Works matching IS 13288067 AND DT 1981 AND VI 23 AND IP 1

Results: 21

Application of Ultramicrotechnique for the Diagnosis of Hereditary Metabolic Diseases.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 44, doi. 10.1111/j.1442-200X.1981.tb01245.x

By:

Suzuki, Yoshiyuki;
Yokota, Shunichiro;
Kobayashi, Noboru;
Kato, Takahiko

Publication type:

Article

Screening for Adenosine Deaminase or Purine Nucleoside Phosphorylase Deficiency and a Report of Two Patients with Adenosine Deaminase Deficiency.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 66, doi. 10.1111/j.1442-200X.1981.tb01248.x

By:

Sakura, Nobuo;
Usui, Tomofusa;
Ito, Kazuhiko

Publication type:

Article

Diagnostic Problems of Disorders of Tyrosine Metabolism.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 77, doi. 10.1111/j.1442-200X.1981.tb01250.x

By:

Nakamura, Norimasa

Publication type:

Article

Instructions to Authors.

Published in:: Pediatrics International, 1981, v. 23, n. 1, p. 132, doi. 10.1111/j.1442-200X.1981.tb01259.x
Publication type:: Article

Clinical Characteristics of Wilson's Disease in Childhood with Special Reference to Fulminant Form.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 107, doi. 10.1111/j.1442-200X.1981.tb01255.x

By:

Arima, Masataka;
Aoki, Tsugutoshi

Publication type:

Article

Genetic Metabolic Diseases-Where Can We Go from Here?

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 4, doi. 10.1111/j.1442-200X.1981.tb01240.x

By:

Landing, Benjamin H.

Publication type:

Article

Impairment of Sulfatide, Acid Mucopolysaccharides and Cholesterol Sulfate Degradation in Cultured Skin Fibroblasts of Patients with Multiple Sulfatase Deficiency (Mukosulfatidosis).

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 101, doi. 10.1111/j.1442-200X.1981.tb01254.x

By:

Eto, Yoshikatsu;
Numaguchi, Shunsuke;
Tahara, Takuhiro;
Tokoro, Toshiharu

Publication type:

Article

Experience and Problems of Newborn Mass Screening for Inborn Errors of Metabolism in Japan.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 24, doi. 10.1111/j.1442-200X.1981.tb01242.x

By:

Kitagawa, Teruo;
Owada, Misao;
Sakiyama, Takeshi;
Kojima, Tomohiko;
Kondo, Wakio

Publication type:

Article

Biochemical Abnormalities in the Wiskott-Aldrich Syndrome: Low Activity of Hexokinase in Lymphocytes.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 72, doi. 10.1111/j.1442-200X.1981.tb01249.x

By:

Ohga, Kazuhiro;
Sakuraba, Hitoshi;
Suzuki, Yoshiyuki;
Kobayashi, Noboru

Publication type:

Article

Copper Deficiency in a Japanese Infant on Milk Formula.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 124, doi. 10.1111/j.1442-200X.1981.tb01257.x

By:

Nishi, Yoshikazu;
Hatano, Shuichi;
Tanaka, Yoshito;
Sakano, Yumiko;
Usui, Tomofusa

Publication type:

Article

Nephrogenic Diabetes Insipidus and Dwarfism: Rare Combination in a Female Patient.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 128, doi. 10.1111/j.1442-200X.1981.tb01258.x

By:

Watanabe, Noriaki;
Inoue, Toshiro;
Shikata, Izuru;
Kukita, Joji;
Okabe, Yasufumi;
Goya, Nagahide

Publication type:

Article

Folate Metabolism in Infantile Type of 5,10 Methlenetetrahydrofolate Reductase Deficiency.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 82, doi. 10.1111/j.1442-200X.1981.tb01251.x

By:

Narisawa, Kuniaki

Publication type:

Article

Mucolipidosis with β-Galactosidase Deficiency: a Type of Sialidosis.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 87, doi. 10.1111/j.1442-200X.1981.tb01252.x

By:

Okada, Shintaro;
Yutaka, Tohru;
Kato, Tomochika;
Inui, Koji;
Yabuuchi, Hyakuji;
Nishigaki, Masanori;
Yamashita, Katsuko;
Chiyo, Hideaki;
Furuyama, Jun-ichi;
Okada, Yoshio

Publication type:

Article

Menkes' Kinky Hair Disease.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 113, doi. 10.1111/j.1442-200X.1981.tb01256.x

By:

Miyao, M.;
Suzue, J.;
Nishikawa, K.;
Toshima, K.;
Kawano, N.;
Sekiguchi, T.;
Okada, K.;
Kuroda, Y.;
Onishi, T.;
Muramatsu, M.;
Kominami, H.;
Lnaba, H.

Publication type:

Article

Human Lymphoid Cell Lines in Biochemical Genetics.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 35, doi. 10.1111/j.1442-200X.1981.tb01243.x

By:

Matsuda, Ichiro;
Akaboshi, Izumi;
Yamamoto, Jiro;
Nagata, Noriyuki

Publication type:

Article

The Characteristic Profiles of Lysosomal Enzyme Activities in Leukocyte Subpopulations of Normal and Pathologic States.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 57, doi. 10.1111/j.1442-200X.1981.tb01247.x

By:

Tanaka, Takeo;
Usui, Tomofusa

Publication type:

Article

Fabry's Disease: Detection of Heterozygotes Using Blastoid Lymphocytes StimuIated by PhytohemaggIutinin.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 39, doi. 10.1111/j.1442-200X.1981.tb01244.x

By:

Sakuraba, Hitoshi;
Ohga, Kazuhiro;
Suzuki, Yoshiyuki

Publication type:

Article

Metabolic Defects of Adrenoleukodystrophy.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 93, doi. 10.1111/j.1442-200X.1981.tb01253.x

By:

Lgarashi, Masahiro

Publication type:

Article

Acompanying information for authors.

Published in:: Pediatrics International, 1981, v. 23, n. 1, p. 134, doi. 10.1111/j.1442-200X.1981.tb01260.x
Publication type:: Article

Fetal Pathology of Lipidoses.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 16, doi. 10.1111/j.1442-200X.1981.tb01241.x

By:

Kamoshita, Shigehiko

Publication type:

Article

Purine Metabolism and Immunodeficiency.

Published in:

Pediatrics International, 1981, v. 23, n. 1, p. 49, doi. 10.1111/j.1442-200X.1981.tb01246.x

By:

Yata, Junichi;
Nakagawa, Toshiro

Publication type:

Article