Search Results - "Dremmen, Marjolein H.G."

Cortical Thickness in Crouzon–Pfeiffer Syndrome: Findings in Relation to Primary Cranial Vault Expansion by Wilson, Alexander T., de Planque, Catherine A., Yang, Sumin S., Tasker, Robert C., van Veelen, Marie-Lise C., Dremmen, Marjolein H.G., Vrooman, Henri A., Mathijssen, Irene M.J.

“…BACKGROUND:Episodes of intracranial hypertension are associated with reductions in cerebral cortical thickness (CT) in syndromic craniosynostosis. Here we…”
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Eye and Orbital Anatomy in Metopic Synostosis by Gaillard, Linda, Puppels, Anna E., Dremmen, Marjolein H.G., Loudon, Sjoukje E., Mathijssen, Irene M.J.

“…Background: Metopic synostosis patients have a high prevalence of orthoptic anomalies, including hyperopia, astigmatism, and amblyopia. We hypothesized altered…”
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Imaging of the Sella and Parasellar Region in the Pediatric Population by Seeburg, Daniel P., MD, PhD, Dremmen, Marjolein H.G., MD, Huisman, Thierry A.G.M., MD

“…Masses in the sella and parasellar region comprise about 10% of all pediatric brain tumors but type and frequency differs from those in adults. Imaging is…”
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Reply: Discussion Cerebral Blood Flow of the Frontal Lobe in Untreated Children with Trigonocephaly versus Healthy Controls: An Arterial Spin Labeling Study by de Planque, Catherine A., Petr, Jan, Gaillard, Linda, Mutsaerts, Henk J.M.M., van Veelen, Marie-Lise C., Versnel, Sarah L., Dremmen, Marjolein H.G., Mathijssen, Irene M.J.

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The Influence of Nonaerated Paranasal Sinuses on DTI Parameters of the Brain in 6- to 9-Year-Old Children by Dremmen, Marjolein H.G., Papp, Dorottya, Hernandez-Tamames, Juan A., Vernooij, Meike W., White, Tonya

“…DTI is prone to susceptibility artifacts. Air in the paranasal sinuses can cause field inhomogeneity, thus affecting measurements. Children often have mucus in…”
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MACF1 Mutations Encoding Highly Conserved Zinc-Binding Residues of the GAR Domain Cause Defects in Neuronal Migration and Axon Guidance by Dobyns, William B., Aldinger, Kimberly A., Ishak, Gisele E., Mirzaa, Ghayda M., Timms, Andrew E., Grout, Megan E., Dremmen, Marjolein H.G., Schot, Rachel, Vandervore, Laura, van Slegtenhorst, Marjon A., Wilke, Martina, Kasteleijn, Esmee, Lee, Arthur S., Barry, Brenda J., Chao, Katherine R., Szczałuba, Krzysztof, Kobori, Joyce, Hanson-Kahn, Andrea, Bernstein, Jonathan A., Carr, Lucinda, D’Arco, Felice, Miyana, Kaori, Okazaki, Tetsuya, Saito, Yoshiaki, Sasaki, Masayuki, Das, Soma, Wheeler, Marsha M., Bamshad, Michael J., Nickerson, Deborah A., Engle, Elizabeth C., Verheijen, Frans W., Doherty, Dan, Mancini, Grazia M.S.

“…To date, mutations in 15 actin- or microtubule-associated genes have been associated with the cortical malformation lissencephaly and variable brainstem…”
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Can neuroimaging measures differentiate the disease course of anorexia nervosa? A systematic review by Bracké, Katrien F.M., Steegers, Cathelijne P.M., van der Harst, Tess, Dremmen, Marjolein H.G., Vernooij, Meike W., White, Tonya J.H., Dieleman, Gwen C.

“…Anorexia nervosa (AN) entails many uncertainties regarding the clinical outcome, due to large heterogeneity in the disease course. AN is associated with global…”
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Cerebral Blood Flow of the Frontal Lobe in Untreated Children with Trigonocephaly versus Healthy Controls: An Arterial Spin Labeling Study by de Planque, Catherine A., Petr, Jan, Gaillard, Linda, Mutsaerts, Henk J. M. M., van Veelen, Marie-Lise C., Versnel, Sarah L., Dremmen, Marjolein H. G., Mathijssen, Irene M. J.

“…Craniofacial surgery is the standard treatment for children with moderate to severe trigonocephaly. The added value of surgery to release restriction of the…”
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The prevalence of incidental findings on pelvis MRI of 8–13-year-old children by de Vreede, Desirée K., Bessems, Johannes H. J. M., Dremmen, Marjolein H. G., Vernooij, Meike W., van der Lugt, Aad, Oei, Edwin H. G.

“…Background The prevalence and clinical relevance of incidental findings (IF(s)) on imaging assessing the pelvis in children has not been well documented…”
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Reply: Cerebral Blood Flow of the Frontal Lobe in Untreated Children with Trigonocephaly versus Healthy Controls: An Arterial Spin Labeling Study by de Planque, Catherine A., Petr, Jan, Gaillard, Linda, Mutsaerts, Henk J. M. M., van Veelen, Marie-Lise C., Versnel, Sarah L., Dremmen, Marjolein H. G., Mathijssen, Irene M. J.

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Silent cerebral infarcts in patients with sickle cell disease: a systematic review and meta-analysis by Houwing, Maite E, Grohssteiner, Rowena L, Dremmen, Marjolein H G, Atiq, Ferdows, Bramer, Wichor M, de Pagter, Anne P J, Zwaan, C Michel, White, Tonya J H, Vernooij, Meike W, Cnossen, Marjon H

“…Silent cerebral infarcts (SCIs) are the most common neurological complication in children and adults with sickle cell disease (SCD). In this systematic review,…”
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Transcutaneous carbon dioxide monitoring during therapeutic hypothermia for neonatal encephalopathy by Gangaram-Panday, Norani H., van Essen, Tanja, van Weteringen, Willem, Dremmen, Marjolein H. G., Goos, Tom G., de Jonge, Rogier C. J., Reiss, Irwin K. M.

“…Background In neonates with post-asphyxial neonatal encephalopathy, further neuronal damage is prevented with therapeutic hypothermia (TH). In addition,…”
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Diffusion tensor imaging of the brain in Pompe disease by van den Dorpel, Jan J. A., Dremmen, Marjolein H. G., van der Beek, Nadine A. M. E., Rizopoulos, Dimitris, van Doorn, Pieter A., van der Ploeg, Ans T., Muetzel, Ryan L., van den Hout, Johanna M. P.

“…Enzyme replacement therapy has drastically changed prospects of patients with Pompe disease, a progressive metabolic myopathy. As classic infantile patients…”
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Intracranial hypertension and cortical thickness in syndromic craniosynostosis by Wilson, Alexander T, Den Ottelander, Bianca K, De Goederen, Robbin, Van Veelen, Marie‐Lise C, Dremmen, Marjolein H G, Persing, John A, Vrooman, Henri A, Mathijssen, Irene M J

“…Aim To evaluate the impact of risk factors for intracranial hypertension (ICH) on cerebral cortex thickness in syndromic craniosynostosis. Method ICH risk…”
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A Systematic Review of Neuromonitoring Modalities in Children Beyond Neonatal Period After Cardiac Arrest by Hunfeld, Maayke, Ketharanathan, Naomi, Catsman, Coriene, Straver, Dirk C. G., Dremmen, Marjolein H. G., Bramer, Wichor, Wildschut, Enno, Tibboel, Dick, Buysse, Corinne

“…Postresuscitation care in children focuses on preventing secondary neurologic injury and attempts to provide (precise) prognostication for both caregivers and…”
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Cerebral cortex maldevelopment in syndromic craniosynostosis by Wilson, Alexander T, Den Ottelander, Bianca K, Van Veelen, Marie‐Lise C, Dremmen, Marjolein HG, Persing, John A, Vrooman, Henri A, Mathijssen, Irene MJ, Tasker, Robert C

“…Aim To assess the relationship of surface area of the cerebral cortex to intracranial volume (ICV) in syndromic craniosynostosis. Method Records of 140…”
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Early MRI diagnosis of Sturge Weber Syndrome type 1 in infants by Catsman-Berrevoets, Coriene E., Koudijs, Suzanne M., Buijze, Michiel S.J., de Laat, Peter C.J., Pasmans, Suzanne G.M.A., Dremmen, Marjolein H.G.

“…Patients with Sturge-Weber syndrome type 1 (SWS1) have a port-wine birthmark (PWB) as cutaneous hallmark. Up to 35% of neonates with a high risk PWB develop…”
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A Diffusion Tensor Imaging Analysis of Frontal Lobe White Matter Microstructure in Trigonocephaly Patients by de Planque, Catherine A., Gaillard, Linda, Vrooman, Henri A., Li, Bo, Bron, Esther E., van Veelen, Marie-Lise C., Mathijssen, Irene M.J., Dremmen, Marjolein H.G.

“…Children with trigonocephaly are at risk for neurodevelopmental disorders. The aim of this study is to investigate white matter properties of the frontal lobes…”
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Cervical ribs and other abnormalities of the vertebral pattern in children with esophageal atresia and anorectal malformations by Schut, Pauline C., Eggink, Alex J., Boersma, Margo, Tibboel, Dick, Wijnen, René M. H., Brosens, Erwin, Dremmen, Marjolein H. G., Cohen-Overbeek, Titia E.

“…Background In mammals the vertebral column has a constant pattern, particularly in the cervical region, which is likely the result of stabilizing selection…”
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Atypical neuroimaging characteristics of hemophagocytic lymphohistiocytosis in infants: a case series of hemorrhagic brain lesions in the deep grey matter by Pak, Neda, Selehnia, Anseh, Hunfeld, Maayke A. W., Lequin, Maarten H., Neuteboom, Rinze F., de Vries, Andrica C. H., Kroon, Andre A., Dremmen, Marjolein H. G.

“…Hemophagocytic lymphohistiocytosis (HLH) is a rare multisystem condition associated with uncontrolled overproduction and infiltration of lymphocytes and…”
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