| Skeletal muscle ultrasound: correlation between fibrous tissue and echo intensity S Pillen, RO Tak, MJ Zwarts, MMY Lammens, KN Verrijp, IMP Arts, ... Ultrasound in medicine & biology 35 (3), 443-446, 2009 | 676 | 2009 |
| Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections AM Bertoli-Avella, E Gillis, H Morisaki, JMA Verhagen, BM De Graaf, ... Journal of the American College of Cardiology 65 (13), 1324-1336, 2015 | 339 | 2015 |
| Development and developmental disorders of the human cerebellum HJ ten Donkelaar, WFA den Dunnen, M Lammens, P Wesseling, ... Clinical neuroembryology: development and developmental disorders of the …, 2023 | 325 | 2023 |
| Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations BPC Van de Warrenburg, M Lammens, CB Lucking, P Denefle, ... Neurology 56 (4), 555-557, 2001 | 299 | 2001 |
| Multiple phenotypes in phosphoglucomutase 1 deficiency LC Tegtmeyer, S Rust, M van Scherpenzeel, BG Ng, ME Losfeld, S Timal, ... New England Journal of Medicine 370 (6), 533-542, 2014 | 292 | 2014 |
| Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies DJ Lefeber, J Schönberger, E Morava, M Guillard, KM Huyben, K Verrijp, ... The American Journal of Human Genetics 85 (1), 76-86, 2009 | 233 | 2009 |
| Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy G Ravenscroft, S Miyatake, VL Lehtokari, EJ Todd, P Vornanen, KS Yau, ... The American Journal of Human Genetics 93 (1), 6-18, 2013 | 228 | 2013 |
| Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness SB Wortmann, FM Vaz, T Gardeitchik, LELM Vissers, GH Renkema, ... Nature genetics 44 (7), 797-802, 2012 | 228 | 2012 |
| Dendritic cell vaccination as postremission treatment to prevent or delay relapse in acute myeloid leukemia S Anguille, AL Van de Velde, EL Smits, VF Van Tendeloo, G Juliusson, ... Blood, The Journal of the American Society of Hematology 130 (15), 1713-1721, 2017 | 227 | 2017 |
| Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis N Dlamini, NC Voermans, S Lillis, K Stewart, EJ Kamsteeg, G Drost, ... Neuromuscular Disorders 23 (7), 540-548, 2013 | 225 | 2013 |
| Nuclear envelope alterations in fibroblasts from LGMD1B patients carrying nonsense Y259X heterozygous or homozygous mutation in lamin A/C gene A Muchir, BG Van Engelen, M Lammens, JM Mislow, E McNally, ... Experimental cell research 291 (2), 352-362, 2003 | 213 | 2003 |
| Neuromuscular involvement in various types of Ehlers–Danlos syndrome NC Voermans, N Van Alfen, S Pillen, M Lammens, J Schalkwijk, ... Annals of Neurology: Official Journal of the American Neurological …, 2009 | 189 | 2009 |
| Mutations in DDHD2, encoding an intracellular phospholipase A1, cause a recessive form of complex hereditary spastic paraplegia JHM Schuurs-Hoeijmakers, MT Geraghty, EJ Kamsteeg, S Ben-Salem, ... The American Journal of Human Genetics 91 (6), 1073-1081, 2012 | 181 | 2012 |
| Autosomal Recessive Dilated Cardiomyopathy due to DOLK Mutations Results from Abnormal Dystroglycan O-Mannosylation DJ Lefeber, APM de Brouwer, E Morava, M Riemersma, ... PLoS genetics 7 (12), e1002427, 2011 | 178 | 2011 |
| Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores N Sambuughin, KS Yau, M Olivé, RM Duff, M Bayarsaikhan, S Lu, ... The American Journal of Human Genetics 87 (6), 842-847, 2010 | 178 | 2010 |
| Thickening of dura surrounding meningiomas: MR features G Wilms, M Lammens, G Marchal, F Van Calenbergh, C Plets, ... Journal of computer assisted tomography 13 (5), 763-768, 1989 | 174 | 1989 |
| Localized 1H NMR spectroscopy in fifty cases of newly diagnosed intracranial tumors P Demaerel, K Johannik, P Van Hecke, C Van Ongeval, S Verellen, ... Journal of computer assisted tomography 15 (1), 67-76, 1991 | 165 | 1991 |
| RYR1‐related myopathies: a wide spectrum of phenotypes throughout life M Snoeck, BGM Van Engelen, B Küsters, M Lammens, R Meijer, ... European journal of neurology 22 (7), 1094-1112, 2015 | 156 | 2015 |
| Clinical neuroembryology: development and developmental disorders of the human central nervous system HJ ten Donkelaar, M Lammens, A Hori, CWRJ Cremers Springer, 2006 | 154 | 2006 |
| Macrophage clustering as a diagnostic marker in sural nerve biopsies of patients with CIDP C Sommer, S Koch, M Lammens, A Gabreëls-Festen, G Stoll, KV Toyka Neurology 65 (12), 1924-1929, 2005 | 151 | 2005 |
