CiNii Articles - NARISAWA Kuniaki

1

Molecular analysis of Japanese patients with cystathionine β-synthase deficiency [in Japanese]

KATSUSHIMA F , OHURA T , SAKAMOTO O , MIYABAYASHI S , IINUMA K , NARISAWA K

日本先天代謝異常学会雑誌 15(2), 250, 1999-10-22

Ichushi Web References (1)
2

Carnitine deficiency associated with cardiomyopathy in a patient with propionic acidemia [in Japanese]

OHURA T , NAKANO O , SUGIYAMA N , IINUMA K , NARISAWA K

日本先天代謝異常学会雑誌 14(2), 216, 1998-10-15

Ichushi Web
3

Analysis of glutamate dehydrogenase activity in lymphoblasts from two children with hyperinsulinism-hyperammonemia syndrome [in Japanese]

OHURA T , ASANUMA A , MORO Y , AIKAWA J , SAKAMOTO O , IGARASHI Y , NARISAWA K , IINUMA K

日本先天代謝異常学会雑誌 14(2), 213, 1998-10-15

Ichushi Web References (3)
4

12. ホロカルボキシラーゼ合成酵素欠損症の遺伝子変異とビオチン反応性 [in Japanese]

成澤邦明

VITAMINS 72(2), 70-71, 1998

J-STAGE
5

Propionic acidemia : mutation analysis of the α-subunit of propionyl CoA carboxylase [in Japanese]

OHURA T , IINUMA K , NARISAWA K

日本先天代謝異常学会雑誌 13(3), 468, 1997-10-15

Ichushi Web
6

Next subjects in inherited metabolic disease research [in Japanese]

NARISAWA Kuniaki , TAKEDA Eiji

日本先天代謝異常学会雑誌 13(3), 385, 1997-10-15

Ichushi Web
7

Disturbances of Amino Acids Metabolism in Infants with Idiopathic Neonatal Hepatitis [in Japanese]

OHURA Toshihiro , ABUKAWA Daiki , AIKAWA Junichiro , NAKAGAWA Michiko , ISHIZAWA Shinobu , TAZAWA Yusaku , NARISAWA Kuinaki , IINUMA Kazuie

日本小児科学会雑誌 101(10), 1522-1525, 1997-10-01

Ichushi Web References (8) Cited by (10)
8

先天性代謝異常症の遺伝子診断 [in Japanese]

成沢邦明

Gene & medicine 1(2), 238-243, 1997-10

Ichushi Web
9

フェニルケトン尿症 (特集最近話題の疾患・症候群) [in Japanese]

成沢邦明

The Journal of pediatric practice 60(7), 1111-1117, 1997-07

Ichushi Web Cited by (1)
10

肝臓内酵素欠損症の遺伝子治療 (特集いま始まった遺伝子治療--何ができ,何が必要か?) [in Japanese]

松原洋一 , 長崎裕 , 成沢邦明

Molecular medicine 34(4), 474-483, 1997-04

Ichushi Web Cited by (1)
11

先天代謝異常と酵素診断 [in Japanese]

成澤邦明

日本先天代謝異常学会雑誌 13(1), 114-115, 1997-03-06
12

先天性疾患の遺伝子診断--出生後確定診断 (特集周産期医療に必要な遺伝子の知識ABC) [in Japanese]

成沢邦明

周産期医学 27(1), 31-35, 1997-01

Ichushi Web
13

10.ホロカルボキシラーゼ合成酵素血症におけるビオチン反応性の機序 : ビタミンB研究委員会第355回会議研究発表要旨 [in Japanese]

成澤邦明

VITAMINS 71(2), 95-96, 1997

J-STAGE Ichushi Web
14

Prenatal diagnosis in high risk pregnancy for X-linked adrenoleukodystrophy [in Japanese]

AIKAWA J , IINUMA K , NARISAWA K

日本先天代謝異常学会雑誌 12(2), 205, 1996-10-15

Ichushi Web References (3)
15

L-carnitine therapy for disorders of propionate metabolism : the outcome of five-year-follow-up in Japan [in Japanese]

SUGIYAMA N , MATSUDA I , WADA Y , NARISAWA K , KIDOUCHI K , KOBAYASHI M , ITO T , ITOH T

日本先天代謝異常学会雑誌 12(2), 186, 1996-10-15

Ichushi Web References (1)
16

ホロカルボキシラーゼ合成酵素欠損症の分子遺伝学的解析 [in Japanese]

成澤邦明

日本先天代謝異常学会雑誌 12(1), 19-26, 1996-05-20

Ichushi Web References (7)
17

Symposium: Development of DNA Test from Chromosome Analysis Department of Biochemical Genetics, Tohoku University, School of Medicine [in Japanese]

NARISAWA Kuniaki , FUNATO Tadao

臨床病理 44(2), 115, 1996-02-25
18

ホロカルボキシラ-ゼ合成酵素(HCS)欠損症の遺伝子異常と遺伝子診断 [in Japanese]

成沢邦明 , 鈴木洋一 , 青木洋子

Japanese journal of clinical medicine 54(1), 259-267, 1996-01

Ichushi Web
19

8.B群ビタミン依存症 : ビタミンB研究委員会 : 第350回記念シンポジウム : B群ビタミン研究の現状と将来展望 [in Japanese]

成澤邦明

VITAMINS 70(5-6), 268-270, 1996

J-STAGE Ichushi Web
20

The Molecular Basis of Holocarboxylase synthetase deficiency, Methylmalonic acidemia and Vitamin B_1 Responsive Pyruvate dehydrogenase deficiency [in Japanese]

NARISAWA Kuniaki

Holocarboxylase synthetase (HCS) plays an essential role in biotin utilization in cells and its deficiency causes biotin-responsive multiple carboxylase deficiency in humans. We have clones the human …

VITAMINS 70(1), 1-8, 1996

J-STAGE Ichushi Web References (4)

成澤邦明 NARISAWA Kuniaki

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成澤 邦明 NARISAWA Kuniaki

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成澤邦明 NARISAWA Kuniaki

Articles:　 1-20 of 49