Pseudotumoral cerebellitis with acute hydrocephalus as a manifestation of EBV infection
Geurten, C., De Bilderling, G., Nassogne, M.-C., Misson, J.-P., Verghote, M.
Published in Revue neurologique (01.01.2018)
Published in Revue neurologique (01.01.2018)
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Dystonia 12: A rare and difficult diagnosis
Leroy, P, Meyer, F, Vaessen, S, Doummar, D, Misson, J-P
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.07.2017)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.07.2017)
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Diastematomyelia: pre- and postnatal multimodal diagnostic approach
Passoglou, V, Tebache, M, Collignon, L, Weerts, E, Misson, J P, Rausin, L
Published in JBR-BTR : organe de la Societe royale belge de radiologie (SRBR) = orgaan van de Koninklijke Belgische Vereniging voor Radiologie (KBVR) (01.11.2011)
Published in JBR-BTR : organe de la Societe royale belge de radiologie (SRBR) = orgaan van de Koninklijke Belgische Vereniging voor Radiologie (KBVR) (01.11.2011)
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Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samples
Van Coster, R. N., Janssens, S., Misson, J.-P., Verloes, A., Leroy, J. G.
Published in Prenatal diagnosis (01.10.1998)
Published in Prenatal diagnosis (01.10.1998)
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Infantile and juvenile presentations of Alexander's disease: a report of two cases
Deprez, M., D'Hooge, M., Misson, J. P., de Leval, L., Ceuterick, C., Reznik, M., Martin, J. J.
Published in Acta neurologica Scandinavica (01.03.1999)
Published in Acta neurologica Scandinavica (01.03.1999)
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Bony syngnathia, vertebral segmentation defect, coloboma, microcephaly and mental retardation: confirmation of Dobrow syndrome and review of syndromal syngnathias
Verloes, A, Raoul, M, Genevieve, D, Sznajer, Y, Demarche, M, Lombet, J, Rigo, V, Misson, J P, Collignon, L, Vanwijck, F, Vanwijck, R
Published in Clinical dysmorphology (01.10.2004)
Published in Clinical dysmorphology (01.10.2004)
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Identification of radial glial cells within the developing murine central nervous system: studies based upon a new immunohistochemical marker
Misson, J P, Edwards, M A, Yamamoto, M, Caviness, Jr, V S
Published in Brain research. Developmental brain research (01.11.1988)
Published in Brain research. Developmental brain research (01.11.1988)
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Multiple peroxisomal enzymatic deficiency disorders. A comparative biochemical and morphologic study of Zellweger cerebrohepatorenal syndrome and neonatal adrenoleukodystrophy
Vamecq, J, Draye, JP, Van Hoof, F, Misson, JP, Evrard, P, Verellen, G, Eyssen, HJ, Van Eldere, J, Schutgens, RB, Wanders, RJ
Published in The American journal of pathology (01.12.1986)
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Published in The American journal of pathology (01.12.1986)
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Heterogeneity of SPONASTRIME dysplasia: delineation of a variant form with severe mental retardation
Verloes, A, Misson, J P, Dubru, J M, Jamblin, P, Le Merrer, M
Published in Clinical dysmorphology (01.07.1995)
Published in Clinical dysmorphology (01.07.1995)
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A disorder of axonal development, necrotizing myopathy, cardiomyopathy, and cataracts: a new familial disease
Lyon, G, Arita, F, Le Galloudec, E, Vallée, L, Misson, J P, Ferrière, G
Published in Annals of neurology (01.02.1990)
Published in Annals of neurology (01.02.1990)
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Listeria monocytogenes sepsis. Fatal course in an immunocompetent child
Mortaji, S, Dacier, P, Mercken, B, Mulder, A, Misson, J P
Published in Revue médicale de Liège (01.07.2019)
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Published in Revue médicale de Liège (01.07.2019)
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