Concurrent uveoretinitis and pineocytoma in a child suggests a causal relationshipILLUM, N; KORF, H. W; JULIAN, K et al.British journal of ophthalmology. 1992, Vol 76, Num 9, pp 574-576, issn 0007-1161Article

Congenital dyserythropoietic anaemia with novel intra-erythroblastic and intra-erythrocytic inclusionsWICKRAMASINGHE, S. N; ILLUM, N; WIMBERLEY, P. D et al.British journal of haematology. 1991, Vol 79, Num 2, pp 322-330, issn 0007-1048Article

Lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous systemILLUM, N; RESKE-NIELSEN, E; SKOUBY, F et al.Neuropediatrics. 1988, Vol 19, Num 4, pp 186-192, issn 0174-304XArticle

Eponymous jacobsen syndrome : Mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in down syndrome. Author's replyTÜMER, Z; HENRIKSEN, A. M; BACHE, I et al.American journal of medical genetics. 2005, Vol 135A, Num 3, pp 339-341, issn 0148-7299, 3 p.Article

Recurrent nodular haemangiomas in Klippel-Trénaunay syndromeILLUM, N; NIELSEN, H. W; SKOV, B. G et al.Acta paediatrica (Oslo). 1992, Vol 81, Num 5, pp 456-458, issn 0803-5253Article

Phenotypical and functional characterization of double-negative (CD4^-CD8^-) αβ T-cell receptor positive cells from an immunodeficient patientILLUM, N; RALFKIAER, E; PALLESEN, G et al.Scandinavian journal of immunology (Print). 1991, Vol 34, Num 5, pp 635-645, issn 0300-9475Article

Primary hyperoxaluria type 1 : clinical manifestations in infancy and prenatal diagnosisILLUM, N; LAVARD, L; DANPURE, C. J et al.Child nephrology and urology. 1992, Vol 12, Num 4, pp 225-227, issn 1012-6694Article

Intravenous immunoglobulin : a single-blind trial in children with Lennox-Gastaut syndromeILLUM, N; TAUDORF, K; HEILMAN, C et al.Neuropediatrics. 1990, Vol 21, Num 2, pp 87-90, issn 0174-304X, 4 p.Article

Ulcerated haemangioma successfully treated with interferon alfa-2b and topical granulocyte-macrophage colony-stimulating factorILLUM, N; KARLSMARK, T; SVEJGAARD, E et al.Dermatology (Basel). 1995, Vol 191, Num 4, pp 315-317, issn 1018-8665Article

A novel form of congeintal dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)]PARSONS, S. F; JONES, J; ANSTEE, D. J et al.Blood. 1994, Vol 83, Num 3, pp 860-868, issn 0006-4971Article

Expression of embryonic ζ-globin and ε-globin chains in a 10-year-old girl with congenital anemiaWOZHAN TANG; SHI-PING CAI; ENG, B et al.Blood. 1993, Vol 81, Num 6, pp 1636-1640, issn 0006-4971Article

Eosinophilic cellulitis: five casesLINDSKOV, R; ILLUM, N; WEISMANN, K et al.Acta dermato-venereologica. 1988, Vol 68, Num 4, pp 325-330, issn 0001-5555Article