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Martin Lammens
Martin Lammens
U.Z. ANTWERPEN
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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
6212009
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
3082015
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
3072023
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
2952001
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
2752014
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
2312009
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
2272012
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
2152013
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
2132013
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
2092003
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
2062017
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
1892009
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
1752012
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
1731989
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
1702011
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
1692010
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
1641991
Development and malformations of the human pyramidal tract
HJ Ten Donkelaar, M Lammens, P Wesseling, A Hori, A Keyser, ...
Journal of neurology 251, 1429-1442, 2004
1492004
Nucleoplasmic LAP2α–lamin A complexes are required to maintain a proliferative state in human fibroblasts
V Pekovic, J Harborth, JLV Broers, FCS Ramaekers, B van Engelen, ...
The Journal of cell biology 176 (2), 163-172, 2007
1462007
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
1432015
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