Lacinski R, Dziadowicz S, Roth C, Ma L, Melemai V, Fitzpatrick B
Front Oncol. 2024; 14:1417459.
PMID: 39493449
PMC: 11527601.
DOI: 10.3389/fonc.2024.1417459.
Iqbal N, Meghani M, Khalid W, Ansari A, Ansari M, Ansari S
Ann Hematol. 2024; 103(8):3243-3246.
PMID: 38976007
DOI: 10.1007/s00277-024-05878-7.
Gallego-Martin T, Prieto-Lloret J, Aaronson P, Rocher A, Obeso A
Antioxidants (Basel). 2019; 8(3).
PMID: 30871199
PMC: 6466535.
DOI: 10.3390/antiox8030062.
Unal S, Karahan F, Arikoglu T, Akar A, Kuyucu S
Turk J Haematol. 2018; 36(1):37-42.
PMID: 30185401
PMC: 6373502.
DOI: 10.4274/tjh.galenos.2018.2018.0230.
Siddiqua T, Ahmad S, Ahsan K, Rashid M, Roy A, Rahman S
Eur J Nutr. 2015; 55(1):281-93.
PMID: 25648738
DOI: 10.1007/s00394-015-0845-x.
Inborn errors of metabolism underlying primary immunodeficiencies.
Parvaneh N, Quartier P, Rostami P, Casanova J, de Lonlay P
J Clin Immunol. 2014; 34(7):753-71.
PMID: 25081841
DOI: 10.1007/s10875-014-0076-6.
Update on transcobalamin deficiency: clinical presentation, treatment and outcome.
Trakadis Y, Alfares A, Bodamer O, Buyukavci M, Christodoulou J, Connor P
J Inherit Metab Dis. 2013; 37(3):461-73.
PMID: 24305960
DOI: 10.1007/s10545-013-9664-5.
Cellular uptake of cobalamin: transcobalamin and the TCblR/CD320 receptor.
Quadros E, Sequeira J
Biochimie. 2013; 95(5):1008-18.
PMID: 23415653
PMC: 3902480.
DOI: 10.1016/j.biochi.2013.02.004.
Transcobalamin II deficiency with methylmalonic aciduria in three sisters.
Bibi H, Gelman-Kohan Z, Baumgartner E, Rosenblatt D
J Inherit Metab Dis. 1999; 22(7):765-72.
PMID: 10518276
DOI: 10.1023/a:1005507204491.
Expression of transcobalamin II mRNA in human tissues and cultured fibroblasts from normal and transcobalamin II-deficient patients.
Li N, Seetharam S, Rosenblatt D, Seetharam B
Biochem J. 1994; 301 ( Pt 2):585-90.
PMID: 7913804
PMC: 1137121.
DOI: 10.1042/bj3010585.
Congenital disorders of vitamin B12 transport and their contributions to concepts. II.
Hall C
Yale J Biol Med. 1981; 54(6):485-95.
PMID: 7342493
PMC: 2596040.
Congenital B12-malabsorption without proteinuria.
Urban C, Mutz I, Kaulfersch W
Blut. 1981; 43(2):71-5.
PMID: 7260408
DOI: 10.1007/BF00320462.
Standardization of nomenclature for transcobalamin II variants.
Frater-Schroder M, Porck H, Eriksson A, Daiger S, Cavalli-Sforza L
Hum Genet. 1982; 61(2):165-6.
PMID: 7129444
DOI: 10.1007/BF00274211.
Neurological involvement in hereditary transcobalamin II deficiency.
Thomas P, Hoffbrand A, SMITH I
J Neurol Neurosurg Psychiatry. 1982; 45(1):74-7.
PMID: 7062075
PMC: 491269.
DOI: 10.1136/jnnp.45.1.74.
Cobalamin deficiency and related disorders in infancy and childhood.
Matthews D, Linnell J
Eur J Pediatr. 1982; 138(1):6-16.
PMID: 7042350
DOI: 10.1007/BF00442320.
Diseases associated with immunosuppression.
HEISE E
Environ Health Perspect. 1982; 43:9-19.
PMID: 7037390
PMC: 1568899.
DOI: 10.1289/ehp.82439.
Impaired immunity: a view of current stigmata and disease evaluation.
LITWIN S
Bull N Y Acad Med. 1981; 57(7):617-30.
PMID: 6944136
PMC: 1805266.
Inheritance and genetic linkage of transcobalamin II.
Yang S, Coleman P, Ochs H, DuPont B
Hum Genet. 1981; 57(3):307-11.
PMID: 6941922
DOI: 10.1007/BF00278950.
Defective adenosylcobalamin synthesis in a case of transcobalamin II deficiency.
Linnell J, Quadros E, Elliott P, Malleson P
J Inherit Metab Dis. 1980; 3(3):95-6.
PMID: 6775148
DOI: 10.1007/BF02312538.
Granulocyte dysfunction in transcobalamin II deficiency responding to leucovorin or hydroxocobalamin-plasma transfusion.
Seger R, Frater-Schroder M, HITZIG W, Wildfeuer A, Linnell J
J Inherit Metab Dis. 1980; 3(1):3-9.
PMID: 6774168
DOI: 10.1007/BF02312515.
