-
1
-
-
33745146118
-
Acquired and inherited disorders of cobalamin and folate in children
-
Whitehead VM. Acquired and inherited disorders of cobalamin and folate in children. Br J Haematol. 2006;134:125-136.
-
(2006)
Br J Haematol.
, vol.134
, pp. 125-136
-
-
Whitehead, V.M.1
-
2
-
-
58549094505
-
Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF
-
Ament AE, Li Z, Sturm AC, et al. Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF. Br J Haematol. 2009;144:622-624.
-
(2009)
Br J Haematol.
, vol.144
, pp. 622-624
-
-
Ament, A.E.1
Li, Z.2
Sturm, A.C.3
-
3
-
-
0033051889
-
Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1
-
Aminoff M, Carter JE, Chadwick RB, et al. Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1. Nat Genet. 1999;21:309-313.
-
(1999)
Nat Genet.
, vol.21
, pp. 309-313
-
-
Aminoff, M.1
Carter, J.E.2
Chadwick, R.B.3
-
4
-
-
0037371866
-
Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia
-
Tanner SM, Aminoff M, Wright FA, et al. Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia. Nat Genet. 2003;33:426-429.
-
(2003)
Nat Genet.
, vol.33
, pp. 426-429
-
-
Tanner, S.M.1
Aminoff, M.2
Wright, F.A.3
-
5
-
-
1442357042
-
The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless
-
Fyfe JC, Madsen M, Hojrup P, et al. The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless. Blood. 2004;103:1573-1579.
-
(2004)
Blood.
, vol.103
, pp. 1573-1579
-
-
Fyfe, J.C.1
Madsen, M.2
Hojrup, P.3
-
6
-
-
20144372885
-
Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene
-
Tanner SM, Li Z, Perko JD, et al. Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene. Proc Natl Acad Sci USA. 2005;102:4130-4133.
-
(2005)
Proc Natl Acad Sci USA.
, vol.102
, pp. 4130-4133
-
-
Tanner, S.M.1
Li, Z.2
Perko, J.D.3
-
7
-
-
0003415792
-
-
AC A. In:Hoffman R BE, Shattil SJ,Furie B, Cohen HJeds. 3rd ed. Philadelphia: Churchill Livingstone
-
AC A. In: Hoffman R BE, Shattil SJ,Furie B, Cohen HJeds. Hematology Basic Principles and Practice. 3rd ed. Philadelphia: Churchill Livingstone; 2000: 446-485.
-
(2000)
Hematology Basic Principles and Practice
, pp. 446-485
-
-
-
8
-
-
73349114634
-
Gastrointestinal abnormalities in vitamin B12 deficient patients with megaloblastic anemia
-
Iqbal SP, Kakepoto GN. Gastrointestinal abnormalities in vitamin B12 deficient patients with megaloblastic anemia. J Coll Physicians Surg Pak. 2009;19:672-673.
-
(2009)
J Coll Physicians Surg Pak.
, vol.19
, pp. 672-673
-
-
Iqbal, S.P.1
Kakepoto, G.N.2
-
9
-
-
0036373131
-
Gastric emptying in patients with vitamin B(12) deficiency
-
Yagci M, Yamac K, Acar K, et al. Gastric emptying in patients with vitamin B(12) deficiency. Eur J Nucl Med Mol Imaging. 2002;29:1125-1127.
-
(2002)
Eur J Nucl Med Mol Imaging.
, vol.29
, pp. 1125-1127
-
-
Yagci, M.1
Yamac, K.2
Acar, K.3
-
10
-
-
10944245290
-
A child with vitamin B12 deficiency presenting with pancytopenia and hyperpigmentation
-
Simsek OP, Gonc N, Gumruk F, et al. A child with vitamin B12 deficiency presenting with pancytopenia and hyperpigmentation. J Pediatr Hematol Oncol. 2004;26:834-836.
-
(2004)
J Pediatr Hematol Oncol.
, vol.26
, pp. 834-836
-
-
Simsek, O.P.1
Gonc, N.2
Gumruk, F.3
-
11
-
-
0018743659
-
Persistence of neutrophil hypersegmentation during recovery from megaloblastic granulopoiesis
-
Nath BJ, Lindenbaum J. Persistence of neutrophil hypersegmentation during recovery from megaloblastic granulopoiesis. Ann Intern Med. 1979;90:757-760.
-
(1979)
Ann Intern Med.
, vol.90
, pp. 757-760
-
-
Nath, B.J.1
Lindenbaum, J.2
-
13
-
-
42349087870
-
Cutaneous lesions and vitamin B12 deficiency: An often-forgotten link
-
Kannan R, Ng MJ. Cutaneous lesions and vitamin B12 deficiency: An often-forgotten link. Can Fam Physician. 2008;54:529-532.
-
(2008)
Can Fam Physician.
, vol.54
, pp. 529-532
-
-
Kannan, R.1
Ng, M.J.2
-
14
-
-
0034973519
-
Generalized hyperpigmentation of the skin due to vitamin B12 deficiency
-
Mori K, Ando I, Kukita A. Generalized hyperpigmentation of the skin due to vitamin B12 deficiency. J Dermatol. 2001;28:282-285.
-
(2001)
J Dermatol.
, vol.28
, pp. 282-285
-
-
Mori, K.1
Ando, I.2
Kukita, A.3
-
15
-
-
34248165629
-
Imerslund-Grasbeck syndrome (selective vitamin B12 malabsorption with proteinuria
-
Grasbeck R. Imerslund-Grasbeck syndrome (selective vitamin B12 malabsorption with proteinuria). Orphanet J Rare Dis. 2006;1:17.
-
(2006)
Orphanet J Rare Dis.
, vol.1
, pp. 17
-
-
Grasbeck, R.1
-
16
-
-
79951581043
-
B12 deficient megaloblastic anemia in a toddler with a history of gastroschisis
-
Marsch AF, Shashidhar H, D'Orazio JA. B12 deficient megaloblastic anemia in a toddler with a history of gastroschisis. J Pediatr. 2011;158:512.
-
(2011)
J Pediatr.
, vol.158
, pp. 512
-
-
Marsch, A.F.1
Shashidhar, H.2
D'Orazio, J.A.3
-
17
-
-
0037370287
-
Improved outcomes in the treatment of gastroschisis using a preformed silo and delayed repair approach
-
discussion 459-464
-
SchlatterM, Norris K, Uitvlugt N, et al. Improved outcomes in the treatment of gastroschisis using a preformed silo and delayed repair approach. J Pediatr Surg. 2003;38:459-464; discussion 459-464.
-
(2003)
J Pediatr Surg.
, vol.38
, pp. 459-464
-
-
Schlatter, M.1
Norris, K.2
Uitvlugt, N.3
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