Search Results - "AKASAKA, Manami"
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Significance of End-Diastolic Forward Flow in Patients With Repaired Tetralogy of Fallot ― Its Interaction With the Left Ventricular Property and End Organ Damage
Published in Circulation Journal (25-12-2023)“…Background: Although right ventricular (RV) enlargement may affect RV diastolic dysfunction assessed by end-diastolic forward flow (EDFF) in patients with…”
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2
Impact of nitrogen metabolism-associated culture pH changes on regulation of Fusarium trichothecene biosynthesis: revision of roles of polyamine agmatine and transcription factor AreA
Published in Current genetics (01-12-2020)“…Fusarium graminearum produces trichothecene mycotoxins in infected grains and axenic liquid culture. A proposed regulatory model of trichothecene biosynthesis…”
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3
Acute encephalopathy in children with tuberous sclerosis complex
Published in Orphanet journal of rare diseases (06-01-2021)“…We examined the clinical manifestations of acute encephalopathy (AE) and identify risk factors for AE in children with tuberous sclerosis complex (TSC). The…”
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4
Effects of Total Parenteral Nutrition on Serum Osmolality and Patent Ductus Arteriosus
Published in Curēus (Palo Alto, CA) (09-07-2024)“…The persistence of high serum osmolality in the early postnatal period is a risk for developing patent ductus arteriosus (PDA). Early aggressive nutrition…”
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5
Usefulness of Early Genetic Diagnosis for Twins With a Family History of Congenital Nephrotic Syndrome
Published in Curēus (Palo Alto, CA) (25-03-2023)“…We reported a dichorionic diamniotic placental twin (DD twin) with a family history of a congenital nephrotic syndrome of the Finnish type (CNF), of which the…”
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6
Chronological T‐wave alternation before and after the onset of arrhythmogenic right ventricular cardiomyopathy
Published in Annals of noninvasive electrocardiology (01-11-2022)“…Identification of arrhythmogenic right ventricular cardiomyopathy (ARVC) during childhood is challenging due to the lack of specific ECG manifestation. We…”
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7
Characteristic proton magnetic resonance spectroscopy in glucose transporter type 1 deficiency syndrome
Published in Pediatrics international (01-10-2018)Get full text
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8
Identification of amino acids negatively affecting Fusarium trichothecene biosynthesis
Published in Antonie van Leeuwenhoek (01-03-2019)“…Nitrogen sources in media have a significant impact on the onset of secondary metabolism in fungi. For transcriptional activation of many nitrogen catabolic…”
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9
GNAO1 mutation-related severe involuntary movements treated with gabapentin
Published in Brain & development (Tokyo. 1979) (01-04-2021)“…Mutations in GNAO1 typically result in neurodevelopmental disorders, including involuntary movements. They may be improved using calcium-channel modulators…”
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10
Long-term outcome of a group of Japanese children with myelin-oligodendrocyte glycoprotein encephalomyelitis without preventive immunosuppressive therapy
Published in Brain & development (Tokyo. 1979) (01-10-2019)“…There is increasing evidence that immunosuppressive therapy is essential for reducing disease activity and avoiding further attacks in patients positive for…”
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11
Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy
Published in Genetics in medicine (01-12-2022)“…Cerebellar hypoplasia and atrophy (CBHA) in children is an extremely heterogeneous group of disorders, but few comprehensive genetic studies have been…”
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Successful Atrial Septal Defect Closure Subsequent to Medical Pulmonary Preconditioning in an Infant With Severe Pulmonary Hypertension Associated With Bronchopulmonary Dysplasia
Published in Curēus (Palo Alto, CA) (30-03-2024)“…While atrial septal defect (ASD) may contribute to right ventricular decompression in patients with severe pulmonary hypertension (PH), the pulmonary…”
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13
Predictive Ability of Combined Factor Scores for Chromosomal Abnormalities in Pregnant Women With Polyhydramnios
Published in Curēus (Palo Alto, CA) (29-12-2022)“…This study investigated factors that can predict chromosomal abnormalities in pregnant women with polyhydramnios. The ability of prenatal factors to predict…”
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14
Familial episodic limb pain in kindreds with novel Nav1.9 mutations
Published in PloS one (17-12-2018)“…We previously performed genetic analysis in six unrelated families with infantile limb pain episodes, characterized by cold-induced deterioration and…”
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15
Case report: Cerebellar swelling and hydrocephalus in familial hemophagocytic lymphohistiocytosis
Published in Frontiers in pediatrics (16-12-2022)“…Familial hemophagocytic lymphohistiocytosis (FHL) is a severe inborn error of immunity caused by a genetic defect that impairs the function of cytotoxic T and…”
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16
Clinical and genetic features of acute encephalopathy in children taking theophylline
Published in Brain & development (Tokyo. 1979) (01-05-2015)“…Abstract Background Theophylline has recently been suspected as a risk factor of acute encephalopathy with biphasic seizures and late reduced diffusion (AESD),…”
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Intellectual outcomes of extremely preterm infants at school age
Published in Pediatrics international (01-05-2017)“…Background The survival rate of extremely preterm (EP) infants (<28 weeks of gestation) has improved dramatically, and there is great interest in the long‐term…”
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18
Reduction in peripheral regulatory T cell population in childhood ocular type myasthenia gravis
Published in Brain & development (Tokyo. 1979) (01-09-2015)“…Abstract Objective Myasthenia gravis (MG) is a T-cell dependent and antibody mediated autoimmune disease. Recent studies of adult patients and animal models…”
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Temporal brain metabolite changes in preterm infants with normal development
Published in Brain & development (Tokyo. 1979) (01-03-2017)“…Abstract Objective Preterm infants are at high risk for developmental delay, epilepsy, and autism spectrum disorders. Some reports have described associations…”
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Successful endoscopic sclerotherapy with bile duct stenting for a vascular malformation neighboring the duodenal papilla in blue rubber bleb nevus syndrome
Published in DEN open (01-04-2022)“…A 14‐year‐old girl, who had been diagnosed with blue rubber bleb nevus syndrome, was referred to our hospital because of iron deficiency anemia…”
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