V. Jogessar

发表

PRIMARY CAUSE OF MEGALOBLASTIC ANAEMIA IN ZIMBABWE

V. Naicker, Z. Chapanduka, Z. Chapanduka, 1994, British journal of haematology.

Nutritional status and dietary intakes of children aged 2-5 years and their caregivers in a rural South African community.

A. Benadé, M. Faber, V. Jogessar, 2001, International journal of food sciences and nutrition.

The effect of different anthelmintic treatment regimens combined with iron supplementation on the nutritional status of schoolchildren in KwaZulu-Natal, South Africa: a randomized controlled trial.

I Kleinschmidt, I. Kleinschmidt, I. Couper, 2001, Transactions of the Royal Society of Tropical Medicine and Hygiene.

Recommendations for the management of adult chronic myeloid leukaemia in South Africa.

P. Ruff, L. Dreosti, V. Louw, 2011, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Neutropenic enterocolitis com- plicating acute lymphoblastic leukaemia

S. Misser, P. Corr, V. Jogessar, 2005 .

βs Haplotypes in various world populations

A. Dimovski, N. Olivieri, D. Loukopoulos, 1992, Human Genetics.

Refractory Castleman's Disease.

P. Jacobs, L. Wood, V. Jogessar, 1998, Hematology.

Estimation and predictive use of the corrected count increment--a proposed clinical guideline.

P. Jacobs, L. Wood, V. Jogessar, 2005, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Distribution of beta-thalassemia mutations in three Asian Indian populations with distant geographical locations.

T. Huisman, S. Wong, E. Baysal, 1994, Hemoglobin.

Guidelines for the treatment of myelodysplastic syndromes (MDS) in South Africa.

P. Ruff, J. Mahlangu, E. Verburgh, 2011, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Combinations of three different forms of alpha-thalassemia in a large Indian family from Durban, South Africa: hematological observations.

Y. Fei, T. Huisman, J. C. Liu, 1992, Acta haematologica.

Hb natal or α2(minus Tyr-Arg)β2: a high oxygen affinity α chain variant with a deleted carboxy-terminus resulting from a TAC → TAA (Tyr→ terminating codon) mutation in codon α140

A. Kutlar, T. Huisman, J. B. Wilson, 1988 .

Long-term evaluation of a micronutrient-fortified biscuit used for addressing micronutrient deficiencies in primary school children

M. Dhansay, C. Lombard, M. V. van Stuijvenberg, 2001, Public Health Nutrition.

Membranous fat necrosis due to subcutaneous elemental mercury injections.

P. Ramdial, V. Jogessar, M. Dada, 1999, The American journal of forensic medicine and pathology.

Thrombocytosis associated with tuberculous peritonitis.

M. C. Kamdar, V. Jogessar, M. A. Omar, 1983, Tubercle.

Pancytopaenia associated with disseminated tuberculosis, reactive histiocytic haemophagocytic syndrome and tuberculous hypersplenism.

V. Gathiram, V. Jogessar, K. Cassim, 1993, Tubercle and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease.

Refractory Castleman's Disease.

P. Jacobs, V. Jogessar, L. Wood, 1998, Hematology.