-
1
-
-
84928862267
-
Peculiar elongated and sickle-shaped red corpuscles in a case of severe anemia
-
Herrick JB. Peculiar elongated and sickle-shaped red corpuscles in a case of severe anemia. Arch Int Med 1910;6:517.
-
(1910)
Arch Int Med
, vol.6
, pp. 517
-
-
Herrick, J.B.1
-
2
-
-
84941816813
-
A study of the erythrocytes in a case of severe anemia with elongated and sickle-shaped red blood corpuscules
-
Emmel VE. A study of the erythrocytes in a case of severe anemia with elongated and sickle-shaped red blood corpuscules. Arch Int Med 1917;20:586.
-
(1917)
Arch Int Med
, vol.20
, pp. 586
-
-
Emmel, V.E.1
-
3
-
-
57749098208
-
Report of a case greatly improved by splenectomy; experimental study of sickle cell formation
-
Hahn EV, Gillespie EB. Report of a case greatly improved by splenectomy; experimental study of sickle cell formation. Arch Int Med 1927;39:233.
-
(1927)
Arch Int Med
, vol.39
, pp. 233
-
-
Hahn, E.V.1
Gillespie, E.B.2
-
4
-
-
0000192487
-
The inheritance of sickle cell anemia in man
-
Neel JV. The inheritance of sickle cell anemia in man. Science 1949;110:64.
-
(1949)
Science
, vol.110
, pp. 64
-
-
Neel, J.V.1
-
5
-
-
0001612986
-
The genetics of sickle-cell trait in a Bantu tribe
-
Lond
-
Beet EA. The genetics of sickle-cell trait in a Bantu tribe. Ann Eugen (Lond) 1949;14:279.
-
(1949)
Ann Eugen
, vol.14
, pp. 279
-
-
Beet, E.A.1
-
6
-
-
0000192486
-
Sickle cell anemia, a molecular disease
-
Pauling L, Itano HA, Singer SJ, Wells IC. Sickle cell anemia, a molecular disease. Science 1949;110:543.
-
(1949)
Science
, vol.110
, pp. 543
-
-
Pauling, L.1
Itano, H.A.2
Singer, S.J.3
Wells, I.C.4
-
7
-
-
1842337282
-
Gene mutations in human haemoglobin: The chemical difference between normal and sickle cell haemoglobin
-
Ingram VM. Gene mutations in human haemoglobin: the chemical difference between normal and sickle cell haemoglobin. Nature 1957;180:326.
-
(1957)
Nature
, vol.180
, pp. 326
-
-
Ingram, V.M.1
-
8
-
-
0002341637
-
A series of cases of splenomegaly in children with anemia and peculiar bone changes
-
Cooley TB, Lee PA. A series of cases of splenomegaly in children with anemia and peculiar bone changes. Trans Am Pediatr Soc 1925;37:29.
-
(1925)
Trans Am Pediatr Soc
, vol.37
, pp. 29
-
-
Cooley, T.B.1
Lee, P.A.2
-
9
-
-
0042076791
-
Racial or familial anemia of children associated with fundamental disturbances of bone and pigment metabolism
-
Whipple GH, Bradford WL. Racial or familial anemia of children associated with fundamental disturbances of bone and pigment metabolism. Am J Dis Child 1932;44:336.
-
(1932)
Am J Dis Child
, vol.44
, pp. 336
-
-
Whipple, G.H.1
Bradford, W.L.2
-
10
-
-
0035676917
-
Towards molecular medicine; reminiscences of the haemoglobin field, 1960-2000
-
Weatherall DJ. Towards molecular medicine; reminiscences of the haemoglobin field, 1960-2000. Br J Haematol 2001;115:729-38.
-
(2001)
Br J Haematol
, vol.115
, pp. 729-738
-
-
Weatherall, D.J.1
-
11
-
-
0036780907
-
Evolutionary and historical aspects of the burden of malaria
-
Carter R, Mendis KN. Evolutionary and historical aspects of the burden of malaria. Clin Microbiol Rev 2002;15:564-94.
-
(2002)
Clin Microbiol Rev
, vol.15
, pp. 564-594
-
-
Carter, R.1
Mendis, K.N.2
-
12
-
-
0000197885
-
The hemolytic effect of primaquine and related compounds: A review
-
Beutler E. The hemolytic effect of primaquine and related compounds: a review. Blood 1959;14:103-39.
-
(1959)
Blood
, vol.14
, pp. 103-139
-
-
Beutler, E.1
-
14
-
-
1342330465
-
Biomedical conflicts of interest: A defence of the sequestration thesis-learning from the cases of Nancy Olivieri and David Healy
-
Schafer A. Biomedical conflicts of interest: a defence of the sequestration thesis-learning from the cases of Nancy Olivieri and David Healy. J Med Ethics 2004;30:8-24.
-
(2004)
J Med Ethics
, vol.30
, pp. 8-24
-
-
Schafer, A.1
-
15
-
-
0031457203
-
A risk-benefit assessment of iron-chelation therapy
-
Porter JB. A risk-benefit assessment of iron-chelation therapy. Drug Saf 1997;17:407-21.
-
(1997)
Drug Saf
, vol.17
, pp. 407-421
-
-
Porter, J.B.1
-
16
-
-
0034889014
-
Inherited haemoglobin disorders: An increasing global health problem
-
Weatherall DJ, Clegg JB. Inherited haemoglobin disorders: an increasing global health problem. Bull World Health Organ 2001;79:704-12.
-
(2001)
Bull World Health Organ
, vol.79
, pp. 704-712
-
-
Weatherall, D.J.1
Clegg, J.B.2
-
17
-
-
0032547518
-
Thalassaemia in Britain: A tale of two communities. Births are rising among British Asians but falling in Cypriots
-
Gill PS, Modell B. Thalassaemia in Britain: a tale of two communities. Births are rising among British Asians but falling in Cypriots. Br Med J 1998;317(7161): 761-2.
-
(1998)
Br Med J
, vol.317
, Issue.7161
, pp. 761-762
-
-
Gill, P.S.1
Modell, B.2
-
19
-
-
0019231070
-
Geographic and ethnic distribution of human hemoglobin variants
-
Winter WP. Geographic and ethnic distribution of human hemoglobin variants. Tex Rep Biol Med 1980;40:179-90.
-
(1980)
Tex Rep Biol Med
, vol.40
, pp. 179-190
-
-
Winter, W.P.1
-
22
-
-
33846958616
-
Phenotypic presentation and underlying mutations in carriers of β-thalassaemia and α-thalassaemia in the Danish immigrant population
-
Manuscript
-
Kornbilt B, Hagve TA, Taaning P, Birgens H. Phenotypic presentation and underlying mutations in carriers of β-thalassaemia and α-thalassaemia in the Danish immigrant population. Manuscript. 2006.
-
(2006)
-
-
Kornbilt, B.1
Hagve, T.A.2
Taaning, P.3
Birgens, H.4
|