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Journal Articles

Molecular analysis of glucose phosphate isomerase deficiency associated with hereditary hemolytic anemia

H Kanno, H Fujii, A Hirono, Y Ishida, S Ohga, Y Fukumoto, K Matsuzawa, S Ogawa, S Miwa

Blood (1996) 88 (6): 2321–2325.

https://doi.org/10.1182/blood.V88.6.2321.bloodjournal8862321

Published: 1996

Journal Articles

Three cases of hereditary nonspherocytic hemolytic anemia associated with red blood cell glutathione deficiency

A Hirono, H Iyori, I Sekine, J Ueyama, H Chiba, H Kanno, H Fujii, S Miwa

Blood (1996) 87 (5): 2071–2074.

https://doi.org/10.1182/blood.V87.5.2071.2071

Published: 1996

Journal Articles

Pyruvate kinase deficiency of mice associated with nonspherocytic hemolytic anemia and cure of the anemia by marrow transplantation without host irradiation

M Morimoto, H Kanno, H Asai, T Tsujimura, H Fujii, Y Moriyama, T Kasugai, A Hirono, Y Ohba, S Miwa

Blood (1995) 86 (11): 4323–4330.

https://doi.org/10.1182/blood.V86.11.4323.bloodjournal86114323

Published: 1995

Journal Articles

Primary structure of murine red blood cell-type pyruvate kinase (PK) and molecular characterization of PK deficiency identified in the CBA strain

H Kanno, M Morimoto, H Fujii, T Tsujimura, H Asai, T Noguchi, Y Kitamura, S Miwa

Blood (1995) 86 (8): 3205–3210.

https://doi.org/10.1182/blood.V86.8.3205.3205

Published: 1995

Journal Articles

Identification of two novel deletion mutations in glucose-6-phosphate dehydrogenase gene causing hemolytic anemia

A Hirono, H Fujii, S Miwa

Blood (1995) 85 (4): 1118–1121.

https://doi.org/10.1182/blood.V85.4.1118.bloodjournal8541118

Published: 1995

Journal Articles

Hereditary hemolytic anemia caused by diverse point mutations of pyruvate kinase gene found in Japan and Hong Kong

H Kanno, DC Wei, LC Chan, H Mizoguchi, M Ando, T Nakahata, K Narisawa, H Fujii, S Miwa

Blood (1994) 84 (10): 3505–3509.

https://doi.org/10.1182/blood.V84.10.3505.3505

Published: 1994

Journal Articles

Nonrandom chromosomal rearrangements of 14q32.3 and 19p13.3 and preferential deletion of 1p in 21 patients with multiple myeloma and plasma cell leukemia

M Taniwaki, K Nishida, T Takashima, H Nakagawa, H Fujii, T Tamaki, C Shimazaki, S Horiike, S Misawa, T Abe

Blood (1994) 84 (7): 2283–2290.

https://doi.org/10.1182/blood.V84.7.2283.2283

Published: 1994

Journal Articles

Molecular study of eight Japanese cases of glucose-6-phosphate dehydrogenase deficiency by nonradioisotopic single-strand conformation polymorphism analysis [see comments]

A Hirono, S Miwa, H Fujii, F Ishida, K Yamada, K Kubota

Blood (1994) 83 (11): 3363–3368.

https://doi.org/10.1182/blood.V83.11.3363.3363

Published: 1994

Journal Articles

Molecular abnormality of erythrocyte pyruvate kinase deficiency in the Amish

H Kanno, SK Ballas, S Miwa, H Fujii, HS Bowman

Blood (1994) 83 (8): 2311–2316.

https://doi.org/10.1182/blood.V83.8.2311.2311

Published: 1994

Journal Articles

G6PD Nara: a new class 1 glucose-6-phosphate dehydrogenase variant with an eight amino acid deletion

A Hirono, H Fujii, M Shima, S Miwa

Blood (1993) 82 (11): 3250–3252.

https://doi.org/10.1182/blood.V82.11.3250.3250

Published: 1993

Journal Articles

Low substrate affinity of pyruvate kinase variant (PK Sapporo) caused by a single amino acid substitution (426 Arg-->Gln) associated with hereditary hemolytic anemia

H Kanno, H Fujii, S Miwa

Blood (1993) 81 (9): 2439–2441.

https://doi.org/10.1182/blood.V81.9.2439.2439

Published: 1993

Journal Articles

A single amino acid substitution (157 Gly----Val) in a phosphoglycerate kinase variant (PGK Shizuoka) associated with chronic hemolysis and myoglobinuria

H Fujii, H Kanno, A Hirono, T Shiomura, S Miwa

Blood (1992) 79 (6): 1582–1585.

https://doi.org/10.1182/blood.V79.6.1582.1582

Published: 1992

Journal Articles

Identical point mutations of the R-type pyruvate kinase (PK) cDNA found in unrelated PK variants associated with hereditary hemolytic anemia

H Kanno, H Fujii, A Hirono, M Omine, S Miwa

Blood (1992) 79 (5): 1347–1350.

https://doi.org/10.1182/blood.V79.5.1347.1347

Published: 1992

Journal Articles

Actions of human interleukin-4/B-cell stimulatory factor-1 on proliferation and differentiation of enriched hematopoietic progenitor cells in culture

Y Sonoda, T Okuda, S Yokota, T Maekawa, Y Shizumi, H Nishigaki, S Misawa, H Fujii, T Abe

Blood (1990) 75 (8): 1615–1621.

https://doi.org/10.1182/blood.V75.8.1615.1615

Published: 1990

Journal Articles

Membrane abnormality in red blood cells with weak type B expression

A Yoshida, H Fujii, V Dave, MJ Cozant, PA Morel

Blood (1980) 56 (5): 881–885.

https://doi.org/10.1182/blood.V56.5.881.881

Published: 1980

NARROW

Molecular analysis of glucose phosphate isomerase deficiency associated with hereditary hemolytic anemia

Three cases of hereditary nonspherocytic hemolytic anemia associated with red blood cell glutathione deficiency

Pyruvate kinase deficiency of mice associated with nonspherocytic hemolytic anemia and cure of the anemia by marrow transplantation without host irradiation

Primary structure of murine red blood cell-type pyruvate kinase (PK) and molecular characterization of PK deficiency identified in the CBA strain

Identification of two novel deletion mutations in glucose-6-phosphate dehydrogenase gene causing hemolytic anemia

Hereditary hemolytic anemia caused by diverse point mutations of pyruvate kinase gene found in Japan and Hong Kong

Nonrandom chromosomal rearrangements of 14q32.3 and 19p13.3 and preferential deletion of 1p in 21 patients with multiple myeloma and plasma cell leukemia

Molecular study of eight Japanese cases of glucose-6-phosphate dehydrogenase deficiency by nonradioisotopic single-strand conformation polymorphism analysis [see comments]

Molecular abnormality of erythrocyte pyruvate kinase deficiency in the Amish

G6PD Nara: a new class 1 glucose-6-phosphate dehydrogenase variant with an eight amino acid deletion

Low substrate affinity of pyruvate kinase variant (PK Sapporo) caused by a single amino acid substitution (426 Arg-->Gln) associated with hereditary hemolytic anemia

A single amino acid substitution (157 Gly----Val) in a phosphoglycerate kinase variant (PGK Shizuoka) associated with chronic hemolysis and myoglobinuria

Identical point mutations of the R-type pyruvate kinase (PK) cDNA found in unrelated PK variants associated with hereditary hemolytic anemia

Actions of human interleukin-4/B-cell stimulatory factor-1 on proliferation and differentiation of enriched hematopoietic progenitor cells in culture

Membrane abnormality in red blood cells with weak type B expression

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American Society of Hematology

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ASH Publications

American Society of Hematology

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