Enzyme Immunoassay (EIA)/Enzyme-Linked Immunosorbent Assay (ELISA) von Lequin, Rudolf M

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The long-term outcome of revision microdiscectomy for recurrent sciatica von Lequin, M. B., Verbaan, D., Schuurman, P. R., Tasche, Saskia, Peul, W. C., Vandertop, W. P., Bouma, G. J.

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The Mammillary Bodies: A Review of Causes of Injury in Infants and Children von Meys, K M E, de Vries, L S, Groenendaal, F, Vann, S D, Lequin, M H

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Progressive damage on high resolution computed tomography despite stable lung function in cystic fibrosis von de Jong, P.A, Nakano, Y, Lequin, M.H, Mayo, J.R, Woods, R, Pare, P.D, Tiddens, H.A.W.M

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Signal Change in the Mammillary Bodies after Perinatal Asphyxia von Molavi, M, Vann, S D, de Vries, L S, Groenendaal, F, Lequin, M

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Imaging Characteristics of CNS Neuroblastoma- FOXR2 : A Retrospective and Multi-Institutional Description of 25 Cases von Tietze, A, Mankad, K, Lequin, M H, Ivarsson, L, Mirsky, D, Jaju, A, Kool, M, Hoff, K V, Bison, B, Löbel, U

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A diffusion tensor imaging analysis of white matter microstructures in non-operated craniosynostosis patients von de Planque, C. A., Florisson, J. M. G., Tasker, R. C., Rijken, B. F. M., van Veelen, M. L. C., Mathijssen, I. M. J., Lequin, M. H., Dremmen, M. H. G.

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Optimal timing of cerebral MRI in preterm infants to predict long-term neurodevelopmental outcome: a systematic review von Plaisier, A, Govaert, P, Lequin, M H, Dudink, J

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Medullary Tegmental Cap Dysplasia: Fetal and Postnatal Presentations of a Unique Brainstem Malformation von Gafner, M, Garel, C, Leibovitz, Z, Valence, S, Krajden Haratz, K, Oegema, R, Mancini, G M S, Heron, D, Bueltmann, E, Burglen, L, Rodriguez, D, Huisman, T A G M, Lequin, M H, Arad, A, Kidron, D, Muqary, M, Gindes, L, Lev, D, Boltshauser, E, Lerman-Sagie, T

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Cognitive outcome of patients with classic infantile Pompe disease receiving enzyme therapy von EBBINK, B. J, AARSEN, F. K, GELDER, C. M. Van, DEN HOUT, J. M. P. Van, WEISGLAS-KUPERUS, N, JAEKEN, J, LEQUIN, M. H, ARTS, W. F. M, DER PLOEG, A. T. Van

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Long-term functional outcome in 167 patients with syndromic craniosynostosis; defining a syndrome-specific risk profile von de Jong, T, Bannink, N, Bredero-Boelhouwer, H.H, van Veelen, M.L.C, Bartels, M.C, Hoeve, L.J, Hoogeboom, A.J.M, Wolvius, E.B, Lequin, M.H, van der Meulen, J.J.N.M, van Adrichem, L.N.A, Vaandrager, J.M, Ongkosuwito, E.M, Joosten, K.F.M, Mathijssen, I.M.J

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Penser l’humain: définitions, descriptions, narrations

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SPORADIC COL4A1 MUTATIONS WITH EXTENSIVE PRENATAL PORENCEPHALY RESEMBLING HYDRANENCEPHALY von MEUWISSEN, M. E. C, DE VRIES, L. S, WESSELS, M. W, MANCINI, G. M. S, VERBEEK, H. A, LEQUIN, M. H, GOVAERT, P. P, SCHOT, R, COWAN, F. M, HENNEKAM, R, RIZZU, P, VERHEIJEN, F. W

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Introduction of Ultra-High-Field MR Imaging in Infants: Preparations and Feasibility von Annink, K V, van der Aa, N E, Dudink, J, Alderliesten, T, Groenendaal, F, Lequin, M, Jansen, F E, Rhebergen, K S, Luijten, P, Hendrikse, J, Hoogduin, H J M, Huijing, E R, Versteeg, E, Visser, F, Raaijmakers, A J E, Wiegers, E C, Klomp, D W J, Wijnen, J P, Benders, M J N L

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The spectrum of structural abnormalities on CT scans from patients with CF with severe advanced lung disease von Loeve, M, van Hal, P Th W, Robinson, P, de Jong, P A, Lequin, M H, Hop, W C, Williams, T J, Nossent, G D, Tiddens, H A

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Characteristic MR Imaging Findings of the Neonatal Brain in RASopathies von Cizmeci, M N, Lequin, M, Lichtenbelt, K D, Chitayat, D, Kannu, P, James, A G, Groenendaal, F, Chakkarapani, E, Blaser, S, de Vries, L S

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Acquisition guidelines and quality assessment tools for analyzing neonatal diffusion tensor MRI data von Heemskerk, A M, Leemans, A, Plaisier, A, Pieterman, K, Lequin, M H, Dudink, J

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Quantitative Differentiation Between Healthy and Disordered Brain Matter in Patients with Neurofibromatosis Type I Using Diffusion Tensor Imaging von van Engelen, S.J.P.M, Krab, L.C, Moll, H.A, de Goede-Bolder, A, Pluijm, S.M.F, Catsman-Berrevoets, C.E, Elgersma, Y, Lequin, M.H

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A New Ultrasound Marker for Bedside Monitoring of Preterm Brain Growth von Roelants, J A, Koning, I V, Raets, M M A, Willemsen, S P, Lequin, M H, Steegers-Theunissen, R P M, Reiss, I K M, Vermeulen, M J, Govaert, P, Dudink, J

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Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly von Breedveld, G, de Coo, I F, Lequin, M H, Arts, W F M, Heutink, P, Gould, D B, John, S W M, Oostra, B, Mancini, G M S

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