Page last updated: 2024-08-24

fluorodeoxyglucose f18 and Autosomal Dominant Hereditary Spastic Paraplegia

fluorodeoxyglucose f18 has been researched along with Autosomal Dominant Hereditary Spastic Paraplegia in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	1 (50.00)	2.80

Authors

Authors	Studies
Banneau, G; Bonnet, C; Bossenmeyer-Pourié, C; Dillier, C; Hocquel, A; Hopes, L; Kaminsky, AL; Kol, B; Lambert, L; Lardin, A; Liao, L; Meyer, M; Michaud, M; Myriam, B; Ravel, JM; Renaud, M; Schmitt, E; Tissier, L; Verger, A; Zhu, F	1
Benti, R; Chiapparini, L; Consonni, M; Di Bella, D; Farina, L; Magri, S; Marotta, G; Pareyson, D; Sagnelli, A; Salsano, E; Scigliuolo, GM; Taroni, F; Tonduti, D	1

Other Studies

2 other study(ies) available for fluorodeoxyglucose f18 and Autosomal Dominant Hereditary Spastic Paraplegia

Article	Year
Reduced penetrance of an eastern French mutation in ATL1 autosomal-dominant inheritance (SPG3A): extended phenotypic spectrum coupled with brain Neurogenetics, 2022, Volume: 23, Issue:4 Topics: Brain; DNA Mutational Analysis; Fluorodeoxyglucose F18; GTP-Binding Proteins; Humans; Membrane Proteins; Mutation; Pedigree; Penetrance; Phenotype; Retrospective Studies; Small Fiber Neuropathy; Spastic Paraplegia, Hereditary	2022
Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findings. Journal of neurology, 2016, Volume: 263, Issue:3 Topics: Brain; Fluorodeoxyglucose F18; Humans; Magnetic Resonance Imaging; Male; Mutation; Positron-Emission Tomography; Spastic Paraplegia, Hereditary; Tubulin; Young Adult	2016

Article

Year

Reduced penetrance of an eastern French mutation in ATL1 autosomal-dominant inheritance (SPG3A): extended phenotypic spectrum coupled with brain

Neurogenetics, 2022, Volume: 23, Issue:4

Topics: Brain; DNA Mutational Analysis; Fluorodeoxyglucose F18; GTP-Binding Proteins; Humans; Membrane Proteins; Mutation; Pedigree; Penetrance; Phenotype; Retrospective Studies; Small Fiber Neuropathy; Spastic Paraplegia, Hereditary

2022

Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findings.

Journal of neurology, 2016, Volume: 263, Issue:3

Topics: Brain; Fluorodeoxyglucose F18; Humans; Magnetic Resonance Imaging; Male; Mutation; Positron-Emission Tomography; Spastic Paraplegia, Hereditary; Tubulin; Young Adult

2016