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

transferrin and Seizures

transferrin has been researched along with Seizures in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19902 (25.00)18.7374
1990's0 (0.00)18.2507
2000's4 (50.00)29.6817
2010's2 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Alfadhel, M; Bolton, M; Dvorak, C; Gadomski, TE; Morava, E; Nelson, SL; Ogunsakin, OA1
Artuch, R; Briones, P; Campistol, J; Cusí, V; García-Cazorla, A; Grunewald, S; Matthijs, G; Pérez-Cerdá, C; Pérez-Dueñas, B; Pineda, M; Poo, P; Schollen, E; Vilaseca, MA1
Cardoso, AL; Costa, P; Culmsee, C; de Almeida, LP; de Lima, MC; Plesnila, N; Simões, S; Wagner, E1
BREIBART, S; EBERLEIN, WR; MELLMAN, WJ1
Beck, MM; Kuenzel, WJ1
Filiano, J; Freeze, HH; Karnes, PS; Kim, S; Mehta, DP; Patterson, MC; Peterson, S; Srikrishna, G; Westphal, V1
Bjerve, KS; Bovim, G; Bråthen, G; Brodtkorb, E1
du Plessis, JA; Erasmus, E; Knoll, DP; Lippert, MM; Mienie, LJ; Pretorius, PJ; van der Westhuizen, FH1

Other Studies

8 other study(ies) available for transferrin and Seizures

ArticleYear
ALG13-CDG in a male with seizures, normal cognitive development, and normal transferrin isoelectric focusing.
    American journal of medical genetics. Part A, 2017, Volume: 173, Issue:10

    Topics: Child, Preschool; Cognition; Congenital Disorders of Glycosylation; Glycosylation; Humans; Isoelectric Focusing; Male; Mutation; N-Acetylglucosaminyltransferases; Seizures; Transferrin

2017
Long-term evolution of eight Spanish patients with CDG type Ia: typical and atypical manifestations.
    European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2009, Volume: 13, Issue:5

    Topics: Adolescent; Adult; Aging; Brain; Child; Child, Preschool; Congenital Disorders of Glycosylation; Disease Progression; DNA Mutational Analysis; Female; Follow-Up Studies; Genotype; Humans; Infant; Infant, Newborn; Kidney; Magnetic Resonance Imaging; Male; Nervous System Diseases; Seizures; Spain; Tomography, X-Ray Computed; Transferrin; Young Adult

2009
Tf-lipoplex-mediated c-Jun silencing improves neuronal survival following excitotoxic damage in vivo.
    Journal of controlled release : official journal of the Controlled Release Society, 2010, Mar-19, Volume: 142, Issue:3

    Topics: Animals; Blotting, Western; Cell Culture Techniques; Cell Survival; Cells, Cultured; Cholesterol; Drug Carriers; Drug Compounding; Fatty Acids, Monounsaturated; Gene Silencing; Glutamic Acid; Humans; Immunohistochemistry; Kainic Acid; Liposomes; Mice; Mice, Inbred C57BL; Neurons; Neuroprotective Agents; Protein Transport; Proto-Oncogene Proteins c-jun; Quaternary Ammonium Compounds; Reverse Transcriptase Polymerase Chain Reaction; RNA, Small Interfering; Seizures; Transferrin

2010
DEVELOPMENTAL RETARDATION ASSOCIATED WITH AN UNBALANCED 13-15/18 TRANSLOCATION.
    Cytogenetics, 1964, Volume: 3

    Topics: Blood Group Antigens; Child; Chromosome Aberrations; Chromosome Disorders; Cryptorchidism; Dermatoglyphics; Erythrocytes; Foot; Hand; Haptoglobins; Humans; Hypospadias; Intellectual Disability; Male; Seizures; Skin; Transferrin

1964
Implication of iron in seizure syndrome of mutant chicks (Gallus domesticus).
    Comparative biochemistry and physiology. A, Comparative physiology, 1983, Volume: 74, Issue:2

    Topics: Animals; Blood Proteins; Brain; Chickens; Hemoglobins; Iron; Male; Mutation; Seizures; Syndrome; Transferrin

1983
Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie)
    The Journal of clinical investigation, 2000, Volume: 105, Issue:2

    Topics: Brain Diseases, Metabolic, Inborn; Carbohydrate Sequence; Cells, Cultured; Congenital Disorders of Glycosylation; Developmental Disabilities; DNA Mutational Analysis; Female; Fibroblasts; Glycoside Hydrolases; Glycosylation; Humans; Infant; Isoelectric Focusing; Isoenzymes; Male; Mannose; Mannosyltransferases; Microcephaly; Molecular Sequence Data; Mutation; Reverse Transcriptase Polymerase Chain Reaction; Seizures; Sequence Deletion; Transferrin

2000
Validity of carbohydrate deficient transferrin and other markers as diagnostic aids in the detection of alcohol related seizures.
    Journal of neurology, neurosurgery, and psychiatry, 2000, Volume: 68, Issue:3

    Topics: Adult; Alcohol Drinking; Alcoholism; Biomarkers; Ethanol; False Negative Reactions; False Positive Reactions; Female; Humans; Male; Middle Aged; Reproducibility of Results; Seizures; Transferrin

2000
An atypical carbohydrate-deficient glycoprotein (CDG) syndrome patient in South Africa.
    South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 2001, Volume: 91, Issue:5

    Topics: Blindness; Congenital Disorders of Glycosylation; Female; Humans; Infant; Intellectual Disability; Isoelectric Focusing; Seizures; South Africa; Transferrin

2001