User profiles for Maarten H. Lequin
Maarten lequinProfessor of Radiology Verified email at texaschildrens.org Cited by 10857 |
Definitions and classification of malformations of cortical development: practical guidelines
Malformations of cortical development are a group of rare disorders commonly manifesting
with developmental delay, cerebral palsy or seizures. The neurological outcome is extremely …
with developmental delay, cerebral palsy or seizures. The neurological outcome is extremely …
[HTML][HTML] The expanding phenotype of COL4A1 and COL4A2 mutations: clinical data on 13 newly identified families and a review of the literature
MEC Meuwissen, DJJ Halley, LS Smit, MH Lequin… - Genetics in …, 2015 - nature.com
Two proα1 (IV) chains, encoded by COL4A1, form trimers that contain, in addition, a proα2 (IV)
chain encoded by COL4A2 and are the major component of the basement membrane in …
chain encoded by COL4A2 and are the major component of the basement membrane in …
[HTML][HTML] Magnetic resonance imaging in children: common problems and possible solutions for lung and airways imaging
Pediatric chest MRI is challenging. High-resolution scans of the lungs and airways are
compromised by long imaging times, low lung proton density and motion. Low signal is a problem …
compromised by long imaging times, low lung proton density and motion. Low signal is a problem …
Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome
…, D Heijsman, T Goldmann, MH Lequin… - Journal of Experimental …, 2016 - rupress.org
Pseudo-TORCH syndrome (PTS) is characterized by microcephaly, enlarged ventricles,
cerebral calcification, and, occasionally, by systemic features at birth resembling the sequelae of …
cerebral calcification, and, occasionally, by systemic features at birth resembling the sequelae of …
Tumour type and size are high risk factors for the syndrome of “cerebellar” mutism and subsequent dysarthria
…, DP y Geuze, PF Paquier, MH Lequin - Journal of Neurology …, 1999 - jnnp.bmj.com
OBJECTIVE “Cerebellar mutis” and subsequent dysarthria (MSD) is a documented complication
of posterior fossa surgery in children. In this prospective study the following risk factors …
of posterior fossa surgery in children. In this prospective study the following risk factors …
Pulmonary disease assessment in cystic fibrosis: comparison of CT scoring systems and value of bronchial and arterial dimension measurements
PURPOSE: To retrospectively compare thin-section computed tomographic (CT) scores
obtained with five scoring systems for assessment of pulmonary disease in children with cystic …
obtained with five scoring systems for assessment of pulmonary disease in children with cystic …
Prospective study on incidence, risk factors, and long-term outcome of osteonecrosis in pediatric acute lymphoblastic leukemia
…, HA de Groot-Kruseman, MH Lequin… - Journal of clinical …, 2011 - ascopubs.org
Purpose We studied cumulative incidence, risk factors, therapeutic strategies, and outcome
of symptomatic osteonecrosis in pediatric patients with acute lymphoblastic leukemia (ALL). …
of symptomatic osteonecrosis in pediatric patients with acute lymphoblastic leukemia (ALL). …
[HTML][HTML] A novel magnetic resonance imaging score predicts neurodevelopmental outcome after perinatal asphyxia and therapeutic hypothermia
Objective To assess the predictive value of a novel magnetic resonance imaging (MRI) score,
which includes diffusion-weighted imaging as well as assessment of the deep grey matter, …
which includes diffusion-weighted imaging as well as assessment of the deep grey matter, …
[PDF][PDF] Mutation in the AP4M1 gene provides a model for neuroaxonal injury in cerebral palsy
…, S Swagemakers, AM Bertoli-Avella, MH Lequin… - The American Journal of …, 2009 - cell.com
Cerebral palsy due to perinatal injury to cerebral white matter is usually not caused by
genetic mutations, but by ischemia and/or inflammation. Here, we describe an autosomal-…
genetic mutations, but by ischemia and/or inflammation. Here, we describe an autosomal-…
Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly
G Breedveld, IF De Coo, MH Lequin… - Journal of medical …, 2006 - jmg.bmj.com
Background: Porencephaly (cystic cavities of the brain) is caused by perinatal vascular
accidents from various causes. Several familial cases have been described and autosomal …
accidents from various causes. Several familial cases have been described and autosomal …