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Author Details

Yoshimitsu Fukushima
Nippon Medical School
1981
340
49
PMIDPaper TitleJournal TitlePublished Year
36866489Clinical utility of <sup>67</sup> Gallium-SPECT/CT for determining osteotomy indication in patients with lower-limb osteomyelitis.Wound Repair Regen2023
37305793Prognostic Implications of Sarcoidosis Granulomasã¿¿- Insights From the Multicenter Registry, the Japanese Cardiac Sarcoidosis Prognostic Study.Circ Rep2023
34822103Serial change in perfusion-metabolism mismatch after coronary artery bypass grafting.Ann Nucl Med2022
35354745Localization of Late Gadolinium Enhancement and Its Association with Ventricular Tachycardia in Patients with Cardiac Sarcoidosis.Int Heart J2022
36540169Multicenter Registry in the Japanese Cardiac Sarcoidosis Prognostic (J-CASP) Study: Baseline Characteristics and Validation of the Non-invasive Approach Using <sup>18</sup>F-FDG PET.Ann Nucl Cardiol2022
36450868Diagnostic performance of quantitative Ga-SPECT/CT for patients with lower-limb osteomyelitis.Eur J Hybrid Imaging2022
34876316Neuropsychological and neurophysiological features of WAGR syndrome: Detailed comprehensive evaluation of a patient with severe intellectual disability and autism spectrum disorder.Brain Dev2022
34902097Correction to: Serial change in perfusion-metabolism mismatch after coronary artery bypass grafting.Ann Nucl Med2022
33884742Heterozygous missense variant in TRPC6 in a boy with rapidly progressive infantile nephrotic syndrome associated with diffuse mesangial sclerosis.Am J Med Genet A2021
32320785Prevalence of atrial FDG uptake and association with atrial arrhythmias in patients with cardiac sarcoidosis.Int J Cardiol2020
31907394Effect of fluctuation of oxygenation on the development of severe retinopathy of prematurity in extremely preterm infants.J Perinatol2020
33324770Clinical Genetics in Japan: Efforts of Human Genetics Societies and Related Organizations.JMA J2020
30941898PIEZO2 deficiency is a recognizable arthrogryposis syndrome: A new case and literature review.Am J Med Genet A2019
30867468Frequency and clinical features of hearing loss caused by STRC deletions.Sci Rep2019
28986773Feasibility of combined risk stratification with coronary CT angiography and stress myocardial SPECT in patients with chronic coronary artery disease.Ann Nucl Med2018
29878129Maternal Uniparental Disomy for Chromosome 20: Physical and Endocrinological Characteristics of Five Patients.J Clin Endocrinol Metab2018
283679054D Flow MR Imaging of Ophthalmic Artery Flow in Patients with Internal Carotid Artery Stenosis.Magn Reson Med Sci2018
29782596Diagnostic performance of hybrid cardiac SPECT/CT imaging for patients with takotsubo cardiomyopathy.Eur J Hybrid Imaging2018
29796285Myelodysplastic syndrome in an infant with constitutional pure duplication 1q41-qter.Hum Genome Var2018
29556942Feasibility of myocardial flow reserve prediction without the use of dynamic data from myocardial perfusion positron emission tomography.Int J Cardiovasc Imaging2018
27873171Prognostic value of lower limb perfusion single-photon emission computed tomography-computed tomography in patients with lower limb atherosclerotic peripheral artery disease.Jpn J Radiol2017
28223668[Genetic Counseling of HBOC and Japanese Organization of HBOC].Gan To Kagaku Ryoho2017
29081981A novel frameshift mutation of <i>SYNE1</i> in a Japanese family with autosomal recessive cerebellar ataxia type 8.Hum Genome Var2017
28711740Early manifestations of epileptic encephalopathy, brain atrophy, and elevation of serum neuron specific enolase in a boy with beta-propeller protein-associated neurodegeneration.Eur J Med Genet2017
27095364Evidence-based clinical practice guidelines for polycystic kidney disease 2014.Clin Exp Nephrol2016
26541773Imaging Angiogenesis Using 99mTc-Macroaggregated Albumin Scintigraphy in Patients with Peripheral Artery Disease.J Nucl Med2016
26481852Elevation 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.Am J Med Genet A2016
26635345Prognostic Value of Myocardial Perfusion SPECT After Intravenous Bolus Administration of Nicorandil in Patients with Acute Ischemic Heart Failure.J Nucl Med2016
27358079Erratum to: Evidence-based clinical practice guidelines for polycystic kidney disease 2014.Clin Exp Nephrol2016
27266115[Therapeutic angiogenesis for refractory peripheral arterial disease (PAD)].Nihon Rinsho2016
27469136Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic Hybridization.Ann Otol Rhinol Laryngol2016
27180792Usefulness of Single Photon Emission Computed Tomography/Computed Tomography Fusion-Hybrid Imaging to Evaluate Coronary Artery Disorders in Patients with a History of Kawasaki Disease.J Nippon Med Sch2016
25423878A novel heterozygous MAP2K1 mutation in a patient with Noonan syndrome with multiple lentigines.Am J Med Genet A2015
26891489[Frontline of vascular regenerative therapy for refractory peripheral arterial diseases].Nihon Jibiinkoka Gakkai Kaiho2015
26090294Estimating Lymphodynamic Conditions and Lymphovenous Anastomosis Efficacy Using (99m)Tc-phytate Lymphoscintigraphy with SPECT-CT in Patients with Lower-limb Lymphedema.Plast Reconstr Surg Glob Open2015
25846547Patients with reduced heart rate response to adenosine infusion have low myocardial flow reserve in (13)N-ammonia PET studies.Int J Cardiovasc Imaging2015
25691411Renal complications in 6p duplication syndrome: microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS).Am J Med Genet A2015
25740237Pseudonormal Corticomedullary Differentiation of the Kidney Assessed on T1-weighted Imaging for Chronic Kidney Disease Patients with Cirrhosis.Magn Reson Med Sci2015
23724928p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small-vessel occlusion in elderly Japanese males.Eur J Neurol2014
25812312[Technical evaluation of medical practice--conversion from things to skill and art. Topics: V. Toward establishment of technical evaluation on medical practice: 4. Informed consent under unusual conditions, 2) Genetic counseling and evaluation of medical treatment fee].Nihon Naika Gakkai Zasshi2014
25478009Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation.Mol Cytogenet2014
24878888Nuclear myocardial perfusion imaging with a cadmium-telluride semiconductor detector gamma camera in patients with acute myocardial infarction.Ann Nucl Med2014
24664492Identification of a novel missense mutation of MAF in a Japanese family with congenital cataract by whole exome sequencing: a clinical report and review of literature.Am J Med Genet A2014
24311518Surgical intervention for esophageal atresia in patients with trisomy 18.Am J Med Genet A2014
24357569Microarray and FISH-based genotype-phenotype analysis of 22 Japanese patients with Wolf-Hirschhorn syndrome.Am J Med Genet A2014
22548404Exome sequencing in a family with an X-linked lethal malformation syndrome: clinical consequences of hemizygous truncating OFD1 mutations in male patients.Clin Genet2013
24419722A definitive diagnosis of mucosa-associated lymphoid tissue lymphoma made at a second biopsy.J Nippon Med Sch2013
23637025Clinical correlations of mutations affecting six components of the SWI/SNF complex: detailed description of 21 patients and a review of the literature.Am J Med Genet A2013
23635952Follow-up nationwide survey on predictive genetic testing for late-onset hereditary neurological diseases in Japan.J Hum Genet2013
23810066Significant suppression of myocardial (18)F-fluorodeoxyglucose uptake using 24-h carbohydrate restriction and a low-carbohydrate, high-fat diet.J Cardiol2013
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Collaborators

Norio Niikawa
Health Sciences University of Hokkaido
Co-authored papers 51
Gen Nishimura
Co-authored papers 18
Yusuke Nakamura
Japanese Foundation for Cancer Research
Co-authored papers 9
Ichiro Matsuda
Health Sciences University of Hokkaido
Co-authored papers 5
Hitoshi Takano
Co-authored papers 5
Shinji Kondo
Co-authored papers 5
Tatsuhiko Tsunoda
The University of Tokyo
Co-authored papers 5
Toshihiro Tanaka
Bioresourse Research Center, Tokyo Medical and Dental University (TMDU)
Co-authored papers 4
Graeme I Bell
Co-authored papers 4
Kenjiro Kosaki
Center for Medical Genetics, Keio University School of Medicine
Co-authored papers 4
Takashi Kadowaki
Co-authored papers 4
Mark F Leppert
University of Utah
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Hui Zhao
Biotechnology Research Institute, Chinese Academy of Agricultural Sciences
Co-authored papers 3
Akihiro Sekine
Graduate School of Medicine, Chiba University
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Clement Adebamowo
Institute for Human Virology
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Toyin Aniagwu
University College Hospital
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Jean E McEwen
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 3
Eiko Suda
National Institute for Environmental Studies.
Co-authored papers 3
Houcan Zhang
Beijing Normal University
Co-authored papers 3
Andy Peiffer
University of Utah, Inc.
Co-authored papers 3
Chibuzor Nkwodimmah
University of Ibadan
Co-authored papers 3
Vivian Ota Wang
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 3
Patricia A Marshall
Case Western Reserve University
Co-authored papers 3
Missy Dixon
Co-authored papers 3
Darryl Macer
American University of Sovereign Nations
Co-authored papers 3
Charles N Rotimi
Center for Research on Genomics and Global Health, National Institutes of Health
Co-authored papers 3
Francis S Collins
University of Michigan ann arbor
Co-authored papers 3
Changqing Zeng
Institute of Biomedical Sciences, Henan Academy of Sciences
Co-authored papers 3
Charmaine D M Royal
Duke University
Co-authored papers 3
IkeOluwapo O Ajayi
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Release 1.2