fluorodeoxyglucose f18 has been researched along with Chromosome Deletion in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (25.00) | 29.6817 |
2010's | 1 (25.00) | 24.3611 |
2020's | 2 (50.00) | 2.80 |
Authors | Studies |
---|---|
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, P | 1 |
Byoun, JT; Cho, JY; Oh, SJ; Rhee, SJ; Yu, ST; Yun, KH | 1 |
Auerbach, M; Burgess, BL; McCannel, TA; Reddy, S | 1 |
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, RM | 1 |
4 other study(ies) available for fluorodeoxyglucose f18 and Chromosome Deletion
Article | Year |
---|---|
Broader phenotypic traits and widespread brain hypometabolism in spinocerebellar ataxia 27.
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.
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.
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.
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 |