Compounds > transferrin
Page last updated: 2024-08-23

transferrin and Adiadochokinesis

transferrin has been researched along with Adiadochokinesis in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's0 (0.00)18.2507
2000's4 (66.67)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Adams, DR; Barritault, J; Brice, A; Clot, F; Ding, JH; Durr, A; Engelke, UF; Huizing, M; Kaneski, CR; Kulkarni, B; Mochel, F; Schiffmann, R; Sedel, F; Seguin, F; Smits, BW; Vanderver, A; Vanier, MT; Verheijen, FW; Wevers, RA; Yang, BZ1
Dahl, N; Dahlqvist, J; Entesarian, M; Gustavson, KH; Melberg, A; Orlén, H; Raininko, R1
McGill, J; O'Sullivan, JD; Schoffer, KL1
Knoers, NA; Kremer, HP; Lefeber, DJ; Leijten, QH; Matthijs, G; Morava, E; Scheffer, H; Vermeer, S; Wevers, RA1
Hayashi, H; Toyoshima, I; Tsubaki, T1
Pascual-Castroviejo, I1

Other Studies

6 other study(ies) available for transferrin and Adiadochokinesis

ArticleYear
Cerebellar ataxia with elevated cerebrospinal free sialic acid (CAFSA).
    Brain : a journal of neurology, 2009, Volume: 132, Issue:Pt 3

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Atrophy; Cells, Cultured; Cerebellar Ataxia; Cerebellum; Child; Child, Preschool; Cohort Studies; Female; Humans; Infant; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Middle Aged; N-Acetylneuraminic Acid; Transferrin

2009
Re-evaluation of the dysequilibrium syndrome.
    Acta neurologica Scandinavica, 2011, Volume: 123, Issue:1

    Topics: Adult; Cerebellar Ataxia; Cerebellum; DNA Mutational Analysis; Female; Humans; Intellectual Disability; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Neurologic Examination; Phosphotransferases (Phosphomutases); Receptors, LDL; Reference Values; Sweden; Transferrin

2011
Congenital disorder of glycosylation type Ia presenting as early-onset cerebellar ataxia in an adult.
    Movement disorders : official journal of the Movement Disorder Society, 2006, Volume: 21, Issue:6

    Topics: Adult; Brain; Cerebellar Ataxia; Congenital Disorders of Glycosylation; Diagnosis, Differential; Glycosylation; Humans; Karyotyping; Magnetic Resonance Imaging; Male; Reference Values; Transferrin

2006
Cerebellar ataxia and congenital disorder of glycosylation Ia (CDG-Ia) with normal routine CDG screening.
    Journal of neurology, 2007, Volume: 254, Issue:10

    Topics: Adolescent; Cerebellar Ataxia; Child; Congenital Disorders of Glycosylation; Female; Fibroblasts; Humans; Isoelectric Focusing; Male; Phosphotransferases (Phosphomutases); Transferrin

2007
[Changes in microheterogeneity of CSF transferrin in patient with amyotrophic lateral sclerosis and spinocerebellar degenerations].
    Rinsho shinkeigaku = Clinical neurology, 1982, Volume: 22, Issue:4

    Topics: Adolescent; Adult; Aged; Amyotrophic Lateral Sclerosis; Cerebellar Ataxia; Humans; Middle Aged; Transferrin

1982
Congenital disorders of glycosylation syndromes.
    Developmental medicine and child neurology, 2002, Volume: 44, Issue:5

    Topics: Asialoglycoproteins; Carbohydrate Metabolism, Inborn Errors; Cerebellar Ataxia; Cerebellum; Child; Child, Preschool; Congenital Disorders of Glycosylation; Female; Glycosylation; Humans; Male; Phosphotransferases (Phosphomutases); Transferrin

2002