메뉴 건너뛰기




Volumn 14, Issue 10, 1999, Pages 621-627

Ocular and oculomotor signs in Joubert syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; APRAXIA; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; DIAGNOSTIC IMAGING; DIFFERENTIAL DIAGNOSIS; DISEASE ASSOCIATION; FEMALE; HUMAN; INFANT; JOUBERT SYNDROME; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; OCULOMOTOR SYSTEM; OPHTHALMOPLEGIA; PRIORITY JOURNAL; SACCADIC EYE MOVEMENT; SMOOTH PURSUIT EYE MOVEMENT; VESTIBULOOCULAR REFLEX;

EID: 0032833611     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/088307389901401001     Document Type: Article
Times cited : (50)

References (23)
  • 1
    • 0014572497 scopus 로고
    • Familial agenesis of the cerebellar vermis. A syndrome of episodic hyperpnea, abnormal eye movements, ataxia, and retardation
    • Joubert M, Eisenring JJ, Robb JP, Andermann F: Familial agenesis of the cerebellar vermis. A syndrome of episodic hyperpnea, abnormal eye movements, ataxia, and retardation. Neurology 1969;19:813-825.
    • (1969) Neurology , vol.19 , pp. 813-825
    • Joubert, M.1    Eisenring, J.J.2    Robb, J.P.3    Andermann, F.4
  • 3
    • 0024784290 scopus 로고
    • Joubert syndrome: A clinico-radiological study
    • Kendall B, Kingsley D, Lambert SR, et al: Joubert syndrome: A clinico-radiological study. Neuroradiology 1990;31:502-506.
    • (1990) Neuroradiology , vol.31 , pp. 502-506
    • Kendall, B.1    Kingsley, D.2    Lambert, S.R.3
  • 4
    • 0025880516 scopus 로고
    • Joubert syndrome: A clinical and pathological description of an affected male and a female fetus from the same sibship
    • van Dorp DB, Palan A, Kwee ML, et al: Joubert syndrome: A clinical and pathological description of an affected male and a female fetus from the same sibship. Am J Med Genet 1991;40:100-104.
    • (1991) Am J Med Genet , vol.40 , pp. 100-104
    • Van Dorp, D.B.1    Palan, A.2    Kwee, M.L.3
  • 5
    • 0024566720 scopus 로고
    • Joubert's syndrome associated with congenital ocular fibrosis and histidinemia
    • Appleton RE, Chitayat D, Jan JE, et al: Joubert's syndrome associated with congenital ocular fibrosis and histidinemia. Arch Neurol 1989;46:579-582.
    • (1989) Arch Neurol , vol.46 , pp. 579-582
    • Appleton, R.E.1    Chitayat, D.2    Jan, J.E.3
  • 7
    • 0019421986 scopus 로고
    • Joubert syndrome: Clinical and polygraphic observations in a further case
    • Boltshauser E, Herdan M, Dumermuth G, Isler W: Joubert syndrome: Clinical and polygraphic observations in a further case. Neuropediatrics 1981;12:181-191.
    • (1981) Neuropediatrics , vol.12 , pp. 181-191
    • Boltshauser, E.1    Herdan, M.2    Dumermuth, G.3    Isler, W.4
  • 8
    • 0025055305 scopus 로고
    • Hidden intelligence of a multiply handicapped child with Joubert syndrome
    • Ziegler AL, Deonna T, Calame A: Hidden intelligence of a multiply handicapped child with Joubert syndrome. Dev Med Child Neurol 1990;32:261-266.
    • (1990) Dev Med Child Neurol , vol.32 , pp. 261-266
    • Ziegler, A.L.1    Deonna, T.2    Calame, A.3
  • 9
    • 0026704824 scopus 로고
    • Congenital oculomotor nerve palsy, cerebellar hypoplasia, and facial capillary hemangioma
    • White WL, Mumma JV, Tomasovic JJ: Congenital oculomotor nerve palsy, cerebellar hypoplasia, and facial capillary hemangioma. Am J Ophthalmol 1992;113:497-500.
    • (1992) Am J Ophthalmol , vol.113 , pp. 497-500
    • White, W.L.1    Mumma, J.V.2    Tomasovic, J.J.3
  • 10
    • 0017577011 scopus 로고
    • Joubert syndrome: Episodic hyperpnea, abnormal eye movements, retardation and ataxia, associated with dysplasia of the cerebellar vermis
    • Boltshauser E, Isler W: Joubert syndrome: Episodic hyperpnea, abnormal eye movements, retardation and ataxia, associated with dysplasia of the cerebellar vermis. Neuropadiatrie 1977;8: 57-66.
    • (1977) Neuropadiatrie , vol.8 , pp. 57-66
    • Boltshauser, E.1    Isler, W.2
  • 12
    • 0025777864 scopus 로고
    • Autistic features in Joubert syndrome: A genetic disorder with agenesis of the cerebellar vermis
    • Holroyd S, Reiss AL, Bryan RN: Autistic features in Joubert syndrome: A genetic disorder with agenesis of the cerebellar vermis. Biol Psychiatry 1991;29:287-294.
    • (1991) Biol Psychiatry , vol.29 , pp. 287-294
    • Holroyd, S.1    Reiss, A.L.2    Bryan, R.N.3
  • 13
    • 0031438402 scopus 로고    scopus 로고
    • "Joubert syndrome" revisited: Key oculomotor signs with magnetic resonance imaging correlation
    • Maria BL, Hoang KB, Tusa RJ, et al: "Joubert syndrome" revisited: Key oculomotor signs with magnetic resonance imaging correlation. J Child Neurol 1997;12:423-430.
    • (1997) J Child Neurol , vol.12 , pp. 423-430
    • Maria, B.L.1    Hoang, K.B.2    Tusa, R.J.3
  • 15
    • 0029920319 scopus 로고    scopus 로고
    • Clinical and MRI correlates in 27 patients with acquired pendular nystagmus
    • Lopez LI, Bronstein AM, Gresty MA, et al: Clinical and MRI correlates in 27 patients with acquired pendular nystagmus. Brain 1996;119:465-472.
    • (1996) Brain , vol.119 , pp. 465-472
    • Lopez, L.I.1    Bronstein, A.M.2    Gresty, M.A.3
  • 16
    • 0028934168 scopus 로고
    • The effect of cerebellar midline lesions on eye movements
    • Büttner U, Straube A: The effect of cerebellar midline lesions on eye movements. Neuro-ophthalmology 1995;15:75-82.
    • (1995) Neuro-ophthalmology , vol.15 , pp. 75-82
    • Büttner, U.1    Straube, A.2
  • 17
    • 0022510566 scopus 로고
    • Vestibulo-ocular reflexes of adventitiously and congenitally blind adults
    • Sherman KR, Keller EL: Vestibulo-ocular reflexes of adventitiously and congenitally blind adults. Invest Ophthalmol Vis Sci 1986;27:1154-1159.
    • (1986) Invest Ophthalmol Vis Sci , vol.27 , pp. 1154-1159
    • Sherman, K.R.1    Keller, E.L.2
  • 18
    • 0021149532 scopus 로고
    • Joubert's syndrome with retinal dysplasia: Neonatal tachypnoea as the clue to a genetic brain-eye malformation
    • King MD, Dudgeon J, Stephenson JB: Joubert's syndrome with retinal dysplasia: Neonatal tachypnoea as the clue to a genetic brain-eye malformation. Arch Dis Child 1984;59:709-718.
    • (1984) Arch Dis Child , vol.59 , pp. 709-718
    • King, M.D.1    Dudgeon, J.2    Stephenson, J.B.3
  • 19
    • 0021685295 scopus 로고
    • The prenatal diagnosis of Joubert's syndrome of familial agenesis of the cerebellar vermis
    • Campbell S, Tsannatos C, Pearce JM: The prenatal diagnosis of Joubert's syndrome of familial agenesis of the cerebellar vermis. Prenat Diagn 1984;4:391-395.
    • (1984) Prenat Diagn , vol.4 , pp. 391-395
    • Campbell, S.1    Tsannatos, C.2    Pearce, J.M.3
  • 20
    • 0032989288 scopus 로고    scopus 로고
    • Molar tooth sign in Joubert syndrome: Clinical, radiologic, and pathologic significance
    • Maria BL, Quisling RG, et al: Molar tooth sign in Joubert syndrome: Clinical, radiologic, and pathologic significance. J Child Neurol 1999;14:368-376.
    • (1999) J Child Neurol , vol.14 , pp. 368-376
    • Maria, B.L.1    Quisling, R.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.