Reversible renal damage due to glue sniffing.

Por King, M D
Publicado em 1981

When not to do a lumbar puncture.

Por King, M D, Stephenson, J B
Publicado em 1988

Joubert's syndrome with retinal dysplasia: neonatal tachypnoea as the clue to a genetic brain-eye malformation.

Por King, M D, Dudgeon, J, Stephenson, J B
Publicado em 1984

Trichothiodystrophy-neurotrichocutaneous syndrome of Pollitt: a report of two unrelated cases.

Por King, M D, Gummer, C L, Stephenson, J B
Publicado em 1984

Carcinoid syndrome: an unusual cause of diarrhoea.

Por King, M D, Young, D G, Hann, I M, Patrick, W J
Publicado em 1985

Solvent encephalopathy.

Por King, M D, Day, R E, Oliver, J S, Lush, M, Watson, J M
Publicado em 1981

Photoaffinity labelling of the active site of the rat glutathione transferases 3-3 and 1-1 and human glutathione transferase A1-1.

Por Cooke, R J, Björnestedt, R, Douglas, K T, McKie, J H, King, M D, Coles, B, Ketterer, B, Mannervik, B
Publicado em 1994

Land Ice Freshwater Budget of the Arctic and North Atlantic Oceans: 1. Data, Methods, and Results

Por Bamber, J. L., Tedstone, A. J., King, M. D., Howat, I. M., Enderlin, E. M., van den Broeke, M. R., Noel, B.
Publicado no J Geophys Res Oceans (2018)

Molecular and Cellular Analysis of the DNA Repair Defect in a Patient in Xeroderma Pigmentosum Complementation Group D Who Has the Clinical Features of Xeroderma Pigmentosum and Co...

Por Broughton, B. C., Thompson, A. F., Harcourt, S. A., Vermeulen, W., Hoeijmakers, J. H. J., Botta, E., Stefanini, M., King, M. D., Weber, C. A., Cole, J., Arlett, C. F., Lehmann, A. R.
Publicado em 1995

PLA2G6-associated neurodegeneration (PLAN): Further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease

Por Illingworth, M.A., Meyer, E., Chong, W.K., Manzur, A.Y., Carr, L.J., Younis, R., Hardy, C., McDonald, F., Childs, A.M., Stewart, B., Warren, D., Kneen, R., King, M.D., Hayflick, S.J., Kurian, M.A.
Publicado em 2014

A second locus for Aicardi‐Goutières syndrome at chromosome 13q14–21

Por Ali, M, Highet, L J, Lacombe, D, Goizet, C, King, M D, Tacke, U, van der Knaap, M S, Lagae, L, Rittey, C, Brunner, H G, van Bokhoven, H, Hamel, B, Oade, Y A, Sanchis, A, Desguerre, I, Cau, D, Mathieu, N, Moutard, M L, Lebon, P, Kumar, D, Jackson, A P, Crow, Y J
Publicado em 2006