M. Kawamura

发表

An instrument capable of grading visual function: results from patients with retinitis pigmentosa.

Makoto Tamai, Miyuki Kawamura, Yuko Wada, 2004, The Tohoku journal of experimental medicine.

rt-PA with Antithrombotic Therapies in a Case with Capsular Warning Syndrome

J. Fujitake, M. Kawamura, Yasuhiro Fuseya, 2017, Internal medicine.

Autosomal dominant macular degeneration associated with 208delG mutation in the FSCN2 gene.

M. Tamai, T. Abe, Y. Wada, 2003, Archives of ophthalmology.

Novel 615delC mutation in the CRX gene in a Japanese family with cone-rod dystrophy.

M. Tamai, Y. Wada, T. Shiono, 2004, American journal of ophthalmology.

Ocular findings in a Japanese family with an Arg41Trp mutation of the CRX gene

M. Tamai, H. Kunikata, Y. Wada, 2003, Graefe's Archive for Clinical and Experimental Ophthalmology.

Microangiopathic hemolytic anemia in a graft-versus-host disease patient treated with cyclosporine A and prednisolone.

T. Horie, Y. Hatta, M. Kawamura, 1992, Internal medicine.

Screening for mutations in CYP4V2 gene in Japanese patients with Bietti's crystalline corneoretinal dystrophy.

M. Tamai, Y. Wada, T. Itabashi, 2005, American journal of ophthalmology.

CLINICAL FEATURES OF JAPANESE FAMILIES WITH A 402DELT OR A 555–556DELAG MUTATION IN CHOROIDEREMIA GENE

M. Tamai, Y. Wada, T. Itabashi, 2004, Retina.

A case of hepatic angiosarcoma diagnosed by laparoscopic liver tumor resection

K. Kami, Koji Takai, M. Miyagawa, 2019, Kanzo.

Sarcomatoid Variant of Primary Cutaneous Anaplastic Large Cell Lymphoma.

K. Ohshima, K. Teye, Y. Natsuaki, 2019, The American Journal of dermatopathology.

Screening of the MERTK gene for mutations in Japanese patients with autosomal recessive retinitis pigmentosa.

K. Nishida, M. Tamai, Y. Wada, 2006, Molecular vision.

Mutations in the pre-mRNA splicing gene, PRPF31, in Japanese families with autosomal dominant retinitis pigmentosa.

Makoto Nakamura, M. Tamai, Y. Wada, 2005, American journal of ophthalmology.

Human TPAPGNADPV LIIFGCFCGF ILIGLILYIS LAIRKRVQET KFGNAFTEED SELVVNYIAK KSFCRRAIEL TLHSLGVSEE LQNKLEDVVI DRNLLILGKI Mouse TPAPGNTDSM FIILGCFCGF ILIGLILCIS LALRRRVQET KFGGAFSEED SQLVVNYRAK KSFCRRAIEL TLQSLGVSEE LQNKLEDVVI DRNLLVLGKV Rat TPAPGNTESM LIILGCFCGF VLMGLILYLS LAIKRRVQET KFGGAFSEED SQLVVNYRA

K. Nishida, M. Tamai, Y. Wada, 2006 .

Novel 2336-2337delCT mutation in RP1 gene in a Japanese family with autosomal dominant retinitis pigmentosa.

M. Tamai, Y. Noda, Y. Wada, 2004, American journal of ophthalmology.

Retinitis pigmentosa associated with ectopia lentis.

M. Tamai, T. Abe, Y. Wada, 2002, Archives of ophthalmology.

Screening for mutations in the IMPDH1 gene in Japanese patients with autosomal dominant retinitis pigmentosa.

M. Tamai, Y. Wada, T. Itabashi, 2005, American journal of ophthalmology.

Clinical Variabity of Patients Associated with RDH5 Gene Mutation

M. Tamai, T. Abe, Y. Wada, 2001 .