Brain and Development

Hypoxic and ischemic disorders of infants and children. Lecture for 38th Meeting of Japanese Society of Child Neurology, Tokyo, Japan, July 1996
pp. 235-239(5)
Author: Johnston M.V.

Improvement of hypertonus after treatment for sleep disturbances in three patients with severe brain damage
pp. 240-244(5)
Authors: Tanaka H.; Araki A.; Ito J.; Tasaki T.; Miyamoto A.; Cho K.

MRI findings and sensorimotor development in infants with bilateral spastic cerebral palsy
pp. 245-253(9)
Authors: Cioni G.; Di Paco M.C.; Bertuccelli B.; Paolicelli P.B.; Canapicchi R.

Differential development of the human cerebellar vermis: immunohistochemical and morphometrical evaluation
pp. 254-257(4)
Authors: Isumi H.; Mizuguchi M.; Takashima S.

Rett syndrome: geographic variation in prevalence in Norway
pp. 258-261(4)
Authors: Skjeldal O.H.; von Tetzchner S.; Aspelund F.; Herder G.A.; Lofterod B.

Treatment of mitochondrial encephalomyopathy with a combination of cytochrome C and vitamins B₁ and B₂
pp. 262-267(6)
Authors: Tanaka J.; Nagai T.; Arai H.; Inui K.; Yamanouchi H.; Goto Y.-i.; Nonaka I.; Okada S.

l-2-Hydroxyglutaric aciduria: clinical, biochemical and magnetic resonance imaging in six Portuguese pediatric patients
pp. 268-273(6)
Authors: Barbot C.; Fineza I.; Diogo L.; Maia M.; Melo J.; Guimaraes A.; Pires M.M.; Cardoso M.L.; Vilarinho L.

The effectiveness of clonazepam on the Rolandic discharges
pp. 274-278(5)
Authors: Mitsudome A.; Ohfu M.; Yasumoto S.; Ogawa A.; Hirose S.; Ogata H.; Yamada T.

Electrophysiological study of myoclonic seizures in children
pp. 279-284(6)
Authors: Oguni H.; Mukahira K.; Uehara T.; Matsuzaki M.; Osawa M.

Two different pathological conditions of photoparoxysmal responses in hereditary dentatorubral-pallidoluysian atrophy
pp. 285-289(5)
Authors: Takahashi Y.; Watanabe M.; Fujiwara T.; Yagi K.; Kondo N.; Orii T.; Seino M.

Developmental and aging changes in the expression of amyloid precursor protein in Down syndrome brains
pp. 290-294(5)
Authors: Arai Y.; Suzuki A.; Mizuguchi M.; Takashima S.

Peroxisomal bifunctional enzyme deficiency: serial neurophysiological examinations of a case
pp. 295-299(5)
Authors: Akaboshi S.; Tomita Y.; Suzuki Y.; Une M.; Sohma O.; Takashima S.; Takeshita K.

Pure red cell aplasia during carbamazepine monotherapy
pp. 300-302(3)
Authors: Tagawa T.; Sumi K.; Uno R.; Itagaki Y.; Fujii F.; Yamaguchi H.

Isolated 3-methylcrotonyl-CoA carboxylase deficiency in a 15-year-old girl
pp. 303-305(3)
Authors: Murayama K.; Kimura M.; Yamaguchi S.; Shinka T.; Kodama K.