syndrome: Clinicopathologic and tissue culture studies of affected siblings. J Neuropathol Exp Neurol1985;44:507-519.
37.
Robbins JH, Brumback RA, Moshell AN: Xeroderma pigmentosum neurologic disease in a complementation group C patient . Clin Res1989;37:114A.