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Items: 19

1.

[Morphological and functional analysis of dento-orofacial complex in monozygotic twins with Duchenne type muscular dystrophy].

Watanabe M, Shimizu K, Nakata S, Watanabe K, Morishita T, Miyoshino S.

Nihon Kyosei Shika Gakkai Zasshi. 1990 Dec;49(6):522-37. Japanese.

PMID:
2133698
2.

Quantitative histologic study of the sural nerve in Lesch-Nyhan syndrome.

Origuchi Y, Miyoshino S, Mishima K, Mine K.

Pediatr Neurol. 1990 Sep-Oct;6(5):353-5.

PMID:
2173615
3.

Adrenoleukodystrophy: abnormality of "tightly bound" fatty acids in the erythrocyte membrane proteins.

Antoku Y, Sakai T, Goto I, Miyoshino S, Iwashita H, Kuroiwa Y.

Neurology. 1985 Oct;35(10):1512-4.

PMID:
4033936
4.

[2 autopsy cases of congenital muscular dystrophy of Fukuyama type--a typical and an atypical cases].

Koga M, Abe M, Tateishi J, Antoku Y, Iwashita H, Miyoshino S.

No To Shinkei. 1984 Nov;36(11):1103-8. Japanese.

PMID:
6525323
5.

Two different modes of enzymatic changes in serum with progression of Duchenne muscular dystrophy.

Aoyagi T, Wada T, Kojima F, Nagai M, Miyoshino S, Umezawa H.

Clin Chim Acta. 1983 Apr;129(2):165-73.

PMID:
6851159
6.

A fluorescent microscopy study of biopsied muscles from infantile neuromuscular disorders.

Miike T, Tamari H, Ohtani Y, Nakamura H, Matsuda I, Miyoshino S.

Acta Neuropathol. 1983;59(1):48-52.

PMID:
6837268
7.

Quantitative histological findings in the sural nerves of neonates.

Origuchi Y, Ishibashi K, Miyoshino S.

Brain Dev. 1982;4(6):474-7.

PMID:
7168485
8.

Xanthine oxidase inhibitor in Duchenne muscular dystrophy.

Tamari H, Ohtani Y, Higashi A, Miyoshino S, Matsuda I.

Brain Dev. 1982;4(2):137-43.

PMID:
6896406
9.

Effect of pyridoxal 5-phosphate on the activity of GOT isozyme in plasma from patients with Duchenne muscular dystrophy.

Ohno H, Taniguchi N, Terayama K, Hirata F, Kawarabayashi T, Miyoshino S, Matsuda I.

Tohoku J Exp Med. 1981 Nov;135(3):333-4.

10.

A clinical and histological study of Ullrich's disease (congenital atonic-sclerotic muscular dystrophy).

Nonaka I, Une Y, Ishihara T, Miyoshino S, Nakashima T, Sugita H.

Neuropediatrics. 1981 Aug;12(3):197-208.

PMID:
7290342
11.

Na+ + K+ ATPase of erythrocyte membranes in Duchenne muscular dystrophy.

Mawatari S, Igisu H, Kuroiwa Y, Miyoshino S.

Neurology. 1981 Mar;31(3):293-7.

PMID:
6259557
12.

Erythrocyte acetylcholinesterase in Duchenne muscular dystrophy.

Igisu H, Mawatari S, Kuroiwa Y, Miyoshino S.

Clin Chim Acta. 1980 Aug 4;105(2):241-7.

PMID:
7398092
13.

Serum vitamin E concentration in patients with severe multiple handicaps treated with anticonvulsants.

Higashi A, Tamari H, Ikeda T, Ohtani Y, Matsukura M, Miyoshino S, Matsuda I.

Pediatr Pharmacol (New York). 1980;1(2):129-34.

PMID:
6213919
14.

Response to transfer factor to immunodeficiency in handicaps treated with phenytoin.

Ikeda T, Higashi A, Matsuda I, Miyoshino S.

Eur J Pediatr. 1979 Sep;132(1):67-8. No abstract available.

PMID:
499256
15.

Delayed cutaneous hypersensitivity in children with severe multiple handicaps treated with phenytoin.

Higashi A, Matsuda I, Sinosuka S, Ohtsuka H, Endo F, Maeda T, Ikeda T, Miyoshino S.

Eur J Pediatr. 1978 Dec 1;129(4):273-8.

PMID:
152707
16.

Mitochondrial fraction of serum glutamic-oxaloacetic transaminase in Duchenne muscular dystrophy.

Matsuda I, Miyoshino S, Miike T, Nagata N, Tamari H, Taniguchi N, Ohno H, Watanabe H.

Clin Chim Acta. 1978 Feb 15;83(3):231-4.

PMID:
624179
17.

An electron microscopical study of the muscle in congenital muscular dystrophy.

Nonaka I, Miyoshino S, Miike T, Ueno T, Usuku G.

Kumamoto Med J. 1972 Jun 30;25(2):68-82. No abstract available.

PMID:
4634534
18.

[The curative results of surgical casectomy for pulmonary tuberculosis].

AMEMIYA S, OGATA T, TAKAGI M, YAMADA K, OISHI M, MIYOSHINO S, MIYAMOTO T, KAKANO Y, TSURUTA S.

Kyobu Geka. 1962 Nov;15:747-50. Japanese. No abstract available.

PMID:
14012551
19.

[On the surgical treatment of pulmonary paragonimiasis].

OISHI M, TAKAGI M, MIYOSHINO S, MIYAMOTO T, TSURUTA S, FUJINO T.

Iryo. 1962 Nov;16:599-603. Japanese. No abstract available.

PMID:
13939713

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