Author

Kanako Kojima

Observed name: K Kojima

Institutions: Tohoku University, Akita University, University of Yamanashi

Observed institutions: Tohoku University, Akita University, Hadassah Medical Center, Tenri Hospital, Kyoto Prefectural University of Medicine, University of Yamanashi

OpenAlex ID: A5111644916

Long-term correction of hyperphenylalaninemia by AAV-mediated gene transfer leads to behavioral recovery in phenylketonuria mice

2004 · S Mochizuki, H Mizukami, et al. · Gene Therapy · 81

Persistent NKH with transient or absent symptoms and a homozygous GLDC mutation

2004 · Stanley H. Korman, Avihu Boneh, et al. · Annals of Neurology · 57

Glycine cleavage system in neurogenic regions

2004 · Akiko Ichinohe, Shigeo Kure, et al. · European Journal of Neuroscience · 56

A novel KCNQ4 one-base deletion in a large pedigree with hearing loss: implication for the genotype–phenotype correlation

2006 · Fumiaki Kamada, Shigeo Kure, et al. · Journal of Human Genetics · 55

Structure and expression of the glycine cleavage system in rat central nervous system

2001 · Yoshiyuki Sakata, Yuji Owada, et al. · Molecular Brain Research · 48

Direct Correlation Between Ischemic Injury and Extracellular Glycine Concentration in Mice With Genetically Altered Activities of the Glycine Cleavage Multienzyme System

2007 · Masaya Oda, Shigeo Kure, et al. · Stroke · 43

Mild variant of nonketotic hyperglycinemia with typical neonatal presentations: mutational and in vitro expression analyses in two patients

2004 · Shigeo Kure, Akiko Ichinohe, et al. · The Journal of Pediatrics · 31

Heterozygous GLDC and GCSH gene mutations in transient neonatal hyperglycinemia

2002 · Shigeo Kure, Kanako Kojima, et al. · Annals of Neurology · 30

Novel mutations in the P-protein (glycine decarboxylase) gene in patients with glycine encephalopathy (non-ketotic hyperglycinemia)

2002 · Jennifer R. Toone, Derek A. Applegarth, et al. · Molecular Genetics and Metabolism · 21

Genetic testing of glycogen storage disease type Ib in Japan: five novel G6PT1 mutations and a rapid detection method for a prevalent mutation W118R

2004 · Kanako Kojima, Shigeo Kure, et al. · Molecular Genetics and Metabolism · 14

Ultrasonographic Findings in Neonates Screened for Congenital Hypothyroidism.

2002 · Kanako Kojima, Eishin Ogawa, et al. · Clinical Pediatric Endocrinology · 3

2003 · Shigeo Kure, Kanako Kojima, et al. · Annals of Neurology

43 Increasing Numbers of Infants With Positive Newborn Screening Results for Congenital Hypothyroidism

2002 · Eishin Ogawa, Kanako Kojima, et al. · Clinical Pediatric Endocrinology

Works count: 13

Citation count: 439

H-index: 10

I10-index: 10