Page last updated: 2024-08-23

transferrin and Intellectual Disability

transferrin has been researched along with Intellectual Disability in 17 studies

Research

Studies (17)

Timeframe	Studies, this research(%)	All Research%
pre-1990	7 (41.18)	18.7374
1990's	2 (11.76)	18.2507
2000's	5 (29.41)	29.6817
2010's	2 (11.76)	24.3611
2020's	1 (5.88)	2.80

Authors

Authors	Studies
Alsharhan, H; Amor, DJ; Bakhtiari, S; Bhoj, EJ; Bilguvar, K; Chen, J; Christodoulou, J; Cogné, B; Daniel, EJP; Deb, W; Donald, T; Edmondson, AC; Freeze, HH; He, M; Jin, SC; Jones, EA; Kruer, MC; Li, D; Ng, BG; Raymond, KM; Sobering, AK; Vassallo, G; Vincent, M; Webster, RI; Werners, AH; Yearwood, KR	1
Aral, B; Bellanné-Chantelot, C; Blair, E; Carmignac, V; Delva, L; Donadieu, J; Droin, N; Duplomb, L; Duvet, S; El Chehadeh-Djebbar, S; Faivre, L; Foulquier, F; Gigot, N; Girodon, F; Jego, G; Klein, A; Lopez, E; Marle, N; Michalski, JC; Philippe, C; Picot, D; Rivière, JB; Solary, E; Thauvin-Robinet, C; Thevenon, J	1
Dahl, N; Dahlqvist, J; Entesarian, M; Gustavson, KH; Melberg, A; Orlén, H; Raininko, R	1
Bubel, S; Hackler, R; Hagenah, J; Hoffmann, GF; Klein, C; Peters, V; Schaefer, JR; Vieregge, P	1
MANN, JD; VALDMANIS, A; VANDYKE, HE	1
BREIBART, S; EBERLEIN, WR; MELLMAN, WJ	1
Holzbach, U; Huber, WD; Huemer, M; Moeslinger, D; Schima, W; Stoeckler-Ipsiroglu, S; Wank, H; Wevers, R	1
Amiel, J; Cormier-Daire, V; Durand, G; Le Merrer, M; Munnich, A; Seta, N; Tan, J; Vuillaumier-Barrot, S	1
du Plessis, JA; Erasmus, E; Knoll, DP; Lippert, MM; Mienie, LJ; Pretorius, PJ; van der Westhuizen, FH	1
Arndt, T; Assmann, B; Hackler, R; Hoffmann, GF; Jaeken, J; Mayatepek, E; Peters, V; Schaefer, JR	1
Agarwal, DP; Benkmann, HG; Goedde, HW; Srivastava, LM	1
Hagberg, B; Jaeken, J; Stibler, H	1
Maehlen, J; Strøm, EH; Strømme, P; Torvik, A	1
Andersson, M; Hagberg, B; Kristiansson, B; Tonnby, B	1
Killian, W; Linkesch, W; Riederer, P	1
Nevo, SS; Sutton, HE	1
Atkins, L; Hazard, GW; Ouellette, EM; Pant, SS	1

Reviews

2 review(s) available for transferrin and Intellectual Disability

Article	Year
Congenital disorders of glycosylation IIa cause growth retardation, mental retardation, and facial dysmorphism. Journal of medical genetics, 2000, Volume: 37, Issue:11 Topics: Child; Child, Preschool; Congenital Disorders of Glycosylation; Diarrhea; Face; Glycoproteins; Growth Disorders; Humans; Intellectual Disability; Male; N-Acetylglucosaminyltransferases; Point Mutation; Transferrin	2000
The carbohydrate-deficient glycoprotein syndrome. A new inherited multisystemic disease with severe nervous system involvement. Acta paediatrica Scandinavica. Supplement, 1991, Volume: 375 Topics: Adolescent; Adult; alpha-Fetoproteins; Amniotic Fluid; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Fetal Blood; Genes, Recessive; Glycoproteins; Humans; Infant; Intellectual Disability; Liver Diseases; Male; Middle Aged; Nervous System Diseases; Prenatal Diagnosis; Transferrin	1991

Article

Year

Congenital disorders of glycosylation IIa cause growth retardation, mental retardation, and facial dysmorphism.

Journal of medical genetics, 2000, Volume: 37, Issue:11

Topics: Child; Child, Preschool; Congenital Disorders of Glycosylation; Diarrhea; Face; Glycoproteins; Growth Disorders; Humans; Intellectual Disability; Male; N-Acetylglucosaminyltransferases; Point Mutation; Transferrin

2000

The carbohydrate-deficient glycoprotein syndrome. A new inherited multisystemic disease with severe nervous system involvement.

Acta paediatrica Scandinavica. Supplement, 1991, Volume: 375

Topics: Adolescent; Adult; alpha-Fetoproteins; Amniotic Fluid; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Fetal Blood; Genes, Recessive; Glycoproteins; Humans; Infant; Intellectual Disability; Liver Diseases; Male; Middle Aged; Nervous System Diseases; Prenatal Diagnosis; Transferrin

1991

Other Studies

15 other study(ies) available for transferrin and Intellectual Disability

Article	Year
ALG13 X-linked intellectual disability: New variants, glycosylation analysis, and expanded phenotypes. Journal of inherited metabolic disease, 2021, Volume: 44, Issue:4 Topics: Congenital Disorders of Glycosylation; Female; Genetic Variation; Glycosylation; Humans; Intellectual Disability; Male; N-Acetylglucosaminyltransferases; Phenotype; Transferrin	2021
Cohen syndrome is associated with major glycosylation defects. Human molecular genetics, 2014, May-01, Volume: 23, Issue:9 Topics: Antigens, CD; Cell Adhesion Molecules; Developmental Disabilities; Electrophoresis, Polyacrylamide Gel; Fibroblasts; Fingers; Glycosylation; Golgi Apparatus; Humans; Intellectual Disability; Intercellular Adhesion Molecule-1; Microcephaly; Muscle Hypotonia; Myopia; Obesity; Retinal Degeneration; RNA Interference; Transferrin; Vesicular Transport Proteins	2014
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
[CDG (congenital disorders of glycosylation). Differential hereditary ataxia in adulthood diagnosis]. Der Nervenarzt, 2002, Volume: 73, Issue:8 Topics: Adult; Brain; Brain Diseases, Metabolic, Inborn; Congenital Disorders of Glycosylation; Diagnosis, Differential; Female; Follow-Up Studies; Humans; Intellectual Disability; Isoelectric Focusing; Magnetic Resonance Imaging; Neuropsychological Tests; Spinocerebellar Degenerations; Syndrome; Transferrin	2002
PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18. American journal of human genetics, 1964, Volume: 16 Topics: 17-Ketosteroids; Adolescent; Adrenal Cortex Hormones; Arm; Blood Group Antigens; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 18; Estrogens; Gonadotropins; Gonadotropins, Pituitary; Haptoglobins; Humans; Intellectual Disability; Transferrin; Urine	1964
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
Budd-Chiari syndrome associated with coagulation abnormalities in a child with carbohydrate deficient glycoprotein syndrome type Ix. The Journal of pediatrics, 2000, Volume: 136, Issue:5 Topics: Blotting, Western; Budd-Chiari Syndrome; Child; Coagulation Protein Disorders; Congenital Disorders of Glycosylation; Consanguinity; Humans; Intellectual Disability; Male; Mannose-6-Phosphate Isomerase; Phosphoglucomutase; Phosphotransferases (Phosphomutases); Portasystemic Shunt, Transjugular Intrahepatic; 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
A new subtype of a congenital disorder of glycosylation (CDG) with mild clinical manifestations. Neuropediatrics, 2001, Volume: 32, Issue:6 Topics: Asialoglycoproteins; Child, Preschool; Congenital Disorders of Glycosylation; Consanguinity; Diagnosis, Differential; Humans; Intellectual Disability; Isoelectric Focusing; Male; Psychomotor Disorders; Transferrin	2001
Studies on the polymorphism of C3, Tf and Bg in Down's syndrome and other diseases. Humangenetik, 1975, Aug-29, Volume: 29, Issue:1 Topics: Complement C3; Complement C4; Complement System Proteins; Down Syndrome; Female; Gene Frequency; Germany, West; Glycoproteins; Hepatolenticular Degeneration; Humans; Intellectual Disability; Male; Myocardial Infarction; Phenotype; Polymorphism, Genetic; Transferrin	1975
[The carbohydrate deficient glycoprotein syndrome]. Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1991, Apr-20, Volume: 111, Issue:10 Topics: Abnormalities, Multiple; Biomarkers; Brain; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Glycoproteins; Humans; Intellectual Disability; Male; Nervous System Diseases; Syndrome; Transferrin	1991
Disialotransferrin developmental deficiency syndrome. Archives of disease in childhood, 1989, Volume: 64, Issue:1 Topics: Adolescent; Adult; Asialoglycoproteins; Child; Child, Preschool; Developmental Disabilities; Facial Expression; Female; Humans; Intellectual Disability; Isoelectric Focusing; Male; Metabolism, Inborn Errors; Nervous System Diseases; Sialoglycoproteins; Syndrome; Transferrin	1989
Serum iron status in Rett syndrome. Brain & development, 1987, Volume: 9, Issue:5 Topics: Adolescent; Adult; Age Factors; Brain Chemistry; Brain Diseases; Child; Child, Preschool; Female; Ferritins; Humans; Infant; Intellectual Disability; Iron; Syndrome; Transferrin	1987
Association between response to typhoid vaccination and known genetic markers. American journal of human genetics, 1968, Volume: 20, Issue:5 Topics: Adolescent; Adult; Antibody Formation; Blood Group Antigens; Blood Protein Electrophoresis; Child; Female; Genetics, Medical; Haptoglobins; Humans; Intellectual Disability; Male; Middle Aged; Polymorphism, Genetic; Transferrin; Typhoid Fever; Vaccination	1968
Two cases with a C-group ring autosome. Annals of human genetics, 1966, Volume: 30, Issue:1 Topics: Blood Group Antigens; Body Height; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Culture Techniques; Fibroblasts; Haptoglobins; Humans; Intellectual Disability; Karyotyping; Leukocytes; Male; Microcephaly; Movement Disorders; Muscles; Transferrin	1966