Page last updated: 2024-08-24

fluorodeoxyglucose f18 and Chromosome Deletion

fluorodeoxyglucose f18 has been researched along with Chromosome Deletion in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's1 (25.00)24.3611
2020's2 (50.00)2.80

Authors

AuthorsStudies
Alshammari, M; Alshammari, T; Bergendal, Å; Di Re, J; Granberg, T; Iwarsson, E; Laezza, F; Lindefeldt, M; Lundin, J; Paucar, M; Savitcheva, I; Solders, G; Svenningsson, P1
Byoun, JT; Cho, JY; Oh, SJ; Rhee, SJ; Yu, ST; Yun, KH1
Auerbach, M; Burgess, BL; McCannel, TA; Reddy, S1
Chen, J; Farrer, M; Gwinn-Hardy, K; Hardy, J; Hussey, J; Hwu, WL; Lincoln, S; Liu, RS; Shan, DE; Sun, CM; Tai, CH; West, A; Wu, RM1

Other Studies

4 other study(ies) available for fluorodeoxyglucose f18 and Chromosome Deletion

ArticleYear
Broader phenotypic traits and widespread brain hypometabolism in spinocerebellar ataxia 27.
    Journal of internal medicine, 2020, Volume: 288, Issue:1

    Topics: Adolescent; Adult; Animals; Attention Deficit Disorder with Hyperactivity; Brain; Chromosome Deletion; Chromosomes, Human, Pair 13; Cognition Disorders; Fibroblast Growth Factors; Fluorodeoxyglucose F18; Genotype; Humans; Immunohistochemistry; Integrin beta1; Magnetic Resonance Imaging; Mice, Knockout; Neuroimaging; Neuropsychological Tests; Pedigree; Phenotype; Positron-Emission Tomography; Prefrontal Cortex; Psychotic Disorders; Radiopharmaceuticals; Spinocerebellar Degenerations; Sweden; Vesicular Inhibitory Amino Acid Transport Proteins; Young Adult

2020
Mid-Aortic Syndrome in Williams-Beuren Syndrome with an Atypical Small-Sized Deletion of Chromosome 7q11.23 Misdiagnosed as Takayasu Arteritis.
    International heart journal, 2021, Jan-30, Volume: 62, Issue:1

    Topics: Adolescent; Adrenergic beta-Antagonists; Angiotensin Receptor Antagonists; Aorta; Aortography; Chromosome Deletion; Computed Tomography Angiography; Diagnostic Errors; Drug Therapy, Combination; Echocardiography; Fluorodeoxyglucose F18; Humans; Hypertension; Male; Microarray Analysis; Positron-Emission Tomography; Takayasu Arteritis; Treatment Outcome; Williams Syndrome

2021
Association of positive dual-modality positron emission tomography/computed tomography imaging of primary choroidal melanoma with chromosome 3 loss and tumor size.
    Retina (Philadelphia, Pa.), 2010, Volume: 30, Issue:1

    Topics: Adult; Aged; Aged, 80 and over; Biopsy, Needle; Choroid Neoplasms; Chromosome Deletion; Chromosomes, Human, Pair 3; Female; Fluorodeoxyglucose F18; Humans; In Situ Hybridization, Fluorescence; Male; Melanoma; Middle Aged; Oligonucleotide Array Sequence Analysis; Polymorphism, Single Nucleotide; Positron-Emission Tomography; Radiopharmaceuticals; Retrospective Studies; Tomography, X-Ray Computed

2010
Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutations.
    Movement disorders : official journal of the Movement Disorder Society, 2002, Volume: 17, Issue:4

    Topics: Adult; Alleles; Asian People; Caudate Nucleus; Chromosome Deletion; Chromosomes, Human, Pair 6; Dominance, Cerebral; Dopamine; Female; Fluorodeoxyglucose F18; Haplotypes; Humans; Ligases; Male; Mutation; Parkinson Disease; Pedigree; Putamen; Receptors, Presynaptic; RNA, Messenger; Taiwan; Tomography, Emission-Computed; Ubiquitin-Protein Ligases

2002