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Movement Disorders: 100 Instructive Cases
Volumn , Issue , 2008, Pages 349-352
An unusual cause of stuttering
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EID: 77950239924     PISSN: None     EISSN: None     Source Type: Book    
DOI: None     Document Type: Chapter
Times cited : (1)
References (8)
  • 1
    • 0000544518 scopus 로고    scopus 로고
    • Lesch-Nyhan disease and its variants
    • Scriver CR, Beaudet AL, Sly WS et al, eds., New York: McGraw-Hill
    • Jinnah HA, Friedmann T. Lesch-Nyhan disease and its variants. In: Scriver CR, Beaudet AL, Sly WS et al, eds. The Metabolic and Molecular Bases of Inherited Disease. New York: McGraw-Hill, 2001: 2537-70.
    • (2001) The Metabolic and Molecular Bases of Inherited Disease , pp. 2537-2570
    • Jinnah, H.A.1    Friedmann, T.2
  • 2
    • 33646227430 scopus 로고    scopus 로고
    • Lesch-Nyhan Disease International Study Group. Delineation of the motor disorder of Lesch-Nyhan disease
    • Jinnah HA, Visser JE, Harris JC et al; Lesch-Nyhan Disease International Study Group. Delineation of the motor disorder of Lesch-Nyhan disease. Brain 2006; 129:1201-17.
    • (2006) Brain , vol.129 , pp. 1201-1217
    • Jinnah, H.A.1    Visser, J.E.2    Harris, J.C.3
  • 3
    • 0033799868 scopus 로고    scopus 로고
    • The spectrum of inherited mutations causing HPRT deficiency: 75 new cases and a review of 196 previously reported cases
    • Jinnah HA, DeGregorio L, Harris JC et al. The spectrum of inherited mutations causing HPRT deficiency: 75 new cases and a review of 196 previously reported cases. Mutat Res2000; 463: 309-26.
    • (2000) Mutat Res , vol.463 , pp. 309-326
    • Jinnah, H.A.1    Degregorio, L.2    Harris, J.C.3
  • 4
    • 0035068003 scopus 로고    scopus 로고
    • The spectrum of hypoxanthine-guanine phosphoribo-syltransferase deficiency: Clinical experience based on 22 patients from 18 Spanish families
    • Puig JG, Torres RJ, Mateos FA et al. The spectrum of hypoxanthine-guanine phosphoribo-syltransferase deficiency: clinical experience based on 22 patients from 18 Spanish families. Medicine 2001; 80:102-12.
    • (2001) Medicine , vol.80 , pp. 102-112
    • Puig, J.G.1    Torres, R.J.2    Mateos, F.A.3
  • 5
    • 0034125082 scopus 로고    scopus 로고
    • Inborn errors of metabolism as a cause of neurological disease in adults: Approach to investigation
    • Gray RGF, Preece MA, Green SH et al. Inborn errors of metabolism as a cause of neurological disease in adults: approach to investigation. J Neurol Neurosurg Psychiatry 2000; 69: 5 - 12.
    • (2000) J Neurol Neurosurg Psychiatry , vol.69
    • Gray, R.1    Preece, M.A.2    Green, S.H.3
  • 6
    • 2542500566 scopus 로고    scopus 로고
    • Stuttering and the basal ganglia circuits: A critical review of possible relations
    • Alm PA. Stuttering and the basal ganglia circuits: a critical review of possible relations. J Commun Disord 2004; 37: 325-69.
    • (2004) J Commun Disord , vol.37 , pp. 325-369
    • Alm, P.A.1
  • 7
    • 0030000377 scopus 로고    scopus 로고
    • Stuttering may be a type of action dystonia
    • Kiziltan G, Akalin MA. Stuttering may be a type of action dystonia. Mov Disord 1996; 11: 278-82.
    • (1996) Mov Disord , vol.11 , pp. 278-282
    • Kiziltan, G.1    Akalin, M.A.2
  • 8
    • 0342699711 scopus 로고    scopus 로고
    • Lesch-Nyhan disease and the basal ganglia
    • Visser JE, Bar PR, Jinnah HA. Lesch-Nyhan disease and the basal ganglia. Brain Res Rev2000; 32: 449-75.
    • (2000) Brain Res Rev , vol.32 , pp. 449-475
    • Visser, J.E.1    Bar, P.R.2    Jinnah, H.A.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.