Hayashi A - Search Results

1

Studies on familial hypotransferrinemia: unique clinical course and molecular pathology.

Hayashi A, Wada Y, Suzuki T, Shimizu A. Hayashi A, et al. Am J Hum Genet. 1993 Jul;53(1):201-13. Am J Hum Genet. 1993. PMID: 8317485 Free PMC article.

2

Monoallelic expression of normal mRNA in the PIT1 mutation heterozygotes with normal phenotype and biallelic expression in the abnormal phenotype.

Okamoto N, Wada Y, Ida S, Koga R, Ozono K, Chiyo H, Hayashi A, Tatsumi K. Okamoto N, et al. Among authors: hayashi a. Hum Mol Genet. 1994 Sep;3(9):1565-8. doi: 10.1093/hmg/3.9.1565. Hum Mol Genet. 1994. PMID: 7833912

3

Decreased blood coagulation activities in carbohydrate-deficient glycoprotein syndrome.

Okamoto N, Wada Y, Kobayashi M, Otani K, Tagawa T, Futagi Y, Imayoshi Y, Hayashi A, Shimizu A, Kato Y. Okamoto N, et al. Among authors: hayashi a. J Inherit Metab Dis. 1993;16(2):435-40. doi: 10.1007/BF00710294. J Inherit Metab Dis. 1993. PMID: 8412004

4

Fetal hemoglobin variants in 80,000 Japanese neonates: high prevalence of Hb F Yamaguchi (A gamma T 80 Asp----Asn).

Wada Y, Fujita T, Kidoguchi K, Hayashi A. Wada Y, et al. Among authors: hayashi a. Hum Genet. 1986 Mar;72(3):196-202. doi: 10.1007/BF00291877. Hum Genet. 1986. PMID: 2420697

5

Neonatal screening and mass-spectrometric analysis of hemoglobin variants in Japan.

Hayashi A, Wada Y, Matsuo T, Katakuse I, Matsuda H. Hayashi A, et al. Acta Haematol. 1987;78(2-3):114-8. doi: 10.1159/000205857. Acta Haematol. 1987. PMID: 3120456

6

Structure and function of a new hemoglobin variant, Hb meilahti (alpha 2 beta 2 36(C2)Pro----Thr), characterized by mass spectrometry.

Wada Y, Ikkala E, Imai K, Matsuo T, Matsuda H, Lehtinen M, Hayashi A, Lehmann H. Wada Y, et al. Among authors: hayashi a. Acta Haematol. 1987;78(2-3):109-13. doi: 10.1159/000205856. Acta Haematol. 1987. PMID: 3120455

7

The genetic studies of familial amyloid polyneuropathy in the Arao district of Japan: II. Studies of genetic markers in blood.

Sakoda S, Suzuki T, Higa S, Ueji M, Kishimoto S, Wada Y, Hayashi A, Matsumoto H, Miyazaki T, Sasazuki T, et al. Sakoda S, et al. Among authors: hayashi a. Jinrui Idengaku Zasshi. 1984 Mar;29(1):51-7. doi: 10.1007/BF01876758. Jinrui Idengaku Zasshi. 1984. PMID: 6205189 No abstract available.

8

Structural analysis of protein variants by mass spectrometry: characterization of haemoglobin providence using a grand-scale mass spectrometer.

Wada Y, Fujita T, Hayashi A, Sakurai T, Matsuo T. Wada Y, et al. Among authors: hayashi a. Biomed Environ Mass Spectrom. 1989 Aug;18(8):563-5. doi: 10.1002/bms.1200180809. Biomed Environ Mass Spectrom. 1989. PMID: 2804442

9

Quantitative analysis of urinary pyroglutamic acid in patients with hyperammonemia.

Nakanishi T, Shimizu A, Saiki K, Fujiwara F, Funahashi S, Hayashi A. Nakanishi T, et al. Among authors: hayashi a. Clin Chim Acta. 1991 Mar 29;197(3):249-55. doi: 10.1016/0009-8981(91)90145-3. Clin Chim Acta. 1991. PMID: 2049866 No abstract available.

10

Urinary organic acids in elderly Japanese patients with ketosis and encephalopathy who have taken panto-yl-gamma-aminobutyrate, calcium salt (calcium hopantenate, HOPA).

Nakanishi T, Funahashi S, Shimizu A, Hayashi A. Nakanishi T, et al. Among authors: hayashi a. Clin Chim Acta. 1990 Apr 13;188(1):85-90. doi: 10.1016/0009-8981(90)90149-m. Clin Chim Acta. 1990. PMID: 2347085 No abstract available.

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