Search Results - "Lequin, M H"

A diffusion tensor imaging analysis of white matter microstructures in non-operated craniosynostosis patients by 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.

“…Purpose In 7 to 15-year-old operated syndromic craniosynostosis patients, we have shown the presence of microstructural anomalies in brain white matter by…”
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Progressive damage on high resolution computed tomography despite stable lung function in cystic fibrosis by de Jong, P.A, Nakano, Y, Lequin, M.H, Mayo, J.R, Woods, R, Pare, P.D, Tiddens, H.A.W.M

“…For effective clinical management of cystic fibrosis (CF) lung disease it is important to closely monitor the start and progression of lung damage. The aim of…”
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Cognitive outcome of patients with classic infantile Pompe disease receiving enzyme therapy by 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

“…Classic infantile Pompe disease affects many tissues, including the brain. Untreated infants die within their first year. Although enzyme-replacement therapy…”
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The spectrum of structural abnormalities on CT scans from patients with CF with severe advanced lung disease by 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

“…In cystic fibrosis (CF), lung disease is the predominant cause of morbidity and mortality. Little is known about the spectrum of structural abnormalities on CT…”
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Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly by 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

“…Background: Porencephaly (cystic cavities of the brain) is caused by perinatal vascular accidents from various causes. Several familial cases have been…”
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SPORADIC COL4A1 MUTATIONS WITH EXTENSIVE PRENATAL PORENCEPHALY RESEMBLING HYDRANENCEPHALY by 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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Resting energy expenditure in children at risk of hypothalamic dysfunction by Van Schaik, J, Burghard, M, Lequin, M H, van Maren, E A, van Dijk, A M, Takken, T, Rehorst-Kleinlugtenbelt, L B, Bakker, B, Meijer, L, Hoving, E W, Fiocco, M, Schouten-van Meeteren, A Y N, Tissing, W J E, van Santen, H M

“…Objective Children with suprasellar brain damage are at risk of hypothalamic dysfunction (HD). HD may lead to decreased resting energy expenditure (REE)…”
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Long-term functional outcome in 167 patients with syndromic craniosynostosis; defining a syndrome-specific risk profile by 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

“…Summary Objective Little is known about the long-term prevalence of elevated intracranial pressure (ICP), obstructive sleep apnoea (OSA), level of education,…”
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Quantitative Differentiation Between Healthy and Disordered Brain Matter in Patients with Neurofibromatosis Type I Using Diffusion Tensor Imaging by 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

“…Hyperintensities on T2-weighted images are seen in the brains of most patients with neurofibromatosis type I (NF-1), but the origin of these unidentified…”
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Primitive neuroectodermal tumours (PNETs) located in the spinal canal; the relevance of classification as central or peripheral PNET : Case report of a primary spinal PNET occurrence with a critical literature review by KAMPMAN, W. A, KROS, J. M, DE JONG, T. H. R, LEQUIN, M. H

“…Intraspinal location of central PNET (cPNET) is very rare. We present a case, critically review all publications of primary intraspinal cPNET occurrence and…”
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The Mammillary Bodies: A Review of Causes of Injury in Infants and Children by Meys, K M E, de Vries, L S, Groenendaal, F, Vann, S D, Lequin, M H

“…Despite their small size, the mammillary bodies play an important role in supporting recollective memory. However, they have typically been overlooked when…”
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Imaging Characteristics of CNS Neuroblastoma- FOXR2 : A Retrospective and Multi-Institutional Description of 25 Cases by Tietze, A, Mankad, K, Lequin, M H, Ivarsson, L, Mirsky, D, Jaju, A, Kool, M, Hoff, K V, Bison, B, Löbel, U

“…The 5th edition of the World Health Organization Classification of CNS tumors defines the CNS neuroblastoma in the group of embryonal tumors. Published…”
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Movement disorder and neuronal migration disorder due to ARFGEF2 mutation by de Wit, M. C. Y., de Coo, I. F. M., Halley, D. J. J., Lequin, M. H., Mancini, G. M. S.

“…We report a child with a severe choreadystonic movement disorder, bilateral periventricular nodular heterotopia (BPNH), and secondary microcephaly based on…”
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Optimal timing of cerebral MRI in preterm infants to predict long-term neurodevelopmental outcome: a systematic review by Plaisier, A, Govaert, P, Lequin, M H, Dudink, J

“…Advances in neonatal neuroimaging have improved detection of preterm brain injury responsible for abnormal neuromotor and cognitive development. Increasingly…”
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Estimation of lung growth using computed tomography by de Jong, P.A, Nakano, Y, Lequin, M.H, Merkus, P.J, Tiddens, H.A, Hogg, J.C, Coxson, H.O

“…Anatomical studies suggest that normal lungs grow by rapid alveolar addition until about 2 yrs of age followed by a gradual increase in alveolar dimensions…”
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Medullary Tegmental Cap Dysplasia: Fetal and Postnatal Presentations of a Unique Brainstem Malformation by 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

“…Medullary tegmental cap dysplasia is a rare brainstem malformation, first described and defined by James Barkovich in his book from 2005 as an anomalous mass…”
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Tumour type and size are high risk factors for the syndrome of “cerebellar” mutism and subsequent dysarthria by Catsman-Berrevoets, Coriene E, Van Dongen, Hugo R, Mulder, Paul G H, y Geuze, Daniel Paz, Paquier, Philippe F, Lequin, Maarten H

“…OBJECTIVE “Cerebellar mutis” and subsequent dysarthria (MSD) is a documented complication of posterior fossa surgery in children. In this prospective study the…”
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Acquisition guidelines and quality assessment tools for analyzing neonatal diffusion tensor MRI data by Heemskerk, A M, Leemans, A, Plaisier, A, Pieterman, K, Lequin, M H, Dudink, J

“…Diffusion tensor imaging is a valuable measure in clinical settings to assess diagnosis and prognosis of neonatal brain development. However, obtaining…”
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Slide tracheoplasty for congenital tracheal stenosis by Koopman, J.P, Bogers, A.J.J.C, Witsenburg, M, Lequin, M.H, Tibboel, D, Hoeve, L.J

“…The aim of this study was to add to the experience of slide tracheoplasty in infants with congenital tracheal stenosis (CTS), to review the recent literature…”
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Diffusion Tensor Imaging and Fiber Tractography in Children with Craniosynostosis Syndromes by Rijken, B F M, Leemans, A, Lucas, Y, van Montfort, K, Mathijssen, I M J, Lequin, M H

“…Patients with craniosynostosis syndromes caused by mutations in FGFR-2, FGFR-3, and TWIST1 genes are characterized by having prematurely fused skull sutures…”
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