N. Aida

发表

Haploinsufficiency of BCL11A associated with cerebellar abnormalities in 2p15p16.1 deletion syndrome

S. Mizuno, K. Kurosawa, Hiroko Shimbo, 2017, Molecular genetics & genomic medicine.

Natural course of neuroblastoma detected by mass screening: s 5-year prospective study at a single institution.

K. Ohnuma, Y. Tanaka, N. Aida, 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Natural C ourse o f N euroblastoma D etected b y Mass S creening: A 5 -Year P rospective S tudy a t a S ingle Institution

Yukichi Tanaka, K. Ohnuma, N. Aida, 2000 .

Monitoring the brain metabolites of children with acute encephalopathy caused by the H1N1 virus responsible for the 2009 influenza pandemic: a quantitative in vivo 1H MR spectroscopy study.

J. Kershaw, T. Obata, H. Osaka, 2012, Magnetic resonance imaging.

Recanalized umbilical vein as a conduit for mesenterico/porto-Rex bypass for patients with extrahepatic portal vein obstruction

N. Aida, M. Shinkai, S. Honda, 2011, Pediatric Surgery International.

[Chronic recurrent multifocal osteomyelitis with interstitial myositis].

N. Aida, T. Miyamae, S. Yokota, 2013, Nihon Rinsho Men'eki Gakkai kaishi = Japanese journal of clinical immunology.

Intracranial Hemorrhage and Tortuosity of Veins Detected on Susceptibility-weighted Imaging of a Child with a Type IV Collagen α1 Mutation and Schizencephaly.

H. Osaka, H. Saitsu, T. Niwa, 2015, Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine.

Impairment of the medullary veins on neonatal subependymal hemorrhage using susceptibility-weighted imaging

T. Niwa, Y. Tachibana, N. Aida, 2010 .

A novel fluorescence in situ hybridization assay for synovial sarcoma.

N. Nagahara, Mio Tanaka, Yukichi Tanaka, 2013, Pathology, research and practice.

Invited. Fukuyama congenital muscular dystrophy: A neuroradiologic review

N. Aida, 1998, Journal of magnetic resonance imaging : JMRI.

Expression analysis of a 17p terminal deletion, including YWHAE, but not PAFAH1B1, associated with normal brain structure on MRI in a young girl

K. Kurosawa, N. Aida, M. Masuno, 2012, American journal of medical genetics. Part A.

Neuropathology of leukoencephalopathy with brainstem and spinal cord involvement and high lactate caused by a homozygous mutation of DARS2

N. Matsumoto, Yukichi Tanaka, N. Miyake, 2013, Brain and Development.

Treatment outcomes and late toxicities in patients with embryonal central nervous system tumors

M. Hata, Tomio Inoue, T. Niwa, 2014, Radiation oncology.

Diffusion-weighted imaging of an atypical teratoid/rhabdoid tumor of the cervical spine.

Mio Tanaka, Yukichi Tanaka, K. Fujita, 2009, Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine.

Urine screening for patients with developmental disabilities detected a patient with creatine transporter deficiency due to a novel missense mutation in SLC6A8

Kyoko Takano, H. Osaka, Hiroko Shimbo, 2014, Brain and Development.

Contiguous deletion of SLC6A8 and BAP31 in a patient with severe dystonia and sensorineural deafness.

N. Matsumoto, H. Osaka, H. Saitsu, 2012, Molecular genetics and metabolism.

Early magnetic resonance detection of cortical necrosis and acute network injury associated with neonatal and infantile cerebral infarction

H. Osaka, T. Niwa, N. Aida, 2014, Pediatric Radiology.

A patient with Pendred syndrome whose goiter progressed with normal serum thyrotropin and iodine organification

K. Fujita, N. Aida, K. Muroya, 2010, American journal of medical genetics. Part A.

Large intracranial vessel occlusive vasculopathy after radiation therapy in children: clinical features and usefulness of magnetic resonance imaging.

N. Aida, M. Kakehi, M. Omura, 1997, International journal of radiation oncology, biology, physics.

1H-MR Spectroscopy of the Early Developmental Brain, Neonatal Encephalopathies, and Neurometabolic Disorders

N. Aida, 2021, Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine.

Intrapulmonary lymph nodes in children versus lung metastases.

Y. Tanaka, N. Aida, H. Nishihira, 1999, Medical and pediatric oncology.

NUT Midline Carcinoma: Report of 2 Cases Suggestive of Pulmonary Origin

Mio Tanaka, Yukichi Tanaka, T. Niwa, 2012, The American journal of surgical pathology.

Possible linkage between specific histological structures and aberrant reactivation of the Wnt pathway in adamantinomatous craniopharyngioma

K. Tachibana, N. Nagahara, Mio Tanaka, 2004, The Journal of pathology.

A prospective study of a long‐term follow‐up of an observation program for neuroblastoma detected by mass screening

Mio Tanaka, Yukichi Tanaka, N. Aida, 2010, Pediatric blood & cancer.

Lack of association of ovariectomy-induced obesity with overeating and the reduction of physical activities

N. Harada, M. Nakatani, T. Wakatsuki, 2019, Biochemistry and biophysics reports.

Late recurrence of neuroblastoma stage 4S with unusual clinicopathologic findings.

Y. Tanaka, N. Aida, T. Kusafuka, 2001, Journal of pediatric surgery.

Congenital absence of the portal vein and role of liver transplantation in children.

K. Tachibana, Y. Tanaka, N. Aida, 2001, Journal of pediatric surgery.

Clinicopathological study of a hilar nodule in the livers of long‐term survivors with biliary atresia

F. Kondo, Yukichi Tanaka, Y. Tanaka, 2001, Pathology international.

Elevation of brain gamma‐aminobutyric acid levels is associated with vigabatrin‐associated brain abnormalities on magnetic resonance imaging

N. Aida, T. Goto, M. Tanabe, 2022, Epilepsy Research.

Neuroradiologic Features in X-linked α-Thalassemia/Mental Retardation Syndrome

N. Okamoto, N. Aida, T. Wada, 2013, American Journal of Neuroradiology.

Contrast-enhanced MRI of an early preosseous lesion of fibrodysplasia ossificans progressiva in a 21-month-old boy.

K. Fujita, G. Nishimura, N. Aida, 2003, AJR. American journal of roentgenology.

Influence of ADORA2A gene polymorphism on leukoencephalopathy risk in MTX‐treated pediatric patients affected by hematological malignancies

S. Ito, N. Aida, K. Urayama, 2016, Pediatric blood & cancer.

Congenital neuroblastoma diagnosed by placental examination.

Y. Tanaka, N. Aida, Y. Toyoda, 1999, Medical and pediatric oncology.

Polyostotic osteolysis and hypophosphatemic rickets with elevated serum fibroblast growth factor 23: A case report

Yukichi Tanaka, G. Nishimura, N. Aida, 2015, American journal of medical genetics. Part A.

Cerebellar MR in Fukuyama congenital muscular dystrophy: polymicrogyria with cystic lesions.

N. Aida, K. Takada, A. Yagishita, 1994, AJNR. American journal of neuroradiology.

Primary cerebellar histiocytic sarcoma in a 17-month-old girl.

Mio Tanaka, Yukichi Tanaka, T. Niwa, 2012, Journal of neurosurgery. Pediatrics.

Congenital neuroblastoma in a patient with partial trisomy of 2p.

N. Matsumoto, Yukichi Tanaka, Toshiyuki Yamamoto, 2006, Journal of pediatric hematology/oncology.

Prophylactic cranial irradiation of acute lymphoblastic leukemia in childhood: Outcomes of late effects on pituitary function and growth in long‐term survivors

K. Tachibana, M. Hata, Tomio Inoue, 2001, International journal of cancer.

Novel USP9X variants in two patients with X-linked intellectual disability

Y. Tsurusaki, Y. Kuroda, K. Kurosawa, 2019, Human Genome Variation.

A novel UBE2A mutation causes X-linked intellectual disability type Nascimento

Y. Tsurusaki, J. Mitsui, K. Kurosawa, 2017, Human Genome Variation.

Imaging and clinical characteristics of children with multiple foci of microsusceptibility changes in the brain on susceptibility-weighted MRI

T. Takahara, T. Kwee, K. Fujita, 2010, Pediatric Radiology.

A rapid screening with direct sequencing from blood samples for the diagnosis of Leigh syndrome

Y. Goto, Kyoko Takano, H. Osaka, 2014, Molecular genetics and metabolism reports.

MR imaging findings in some rare neurological complications of paediatric cancer

T. Niwa, N. Aida, Y. Kurihara, 2018, Insights into Imaging.

Imaging of Cystic Lung Lesions in Infants Using Pointwise Encoding Time Reduction with Radial Acquisition (PETRA)

T. Niwa, N. Aida, K. Nozawa, 2018, Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine.

Apparent diffusion coefficient values predict outcomes of abusive head trauma

N. Aida, K. Tanoue, K. Matsui, 2013, Acta paediatrica.

MR findings of bowlegs in toddlers

G. Nishimura, N. Aida, T. Iwasawa, 1999, Pediatric Radiology.

Usefulness of pancreatic ultrasonography in the diagnosis of Shwachman‐Bodian‐Diamond syndrome

K. Tachibana, N. Aida, M. Adachi, 2005, Acta paediatrica.

Congenital Absence of the Portal Vein: Clinical and Radiologic Findings

K. Tachibana, K. Fujita, Tomio Inoue, 2002, Journal of computer assisted tomography.

Unilateral glomerulocystic kidney disease associated with tuberous sclerosis complex in a neonate

Mio Tanaka, Yukichi Tanaka, N. Aida, 2012, Pathology international.

Massive Enlargement of an Ovarian Follicle after Administration of Nasal GnRH Analogue in Two Girls with Central Precocious Puberty

K. Tachibana, N. Aida, M. Adachi, 1999 .

Trigonocephaly in a boy with paternally inherited deletion 22q11.2 syndrome

N. Matsumoto, Toshiyuki Yamamoto, K. Kurosawa, 2006, American journal of medical genetics. Part A.

Radiation therapy for life- or function-threatening infant hemangioma.

M. Hata, N. Aida, I. Ogino, 2001, Radiology.

Arteriovenous malformations of the kidneys: diagnosis and follow-up with color Doppler sonography in six patients.

N. Aida, S. Takebayashi, K. Matsui, 1991, AJR. American journal of roentgenology.

Scurvy in a child with autism: magnetic resonance imaging and pathological findings.

Mio Tanaka, Yukichi Tanaka, T. Niwa, 2012, Journal of pediatric hematology/oncology.

In vivo estimation of gamma‐aminobutyric acid levels in the neonatal brain

M. Umeda, T. Obata, K. Murata, 2016, NMR in biomedicine.

Altered brain metabolite concentration and delayed neurodevelopment in preterm neonates

T. Obata, H. Kawaguchi, N. Aida, 2021, Pediatric Research.

Neuroimaging findings of inborn errors of metabolism: urea cycle disorders, aminoacidopathies, and organic acidopathies

Y. Nakata, N. Aida, T. Moritani, 2023, Japanese Journal of Radiology.

A postzygotic NRAS mutation in a patient with Schimmelpenning syndrome

Yukichi Tanaka, N. Okamoto, T. Niihori, 2015, American journal of medical genetics. Part A.

Papillary carcinoma with extensive squamous metaplasia arising from thyroglossal duct cyst in an 11-year-old girl: significance of differentiation from squamous cell carcinoma: a case report.

Mio Tanaka, Yukichi Tanaka, N. Aida, 2011, Journal of pediatric surgery.

Osteopathia striata, short stature, and characteristic facies: a previously unknown skeletal dysplasia

M. Masuno, K. Tachibana, G. Nishimura, 1997, European Journal of Pediatrics.

Currarino triad with a terminal deletion 7q35-->qter.

M. Masuno, Y. Kuroki, Y. Tanaka, 1996, Journal of medical genetics.

Pleuropulmonary blastoma in extrapulmonary lung tissue: A case report

Mio Tanaka, Yukichi Tanaka, N. Aida, 2014 .

Two Japanese patients with Leigh syndrome caused by novel SURF1 mutations

Kyoko Takano, H. Osaka, A. Ohtake, 2012, Brain and Development.

Hypofractionated radiotherapy in children with diffuse intrinsic pontine glioma

Mio Tanaka, Yukichi Tanaka, N. Aida, 2019, Pediatrics international : official journal of the Japan Pediatric Society.

Causative novel PNKP mutations and concomitant PCDH15 mutations in a patient with microcephaly with early-onset seizures and developmental delay syndrome and hearing loss

N. Matsumoto, Kyoko Takano, N. Miyake, 2014, Journal of Human Genetics.

A severe form of Ellis-van Creveld syndrome caused by novel mutations in EVC2

Y. Tsurusaki, Y. Kuroda, G. Nishimura, 2019, Human Genome Variation.

Concurrent Ewing Sarcoma Family of Tumors and Fibrous Dysplasia: Possible Diagnostic Pitfall

Mio Tanaka, Yukichi Tanaka, N. Aida, 2007, Journal of pediatric hematology/oncology.

Treatment outcomes and late toxicities in patients with embryonal central nervous system tumors

M. Hata, Tomio Inoue, T. Niwa, 2014, Radiation oncology.

Analysis of Multiple B-Value Diffusion-Weighted Imaging in Pediatric Acute Encephalopathy

T. Obata, Tomio Inoue, T. Niwa, 2013, PloS one.

Twin pregnancy with chromosomal abnormalities mimicking a gestational trophoblastic disorder and coexistent foetus on ultrasound

H. Kurahashi, M. Kuroda, N. Aida, 2018, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Congenital primitive epithelial tumor of the liver showing focal rhabdoid features, placental involvement, and clinical features mimicking multifocal hemangioma or stage 4S neuroblastoma.

M. Masuno, K. Ohnuma, Y. Tanaka, 2000, Human pathology.

A cloverleaf skull syndrome probably of Beare-Stevenson type associated with Chiari malformation

S. Ito, N. Aida, Masami Suzuki, 1996, Brain and Development.

A small pons as a characteristic finding in Down syndrome: A quantitative MRI study

Tomio Inoue, T. Niwa, N. Aida, 2017, Brain and Development.

Transient Hyperintensity in the Subthalamic Nucleus and Globus Pallidus of Newborns on T1-Weighted Images

T. Taoka, K. Kichikawa, T. Akashi, 2011, American Journal of Neuroradiology.

Diffusion-weighted imaging of retroperitoneal malignant peripheral nerve sheath tumor in a patient with neurofibromatosis type 1.

Yukichi Tanaka, K. Fujita, Tomio Inoue, 2008, Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine.

DiŠusion-weighted Imaging of Retroperitoneal Malignant Peripheral Nerve Sheath Tumor in a Patient with Neuroˆbromatosis Type 1

Yukichi Tanaka, K. Fujita, Tomio Inoue, 2008 .

Diagnostic utility of whole exome sequencing in patients showing cerebellar and/or vermis atrophy in childhood

N. Matsumoto, Y. Eto, N. Miyake, 2013, neurogenetics.

Neuroimaging findings in Joubert syndrome with C5orf42 gene mutations: A milder form of molar tooth sign and vermian hypoplasia

N. Matsumoto, H. Osaka, Toshifumi Suzuki, 2017, Journal of the Neurological Sciences.

Diagnostic utility of whole exome sequencing in patients showing cerebellar and/or vermis atrophy in childhood

N. Matsumoto, Y. Eto, N. Miyake, 2013, neurogenetics.

Toriello-Carey syndrome with endocardial fibroelastosis.

M. Masuno, Y. Kuroki, Y. Tanaka, 1999, American journal of medical genetics.

Endocrine and radiological studies in patients with molecularly confirmed CHARGE syndrome.

K. Kosaki, K. Fujita, K. Kurosawa, 2008, The Journal of clinical endocrinology and metabolism.

Abnormal Basiocciput Development in CHARGE Syndrome

K. Fujita, T. Niwa, G. Nishimura, 2009, American Journal of Neuroradiology.

Spinal Teratoid/Rhabdoid Tumor: Use of Diffusion – Weighted Imaging for Diagnosis

T. Takahara, T. Kwee, T. Niwa, 2012 .

Congenital anomaly of cervical vertebrae is a major complication of Rubinstein–Taybi syndrome

N. Okamoto, Toshiyuki Yamamoto, G. Nishimura, 2005, American journal of medical genetics. Part A.

Anaplastic sarcoma of the kidney with chromosomal abnormality: first report on cytogenetic findings.

Mio Tanaka, Yukichi Tanaka, T. Niwa, 2010, Human pathology.

Indocyanine green lymphography for congenital lymphatic dysplasia with tuberous sclerosis complex: A case report

N. Aida, Y. Kaneshi, J. Shibasaki, 2020, Pediatrics international : official journal of the Japan Pediatric Society.

A new case of GABA transaminase deficiency facilitated by proton MR spectroscopy

T. Obata, H. Osaka, K. Kurosawa, 2010, Journal of Inherited Metabolic Disease.

Acute gastric outlet obstruction following the administration of prostaglandin: an additional case

G. Nishimura, N. Aida, M. Ohta, 1997, Pediatric Radiology.

Asymptomatic radiation-induced telangiectasia in children after cranial irradiation: frequency, latency, and dose relation.

K. Fujita, M. Hata, Tomio Inoue, 2004, Radiology.

MRI findings of dysplasia epiphysealis hemimelica

G. Nishimura, N. Aida, T. Iwasawa, 2005, Pediatric Radiology.

Computed tomography of intracranial chondroma with emphasis on delayed contrast enhancement.

N. Aida, T. Maehara, K. Tanohata, 1987, Journal of computer assisted tomography.

New Congenital Malformation Syndrome with Severe Short Stature, Craniosynostosis, and Generalized Osseous Dysplasia in Two Siblings; New Osseous Dysplasia in Two Siblings

K. Tachibana, G. Nishimura, N. Aida, 1994 .

Syndromes associated with vascular tumors and malformations: a pictorial review.

T. Niwa, N. Aida, Y. Saida, 2013, Radiographics : a review publication of the Radiological Society of North America, Inc.

Acute hemicerebellitis in a pediatric patient: a case report of a serial MR spectroscopy study

T. Obata, Tadahiro Mitani, H. Osaka, 2012, Acta radiologica.

Symmetrical central tegmental tract (CTT) hyperintense lesions on magnetic resonance imaging in children

S. Yoshida, K. Hayakawa, A. Yamamoto, 2008, European Radiology.

Susceptibility-Weighted Imaging Findings of Cortical Laminar Necrosis in Pediatric Patients

K. Fujita, Tomio Inoue, T. Niwa, 2008, American Journal of Neuroradiology.

A Japanese girl with an early-infantile onset vanishing white matter disease resembling Cree leukoencephalopathy

N. Matsumoto, Kyoko Takano, Y. Tsurusaki, 2015, Brain and Development.

Incomplete Growth Hormone Secretion with Pituitary Stalk Transection and Syringomyelia

K. Tachibana, N. Aida, Y. Asakura, 1993 .

Treatment outcomes, growth height, and neuroendocrine functions in patients with intracranial germ cell tumors treated with chemoradiation therapy.

M. Hata, Tomio Inoue, T. Niwa, 2012, International journal of radiation oncology, biology, physics.

Effectiveness of Corticosteroid Therapy for Acute Neurological Symptoms in Incontinentia Pigmenti.

N. Aida, Seiichi Tomotaki, J. Shibasaki, 2016, Pediatric neurology.

Interhemispheric Lipoma, Callosal Anomaly, and Malformations of Cortical Development: A Case Series

L. D. de Vries, M. Lequin, T. Niwa, 2016, Neuropediatrics.

Congenital dyserythropoietic anemia type 1 with fetal onset of severe anemia.

Y. Tanaka, N. Aida, R. Ijiri, 2001, Journal of pediatric hematology/oncology.

Predictive value of early radiological findings in inflicted traumatic brain injury

N. Aida, K. Nozawa, K. Tanoue, 2012, Acta paediatrica.

Comparison of Predictive Values of Magnetic Resonance Biomarkers Based on Scan Timing in Neonatal Encephalopathy Following Therapeutic Hypothermia.

T. Niwa, N. Aida, N. Morisaki, 2021, The Journal of pediatrics.

K. Tachibana, K. Tanaka, Y. Tanaka, 2000, Transplantation proceedings.

Pericardial hemangioma presenting fetal cardiac tamponade and postnatal bronchostenosis

N. Aida, M. Shinkai, T. Nishi, 2004, Pediatric Surgery International.

Biliary rhabdomyosarcoma

N. Aida, N. Kitagawa, 2007, Pediatric Radiology.

Persistent Hyperplastic Primary Vitreous with Microphthalmia and Coloboma in a Patient with Okur-Chung Neurodevelopmental Syndrome

K. Kosaki, Y. Kuroda, K. Kurosawa, 2021, Molecular Syndromology.

Mutations in the glutaminyl-tRNA synthetase gene cause early-onset epileptic encephalopathy

N. Matsumoto, A. Yamashita, N. Miyake, 2014, Journal of Human Genetics.

Novel AMER1 frameshift mutation in a girl with osteopathia striata with cranial sclerosis

Y. Tsurusaki, K. Kurosawa, N. Aida, 2018, Congenital anomalies.

A Child with Three Episodes of Reversible Splenial Lesion

J. Takanashi, H. Osaka, N. Aida, 2012, Neuropediatrics.

Visualization of the airway in infants with MRI using pointwise encoding time reduction with radial acquisition (PETRA)

T. Niwa, N. Aida, K. Nozawa, 2017, Journal of magnetic resonance imaging : JMRI.

Changes in Brain Metabolite Concentrations after Neonatal Hypoxic-ischemic Encephalopathy.

N. Aida, J. Shibasaki, K. Toyoshima, 2018, Radiology.

Brain MRI findings of older patients with Pallister–Killian syndrome

Y. Kuroki, K. Kurosawa, N. Aida, 2006, Brain and Development.

Microscopic intraosseous extension of osteosarcoma: assessment on dynamic contrast-enhanced MRI

Yukichi Tanaka, G. Nishimura, N. Aida, 1997, Skeletal Radiology.

Clinical characteristics and outcomes of Möbius syndrome in a children's hospital.

Kenji Kurosawa, Noriko Aida, Jun Shibasaki, 2014, Pediatric neurology.

Periventricular nodular heterotopia is related to severity of the hindbrain deformity in Chiari II malformation

T. Nagaoka, T. Niwa, N. Aida, 2012, Pediatric Radiology.

A case of infantile Alexander disease diagnosed by magnetic resonance imaging and genetic analysis

T. Taoka, S. Tsujino, M. Shima, 2007, Brain and Development.

Brain MR in Fukuyama congenital muscular dystrophy.

N. Aida, N. Kobayashi, K. Takada, 1996, AJNR. American journal of neuroradiology.

Transient ischemic attack-like episodes without stroke-like lesions in MELAS

H. Osaka, N. Aida, T. Wada, 2013, Pediatric Radiology.

Noonan syndrome and cavernous hemangioma of the brain.

M. Masuno, Y. Kuroki, S. Yamanaka, 1999, American journal of medical genetics.

WDR45 mutations in three male patients with West syndrome

N. Matsumoto, Kyoko Takano, N. Miyake, 2016, Journal of Human Genetics.

Aggregate formation analysis of GFAPR416W found in one case of Alexander disease

Kyoko Takano, H. Osaka, Hiroko Shimbo, 2019, Brain and Development.

Quiet T1-Weighted Pointwise Encoding Time Reduction with Radial Acquisition for Assessing Myelination in the Pediatric Brain

K. Murata, T. Obata, T. Niwa, 2016, American Journal of Neuroradiology.

A distinct subtype of “metatropic dysplasia variant” characterised by advanced carpal skeletal age and subluxation of the radial heads

K. Ozono, G. Nishimura, N. Aida, 1998, Pediatric Radiology.

Novel COL4A1 mutation in a fetus with early prenatal onset of schizencephaly

Y. Tsurusaki, K. Kurosawa, N. Aida, 2018, Human Genome Variation.

[A case of ureteral polyp prolapsing into bladder in a 3-year-old boy].

Y. Tanaka, N. Aida, S. Nosaka, 1998, Hinyokika kiyo. Acta urologica Japonica.

Effective performance of T(1)-weighted FLAIR Imaging with BLADE in pediatric brains.

T. Nagaoka, T. Takahara, T. Kwee, 2012, Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine.

Clinicopathologic study of mass-screened neuroblastoma with special emphasis on untreated observed cases: a possible histologic clue to tumor regression.

Y. Tanaka, N. Aida, T. Momoi, 2000, The American journal of surgical pathology.

Magnetic Resonance Imaging Regional T1 Abnormalities at Term Accurately Predict Motor Outcome in Preterm Infants

Yoshiaki Sato, N. Aida, A. Oka, 2007, Pediatrics.

MR imaging of perinatal brain damage: comparison of clinical outcome with initial and follow-up MR findings.

G. Nishimura, N. Aida, M. Takeuchi, 1998, AJNR. American journal of neuroradiology.

Normal lactate concentration range in the neonatal brain.

T. Obata, Y. Tachibana, N. Aida, 2016, Magnetic resonance imaging.

T. Niwa, N. Aida, Y. Imai, 2015, Brain and Development.

Anatomic dependency of phase shifts in the cerebral venous system of neonates at susceptibility‐weighted MRI

T. Obata, T. Takahara, T. Kwee, 2011, Journal of magnetic resonance imaging : JMRI.

Novel CUL7 biallelic mutations alter the skeletal phenotype of 3M syndrome

Y. Tsurusaki, G. Nishimura, K. Kurosawa, 2020, Human Genome Variation.

Cystic lesion of the buttock communicating with the lateral side of the posterior urethra.

N. Aida, Y. Sasaki, M. Matsumura, 1994, Journal of Urology.

Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation, and CNS structural anomalies: another observation.

M. Masuno, Y. Kuroki, G. Nishimura, 2000, Clinical Dysmorphology.

Elevation of neuron specific enolase and brain iron deposition on susceptibility‐weighted imaging as diagnostic clues for beta‐propeller protein‐associated neurodegeneration in early childhood: Additional case report and review of the literature

Y. Fukushima, Kyoko Takano, N. Aida, 2016, American journal of medical genetics. Part A.

Combined pituitary hormone deficiency with unique pituitary dysplasia and morning glory syndrome related to a heterozygous PROKR2 mutation

N. Aida, K. Muroya, T. Hasegawa, 2015, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Neonatal Brain Metabolite Concentrations: An In Vivo Magnetic Resonance Spectroscopy Study with a Clinical MR System at 3 Tesla

T. Obata, N. Aida, H. Tsuji, 2013, PloS one.

Serial Magnetic Resonance Imaging and 1H-Magnetic Resonance Spectroscopy in GABA Transaminase Deficiency: A Case Report.

N. Aida, T. Goto, Y. Tsuyusaki, 2019, JIMD reports.

Serial Magnetic Resonance Imaging and 1 H-Magnetic Resonance Spectroscopy in GABA Transaminase Deficiency: A Case Report

N. Aida, T. Goto, Y. Tsuyusaki, 2018 .

[Imaging diagnosis of abusive head trauma/shaken baby syndrome].

N. Aida, 2011, No shinkei geka. Neurological surgery.

Neonatal case of classic maple syrup urine disease: Usefulness of 1H‐MRS in early diagnosis

N. Aida, K. Muroya, T. Hasegawa, 2014, Pediatrics international : official journal of the Japan Pediatric Society.

White matter microstructural changes in tuberous sclerosis: Evaluation by neurite orientation dispersion and density imaging (NODDI) and diffusion tensor images

H. Kawai, T. Taoka, S. Naganawa, 2020, Scientific Reports.

Paradoxical increase in seizure frequency with valproate in nonketotic hyperglycinemia

H. Osaka, S. Kure, Hiroko Shimbo, 2012, Brain and Development.