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1

Glycine cleavage system in astrocytes

Kohji Sato, Sigetaka Yoshida, Kazuko Fujiwara, Keiya Tada, Masaya Tohyama

Journal:

Year:

1991

Language:

english

File:

PDF, 5.73 MB

english, 1991

2

Inborn Metabolic Diseases || Organic Acidemias

Fernandes, John, Saudubray, Jean-Marie, Tada, Keiya

Year:

1990

Language:

english

File:

PDF, 3.34 MB

english, 1990

3

Hyperornithinemia with gyrate atrophy of the choroid and retina: A disturbance in de novo formation of proline.

SAITO, TAKASHI, OMURA, KIYOSHI, HAYASAKA, SEIJI, NAKAJIMA, HISAO, MIZUNO, KATSUYOSHI, TADA, KEIYA

Journal:

The Tohoku Journal of Experimental Medicine

Year:

1981

Language:

english

File:

PDF, 2.80 MB

english, 1981

4

Prenatal diagnosis of non-ketotic hyperglycinaemia: enzymatic diagnosis in 28 families and DNA diagnosis detecting prevalent Finnish and Israeli–Arab mutations

Shigeo Kure, Marie-Odile Rolland, Jaako Leisti, Hanna Mandel, Yoshiyuki Sakata, Keiya Tada, Yoichi Matsubara, Kuniaki Narisawa

Journal:

Prenatal Diagnosis

Year:

1999

Language:

english

File:

PDF, 124 KB

english, 1999

5

Establishment and characterization of a human acute monocytic leukemia cell line (THP-1)

Shigeru Tsuchiya, Michiko Yamabe, Yoshiko Yamaguchi, Yasuko Kobayashi, Tasuke Konno, Keiya Tada

Journal:

International Journal of Cancer

Year:

1980

Language:

english

File:

PDF, 523 KB

english, 1980

6

Isolation and characterization of a blood group active glycopeptide from porcine aorta

Junichiro Aikawa, Mamoru Isemura, Hiroshi Manakata, Masaki Kikuchi, Keiya Tada, Zensaku Yosizawa

Journal:

International Journal of Biochemistry

Year:

1985

Language:

english

File:

PDF, 606 KB

english, 1985

7

Leukoencephalopathy in childhood hematopoietic neoplasm caused by moderate-dose methotrexate and prophylactic cranial radiotherapy—An MR analysis

Ko Matsumoto, Shoki Takahashi, Atsushi Sato, Masue Imaizumi, Shuichi Higano, Kiyohiko Sakamoto, Hiroshi Asakawa, Keiya Tada

Journal:

International Journal of Radiation Oncology*Biology*Physics

Year:

1995

Language:

english

File:

PDF, 1.23 MB

english, 1995

8

A novel splicing mutation in propionic acidemia associated with a tetranucleotide direct repeat in the PCCB gene

Toshihiro Ohura, Kuniaki Nariwasa, Keiya Tada, Kazuie Iisnuma

Journal:

Year:

1995

Language:

english

File:

PDF, 167 KB

english, 1995

9

Cerebral glucose utilization in pediatric neurological disorders determined by positron emission tomography

Kazuhiko Yanai, Kazuie Iinuma, Taiju Matsuzawa, Masatoshi Ito, Shigeaki Miyabayashi, Kuniaki Narisawa, Tatsuo Ido, Kenji Yamada, Keiya Tada

Journal:

European Journal of Nuclear Medicine and Molecular Imaging

Year:

1987

Language:

english

File:

PDF, 1.03 MB

english, 1987

10

Dystrophin immunohistochemistry in a symptomatic carrier of becker muscular dystrophy

Kazuhiro Haginoya, Katsuya Yamamoto, Kazuie Iinuma, Toshiro Yanagisawa, Yu Ichinohasama, Michie Shimmoto, Yoshiyuki Suzuki, Keiya Tada

Journal:

Journal of Neurology

Year:

1991

Language:

english

File:

PDF, 989 KB

english, 1991

11

A new method for screening for hyperammonemia

Keiya Tada, Kiyoshi Okuda, Kyoko Watanabe, Yasuo Iimura, Shigeki Yamada

Journal:

European Journal of Pediatrics

Year:

1979

Language:

english

File:

PDF, 480 KB

english, 1979

12

Congenital lactic acidosis due to pyruvate carboxylase deficiency: Absence of an inhibitor of TPP-ATP phosphoryl transferase

Keiya Tada, Goro Takada, Kiyoshi Omura, Yoshinori Itokawa

Journal:

European Journal of Pediatrics

Year:

1978

Language:

english

File:

PDF, 367 KB

english, 1978

13

α-l-Iduronidase activity in leukocytes: Diagnosis of homozygotes and heterozygotes of the Hurler syndrome

Kiyoshi Omura, Shinobu Higami, Keiya Tada

Journal:

European Journal of Pediatrics

Year:

1976

Language:

english

File:

PDF, 173 KB

english, 1976

14

Hyperalaninemia, hyperpyruvicemia and lactic acidosis due to pyruvate carboxylase deficiency of the liver; Treatment with thiamine and lipoic acid

Hatae Maesaka, Kazuhiko Komiya, Kazuaki Misugi, Keiya Tada

Journal:

European Journal of Pediatrics

Year:

1976

Language:

english

File:

PDF, 1.25 MB

english, 1976

15

Genetic heterogeneity of propionic acidemia: Analysis of 15 Japanese patients

Toshihiro Ohura, Shigeaki Miyabayashi, Kuniaki Narisawa, Keiya Tada

Journal:

Year:

1991

Language:

english

File:

PDF, 522 KB

english, 1991

16

The molecular defect in propionic acidemia: Exon skipping caused by an 8-bp deletion from an intron in the PCCB allele

Toshihiro Ohura, Masato Ogasawara, Hiroyuki Ikeda, Kuniaki Narisawa, Keiya Tada

Journal:

Year:

1993

Language:

english

File:

PDF, 1.09 MB

english, 1993

17

Glycogen storage disease type Ib: A defect in the glucose-6-phosphate transport system in microsomal membrane

Journal:

Journal of Human Genetics

Year:

1984

Language:

english

File:

PDF, 565 KB

english, 1984

18

A family of adenosine deaminase deficiency with severe combined immunodeficiency

Shigeru Tsuchiya, Kuniaki Narisawa, Tasuke Konno, Keiya Tada

Journal:

Journal of Human Genetics

Year:

1979

Language:

english

File:

PDF, 187 KB

english, 1979

19

PstI fragment polymorphism in the gene of the human ATP synthase beta subunit

Kiyoshi Hasegawa, Shigeo Ohta, Kuniaki Narisawa, Keiya Tada, Yasuo Kagawa

Journal:

Journal of Human Genetics

Year:

1987

Language:

english

File:

PDF, 721 KB

english, 1987

20

Nonketotic hyperglycinemia: Biochemical, molecular, and neurological aspects

Shigeo Kure, Keiya Tada, Kuniaki Narisawa

Journal:

Journal of Human Genetics

Year:

1997

Language:

english

File:

PDF, 589 KB

english, 1997

21

A missense mutation (His42Arg) in the T-protein gene from a large Israeli-Arab kindred with nonketotic hyperglycinemia

S. Kure, Hanna Mandel, Marie-Odile Rolland, Yoshiyuki Sakata, Toshikatsu Shinka, Aryeb Drugan, Avihu Boneh, Keiya Tada, Yoichi Matsubara, Kuniaki Narisawa

Journal:

Year:

1998

Language:

english

File:

PDF, 131 KB

english, 1998

22

A one-base deletion (183delC) and a missense mutation (D276H) in the T-protein gene from a Japanese family with nonketotic hyperglycinemia

S. Kure, Toshikatsu Shinka, Yoshiyuki Sakata, Narasaki Osamu, Masaru Takayanagi, Keiya Tada, Yoichi Matsubara, Kuniaki Narisawa

Journal:

Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 236 KB

english, 1998

23

Founders of Child Neurology in Japan – Keiya Tada

Keiya Tada, Kenji Nihei

Journal:

Brain and Development

Year:

2004

Language:

english

File:

PDF, 82 KB

english, 2004

24

Depletion of Cerebral D-Serine in Non-Ketotic Hyperglycinemia: Possible Involvement of Glycine Cleavage System in Control of Endogenous D-Serine

Hisayuki Iwama, Katsunobu Takahashi, Shigeo Kure, Fumihiko Hayashi, Kuniaki Narisawa, Keiya Tada, Masashi Mizoguchi, Sachio Takashima, Urara Tomita, Toru Nishikawa

Journal:

Biochemical and Biophysical Research Communications

Year:

1997

Language:

english

File:

PDF, 75 KB

english, 1997

25

The impaired expression of glycine decarboxylase in patients with hyperglycinemias

Akihiro Kume, Shigeo Kure, Keiya Tada, Koichi Hiraga

Journal:

Biochemical and Biophysical Research Communications

Year:

1988

Language:

english

File:

PDF, 750 KB

english, 1988

26

Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency

Yoichi Matsubara, Kuniaki Narisawa, Shigeaki Miyabayashi, Keiya Tada, Paul M. Coates, Claude Bachmann, Louis J. Elsas II, Rodney J. Pollitt, William J. Rhead, Charles R. Roe

Journal:

Biochemical and Biophysical Research Communications

Year:

1990

Language:

english

File:

PDF, 706 KB

english, 1990

27

Glutamate triggers internucleosomal DNA cleavage in neuronal cells

Shigeo Kure, Teiji Tominaga, Takashi Yoshimoto, Keiya Tada, Kuniaki Narisawa

Journal:

Biochemical and Biophysical Research Communications

Year:

1991

Language:

english

File:

PDF, 1.13 MB

english, 1991

28

Structural and expression analyses of normal and mutant mRNA encoding glycine decarboxylase: Three-base deletion in mRNA causes nonketotic hyperglycinemia

Shigeo Kure, Kuniaki Narisawa, Keiya Tada

Journal:

Biochemical and Biophysical Research Communications

Year:

1991

Language:

english

File:

PDF, 881 KB

english, 1991

29

Gyrate atrophy of the choroid and retina: decreased ornithine aminotransferase concentration in cultured skin fibroblasts from patients

Toshihiro Ohura, Eiki Kominami, Keiya Tada, Nobuhiko Katunuma

Journal:

Clinica Chimica Acta

Year:

1984

Language:

english

File:

PDF, 582 KB

english, 1984

30

Assay of methylmalonyl CoA mutase with high-performance liquid chromatography

Masahiro Kikuchi, Hiroshi Hanamizu, Kuniaki Narisawa, Keiya Tada

Journal:

Clinica Chimica Acta

Year:

1989

Language:

english

File:

PDF, 440 KB

english, 1989

31

Enzymatic diagnosis of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency with high-performance liquid chromatography

Masahiro Kikuchi, Kuniaki Narisawa, Keiya Tada, Laurence Sweetman

Journal:

Clinica Chimica Acta

Year:

1990

Language:

english

File:

PDF, 325 KB

english, 1990

32

One of the two genomic copies of the glycine decarboxylase cDNA has been deleted at a 5′ region in a patient with nonketotic hyperglycinemia

Toshihiro Sakakibara, Hirohisa Koyata, Yoshihisa Ishiguro, Shigeo Kure, Akihiro Kume, Keiya Tada, Koichi Hiraga

Journal:

Biochemical and Biophysical Research Communications

Year:

1990

Language:

english

File:

PDF, 1.12 MB

english, 1990

33

A direct evidence for defect in glucose-6-phosphate transport system in hepatic microsomal membrane of glycogen storage disease type Ib

Yutaka Igarashi, Seiichi Kato, Kuniaki Narisawa, Keiya Tada, Yoshio Amano, Tetsuo Mori, Shin Takeuchi

Journal:

Biochemical and Biophysical Research Communications

Year:

1984

Language:

english

File:

PDF, 218 KB

english, 1984

34

Enzymatic diagnosis of nonketotic hyperglycinemia with lymphoblasts

Shigeo Kure, Kunlaki Narisawa, Keiya Tada

Journal:

The Journal of Pediatrics

Year:

1992

Language:

english

File:

PDF, 315 KB

english, 1992

35

Prenatal diagnosis of nonketotic hyperglycinemia: Enzymatic analysis of the glycine cleavage system in chorionic villi

Kiyoshi Hayasaka, Keiya Tada, Noboru Fueki, Junichiro Aikawa

Journal:

The Journal of Pediatrics

Year:

1990

Language:

english

File:

PDF, 171 KB

english, 1990

36

A new variant of glycogen storage disease Type I probably due to a defect in the glucose-6-phosphate transport system

Kuniaki Narisawa, Yutaka Igarashi, Hiromi Otomo, Keiya Tada

Journal:

Biochemical and Biophysical Research Communications

Year:

1978

Language:

english

File:

PDF, 265 KB

english, 1978

37

Glycogen storage disease type Ib: A new model of genetic disorders involving the transport system of intracellular membrane

Keiya Tada, Kuniaki Narisawa, Yutaka Igarashi, Seiichi Kato

Journal:

Biochemical Medicine

Year:

1985

Language:

english

File:

PDF, 487 KB

english, 1985

38

Treatment of Phenylketonuria during Early Infancy

Hisao Aoki, Akemi Mori, Gen Ishiki, Keiya Tada, Toshiaki Oura, Kunio Fujii

Journal:

Pediatrics International

Year:

1976

Language:

english

File:

PDF, 45 KB

english, 1976

39

Treatment of Inborn Errors of Metabolism

Journal:

Pediatrics International

Year:

1980

Language:

english

File:

PDF, 365 KB

english, 1980

40

Neonatal Propionic Acidemia

Noriko Kanno, Masaaki Yamada, Toshio Kawano, Tatsuo Naitoh, Tsugutoshi Aoki, Kuniaki Narisawa, Keiya Tada

Journal:

Pediatrics International

Year:

1981

Language:

english

File:

PDF, 77 KB

english, 1981

41

Prenatal Diagnosis for Inborn Errors of Metabolism in Japan

Teruo Kitagawa, Momoko Saito, Masataka Arima, Yoshikatsu Eto, Tadao Orii, Tomokazu Kusunoki, Yoshiyuki Suzuki, Keiya Tada, Seishiro Tarui, Momoji Yabuuchi

Journal:

Pediatrics International

Year:

1983

Language:

english

File:

PDF, 73 KB

english, 1983

42

Metabolism: Molecular Lesion of Nonketotic Hyperglycinemia

Keiya Tada, Kiyoshi Hayasaka

Journal:

Pediatrics International

Year:

1985

Language:

english

File:

PDF, 247 KB

english, 1985

43

Treatment of Cystinosis: Decrease in Content of Free Cystine in Leukocytes and Alleviation of Progressive Renal Failure by Treatment with Riboflavin

Kiyoshi Hayasaka, Kuniaki Narisawa, Takashi Saitoh, Hirohiko Numakura, Kaoru Fukuda, Seiichi Kato, Toshiyuki Tayama, Keiya Tada

Journal:

Pediatrics International

Year:

1986

Language:

english

File:

PDF, 263 KB

english, 1986

44

Site Specific Mapping of Chromosome 21 Gene Probes and the Study of Down Syndrome

Hiroshi Nakai, Paul C. Watkins, Mary G. Byers, Thomas B. Shows, Keiya Tada

Journal:

Pediatrics International

Year:

1987

Language:

english

File:

PDF, 411 KB

english, 1987

45

Prenatal Diagnosis in High Risk Pregnancies for Zellweger Syndrome

Junichiro Aikawa, Koji Sato, Shigeaki Miyabayashi, Keiya Tada, Kuniaki Narisawa, Nobukazu Chida, Takashi Hashimoto

Journal:

Pediatrics International

Year:

1992

Language:

english

File:

PDF, 377 KB

english, 1992

46

Lack of Subunit II of Cytochrome c Oxidase in a Patient with Mitochondrial Myopathy

MASASHI TANAKA, MORIMITSU NISHIKIMI, TAKAYUKI OZAWA, SHIGEAKI MIYABAYASHI, KEIYA TADA

Journal:

Annals of the New York Academy of Sciences

Year:

1986

Language:

english

File:

PDF, 99 KB

english, 1986

47

Physiological significance of glycine cleavage system in human liver as revealed by the study of a case of hyperglycinemia

Tadashi Yoshida, Goro Kikuchi, Keiya Tada, Kuniaki Narisawa, Tsuneo Arakawa

Journal:

Biochemical and Biophysical Research Communications

Year:

1969

Language:

english

File:

PDF, 360 KB

english, 1969

48

Neutropenia in type IB glycogen storage disease

Kuniaki Narisawa, Keiya Tada, Takeshi Kuzuya

Journal:

The Journal of Pediatrics

Year:

1981

Language:

english

File:

PDF, 190 KB

english, 1981

49

Intellectual development in patients with untreated histidinemia: A collaborative study group of neonatal screening for inborn errors of metabolism in Japan

Keiya Tada, Hiraku Tateda, Schinichiro Arashima, Kaoru Sakai, Teruo Kitagawa, Kikumaro Aoki, Seizo Suwa, Masahiko Kawamura, Toshiaki Oura, Masashi Takesada, Yasuhiro Kuroda, Fumio Yamashita, Ichiro Ma

Journal:

The Journal of Pediatrics

Year:

1982

Language:

english

File:

PDF, 177 KB

english, 1982

50

Diagnosis of variant forms of hyperphenylalaninemia using filter paper spots of urine

Kuniaki Narisawa, Hiroshi Hayakawa, Nobuhiro Arai, Nobutake Matsuo, Takeo Tanaka, Kenji Naritomi, Keiya Tada

Journal:

The Journal of Pediatrics

Year:

1983

Language:

english

File:

PDF, 277 KB

english, 1983