Serial electrophysiologic studies in rhesus monkeys with Krabbe disease

Muscle and Nerve

Volumn 32, Issue 2, 2005, Pages 185-190

  Weimer, Maria B ^a   Gutierrez, Amparo ^a   Baskin, Gary B ^b   Borda, Juan T ^c   Veazey, Ronald S ^c   Myers, Leann ^d   Phillippi Falkenstein, Kathrine M ^c   Bunnell, Bruce A ^c   Ratterree, Marion S ^c   England, John D ^e  

^a LOUISIANA STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b CHARLES RIVER LABORATORIES   (United States)

^c TULANE NATIONAL PRIMATE RESEARCH CENTER   (United States)

^d TULANE UNIVERSITY   (United States)

^e Billings Clinic Red Lodge   (United States)

Author keywords

Demyelination; Dysmyelination; Krabbe disease; Nerve conduction studies; Primate

Indexed keywords

ADOLESCENT; AGED; ARTICLE; CENTRAL NERVOUS SYSTEM; DEMYELINATION; DISEASE COURSE; ELECTROPHYSIOLOGY; GLOBOID CELL LEUKODYSTROPHY; HETEROZYGOSITY; HOMOZYGOSITY; LEUKODYSTROPHY; MACACA; MEDIAN NERVE; MYELIN DEFICIENCY; NERVE CONDUCTION; NONHUMAN; PERIPHERAL NERVOUS SYSTEM; PRIORITY JOURNAL; RHESUS MONKEY; TIBIAL NERVE; ULNAR NERVE;

ACTION POTENTIALS; AGE FACTORS; AGING; ANIMALS; DEMYELINATING DISEASES; ELECTRODIAGNOSIS; LEUKODYSTROPHY, GLOBOID CELL; MACACA MULATTA; MEDIAN NERVE; NERVE FIBERS, MYELINATED; NEURAL CONDUCTION; PERIPHERAL NERVES; PERIPHERAL NERVOUS SYSTEM DISEASES; TIBIAL NERVE; ULNAR NERVE;

EID: 23044459533     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/mus.20350     Document Type: Article

References (20)

1. Baskin GB, Alroy J, Li Y-T, Dayal Y, Raghavan SS, Sharer L. Galactosylceramide-lipidosis in rhesus monkeys. Lab Invest 1989;60:7A.
2. Baskin GB, Ratterree M, Davison BB, Falkenstein KP, Clarke MR, England JD, et al. Genetic galactocerebrosidase deficiency (globoid cell leukodystrophy, Krabbe disease) in rhesus monkeys (Macaca mulatta). Lab Anim Sci 1998;48:476-482.
3. Berciano J, Combarros O, Calleja J, Polo JM, Leno C. The application of nerve conduction and clinical studies to genetic counseling in hereditary motor and sensory neuropathy type I. Muscle Nerve 1989;12:302-306.
4. Dunn H, Lake B, Dolman C, Wilson J. The neuropathy of Krabbe's infantile cerebral sclerosis. Brain 1969;92:329-344.
5. England JD, Bohm RP Jr, Roberts ED, Phillip MT. Mononeuropathy multiplex in rhesus monkeys with chronic Lyme disease. Ann Neurol 1997;41:375-384.
6. Gutmann L, Fakadej A, Riggs JE. Evolution of nerve conduction abnormalities in children with dominant hypertrophic neuropathy of the Charcot-Marie-Tooth type. Muscle Nerve 1983;6:515-519.
7. Hagberg B, Kollberg H, Sourander P, Akesson H. Infantile globoid cell leucodystrophy (Krabbe's disease). Neuropadiatrie 1969;1:74-88.
8. Korn-Lubetzki I, Dor-Wollman T, Soffer D, Raas-Rothschild A, Hurvitz H, Nevo Y. Early peripheral nervous system manifestations of infantile Krabbe disease. Pediatr Neurol 2003;28:115-118.
9. Krivit W, Shapiro EG, Peters C, Wagner JE, Cornu G, Kurtzberg J, et al. Hematopoietic stem-cell transplantation in globoid-cell leukodystrophy. N Engl J Med 1998;338:1119-1126.
10. Lieberman J, Oshtory M, Taylor R, Dreyfus P. Peripheral neuropathy as an early manifestation of Krabbe's disease. Arch Neurol 1980;37:446-447.
11. Luzi P, Rafi MA, Victoria T, Baskin GB, Wenger DA. Characterization of the rhesus monkey galactocerebrosidase (GALC) cDNA and gene and identification of the mutation causing globoid cell leukodystrophy (Krabbe disease) in this primate. Genomics 1997;42:319-324.
12. Lyon G, Adams R, Kolodny EH. Neurology of hereditary metabolic diseases of children. New York: McGraw-Hill; 1996. p 7-70.
13. Robaglia-Schlupp A, Pizant J, Norreel J-C, Passage E, Saberan-Djoneidi D, Ansaldi JL, et al. PMP22 overexpression causes dysmyelination in mice. Brain 2002;125:2213-2221.
14. Roy EP III, Gutmann L, Riggs JE. Longitudinal conduction studies in hereditary motor and sensory neuropathy type I. Muscle Nerve 1989;12:52-55.
15. Sourander P, Olsson Y. Peripheral neuropathy in globoid cell leukodystrophy (morbus Krabbe). Acta Neuropathol (Berl) 1968;11:69-81.
16. Suzuki K, Suzuki K. Genetic galactosylceramidase deficiency (globoid cell leukodystrophy, Krabbe disease) in different mammalian species. Neurochem Pathol 1985;3:53-68.
17. Suzuki K, Suzuki Y. Globoid cell leucodystrophy (Krabbe disease): deficiency of galactocerebrosidase β-galactosidase. Proc Natl Acad Sci USA 1970;66:302-309.
18. Svennerholm L, Vanier MT, Mansson J-E. Krabbe disease: a galactosylsphingosine (psychosine) lipidosis. J Lipid Res 1980;21:53-64.
19. Zafeiriou D, Anastasiou A, Michelakaki E, Augoustidou-Savvopoulou P, Katzos G, Kontopoulos E. Early infantile Krabbe disease: deceptively normal magnetic resonance imaging and serial neurophysiological studies. Brain Dev 1997;19:488-491.
20. Zafeiriou D, Michelakaki E, Anastasiou A, Gombakis N, Kontopoulos E. Serial MRI and neurophysiological studies in late-infantile Krabbe disease. Pediatr Neurol 1996;15:240-244.