Hideo Sasai

Gifu University

Japan

Research Interests

Explore related searches

Professors in Japan

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

Articles (14)

Year:

2024

Year:

2023

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2020

Year:

2020

Year:

2020

Year:

2020

Year:

2020

Year:

2020

Year:

2020

Collaborators (4)

Masatake Osawa

Professor

Gifu University

JAPAN

View details

Tomohiro Hori

department of pediatrics university of cincinnati college of medicine cincinnati ohio usa

JAPAN

View details

Hideki Matsumoto

Gifu University

JAPAN

View details

Satoshi Okada

Professor

Hiroshima University

JAPAN

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Hideo Sasai

Research Interests

Explore related searches

Contact this professor

Articles (14)

Using the C14:1/Medium-Chain Acylcarnitine Ratio Instead of C14:1 to Reduce False-Positive Results for Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency in Newborn Screening in Japan

Newborn Screening with (C16 + C18:1)/C2 and C14/C3 for Carnitine Palmitoyltransferase II Deficiency throughout Japan Has Revealed C12/C0 as an Index of Higher Sensitivity and Specificity

In vitro functional analysis of four variants of human asparagine synthetase.

Endoscopic third ventriculostomy for hydrocephalus in a patient with achondroplasia: a case report and literature review

Propranolol for infantile hemangiomas with hyperinsulinemic hypoglycemia

Advanced Diagnostic System and Introduction of Newborn Screening of Adrenoleukodystrophy and Peroxisomal Disorders in Japan

Current Perspectives on Neonatal Screening for Propionic Acidemia in Japan: An Unexpectedly High Incidence of Patients with Mild Disease Caused by a Common <i>PCCB</i> Variant

Deficiency of 3‐hydroxybutyrate dehydrogenase (BDH1) in mice causes low ketone body levels and fatty liver during fasting

Japanese patients with mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: <i>In vitro</i> functional analysis of five novel <i>HMGCS2</i> mutations.

Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemia (Genetics in Medicine, (2019), 21, 6, (1286-1294), 10.1038/s41436-018-0340-x)

Neonatal bacteremia caused by emm type 80 group A Streptococcus: A case report

Novel HADHB mutations in a patient with mitochondrial trifunctional protein deficiency

Retrospective evaluations revealed pre-symptomatic citrulline concentrations measured by newborn screening were significantly low in late-onset ornithine transcarbamylase deficiency patients

Short-chain enoyl-CoA hydratase deficiency causes prominent ketoacidosis with normal plasma lactate levels: A case report

Collaborators (4)

Masatake Osawa

Tomohiro Hori

Hideki Matsumoto

Satoshi Okada

Make your next move.