Keiko Tsukamoto
Overview
Explore the profile of Keiko Tsukamoto including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
29
Citations
396
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Uehara Y, Wada Y, Iwasaki Y, Yoneda K, Ikuta Y, Amari S, et al.
BMC Pediatr
. 2021 Apr;
21(1):161.
PMID: 33823829
Background: Systemic juvenile xanthogranuloma is a very rare disease typically presents as skin lesions with yellow papules or nodules and is sometimes fatal. We report a case of congenital neonatal...
2.
Fujino S, Maruyama H, Tsukamoto K, Ono H, Isayama T, Ito Y
AJP Rep
. 2020 Dec;
10(4):e403-e407.
PMID: 33294285
Congenital complete atrioventricular block (CCAVB) associated with congenital chylothorax is a rare finding that has been reported in only one case in the literature. We report here the case of...
3.
Matsushima S, Ozawa K, Sugibayashi R, Ogawa K, Tsukamoto K, Miyazaki O, et al.
Prenat Diagn
. 2020 May;
40(8):1013-1019.
PMID: 32362029
Background: Data on neurodevelopmental outcomes of children surviving after fetoscopic laser surgery (FLS) for twin-to-twin transfusion syndrome (TTTS) are scarce. Methods: We retrospectively investigated children surviving after FLS for TTTS...
4.
Shibata Y, Maruyama H, Hayashi T, Ono H, Wada Y, Fujinaga H, et al.
AJP Rep
. 2019 Jul;
9(3):e213-e217.
PMID: 31304050
Most cardiac rhabdomyomas with tuberous sclerosis (TS) are asymptomatic and spontaneously regress. However, some cases require surgical intervention due to arrhythmia and severe obstruction of cardiac inflow or outflow. We...
5.
Amari S, Tsukamoto K, Ishiguro A, Yanagi K, Kaname T, Ito Y
Eur J Med Genet
. 2019 Apr;
63(2):103646.
PMID: 30965144
We describe herein an extremely severe case of Aicardi-Goutières syndrome 7 (AGS7). The female patient was the daughter of nonconsanguineous parents and developed cardiomegaly, pericardial effusion, splenomegaly, and intracranial calcification...
6.
Watanabe T, Ohno M, Tahara K, Tomonaga K, Fuchimoto Y, Fujino A, et al.
J Pediatr Surg
. 2018 Sep;
53(12):2390-2393.
PMID: 30227995
Background/purpose: Differences in clinical features between congenital pulmonary airway malformation (CPAM) and bronchial atresia (BA) have not yet been clearly described. Methods: We retrospectively reviewed 112 patients with a pathological...
7.
Ichimiya Y, Wada Y, Kunishima S, Tsukamoto K, Kosaki R, Sago H, et al.
J Med Case Rep
. 2018 Jan;
12(1):3.
PMID: 29307309
Background: 11q23 deletion syndrome, also known as Jacobsen syndrome, is characterized by growth retardation, psychomotor retardation, facial dysmorphism, multiple congenital abnormalities, and thrombocytopenia. In 11q23 deletion syndrome, it is often...
8.
Ito A, Fujinaga H, Matsui S, Tago K, Iwasaki Y, Fujino S, et al.
AJP Rep
. 2018 Jan;
7(4):e234-e237.
PMID: 29302380
Congenital diaphragmatic hernia (CDH) is fatal in severe cases of pulmonary hypoplasia. We experienced a fatal case of pulmonary hypoplasia due to CDH, thoracic myelomeningocele (MMC), and thoracic dysplasia. This...
9.
Soshi M, Maeda K, Isoda S, Tsukamoto K
J Gen Fam Med
. 2017 Dec;
18(6):487-488.
PMID: 29264105
No abstract available.
10.
Watanabe T, Amari S, Tsukamoto K, Ito Y, Tomizawa D, Yoshioka T, et al.
Pediatr Int
. 2017 Apr;
59(4):515-518.
PMID: 28401746
Neonates with Down syndrome are at risk of developing transient abnormal myelopoiesis (TAM), which is characterized by transient clonal myeloproliferation of the blast cells. TAM can resolve spontaneously, but some...