Browsing by Author "Lammens, M.M.Y."

Now showing items 1-50 of 100

The enteric nervous system and the musculature of the colon are altered in patients with spina bifida and spinal cord injury
Braber-Ymker, M. den; Lammens, M.M. ; Putten, M.J.A.M. van; Nagtegaal, I.D.
2017, Article / Letter to editor (Virchows Archiv, vol. 470, iss. 2, (2017), pp. 175-184)
Intranuclear Aggregates Precede Clinical Onset in Oculopharyngeal Muscular Dystrophy
Sluijs, B.M. van der ; Raz, V.; Lammens, M.M. ; Heuvel, L.P.W.J. van den ; Voermans, N.C. ; Engelen, B.G.M. van
2016, Article / Letter to editor (Journal of Neuromuscular Diseases, vol. 3, iss. 1, (2016), pp. 101-109)
RYR1-related myopathies: a wide spectrum of phenotypes throughout life
Snoeck, M.; Engelen, B.G.M. van ; Kusters, B. ; Lammens, M.M. ; Meijer, R.; Molenaar, J.P.F. ; Raaphorst, J.; Verschuuren-Bemelmans, C.C.; Straathof, C.S.; Sie, L.T.L. ; Coo, I.F.M. de; Pol, W.L. van der; Visser, M de; Scheffer, H. ; Treves, S.; Jungbluth, H.; Voermans, N.C. ; Kamsteeg, E.J. et al. sine al.
2015, Article / Letter to editor (European Journal of Neurology, vol. 22, iss. 7, (2015), pp. 1094-1112)
A novel mitochondrial DNA m.7507A>G mutation is only pathogenic at high levels of heteroplasmy
McCann, B.J.; Tuppen, H.A.; Kusters, B. ; Lammens, M.M.Y. ; Smeitink, J.A.M. ; Taylor, R.W.; Rodenburg, R.J.T. ; Wortmann, S.B.
2015, Article / Letter to editor (Neuromuscular Disorders, vol. 25, iss. 3, (2015), pp. 262-267)
Experimental treatment of NRAS-mutated neurocutaneous melanocytosis with MEK162, a MEK-inhibitor
Kusters-vandevelde, H.V.; Willemsen, A.E.C.A.B. ; Groenen, P.J.T.A. ; Kusters, B. ; Lammens, M.M. ; Wesseling, P. ; Djafarihamedani, M.; Rijntjes, J. ; Delye, H.H. ; Willemsen, M.A. ; Herpen, C.M.L. van ; Blokx, W.A.M. et al. sine al.
2014, Article / Letter to editor (Acta Neuropathologica Communications, vol. 2, iss. 1, (2014), pp. 41)
Clinical and biochemical features guiding the diagnostics in neurometabolic cutis laxa
Gardeitchik, T. ; Mohamed, M.; Fischer, B.; Lammens, M.M. ; Lefeber, D.J. ; Lace, B.; Parker, M.; Kim, K.J.; Lim, B.C.; Haberle, J.; Garavelli, L.; Jagadeesh, S.; Kariminejad, A.; Guerra, D.; Leao, M.; Keski-Filppula, R.; Brunner, H.G. ; Nijtmans, L.G.J. ; Heuvel, B. van den ; Wevers, R.A. ; Kornak, U.; Morava, E. et al. sine al.
2014, Article / Letter to editor (European Journal of Human Genetics, vol. 22, iss. 7, (2014), pp. 888-895)
Fetal brain lesions in tuberous sclerosis complex: TORC1 activation and inflammation
Prabowo, A.S.; Anink, J.J.; Lammens, M.M. ; Nellist, M.; Ouweland, A.M.W. van den; Adle-Biassette, H.; Sarnat, H.B.; Flores-Sarnat, L.; Crino, P.B.; Aronica, E.
2013, Article / Letter to editor (Brain Pathology, vol. 23, iss. 1, (2013), pp. 45-59)
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis
Dlamini, N.; Voermans, N.C. ; Lillis, S.; Stewart, K.; Kamsteeg, E.J. ; Drost, G. ; Quinlivan, R.; Snoeck, M.; Norwood, F.; Radunovic, A.; Straub, V.; Roberts, M.J. ; Vrancken, A.F.; Pol, W.L. van der; Coo, R.I. de; Manzur, A.Y.; Yau, S.; Abbs, S.; King, A.; Lammens, M.M.Y. ; Hopkins, P.M.; Mohammed, S.; Treves, S.; Muntoni, F.; Wraige, E.; Davis, M.R.; Engelen, B.G.M. van ; Jungbluth, H. et al. sine al.
2013, Article / Letter to editor (Neuromuscular Disorders, vol. 23, iss. 7, (2013), pp. 540-548)
A novel late-onset axial myopathy associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Loseth, S.; Voermans, N.C. ; Torbergsen, T.; Lillis, S.; Jonsrud, C.; Lindal, S.; Kamsteeg, E.J. ; Lammens, M.M.Y. ; Broman, M.; Dekomien, G.; Maddison, P.; Muntoni, F.; Sewry, C.; Radunovic, A.; Visser, M. de; Straub, V.; Engelen, B.G.M. van ; Jungbluth, H. et al. sine al.
2013, Article / Letter to editor (Journal of Neurology, vol. 260, iss. 6, (2013), pp. 1504-1510)
Symptomatic lipid storage in carriers for the PNPLA2 gene
Janssen, M.C.H. ; Engelen, B.G.M. van ; Kapusta, L. ; Lammens, M.M. ; Dijk, M.; Fischer, J.; Graaf, M. van der ; Wevers, R.A. ; Fahrleitner, M.; Zimmermann, R.; Morava, E. et al. sine al.
2013, Article / Letter to editor (European Journal of Human Genetics, vol. 21, iss. 8, (2013), pp. 807-815)
Late-onset post-irradiation vasculopathy of the posterior cerebral vasculature.
Ameele, J. van den; Sieben, A.; Broecke, C. van den; Boterberg, T.; Defreyne, L.; Achten, E.; Lammens, M.M.Y. ; Hemelsoet, D.
2012, Article / Letter to editor (Acta Neurologica Belgica, vol. 112, iss. 1, (2012), pp. 101-104)
Correlation between contrast enhancement on intraoperative magnetic resonance imaging and histopathology in glioblastoma
Kubben, P.; Wesseling, P. ; Lammens, M.M.Y. ; Schijns, O.; ter Laal-Poort, M.; van Overbeeke, J.; van Santbrink, H.
2012, Article / Letter to editor (Surgical Neurology International, vol. 3, iss. 1, (2012), pp. 158)
Mutations in TPM2 and congenital fibre type disproportion
Clarke, N.F.; Waddell, L.B.; Sie, L.T.L. ; van Bon, B.W. ; McLean, C.; Clark, D.; Kornberg, A.; Lammens, M.M. ; North, K.N.
2012, Article / Letter to editor (Neuromuscular Disorders, vol. 22, iss. 11, (2012), pp. 955-958)
Neuropathology in classical and variant ataxia-telangiectasia.
Verhagen, M.M.M. ; Martin, J.J.; Deuren, M. van ; Ceuterick-de Groote, C.; Weemaes, C.M.R. ; Kremer, B. ; Taylor, M.A.; Willemsen, M.A.A.P. ; Lammens, M.M.Y.
2012, Article / Letter to editor (Neuropathology, vol. 32, iss. 3, (2012), pp. 234-244)
Processing of nerve biopsies: a practical guide for neuropathologists.
Weis, J.; Brandner, S.; Lammens, M.M.Y. ; Sommer, C.; Vallat, J.M.
2012, Article / Letter to editor (Clinical Neuropathology, vol. 31, iss. 1, (2012), pp. 7-23)
Mitochondrial DNA m.3242G > A mutation, an under diagnosed cause of hypertrophic cardiomyopathy and renal tubular dysfunction?
Wortmann, S.B.; Champion, M.P.; Heuvel, L.P. van den ; Barth, H.; Trutnau, B.; Craig, K.; Lammens, M.M. ; Schreuder, M.F. ; Taylor, R.W.; Smeitink, J.A.M. ; Wevers, R.A. ; Rodenburg, R.J.T. ; Morava, E. et al. sine al.
2012, Article / Letter to editor (European Journal of Medical Genetics, vol. 55, iss. 10, (2012), pp. 552-556)
Brody syndrome: A clinically heterogeneous entity distinct from Brody disease: A review of literature and a cross-sectional clinical study in 17 patients
Voermans, N.C. ; Laan, A.E.; Oosterhof, A. ; Kuppevelt, A.H.M.S.M. van ; Drost, G. ; Lammens, M.M. ; Kamsteeg, E.J. ; Scotton, C.; Gualandi, F.; Guglielmi, V.; Heuvel, L.P. van den ; Vattemi, G.; Engelen, B.G.M. van et al. sine al.
2012, Article / Letter to editor (Neuromuscular Disorders, vol. 22, iss. 11, (2012), pp. 944-954)
Intramuscular fibrous tissue determines muscle echo intensity in amyotrophic lateral sclerosis.
Arts, I.M.P. ; Schelhaas, H.J. ; Verrijp, K.C.; Zwarts, M.J. ; Overeem, S. ; Laak, J.A.W.M. van der ; Lammens, M.M.Y. ; Pillen, S.
2012, Article / Letter to editor (Muscle and Nerve, vol. 45, iss. 3, (2012), pp. 449-450)
Myopathy in a 20-year-old female patient with D4ST-1 deficient Ehlers-Danlos syndrome due to a homozygous CHST14 mutation.
Voermans, N.C. ; Kempers, M.; Lammens, M.M.Y. ; Alfen, N. van ; Janssen, M.C.H. ; Bonnemann, C.; Engelen, B.G.M. van ; Hamel, B.C.J.
2012, Article / Letter to editor (American Journal of Medical Genetics. Part A, vol. 158A, iss. 4, (2012), pp. 850-855)
Congenital myopathy caused by a novel missense mutation in the CFL2 gene.
Ockeloen, C.W. ; Gilhuis, H.J.; Pfundt, R.; Kamsteeg, E.J. ; Agrawal, P.B.; Beggs, A.H.; Hama-Amin, A.D.; Diekstra, A.; Knoers, N.V.A.M. ; Lammens, M.M. ; Alfen, N. van et al. sine al.
2012, Article / Letter to editor (Neuromuscular Disorders, vol. 22, iss. 7, (2012), pp. 632-639)
Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness.
Wortmann, S.B.; Vaz, F.M.; Gardeitchik, T. ; Vissers, L.E.L.M. ; Renkema, G.H. ; Schuurs-Hoeijmakers, J.H.M. ; Kulik, W.; Lammens, M.M.Y. ; Christin, C.; Kluijtmans, L.A.J. ; Rodenburg, R.J.T. ; Nijtmans, L.G.J. ; Grunewald, A.; Klein, C.; Gerhold, J.M.; Kozicz, L.T. ; Hasselt, P.M. van; Harakalova, M.; Kloosterman, W.; Baric, I.; Pronicka, E.; Ucar, S.K.; Naess, K.; Singhal, K.K.; Krumina, Z.; Gilissen, C.F.H.A. ; Bokhoven, J.H.L.M. van ; Veltman, J.A. ; Smeitink, J.A.M. ; Lefeber, D.J. ; Spelbrink, J.N. ; Wevers, R.A. ; Morava, E. ; Brouwer, A.P.M. de et al. sine al.
2012, Article / Letter to editor (Nature Genetics, vol. 44, iss. 7, (2012), pp. 797-802)
Mutations in DDHD2, Encoding an Intracellular Phospholipase A(1), Cause a Recessive Form of Complex Hereditary Spastic Paraplegia
Schuurs-Hoeijmakers, J.H.M. ; Geraghty, M.T.; Kamsteeg, E.J. ; Ben-Salem, S.; Bot, S.T. de ; Nijhof, B.; van de, V., II; Graaf, M. van der ; Nobau, A.C.; Otte-Holler, I. ; Vermeer, S. ; Smith, A.C.; Humphreys, P.; Schwartzentruber, J.; Consortium, F.C.; Ali, B.R.; Al-Yahyaee, S.A.; Tariq, S.; Pramathan, T.; Bayoumi, R.; Kremer, H.P.H. ; Warrenburg, B.P.C. van de ; van den Akker, W.M.; Gilissen, C.F.H.A. ; Veltman, J.A. ; Janssen, I.M. ; Vulto-van Silfhout, A.T. ; van der Velde-Visser, S.; Lefeber, D.J. ; Diekstra, A.; Erasmus, C.E. ; Willemsen, M.A.A.P. ; Peart-Vissers, L.E.L.M. ; Lammens, M.M.Y. ; Bokhoven, J.H.L.M. van ; Brunner, H.G. ; Wevers, R.A. ; Schenck, A. ; Al-Gazali, L.; Vries, L.B.A. de ; Brouwer, A.P.M. de et al. sine al.
2012, Article / Letter to editor (American Journal of Human Genetics, vol. 91, iss. 6, (2012), pp. 1073-1081)
169th ENMC International Workshop Rare Structural Congenital Myopathies 6-8 November 2009, Naarden, The Netherlands.
Goebel, H.H.; Bonnemann, C.G.; Lammens, M.M.Y. ; et al.
2011, Article / Letter to editor (Neuromuscular Disorders, vol. 21, iss. 5, (2011), pp. 363-374)
Increased axonal ribosome numbers in CMT diseases.
Verheijen, M.H.; Lammens, M.M.Y. ; Ceuterick-de Groote, C.; Timmerman, V.; Jonghe, P. de; King, R.H.; Smit, A.B.; Minnen, J. van
2011, Article / Letter to editor (Journal of the Peripheral Nervous System, vol. 16, iss. 1, (2011), pp. 71-73)
Scoliosis surgery in a patient with "de novo" myosin storage myopathy.
Stalpers, X.; Verrips, A. ; Braakhekke, J.; Lammens, M.M.Y. ; Wijngaard, A. van den; Mostert, A.
2011, Article / Letter to editor (Neuromuscular Disorders, vol. 21, iss. 11, (2011), pp. 812-815)
Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores.
Sambuughin, N.; Yau, K.S.; Duff, R.M.; Bayarsaikhan, M.; Lu, S.J.; Gonzalez-Mera, L.; Sivadorai, P.; Nowak, K.J.; Ravenscroft, G.; Mastaglia, F.L.; North, K.N.; Ilkovski, B.; Kremer, H. ; Lammens, M.M. ; Engelen, B.G.M. van ; Fabian, V.; Lamont, P.; Davis, M.R.; Laing, N.G.; Goldfarb, L.G. et al. sine al.
2011, Article / Letter to editor (American Journal of Human Genetics, vol. 87, (2011), pp. 842)
The phenotype of the Gly94fsX222 PMP22 insertion
Vries, S.D. de; Verhamme, C.; Ruissen, F. van; Paassen, B.W. van; Arts, W.F.M.; Kerkhoff, H.; Engelen, B.G.M. van ; Lammens, M.M.Y. ; Visser, M. de; Baas, F.; Kooi, A.J. van der et al. sine al.
2011, Article / Letter to editor (Journal of the Peripheral Nervous System, vol. 16, iss. 2, (2011), pp. 113-118)
Uw Diagnose?
Wilbers, J. ; Goraj, B.M. ; Lammens, M.M.Y. ; Dijk, E.J. van
2011, Article / Letter to editor (Tijdschrift voor Neurologie & Neurochirurgie, vol. 112, (2011), pp. 84-86)
Restoration of complex V deficiency caused by a novel deletion in the human TMEM70 gene normalizes mitochondrial morphology
Jonckheere, A.I. ; Huigsloot, M. ; Lammens, M.M.Y. ; Jansen, J.; Heuvel, L.P.W.J. van den ; Spiekerkoetter, U.; Kleist-Retzow, J.C. von; Forkink, M. ; Koopman, W.J.H. ; Szklarczyk, R.J. ; Huynen, M.A. ; Fransen, J. ; Smeitink, J.A.M. ; Rodenburg, R.J.T. et al. sine al.
2011, Article / Letter to editor (Mitochondrion, vol. 11, iss. 6, (2011), pp. 954-963)
Mild muscular features in tenascin-x knockout mice, a model of ehlers-danlos syndrome
Voermans, N.C. ; Verrijp, K. ; Eshuis, L.; Balemans, M.C.M. ; Egging, D.F. ; Sterrenburg, E.; Rooij, I.A.L.M. van ; Laak, J.A.W.M. van der ; Schalkwijk, J. ; Maarel, S. van der; Lammens, M.M.Y. ; Engelen, B.G.M. van et al. sine al.
2011, Article / Letter to editor (Connective Tissue Research, vol. 52, iss. 5, (2011), pp. 422-432)
Autosomal Recessive Dilated Cardiomyopathy due to DOLK Mutations Results from Abnormal Dystroglycan O-Mannosylation.
Lefeber, D.J. ; Brouwer, A.P.M. de ; Morava, E. ; Riemersma, M. ; Schuurs-Hoeijmakers, J.H.M. ; Absmanner, B.; Verrijp, K. ; Akker, W.M.R. van den; Huijben, K.; Steenbergen, G.C. ; Reeuwijk, J. van ; Jozwiak, A.; Zucker, N.; Lorber, A.; Lammens, M.M.Y. ; Knopf, C.; Bokhoven, H. van ; Grunewald, S. ; Lehle, L.; Kapusta, L. ; Mandel, H.; Wevers, R.A. et al. sine al.
2011, Article / Letter to editor (Plos Genetics, vol. 7, iss. 12, (2011), pp. e1002427)
Mitochondrial dysfunction and organic aciduria in five patients carrying mutations in the Ras-MAPK pathway
Kleefstra, T. ; Wortmann, S.B.; Rodenburg, R.J.T. ; Bongers, M.H.F. ; Hadzsiev, K.; Noordam, C. ; Heuvel, L.P.W.J. van den ; Nillesen, W.M.; Hollody, K.; Gillessen-Kaesbach, G.; Lammens, M.M.Y. ; Smeitink, J.A.M. ; Burgt, C.J.A.M. van der ; Morava, E. et al. sine al.
2011, Article / Letter to editor (European Journal of Human Genetics, vol. 19, iss. 2, (2011), pp. 138-144)
Urinary dopamine in aromatic L-amino acid decarboxylase deficiency: the unsolved paradox.
Wassenberg, T.; Willemsen, M.H. ; Geurtz, P.B.; Lammens, M.M.Y. ; Verrijp, K. ; Wilmer, M.J.G. ; Lee, W.T.; Wevers, R.A. ; Verbeek, M.M.
2010, Article / Letter to editor (Molecular Genetics and Metabolism, vol. 101, iss. 4, (2010), pp. 349-356)
Peripheral Nerve Society Guideline on processing and evaluation of nerve biopsies.
Sommer, C.L.; Brandner, S.; Dyck, P.J.; Harati, Y.; LaCroix, C.; Lammens, M.M.Y. ; Magy, L.; Mellgren, S.I.; Morbin, M.; Navarro, C; Powell, H.C.; Schenone, A.E.; Tan, E.; Urtizberea, A.; Weis, J. et al. sine al.
2010, Article / Letter to editor (Journal of the Peripheral Nervous System, vol. 15, iss. 3, (2010), pp. 164-175)
A de novo p.Asp18Asn mutation in TREX1 in a patient with Aicardi-Goutieres syndrome.
Haaxma, C.A. ; Crow, Y.J.; Steensel, M.A.M. van ; Lammens, M.M.Y. ; Rice, G.I.; Verbeek, M.M. ; Willemsen, M.H.
2010, Article / Letter to editor (American Journal of Medical Genetics. Part A, vol. 152A, iss. 10, (2010), pp. 2612-2617)
Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores.
Sambuughin, N.; Yau, K.S.; Olive, M.; Duff, R.M.; Bayarsaikhan, M.; Lu, S.; Gonzalez-Mera, L.; Sivadorai, P.; Nowak, K.J.; Ravenscroft, G.; Mastaglia, F.L.; North, K.N.; Ilkovski, B.; Kremer, J.M.J. ; Lammens, M.M.Y. ; Engelen, B.G.M. van ; Fabian, V.; Lamont, P.; Davis, M.R.; Laing, N.G.; Goldfarb, L.G. et al. sine al.
2010, Article / Letter to editor (American Journal of Human Genetics, vol. 87, iss. 6, (2010), pp. 842-847)
Clinical features, lectin staining, and a novel GNE frameshift mutation in hereditary inclusion body myopathy.
Voermans, N.C. ; Guillard, M. ; Doedee, R.; Lammens, M.M.Y. ; Huizing, M.; Padberg, G.W.A.M. ; Wevers, R.A. ; Engelen, B.G.M. van ; Lefeber, D.J.
2010, Article / Letter to editor (Clinical Neuropathology, vol. 29, iss. 2, (2010), pp. 71-77)
Cardiac biplane strain imaging: initial in vivo experience.
Lopata, R.G.P. ; Nillesen, M.M. ; Verrijp, C.N. ; Singh, S.K. ; Lammens, M.M.Y. ; Laak, J.A.W.M. van der ; Wetten, H.B. van ; Thijssen, J.M. ; Kapusta, L. ; Korte, C.L. de
2010, Article / Letter to editor (Physics in Medicine and Biology, vol. 55, iss. 4, (2010), pp. 963-979)
TDP-43 accumulation is common in myopathies with rimmed vacuoles.
Kusters, B. ; Hoeve, B.J.A. van ; Schelhaas, H.J. ; Laak, H.J. ter ; Engelen, B.G.M. van ; Lammens, M.M.Y.
2009, Article / Letter to editor (Acta Neuropathologica, vol. 117, iss. 2, (2009), pp. 209-211)
Myopathy and polyneuropathy in an adolescent with the kyphoscoliotic type of Ehlers-Danlos syndrome.
Voermans, N.C. ; Bonnemann, C.G.; Lammens, M.M.Y. ; Engelen, B.G.M. van ; Hamel, B.C.J.
2009, Article / Letter to editor (American Journal of Medical Genetics. Part A, vol. 149A, iss. 10, (2009), pp. 2311-2316)
[Metabolic myopathies - an overview]
Lammens, M.M.Y. ; Schoser, B.
2009, Article / Letter to editor (Pathologe, vol. 30, iss. 5, (2009), pp. 370-378)
Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects.
Paepe, B. De; Smet, J.; Lammens, M.M.Y. ; Seneca, S.; Martin, J.J.; Bleecker, J. De; Meirleir, L. de; Lissens, W.; Coster, R. van
2009, Article / Letter to editor (Journal of Clinical Pathology : the Journal of the Association of Clinical Pathologists, vol. 62, iss. 2, (2009), pp. 172-176)
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy.
Claeys, K.G.; Zuchner, S.; Kennerson, M.; Berciano, J.; Garcia, A.; Verhoeven, K.; Storey, E.; Merory, J.R.; Bienfait, H.M.; Lammens, M.M.Y. ; Nelis, E.; Baets, J.; Vriendt, E. De; Berneman, Z.N.; Veuster, I. De; Vance, J.M.; Nicholson, G.; Timmerman, V.; Jonghe, P. de et al. sine al.
2009, Article / Letter to editor (Brain, vol. 132, iss. Pt 7, (2009), pp. 1741-1752)
Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies.
Lefeber, D.J. ; Schonberger, J.; Morava, E. ; Guillard, M. ; Huyben, C.M.L.C. ; Verrijp, K. ; Grafakou, O.; Evangeliou, A.; Preijers, F.W.M.B. ; Manta, P.; Yildiz, J.; Grunewald, S. ; Spilioti, M.; Elzen, C. van den; Klein, D.; Hess, D.; Ashida, H.; Hofsteenge, J.; Maeda, Y.; Heuvel, L.P.W.J. van den ; Lammens, M.M.Y. ; Lehle, L.; Wevers, R.A. et al. sine al.
2009, Article / Letter to editor (American Journal of Human Genetics, vol. 85, iss. 1, (2009), pp. 76-86)
Congenital monomelic muscular hypertrophy of the upper extremity.
Gilhuis, H.J.; Zophel, O.T.; Lammens, M.M.Y. ; Zwarts, M.J.
2009, Article / Letter to editor (Neuromuscular Disorders, vol. 19, iss. 10, (2009), pp. 714-717)
Skeletal muscle ultrasound: correlation between fibrous tissue and echo intensity.
Pillen, S. ; Tak, R.O. ; Zwarts, M.J. ; Lammens, M.M.Y. ; Verrijp, K. ; Arts, I.M.P. ; Laak, J.A.W.M. van der ; Hoogerbrugge, P.M. ; Engelen, B.G.M. van ; Verrips, A.
2009, Article / Letter to editor (Ultrasound in Medicine and Biology, vol. 35, iss. 3, (2009), pp. 443-446)
Development of the human cerebellum and its disorders.
Donkelaar, H.J. ten ; Lammens, M.M.Y.
2009, Article / Letter to editor (Clinics in Perinatology, vol. 36, iss. 3, (2009), pp. 513-530)
Neuromuscular features in Marfan syndrome.
Voermans, N.C. ; Timmermans, J. ; Alfen, N. van ; Pillen, S. ; Akker, J.W. op den ; Lammens, M.M.Y. ; Zwarts, M.J. ; Rooij, I.A.L.M. van ; Hamel, B.C.J. ; Engelen, B.G.M. van
2009, Article / Letter to editor (Clinical Genetics, vol. 76, iss. 1, (2009), pp. 25-37)
Neuromuscular involvement in various types of Ehlers-Danlos syndrome.
Voermans, N.C. ; Alfen, N. van ; Pillen, S. ; Lammens, M.M.Y. ; Schalkwijk, J. ; Zwarts, M.J. ; Rooij, I.A.L.M. van ; Hamel, B.C.J. ; Engelen, B.G.M. van
2009, Article / Letter to editor (Annals of Neurology, vol. 65, iss. 6, (2009), pp. 687-697)
Sporadic late-onset nemaline myopathy effectively treated by melphalan and stem cell transplant.
Voermans, N.C. ; Minnema, M.C.; Lammens, M.M.Y. ; Schelhaas, H.J. ; Kooi, A.V.; Lokhorst, H.M.; Engelen, B.G.M. van
2008, Article / Letter to editor (Neurology, vol. 71, iss. 7, (2008), pp. 532-534)

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