S. Morikawa

发表

Paramyotonia congenita: From clinical diagnosis to in silico protein modeling analysis

Y. Takeshima, H. Nishio, M. Matsuo, 2012, Pediatrics international : official journal of the Japan Pediatric Society.

Generalized epilepsy with febrile seizures plus (GEFS+) spectrum: Clinical manifestations and SCN1A mutations in Indonesian patients

Gunadi, H. Nishio, M. Matsuo, 2010, Epilepsy Research.

Quantitative evaluation of ventricular dilatation using computed tomography in infants with congenital cytomegalovirus infection

N. Inoue, S. Kawano, K. Iijima, 2014, Brain and Development.

Minimal residual disease monitoring in neuroblastoma patients based on the expression of a set of real-time RT-PCR markers in tumor-initiating cells.

Y. Takeshima, H. Nishio, M. Matsuo, 2013, Oncology reports.

Minimal residual disease monitoring in neuroblastoma patients based on the expression of a set of real-time RT-PCR markers in tumor-initiating cells TRI

Y. Takeshima, H. Nishio, M. Matsuo, 2013 .

Herbal Medicine Containing Licorice May Be Contraindicated for a Patient with an HSD11B2 Mutation

Gunadi, M. Hirai, N. Sasaki, 2011, Evidence-based complementary and alternative medicine : eCAM.

Diagnosis of spinal muscular atrophy via high-resolution melting analysis symmetric polymerase chain reaction without probe: a screening evaluation for SMN1 deletions and intragenic mutations.

H. Nishio, M. Matsuo, Noriyuki Nishimura, 2011, Genetic testing and molecular biomarkers.

Epigallocatechin gallate inhibits sphere formation of neuroblastoma BE(2)-C cells

Y. Takeshima, H. Nishio, M. Matsuo, 2012, Environmental Health and Preventive Medicine.

Identification of N-acetyl Proline-Glycine-Proline (acPGP) in human serum of adults and newborns by liquid chromatography-tandem mass spectrometry.

M. Matsuo, A. Takeuchi, K. Saiki, 2009, Clinica chimica acta; international journal of clinical chemistry.

Renin is activated in monochorionic diamniotic twins with birthweight discordance who do not have twin-to-twin transfusion syndrome

M. Morizane, M. Matsuo, S. Morikawa, 2012, Journal of Perinatology.

Genetic disorders associated with neonatal jaundice

H. Nishio, M. Matsuo, Noriyuki Nishimura, 2010 .

Does thrombocytopenia contribute to patent ductus arteriosus?

M. Matsuo, I. Morioka, S. Morikawa, 2011, Nature Medicine.

Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patients

Y. Tohyama, Y. Takeshima, H. Nishio, 2014, Brain and Development.

A case of severe hydrops fetalis with chylothorax, a nodular lesion in the liver, and unilateral multicystic kidney

M. Matsuo, M. Enomoto, I. Morioka, 2009 .

Spinal Muscular Atrophy: From Gene Discovery to Clinical Trials

Y. Tohyama, Y. Takeshima, H. Nishio, 2013, Annals of human genetics.

Valproic acid increases SMN2 expression and modulates SF2/ASF and hnRNPA1 expression in SMA fibroblast cell lines

Gunadi, N. Sasaki, Y. Takeshima, 2012, Brain and Development.

Rab15 alternative splicing is altered in spheres of neuroblastoma cells.

Y. Takeshima, H. Nishio, M. Matsuo, 2012, Oncology reports.

Novel treatment strategy for Japanese newborns with high serum unbound bilirubin

S. Kawano, K. Iijima, I. Morioka, 2013, Pediatrics international : official journal of the Japan Pediatric Society.

Is bilirubin/albumin ratio correlated with unbound bilirubin concentration?

H. Nishio, M. Matsuo, I. Morioka, 2012, Pediatrics International.

Correlation and precision of serum free bilirubin concentrations determined by single and two peroxidase concentration methods in term or late-preterm newborn infants using a FDA-approved analyzer.

H. Nishio, M. Matsuo, I. Morioka, 2012, Clinical laboratory.

Hypoalbuminemia following Abdominal Surgery Leads to High Serum Unbound Bilirubin Concentrations in Newborns Soon after Birth

M. Matsuo, I. Morioka, S. Morikawa, 2010, Neonatology.

A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome.

Y. Takeshima, H. Nishio, M. Matsuo, 2011, The Kobe journal of medical sciences.

A Homozygous Mutation in UGT 1 A 1 Exon 5 May Be Responsible for Persistent Hyperbilirubinemia in a Japanese Girl with Gilbert ’ s Syndrome

Y. Takeshima, H. Nishio, M. Matsuo, 2011 .

A Polymorphic Mutation, c.-3279T>G, in the UGT1A1 Promoter Is a Risk Factor for Neonatal Jaundice in the Malay Population

M. Hirai, H. Nishio, M. Matsuo, 2010, Pediatric Research.

Severely high serum unbound bilirubin level after abdominal surgery in a newborn

H. Nishio, K. Iijima, I. Morioka, 2013, Pediatrics international : official journal of the Japan Pediatric Society.

Culture-Proven Neonatal Sepsis in Japanese Neonatal Care Units in 2006–2008

H. Nishio, M. Matsuo, M. Kugo, 2012, Neonatology.

Rab15 expression correlates with retinoic acid-induced differentiation of neuroblastoma cells.

Y. Takeshima, H. Nishio, M. Matsuo, 2011, Oncology reports.

Spinal muscular atrophy patient detection and carrier screening using dried blood spots on filter paper.

H. Nishio, N. Harahap, D. K. Nurputra, 2012, Genetic testing and molecular biomarkers.

Rab15 expression correlates with retinoic acid-induced differentiation of neuroblastoma cells.

Y. Takeshima, H. Nishio, M. Matsuo, 2011, Oncology reports.