72 |
Inui K, Furukawa M, Okada S, Yabuuchi H. |
Metabolism of cerebroside sulfate and subcellular
distribution of its metabolites in
cultured
skin fibroblasts from controls, metachromatic
leukodystrophy, and globoid cell leukodystrophy. |
J Clin Invest |
81 |
310-317 |
1988 |
|
|
|
|
|
|
73 |
Taniike M, Inui K, Shinoda K, Okada S, Shiotani
Y, Yabuuchi H. |
Correlation of subcellular localization of
disease-specific inclusions and sphingolipid
activator protein-1 (SAP-1) in sulfatide
sulfatase-deficient fibroblasts. |
Acta Histochem Cytochem |
21 |
565-573 |
1988 |
|
|
|
|
|
|
74 |
Nishimoto J, Inui K, Okada S, Ishigami W,
Hirota S, Yamano T, Yabuuchi H. |
A family with pseudodeficiency of acid α-glucosidase. |
Clin Genet |
33 |
254-261 |
1988 |
|
|
|
|
|
|
75 |
Okada S, Handa M, Hashimoto T, Nishimoto
J, Inui K, Furukawa M, Furuyama J,
Yabuuchi
H, Tate M, Gasa S, Makita A |
Biochemical studies on lymphoblastoid cell
with inherited N-acetyl-glucosamine
1-phospho-transferase
deficiency (I-cell disease). |
Biochem Int |
17 |
375-3834 |
1988 |
|
|
|
|
|
|
76 |
萱谷 太、小川 実、佐野 哲也、中島 徹、松下 亨、高田 慶応、三上 泰司、西本 潤史、乾 幸治、岡田 伸太郎、薮内 百治、松田 輝、中埜 粛、川島 康生、牧 一郎 |
乳時期に僧帽弁閉鎖不全が急速に進行したHurler症候群の1例 |
日本小児科学会雑誌 |
92 |
2437-2443 |
1988 |
|
|
|
|
|
|
77 |
河 敬世、池田 輝生、岡田 伸太郎、乾 幸治、田川 哲三、高田 和夫、内村 伸生、覚道 健一、中川 公彦、岡田 正、薮内 百治 |
低血糖症を合併した肝芽腫の1例 |
日本小児外科学会雑誌 |
16 |
1111-1116 |
1988 |
|
|
|
|
|
|
78 |
Okada S, Inui K, Furukawa M, Midorikawa M,
Nishimoto J, Yabuuchi H, Kato T, Watanabe
M, Gasa S, Makita A |
Biochemical heterogeneity in I-cell disease.
Sucrose-loading test classifies two
distinct
subtypes. |
Enzyme |
38 |
267-272 |
1987 |
|
|
|
|
|
|
79 |
Inui K, Furukawa M, Nishimoto J, Okada S,
Yabuuchi H |
Metabolism of cerebroside sulphate and subcellular
distribution of its metabolites in
cultured
skin fibroblasts derived from control,
metachromatic
leukodystrophy, globoid cell leukodystophy
and Farber disease. |
J Inher Metab Dis |
10 |
293-296 |
1987 |