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1.

Haemoglobin D in Jamaica

Milner, Paul F. A.

West Indian med. j ; 12(2): 141, June 1963.

Article in English | MedCarib | ID: med-7449

2.

Oxygen transport in sickle cell anemia

Milner, Paul F. A.

Arch Intern Med ; 133(4): 565-72, 1974.

Article in English | MedCarib | ID: med-8175

3.

High incidence of haemoglobin G[Accra] in a rural district in Jamaica

Milner, Paul F. A.

J Med Genet ; 4(2): 88-90, June 1967.

Article in English | MedCarib | ID: med-9922

4.

Modern laboratory methods in clinical haematology: the assay of serum vitamin B12

Milner, Paul F. A.

West Indian med. j ; 14(4): 230-40, Dec. 1965.

Article in English | MedCarib | ID: med-10702

5.

Glucose-6-phosphate dehydrogenase deficiency and methaemoglobin reduction in sickle cell anaemia - abstract only

Milner, Paul F. A; Seakins, Michael.

West Indian med. j ; 17(4): 248, Dec. 1968.

Article in English | MedCarib | ID: med-7599

6.

Urinary figlu and serum B12 levels in patients with anemia

Henry, Mervyn U; Milner, Paul F. A.

West Indian med. j ; 13(2): 139, Mar. 1964.

Article in English | MedCarib | ID: med-7414

7.

Hereditary hypochromic anaemia with iron loading

Irvine, Ronald A; Milner, Paul F. A.

West Indian med. j ; 13(2): 138, Mar. 1964.

Article in English | MedCarib | ID: med-7416

8.

Alpha thalassaemia phenotypes

Ahern, Edgar J; Milner, Paul F. A.

West Indian med. j ; 17(4): 250, Dec. 1968.

Article in English | MedCarib | ID: med-7550

9.

Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemia

Bertles, John F; Milner, Paul F. A.

J Clin Invest ; 47(8): 1731-41, Aug. 1968.

Article in English | MedCarib | ID: med-12189

10.

The management of leg ulcers in sickle cell anaemia

Walshe, Margaret M; Milner, Paul F. A.

West Indian med. j ; 16(1): 10-6, Mar. 1967.

Article in English | MedCarib | ID: med-10837

11.

Neonatal jaundice in Jamaican children

Miller, Colin G; Milner, Paul F. A; Sue, S. L.

West Indian med. j ; 12(2): 142, June 1963.

Article in English | MedCarib | ID: med-7448

12.

Haemoglobin concentration, eosinophilia and intestinal helminths in children in rural Jamaica

Ashcroft, Michael T; Milner, Paul F. A; Wood, C. W.

Trans R Soc Trop Med Hyg ; 63(6): 811-20, 1969.

Article in English | MedCarib | ID: med-14574

13.

The irreversibly sickled cell: a determinant of haemolysis in sickle cell anaemia

Serjeant, Graham R; Serjeant, Beryl E; Milner, Paul F. A.

Br J Haematol ; 17(6): 527-33, 1969.

Article in English | MedCarib | ID: med-14747

14.

Pregnancy and homozygous haemoglobin C disease

Anderson, Mavis F; Bluestone, Rodney; Milner, Paul F. A.

J Obstet Gynaecol Br Commonw ; 74(5): 694-6, Oct. 1967.

Article in English | MedCarib | ID: med-15699

15.

A comparison between the characteristics of Jamaican adults with normal hemoglobin and those with sickle cell trait

Ashcroft, Michael T; Miall, William E; Milner, Paul F. A.

Am J Epidemiol ; 90(3): 236-43, Sept. 1969.

Article in English | MedCarib | ID: med-12452

16.

Haematological levels in Jamaican infants

Grantham McGregor, Sally M; Desai, Patricia; Milner, Paul F. A.

Arch Dis Child ; 49(7): 525-30, July 1974.

Article in English | MedCarib | ID: med-13051

17.

The metabolism of iron-dextran given as a total-dose infusion to iron deficient Jamaican subjects

Wood, J. K; Milner, Paul F. A; Pathak, Upendra N.

Br J Haematol ; 14(2): 119-29, Feb. 1968.

Article in English | MedCarib | ID: med-13075

18.

Haemoglobin H disease caused by alpha-thalassaemia and a new abnormal haemoglobin with an elongated alpha-chain (Hb constant spring) - abstract

Milner, Paul F. A; Weatherall, David J; Clegg, John B.

West Indian med. j ; 20(4): 266, Dec. 1971.

Article in English | MedCarib | ID: med-6324

19.

Absorption of dietary iron and ferrous ascorbate by infants - abstract

Ashworth, Ann; Milner, Paul F. A; Waterlow, John C.

West Indian med. j ; 18(2): 123, June 1969.

Article in English | MedCarib | ID: med-6419

20.

Haemoglobin-H disease due to a unique haemoglobin variant with an elongated O-chain

Milner, Paul F. A; Clegg, John B; Weatherall, David J.

Lancet ; 1(7702): 729-32, Apr. 10, 1971.

Article in English | MedCarib | ID: med-867

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Haemoglobin D in Jamaica

Oxygen transport in sickle cell anemia

High incidence of haemoglobin G[Accra] in a rural district in Jamaica

Modern laboratory methods in clinical haematology: the assay of serum vitamin B12

Glucose-6-phosphate dehydrogenase deficiency and methaemoglobin reduction in sickle cell anaemia - abstract only

Urinary figlu and serum B12 levels in patients with anemia

Hereditary hypochromic anaemia with iron loading

Alpha thalassaemia phenotypes

Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemia

The management of leg ulcers in sickle cell anaemia

Neonatal jaundice in Jamaican children

Haemoglobin concentration, eosinophilia and intestinal helminths in children in rural Jamaica

The irreversibly sickled cell: a determinant of haemolysis in sickle cell anaemia

Pregnancy and homozygous haemoglobin C disease

A comparison between the characteristics of Jamaican adults with normal hemoglobin and those with sickle cell trait

Haematological levels in Jamaican infants

The metabolism of iron-dextran given as a total-dose infusion to iron deficient Jamaican subjects

Haemoglobin H disease caused by alpha-thalassaemia and a new abnormal haemoglobin with an elongated alpha-chain (Hb constant spring) - abstract

Absorption of dietary iron and ferrous ascorbate by infants - abstract

Haemoglobin-H disease due to a unique haemoglobin variant with an elongated O-chain