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NEUROLOGICAL DISORDERS
Author(s) -
G J Hankey,
S F Berkovic
Publication year - 1969
Publication title -
developmental medicine and child neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.658
H-Index - 143
eISSN - 1469-8749
pISSN - 0012-1622
DOI - 10.1111/j.1469-8749.1969.tb01553.x
Subject(s) - citation , medicine , psychology , computer science , library science
963. ADLER, J. B., PATTERSON, R. L. (1967) ‘Erb’s palsy. Long term results of treatment in eightyeight cases.’ J. Bone Jt Surg., 49A, 1052-1064. ALTHER, E. (1968) ‘Cerebrospinal fluid absorption deficit.’ (German.) Dtsch. med. Wschr., 93, 1270-1 276. BELLANTI, J. A., GUIN, G. H., GRASSI, R. M., OLSON, L. C. (1968) ‘Herpes simplex encephalitis, brain biopsy and treatment with 5-iodo-2-deoxyuridine.’ J, Pediat., 72, 266-275. BLATTNER, . J. (1967) ‘Subacute sclerosing encephalitis.’ J. Pediat., 71, 910-913. BROWN, J. (1967) ‘Cerebellar tumors in children.’ Proc. Mayo Clin., 42, 51 1-516. BURRY, V. F., HELLERSTEIN, F. (1968) ‘Preventable convulsions in children with meningitis.’ G.P. (Kansas), 37, (l), 107-111. CLAUSEN, J. MELCHIOR, J. C. (1967) ‘Treatment of metachromatic leucodystrophy.’ Lancet, ii, 834. (Letter.) CLAYTON, B. E., DOBBS, R. H., PATRICK, A. D. (1967) ‘Leigh‘s subacute necrotising encephalopathy : clinical and biochemical study with special reference to therapy with lipoate.’ Arch. Dis. Childh., 42, 467-478. CROMPTON, M. R. (1968) ‘Alpers’ disease, a variant of Creutzfeldt-Jakob disease and subacute spongiform encephalopathy.’ Acta neuropath. (Bed.), 10, 99-104. DANO, G. (1968) ‘Acute cerebellar ataxia associated with Herpes simplex virus infection.’ Actu paediat. scand., 57, 151-152. DASTUR, D. K., LALITHA, V. S., PRABHAKAR, V. (1968) ‘Pathological analysis of intracranial space-occupying lesions in 1,000 cases including children. I. Age, sex patterns; and the tuberculomas.’ J. neurol. Sci., 6, 575-592. DEPRES, P., HEROUIN, CL., SERINGE, PH. (1968) ‘Myoclonic encephalopathy with opisthotonus.’ (French.) Sem. H6p. Paris (Ann. pbdiat.), 44, 185-193. DIEBOLD, K., HAFNER, H., VOGEL, F., SCHALT, E. (1968) ‘A myoclonic variant of familial amaurotic idiocy.’ (German.) Humangenetik, 5, 119-164. DIEKMAN, L., HUTHER, W., PFEIFFER, R. A. (1967) ‘Unusual manifestations of neurofibromatosis (von Recklinghausen’s disease) in childhood.’ (German.) Z. Kinderheilk., 101,

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