K. Okajima

J. Tyson, S. Malcolm, T. Niwa, 2002, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Increase of protein synthesis by uridine supplement in lectin-stimulated peripheral blood lymphocytes and EB virus-transformed B cell line of hereditary orotic aciduria type I.

K. Okajima, M. Suchi, M. Yazaki, 1987, The Tohoku journal of experimental medicine.

Characterization of Point Mutations in Two Hereditary Orotic

M. E. Hodgson, K. Okajima, S. Sumi, 2006 .

FOXG1 mutations in Japanese patients with the congenital variant of Rett syndrome

K. Okajima, A. Miyamoto, A. Araki, 2012, Clinical genetics.

A case of primary familial congenital polycythemia with a novel EPOR mutation: possible spontaneous remission/alleviation by menstrual bleeding

H. Azuma, N. Hatakeyama, K. Okajima, 2018, International Journal of Hematology.

Virological analysis of a regional mumps outbreak in the northern island of Japan-mumps virus genotyping and clinical description.

H. Azuma, A. Kato, K. Okajima, 2013, Japanese journal of infectious diseases.

Male siblings with dyserythropoiesis, microcephaly and intrauterine growth retardation.

M. Shamoto, K. Okajima, T. Ito, 2002, Clinical dysmorphology.

Genomic organization, expression, and chromosome location of the human SNAIL gene (SNAI1) and a related processed pseudogene (SNAI1P).

E. Jabs, K. Okajima, M. Schertzer, 1999, Genomics.

Enhancement of S-100β protein in blood of patients with down’s syndrome

F. Suzuki, Kanefusa Kato, T. Yamanaka, 2008, Journal of Molecular Neuroscience.

Molecular cloning of the human UMP synthase gene and characterization of point mutations in two hereditary orotic aciduria families.

M. E. Hodgson, K. Okajima, S. Sumi, 1997, American journal of human genetics.

Mutations of the E1beta subunit gene (PDHB) in four families with pyruvate dehydrogenase deficiency.

D. Kerr, M. Patel, C. Prasad, 2008, Molecular genetics and metabolism.

A haploinsufficiency of FOXG1 identified in a boy with congenital variant of Rett syndrome

K. Okajima, A. Kumakura, D. Hata, 2014, Brain and Development.

89 Polymorphisms or pathogenic mutations? Re-evaluation of several PDHA1 mutations by protein structural modeling

D. Kerr, K. Okajima, 2007 .

Somatic mosaicism in a male with an exon skipping mutation in PDHA1 of the pyruvate dehydrogenase complex results in a milder phenotype.

D. Kerr, M. Warman, K. Okajima, 2006, Molecular genetics and metabolism.

Clinical and Biochemical Findings of a Patient with Thanatophoric Dysplasia Type I: Additional Finding of Dicarboxylic Aciduria

J. Tyson, S. Malcolm, T. Niwa, 2002 .

Multiple enzyme defects in mitochondria of a case with congenital lactic acidosis and hyperammonaemia

H. Togari, Y. Wada, E. Naito, 1992, Journal of Inherited Metabolic Disease.

Sensitive enzyme immunoassay for human aldolase A.

N. Kurobe, K. Okajima, K. Shimizu, 1989, Clinica chimica acta; international journal of clinical chemistry.

Does Amniotomy Influence the Prognosis of Babies in Cases with Severe Chorioamnionitis?

K. Okajima, K. Suzumori, Yoshikatsu Suzuki, 2000, Fetal Diagnosis and Therapy.

A Screening Method for Dihydropyrimidine Dehydrogenase Deficiency with Colorimetric Detection of Urinary Uracil

K. Okajima, M. Suchi, Y. Wada, 1988 .

In vitro culture of bovine spermatocytes on murine testicular somatic cells

K. Okajima, K. Goto, S. Ookutsu, 1997 .