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Nobuo Okumura
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Nobuo Okumura
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Nobuo Okumura
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1
Hereditary Fibrinogen Aα-Chain Amyloidosis in Asia: Clinical and Molecular Characteristics
by
Masahide Yazaki
,
Tsuneaki Yoshinaga
,
Yoshiki Sekijima
,
Fuyuki Kametani
,
Nobuo
Okumura
Published 2018-01-01
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Article
2
A Novel Mutation in the Fibrinogen Bβ Chain (c.490G>A; End of Exon 3) Causes a Splicing Abnormality and Ultimately Leads to Congenital Hypofibrinogenemia
by
Chiaki Taira
,
Kazuyuki Matsuda
,
Shinpei Arai
,
Mitsutoshi Sugano
,
Takeshi Uehara
,
Nobuo
Okumura
Published 2017-11-01
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Article
3
Recombinant γY278H Fibrinogen Showed Normal Secretion from CHO Cells, but a Corresponding Heterozygous Patient Showed Hypofibrinogenemia
by
Tomu Kamijo
,
Takahiro Kaido
,
Masahiro Yoda
,
Shinpei Arai
,
Kazuyoshi Yamauchi
,
Nobuo
Okumura
Published 2021-05-01
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Article
4
Congenital Hypofibrinogenemia in a Neonate with a Novel Mutation in the <i>FGB</i> Gene
by
Jun Shinozuka
,
Nobuo
Okumura
,
Mayumi Nagasawa
,
Motokazu Nishikado
,
Sayaka Kadowaki
,
Itsuro Katsuda
,
Shinsaku Imashuku
Published 2021-03-01
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Article
5
A Novel Amino Acid Substitution, Fibrinogen Bβp.Pro234Leu, Associated with Hypofibrinogenemia Causing Impairment of Fibrinogen Assembly and Secretion
by
Takahiro Kaido
,
Masahiro Yoda
,
Tomu Kamijo
,
Shinpei Arai
,
Chiaki Taira
,
Yumiko Higuchi
,
Nobuo
Okumura
Published 2020-12-01
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Article
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