Search Results - "Otani, Katsuki"
-
1
Investigating ice surfaces formed near the freezing point in the vapor phase via atomic force microscopy
Published in Japanese Journal of Applied Physics (01-08-2019)“…An atomic force microscope (AFM) using a qPlus sensor was developed to observe ice surfaces grown near the freezing point in the vapor phase. The AFM system…”
Get full text
Journal Article -
2
Early-onset Marfan syndrome with a novel missense mutation: A case report
Published in Journal of cardiology cases (01-06-2023)“…Early-onset Marfan syndrome (eoMFS) progresses rapidly, starting during the neonatal period, causes severe clinical disease, and has a poor prognosis. The…”
Get full text
Journal Article -
3
MYH7 mutation identified by next-generation sequencing in three infant siblings with bi-ventricular noncompaction presenting with restrictive hemodynamics: A report of three siblings with a severe phenotype and poor prognosis
Published in Journal of cardiology cases (01-04-2019)“…Noncompaction of the ventricular myocardium (NVM) is a genetically heterogeneous cardiomyopathy. Various mutations associated with NVM have been identified in…”
Get full text
Journal Article -
4
Association of Multiple Gene Polymorphisms Including Homozygous NUDT15 R139C With Thiopurine Intolerance During the Treatment of Acute Lymphoblastic Leukemia
Published in Journal of pediatric hematology/oncology (01-11-2021)“…Although thiopurine is a crucial drug for treating acute lymphoblastic leukemia, individual variations in intolerance are observed due to gene polymorphisms. A…”
Get full text
Journal Article -
5
Association of Multiple Gene Polymorphisms Including Homozygous NUDT15 R139C With Thiopurine Intolerance During the Treatment of Acute Lymphoblastic Leukemia
Published in Journal of pediatric hematology/oncology (31-03-2021)“…Although thiopurine is a crucial drug for treating acute lymphoblastic leukemia, individual variations in intolerance are observed due to gene polymorphisms. A…”
Get full text
Journal Article -
6
MYH7 mutation identified by next-generation sequencing in three infant siblings with bi-ventricular noncompaction presenting with restrictive hemodynamics
Published in Journal of cardiology cases (01-04-2019)“…Noncompaction of the ventricular myocardium (NVM) is a genetically heterogeneous cardiomyopathy. Various mutations associated with NVM have been identified in…”
Get full text
Journal Article -
7
Early-onset Marfan syndrome with a novel missense mutation: A case report
Published in Journal of cardiology cases (01-06-2023)“…Early-onset Marfan syndrome (eoMFS) progresses rapidly, starting during the neonatal period, causes severe clinical disease, and has a poor prognosis. The…”
Get full text
Report -
8
MYH7 mutation identified by next-generation sequencing in three infant siblings with bi-ventricular noncompaction presenting with restrictive hemodynamics: A report of three siblings with a severe phenotype and poor prognosis
Published in Journal of cardiology cases (01-04-2019)Get full text
Report