Case of adrenoleukodystrophy (ALD) with clinical features of olivopontocerebellar atrophy
Tsuchida, H.; Ohno, T.; Fukuhara, N.; Miyatake, T.
Rinsho Shinkeigaku 23(6): 489-494
1983
ISSN/ISBN: 0009-918X PMID: 6652994 Document Number: 209286
Document emailed within 1 workday
Related Documents
Takada, K.; Onoda, K.; Takahashi, K.; Nakamura, H.; Taketomi, T. 1987: An adult case of adrenoleukodystrophy with features of olivo-ponto-cerebellar atrophy: I. Clinical and pathological studies Japanese Journal of Experimental Medicine 57(1): 53-58Caplan, L.R. 1984: Clinical features of sporadic (Dejerine-Thomas) olivopontocerebellar atrophy Advances in Neurology 41: 217-224
Chou, S.M.; Gilbert, E.F.; Chun, R.W.; Laxova, R.; Tuffli, G.A.; Sufit, R.L.; Krassikot, N. 1990: Infantile olivopontocerebellar atrophy with spinal muscular atrophy (infantile OPCA + SMA) Clinical Neuropathology 9(1): 21-32
Janati, A.; Metzer, W.S.; Archer, R.L.; Nickols, J.; Raval, J. 1989: Blepharospasm associated with olivopontocerebellar atrophy Journal of Clinical Neuro-Ophthalmology 9(4): 281-284
Huang, Y.P.; Plaitakis, A. 1984: Morphological changes of olivopontocerebellar atrophy in computed tomography and comments on its pathogenesis Advances in Neurology 41: 39-85
Yazawa, R.; Kondo, T.; Miyashita, T.; Koide, Y.; Andoh, T.; Yamada, Y. 2004: Anesthetic management of a patient with olivopontocerebellar atrophy using heart rate variability (HRV) Masui. Japanese Journal of Anesthesiology 53(1): 55-58
Konagaya, M.; Sakai, M.; Matsuoka, Y.; Goto, Y.; Hashizume, Y. 1998: An autopsied case of multiple system atrophy with remarkable cerebral atrophy Rinsho Shinkeigaku 38(7): 673-679
Washington, C.; Gore, E. 1991: Wadia type olivopontocerebellar degeneration: a case history and review of literature Journal of the Mississippi State Medical Association 32(7): 255-257
Tsuda, N.; Yamamoto, K.; Fukusako, T.; Morimatsu, M. 1991: A case of unilateral lingual atrophy and ipsilateral muscular atrophy supplied by trigeminal nerve--in relation to progressive facial hemiatrophy Rinsho Shinkeigaku 31(9): 1007-1009
Mingorance Delgado, A.; Tabernero Pérez, C.; Tapia Muñoz, J.; Martín Aguado, M.J.; Lloret Sempere, T.; Flores Serrano, J. 1999: X-linked adrenoleukodystrophy. A case report Anales Espanoles de Pediatria 50(5): 509-512
Suzuki, S.; Kitaguchi, T.; Tabira, T.; Goto, I.; Kuroiwa, Y. 1983: Case of adrenoleukodystrophy presenting as spinocerebellar degeneration Rinsho Shinkeigaku 23(8): 678-682
Seok, H.Y.; Eun, M.-Y.; Park, K.-W.; Yu, S.-W. 2011: FDG-PET and MRi features in multiple system atrophy Acta Neurologica Belgica 111(1): 76-77
De León-Silva, T.J.; Vázquez-Lara, J.; Coronado-Garza, M.A.; Hinojosa-Lezama, M. 1989: Adrenoleukodystrophy. Diagnosis of a typical case using magnetic resonance Boletin Medico del Hospital Infantil de Mexico 46(10): 681-683
Marche, C.; Bocquet, L.; Mignon, M.; Preel, J.L. 1974: Malabsorption syndrome with mesenteric lymph node cavitation and splenic atrophy. Apropos of a new anatomo-clinical case La Semaine des Hopitaux: Organe Fonde Par l'Association d'Enseignement Medical des Hopitaux de Paris 50(13): 879-886
Tanaka, M.; Tanaka, Y.; Hamano, S.; Nara, T.; Imai, M. 1997: A case of PEHO (progressive encephalopathy with edema, hypsarrhythmia and optic atrophy) syndrome: changes in clinical and neuroradiological findings No to Hattatsu 29(6): 488-493
Kanakis, D.; Wördehoff, H.; Heinrichs, T.; Kirches, E.; Dietzmann, K.; Mawrin, C. 2002: Post-traumatic atrophy of the olfactory tract: clinicopathological features Advances in Clinical Pathology: the Official Journal of Adriatic Society of Pathology 6(3-4): 113-118
Vetshev, P.S.; Zaĭrat'iants, O.V.; Ippolitov, I.K.; Belokrinitskiĭ, D.V.; Shkrob, L.O.; Khodzhaev, Z.S.; Kurochkin, A.V. 1991: Clinico-immunological features of generalized myasthenia in patients with hyperplasia and atrophy of the thymus gland Klinicheskaia Meditsina 69(12): 78-83
Sutovský, S.; Kolníková, M.; Petrovic, Róbert.; Kollár, B.; Siarnik, P.; Chandoga, Ján.; Fischerová, Mária.; Turcáni, P. 2014: Differing clinical presentations of two unrelated cases of X-linked adrenoleukodystrophy with identical mutation Y296C in the ABCD1 gene Neuro Endocrinology Letters 35(5): 411-416
Ohori, N.; Yamashita, Y.; Ohnishi, A. 1999: A case of adult cerebral X-linked adrenoleukodystrophy (X-ALD) accompanying typical hypertrophic neuropathy with marked onion-bulb formation Rinsho Shinkeigaku 39(11): 1144-1146
De Martino, A.; Botta, G.; Testi, W.; Signorini, A. 1988: Clinical features of a case of cysts of the hepatogastric ligament Minerva Chirurgica 43(15-16): 1287-1289