Mitsuru Ikeno
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Explore the profile of Mitsuru Ikeno including associated specialties, affiliations and a list of published articles.
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Articles
39
Citations
154
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Recent Articles
1.
Nakazawa M, Abe S, Ikeno M, Shima T, Shimizu T, Okumura A
Brain Dev
. 2023 Oct;
46(1):10-17.
PMID: 37884431
Background: Adenovirus is a major pathogen causing febrile illness among children. It may also cause acute encephalitis/encephalopathy. This study aimed to elucidate the clinical features of adenovirus-associated encephalitis/encephalopathy (AdVE) among...
2.
Tanimoto R, Ikuse T, Ito N, Sato H, Kasai Y, Yamada H, et al.
Medicina (Kaunas)
. 2023 Apr;
59(4).
PMID: 37109684
The frequency of split cord malformation (SCM) is approximately 1 in 5000 births; however, patients are rarely diagnosed with SCM in the neonatal period. Moreover, there have been no reports...
3.
Masunaga Y, Nishimura G, Takahashi K, Hishiyama T, Imamura M, Kashimada K, et al.
Sci Rep
. 2022 Oct;
12(1):17079.
PMID: 36224347
We report clinical and molecular findings in three Japanese patients with N-acetylneuraminic acid synthetase-congenital disorder of glycosylation (NANS-CDG). Patient 1 exhibited a unique constellation of clinical features including marked hydrocephalus,...
4.
Kirino S, Suzuki M, Ogawa T, Takasawa K, Adachi E, Gau M, et al.
Eur J Med Genet
. 2022 Sep;
65(11):104623.
PMID: 36116699
AMOTL1 is a member of the Motin protein family and localizes to tight junctions and is involved in cell polarity and paracellular permeability. Pathological variants have been reported in three...
5.
Yakabe A, Ikuse T, Ito N, Yamada H, Saito N, Kitamura Y, et al.
Hum Genome Var
. 2022 Jun;
9(1):24.
PMID: 35688819
A 2-day-old neonate presented with seizures, multiple intracranial hemorrhages, and bilateral congenital cataracts. Targeted next-generation sequencing of the collagen type IV alpha 1 chain (COL4A1) gene revealed a heterozygous de...
6.
Numoto S, Kurahashi H, Sato A, Kubota M, Shiihara T, Okanishi T, et al.
Orphanet J Rare Dis
. 2021 Jan;
16(1):5.
PMID: 33407677
Objective: We examined the clinical manifestations of acute encephalopathy (AE) and identify risk factors for AE in children with tuberous sclerosis complex (TSC). Methods: The clinical data of 11 children...
7.
Sato A, Suzuki T, Ikeno M, Takeda J, Yamamoto Y, Shinohara M, et al.
Eur J Med Genet
. 2020 Jul;
63(10):104005.
PMID: 32693209
9p duplication syndrome is a common congenital anomaly syndrome with specific facial features, mental and developmental retardations, and characteristic fingers. Pure 9p duplication without other chromosomal structural variations is very...
8.
Andica C, Hagiwara A, Hori M, Kamagata K, Koshino S, Maekawa T, et al.
J Neuroradiol
. 2019 Mar;
46(4):268-275.
PMID: 30853545
Quantitative magnetic resonance imaging (MRI) with multislice, multi-echo, and multi-delay acquisition enables simultaneous quantification of R and R relaxation rates, proton density, and the B field in a single acquisition,...
9.
Shima T, Okumura A, Kurahashi H, Numoto S, Abe S, Ikeno M, et al.
Brain Dev
. 2019 Feb;
41(3):263-270.
PMID: 30798941
Background: Norovirus is a major pathogen of gastroenteritis and is known to cause encephalitis/encephalopathy. The aim of this national survey was to clarify the clinical features of norovirus-associated encephalitis/encephalopathy (NoVE)...
10.
Andica C, Hagiwara A, Nakazawa M, Kumamaru K, Hori M, Ikeno M, et al.
Magn Reson Med Sci
. 2016 Dec;
16(2):91-92.
PMID: 28003620
No abstract available.