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Cancer|May 20, 1998
Hemophagocytic syndrome in five patients with Epstein-Barr virus negative B-cell lymphomaT Ohno, N Miyake, S Hada, et al.
Clinical Genetics|May 3, 2014
Mutations in COG2 encoding a subunit of the conserved oligomeric golgi complex cause a congenital disorder of glycosylationH Kodera, N Ando, I Yuasa, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|June 1, 1992
[Cold agglutinin hemolytic anemia complicating mycoplasma pneumonia]F Inoue, N Miyake, M Yamasowa, et al.
Nihon Jinzo Gakkai Shi|September 1, 1996
[A case of myeloperoxidase-specific antineutrophil cytoplasmic antibody (MPO-ANCA)-related glomerulonephritis associated with Cogan's syndrome]M Suzuki, Y Arimura, S Minoshima, et al.
Clinical Genetics|June 12, 2018
Bilateral cerebellar cysts and cerebral white matter lesions with cortical dysgenesis: Expanding the phenotype of LAMB1 gene mutationsT Okazaki, Y Saito, T Hayashida, et al.
Clinical Genetics|August 4, 2017
A case of atypical Kabuki syndrome arising from a novel missense variant in HNRNPKN Miyake, M Inaba, S Mizuno, et al.
Nihon Shokakibyo Gakkai Zasshi = the Japanese Journal of Gastro-Enterology|January 16, 1999
[A clinical study on the cases of ischemic colitis: comparison of clinical images based on time from onset of the disease to detection of bloody stool]T Tsukamoto, F Inoue, K Azuma, et al.
Letters in Applied Microbiology|March 12, 2014
Development of loop-mediated isothermal amplification assay for the detection of Pythium myriotylumS Fukuta, R Takahashi, S Kuroyanagi, et al.
Clinical Genetics|October 5, 2017
A novel missense mutation affecting the same amino acid as the recurrent PACS1 mutation in Schuurs-Hoeijmakers syndromeN Miyake, S Ozasa, H Mabe, et al.
Clinical Genetics|April 5, 2014
De novo EEF1A2 mutations in patients with characteristic facial features, intellectual disability, autistic behaviors and epilepsyJ Nakajima, N Okamoto, J Tohyama, et al.
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