Kanzaki A - Search Results

1

Multiple cerebral infarctions in a patient with refractory idiopathic thrombocytopenic purpura.

Otsuki T, Funakawa T, Sugihara T, Kanzaki A, Wada H, Inoue T, Yamada O, Ueki A, Yawata Y. Otsuki T, et al. Among authors: kanzaki a. J Intern Med. 1997 Mar;241(3):249-52. doi: 10.1046/j.1365-2796.1997.72899000.x. J Intern Med. 1997. PMID: 9104439 Free article.

2

[The complete band4.2 deficiency in human red cells].

Kanzaki A, Inoue T, Wada H, Yawata Y. Kanzaki A, et al. Nihon Rinsho. 1996 Sep;54(9):2492-501. Nihon Rinsho. 1996. PMID: 8890584 Review. Japanese.

3

Hereditary stomatocytosis: phenotypical expression of sodium transport and band 7 peptides in 44 cases.

Kanzaki A, Yawata Y. Kanzaki A, et al. Br J Haematol. 1992 Sep;82(1):133-41. doi: 10.1111/j.1365-2141.1992.tb04605.x. Br J Haematol. 1992. PMID: 1419788

4

[Cytoskeleton anomalies in disorders of red cell membrane proteins].

Kanzaki A, Wada H, Yawata Y. Kanzaki A, et al. Rinsho Ketsueki. 1991 Jun;32(6):573-9. Rinsho Ketsueki. 1991. PMID: 1832469 Japanese.

5

Evolution and development of membrane components in erythroid precursor cells in newly-developed two phase culture system.

Yawata Y, Wada H, Kanzaki A, Yamada O. Yawata Y, et al. Among authors: kanzaki a. Biomed Biochim Acta. 1990;49(2-3):S76-81. Biomed Biochim Acta. 1990. PMID: 2386532

6

Uniquely higher incidence of isolated or combined deficiency of band 3 and/or band 4.2 as the pathogenesis of autosomal dominantly inherited hereditary spherocytosis in the Japanese population.

Inoue T, Kanzaki A, Yawata A, Wada H, Okamoto N, Takahashi M, Sugihara T, Yamada O, Yawata Y. Inoue T, et al. Among authors: kanzaki a. Int J Hematol. 1994 Dec;60(4):227-38. Int J Hematol. 1994. PMID: 7894027

7

Red cell membrane disorders in the Japanese population: clinical, biochemical, electron microscopic, and genetic studies.

Yawata Y, Kanzaki A, Inoue T, Ata K, Wada H, Okamoto N, Higo I, Yawata A, Sugihara T, Yamada O. Yawata Y, et al. Among authors: kanzaki a. Int J Hematol. 1994 Jul;60(1):23-38. Int J Hematol. 1994. PMID: 7919236 Review.

8

[Concordant improvement of progressive systemic sclerosis and chronic myelogenous leukemia with interferon-alpha treatment].

Watanabe S, Sugihara T, Takahashi M, Ata K, Kanzaki A, Yamada O, Yawata Y. Watanabe S, et al. Among authors: kanzaki a. Rinsho Ketsueki. 1994 Sep;35(9):895-7. Rinsho Ketsueki. 1994. PMID: 7967060 Japanese.

9

Homozygous missense mutation (band 3 Fukuoka: G130R): a mild form of hereditary spherocytosis with near-normal band 3 content and minimal changes of membrane ultrastructure despite moderate protein 4.2 deficiency.

Inoue T, Kanzaki A, Kaku M, Yawata A, Takezono M, Okamoto N, Wada H, Sugihara T, Yamada O, Katayama Y, Nagata N, Yawata Y. Inoue T, et al. Among authors: kanzaki a. Br J Haematol. 1998 Sep;102(4):932-9. doi: 10.1046/j.1365-2141.1998.00868.x. Br J Haematol. 1998. PMID: 9734643 Free article.

10

Late expression of red cell membrane protein 4.2 in normal human erythroid maturation with seven isoforms of the protein 4.2 gene.

Wada H, Kanzaki A, Yawata A, Inoue T, Kaku M, Takezono M, Sugihara T, Yamada O, Yawata Y. Wada H, et al. Among authors: kanzaki a. Exp Hematol. 1999 Jan;27(1):54-62. doi: 10.1016/s0301-472x(98)00014-9. Exp Hematol. 1999. PMID: 9923444 Free article.

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