Imperial College London

ProfessorKathMaitland

Faculty of MedicineDepartment of Surgery & Cancer

Professor of Tropical Paediatric Infectious Disease
 
 
 
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Contact

 

k.maitland CV

 
 
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Location

 

Based full-time at KEMRI/Wellcome Programme, KenyaQueen Elizabeth and Queen Mary HospitalSt Mary's Campus

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Summary

 

Publications

Publication Type
Year
to

258 results found

Schapira A, 1998, More on malaria transmissibility, PARASITOLOGY TODAY, Vol: 14, Pages: 293-293, ISSN: 0169-4758

Journal article

Maitland K, Williams TN, 1998, Malaria mortality: The Pacific enigma, PARASITOLOGY TODAY, Vol: 14, Pages: 258-259, ISSN: 0169-4758

Journal article

Williams TN, Maitland K, Martin PMV, Weatherall DJ, Clegg JBet al., 1998, Splenic size in homozygous α<SUP>+</SUP> thalassaemia, BRITISH JOURNAL OF HAEMATOLOGY, Vol: 100, Pages: 611-612, ISSN: 0007-1048

Journal article

Barnardo MCNM, Welsh KI, Vilches C, Maitland K, Bunce Met al., 1998, Allele-specific HLA-B(*)15 typing by PCR-SSP and its application to four distinct ethnic populations, Tissue Antigens, Vol: 51, Pages: 293-300, ISSN: 0001-2815

We present a set of primer mixes for the allele-specific typing of the HLA-B(*)15 group by PCR-SSP. The set comprises 46 primer mixes which are designed to unequivocally resolve all but two of the 666 possible combinations of the B(*)15 alleles, B(*)1501-37 (B(*)1536 sequence unavailable). A core subset of 34 of the 46 mixes can be used alone to give a high resolution B(*)15 typing set. This allows for the identification of each B(*)15 allele when present as the only B(*)15 allele and the majority of the possible B(*)15 homozygotic combinations. The method was validated using reference DNA samples and the B(*)15 allele frequency in 4 distinct ethnic populations was investigated. The results show that these populations contain predominantly mutually exclusive sets of B(*)15 alleles.

Journal article

Rees DJ, 1998, Alpha thalassaemia is associated with increased soluble transferrin receptor levels, British Journal of Haematology, Vol: 103, Pages: 365-369

Journal article

Maitland K, Williams TN, Kotecka BM, Edstein MD, Rieckmann KHet al., 1997, Plasma chloroquine concentrations in young and older malaria patients treated with chloroquine, ACTA TROPICA, Vol: 66, Pages: 155-161, ISSN: 0001-706X

Journal article

Maitland K, Williams TN, Peto TEA, Day KP, Clegg JB, Weatherall DJ, Bowden DKet al., 1997, Absence of malaria-specific mortality in children in an area of hyperendemic malaria, TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, Vol: 91, Pages: 562-566, ISSN: 0035-9203

Journal article

Williams TN, Maitland K, Phelps L, Bennett S, Peto TE, Viji J, Timothy R, Clegg JB, Weatherall DJ, Bowden DKet al., 1997, Plasmodium vivax: a cause of malnutrition in young children, QJM, Vol: 90, Pages: 751-757, ISSN: 1460-2725

We studied the aetiology of malnutrition in a cohort of 1511 children < 10 years old in Espiritu Santo, Vanuatu. Malnutrition was categorized using standard anthropometric criteria as: underweight [weight-for-age (WA) Z score < -2], wasting [weight-for-height (WH) Z < -2], or stunting [height-for-age (HA) Z < -2]. On multiple logistic regression analysis, the only factors significantly associated with wasting were age < 5 years [OR (95% CI) 1.8 (1.2-2.9), p = 0.01] and having suffered one or more episodes of clinical P. vivax malaria in the 6 months preceding nutritional assessment [OR 2.4 (1.3-4.4), p = 0.006]. The incidence of P. vivax infection was significantly higher during the 6 months preceding assessment in underweight vs. non-underweight children [incidence rate ratio (IRR) 2.6 (1.5-4.4), p < or = 0.0001). These groups had similar incidences of clinical P. falciparum infection during the same period [IRR 1.1 (0.57-2.1) p = 0.8] and of either species during the 6 months following assessment [IRR P. vivax 1.3 (0.9-2.0) p = 0.2; IRR P. falciparum 1.3 (0.9-1.9) p = 0.2]. In these children, P. vivax malaria was a major predictor of acute malnutrition; P. falciparum was not. Wasting neither predisposed to nor protected against malaria of either species. Although P. vivax malaria is generally regarded as benign, it may produce considerable global mortality through malnutrition.

Journal article

Bryan JH, Burwell C, Maitland K, Williams Tet al., 1996, Culicine mosquitoes (Diptera: Culicidae) attracted to humans on Espiritu Santo, Vanuatu, MEDICAL AND VETERINARY ENTOMOLOGY, Vol: 10, Pages: 101-102, ISSN: 0269-283X

Journal article

Williams DK, 1996, Red blood cell phenotypes in the α + thalassaemias from early childhood to maturity, British Journal of Haematology, Vol: 95, Pages: 266-272

Journal article

Williams JB, 1996, High incidence of malaria in α-thalassaemic children, Nature, Vol: 383, Pages: 522-525

Journal article

Maitland K, Williams TN, Bennett S, Newbold CI, Peto TE, Viji J, Timothy R, Clegg JB, Weatherall DJ, Bowden DKet al., 1996, The interaction between Plasmodium falciparum and P. vivax in children on Espiritu Santo island, Vanuatu, Trans R Soc Trop Med Hyg, Vol: 90, Pages: 614-620, ISSN: 0035-9203

Studies of the prevalence and incidence of malaria were conducted in children < 10 years old living in 10 rural villages on the island of Espiritu Santo, Vanuatu, south-west Pacific. Malaria prevalence remained stable at 30% throughout the year but the relative contributions of the 2 major species were highly dependent on season. Plasmodium falciparum predominated in the long wet season (November-May) and P. vivax in the dry season (June-October). Case definitions for malaria, derived using a multiple logistic regression method, showed that parasite densities associated with clinical disease were low; case definitions for P. falciparum (> 1000 parasites/microL in children > 1 year old and > 500 microL in infants) and P. vivax (> 500 parasites/microL at all ages) were both associated with a specificity and sensitivity of > 90%. Like prevalence data, malaria morbidity was highly seasonal; 80% of clinical P. falciparum infections occurred in the wet season and 66% of clinical P. vivax in the dry season. Mixed infections were rare. Malaria was important cause of morbidity with children < 5 years old experiencing 1.3-3.0 episodes of clinical malaria per year and 23% of fevers being attributable to malaria in this age group. Children aged 5-9 years continued to suffer one episode of clinical malaria per year. The peak incidence of P. vivax malaria occurred earlier in life than the peak incidence of P. falciparum malaria. The possible interactions between these 2 parasite species are discussed.

Journal article

BRINDLE PM, MAITLAND K, WILLIAMS TN, GANCZAKOWSKI MEet al., 1995, A SURVEY FOR THE RARE BLOOD-GROUP ANTIGEN VARIANTS, EN(A-), GERBICH NEGATIVE AND DUFFY NEGATIVE ON ESPIRITU-SANTO, VANUATU IN THE SOUTH-PACIFIC, HUMAN HEREDITY, Vol: 45, Pages: 211-214, ISSN: 0001-5652

Journal article

Williams DH, 1995, Malaria sporozoite rates for Anopheles farauti s.s. Laveran (Diptera: Culicidae) from Vanuatu, Annals of Tropical Medicine and Parasitology, Vol: 89, Pages: 305-307

Journal article

Ganczakowski DJ, 1995, Thalassaemia in Vanuatu, South-West Pacific: Frequency and haematological phenotypes of young children, British Journal of Haematology, Vol: 89, Pages: 485-495

Journal article

Maitland K, How Do We Treat Children with Severe Malaria?, Advances in Experimental Medicine and Biology, Publisher: Springer US, Pages: 9-21, ISBN: 9780387317830

Book chapter

Maitland K, Wills B, Tropical infections: malaria and dengue, Infectious Diseases in the Pediatric Intensive Care Unit, Editors: Nadel, Giroir P, London, Publisher: Springer-Verlag

Book chapter

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