M
Martin Lammens
Researcher at University of Antwerp
Publications - 233
Citations - 8219
Martin Lammens is an academic researcher from University of Antwerp. The author has contributed to research in topics: Myopathy & Muscle biopsy. The author has an hindex of 49, co-authored 219 publications receiving 7213 citations. Previous affiliations of Martin Lammens include Catholic University of Leuven & Catharina Ziekenhuis.
Papers
More filters
Journal ArticleDOI
Skeletal muscle ultrasound: correlation between fibrous tissue and echo intensity.
Sigrid Pillen,Ramon O. Tak,Machiel J. Zwarts,Martin Lammens,Kiek Verrijp,Ilse M.P. Arts,Jeroen van der Laak,Peter M. Hoogerbrugge,Baziel G.M. van Engelen,Aad Verrips +9 more
TL;DR: The high correlation between interstitial fibrous tissue and EI makes ultrasound a reliable method to determine severity of structural muscle changes, and it is concluded that Fibrous tissue causes increased muscle EI.
Journal ArticleDOI
Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations
B.P.C. van de Warrenburg,Martin Lammens,C. B. Lücking,Patrice Denefle,Pieter Wesseling,Jan Booij,Peter Praamstra,Niall Quinn,Alexis Brice,Martin W.I.M. Horstink +9 more
TL;DR: A Dutch family with autosomal recessive early-onset parkinsonism showed a heterozygous missense mutation in combination with aheterozygous exon deletion in the parkin gene, which pathologically showed neuronal loss in parts of the spinocerebellar system, in addition to selective loss of dopaminergic neurons in the substantia nigra pars compacta.
Journal ArticleDOI
Development and developmental disorders of the human cerebellum.
TL;DR: In this review the development of the cerebellum and some of its more frequent developmental disorders, such as the Dandy-Walker and related midline malformations, and the pontocerebellar hypoplasias are discussed.
Journal ArticleDOI
Multiple Phenotypes in Phosphoglucomutase 1 Deficiency
Laura C. Tegtmeyer,Stephan Rust,Monique van Scherpenzeel,Bobby G. Ng,Marie-Estelle Losfeld,Sharita Timal,Kimiyo Raymond,Ping He,Mie Ichikawa,Joris A. Veltman,Karin Huijben,Yoon S. Shin,Vandana Sharma,Maciej Adamowicz,Martin Lammens,Janine Reunert,Anika Witten,Esther Schrapers,Gert Matthijs,Jaak Jaeken,Daisy Rymen,Tanya Stojkovic,Pascal Laforêt,François Petit,Olivier Aumaître,Elżbieta Czarnowska,Monique Piraud,Teodor Podskarbi,Charles A. Stanley,Reuben Matalon,Patricie Burda,Soraya Seyyedi,V. Debus,Piotr Socha,Jolanta Sykut-Cegielska,Francjan J. van Spronsen,Linda De Meirleir,Pietro Vajro,Terry J. DeClue,Can Ficicioglu,Yoshinao Wada,Ron A. Wevers,Dieter Vanderschaeghe,Nico Callewaert,Ralph Fingerhut,Emile Van Schaftingen,Hudson H. Freeze,Eva Morava,Dirk Lefeber,Thorsten Marquardt +49 more
TL;DR: In this paper, the authors evaluated patients who had a novel recessive disorder of glycosylation, with a range of clinical manifestations that included hepatopathy, bifid uvula, malignant hyperthermia, hypogonadotropic hypogono-morphosis, growth retardation, hypoglycemia, myopathy, dilated cardiomyopathy, and cardiac arrest.
Journal ArticleDOI
Mutations in a TGF-β ligand, TGFB3, cause syndromic aortic aneurysms and dissections.
Aida M. Bertoli-Avella,Elisabeth Gillis,Hiroko Morisaki,Judith M.A. Verhagen,Bianca M. de Graaf,Gerarda van de Beek,Elena M. Gallo,Boudewijn P.T. Kruithof,Hanka Venselaar,Loretha Myers,Steven Laga,Alexander J Doyle,Gretchen L. Oswald,Gert W. A. van Cappellen,Itaru Yamanaka,Robert van der Helm,Berna Beverloo,Annelies de Klein,Luba M. Pardo,Martin Lammens,Christina Evers,Koenraad Devriendt,Michiel Dumoulein,Janneke Timmermans,Hennie T. Brüggenwirth,Frans W. Verheijen,Inez Rodrigus,Gareth Baynam,Marlies Kempers,Johan Saenen,Emeline M. Van Craenenbroeck,Kenji Minatoya,Ritsu Matsukawa,Takuro Tsukube,Noriaki Kubo,Robert M.W. Hofstra,Marie J ose Goumans,Jos A. Bekkers,Jolien W. Roos-Hesselink,Ingrid M.B.H. van de Laar,Harry C. Dietz,Lut Van Laer,Takayuki Morisaki,Marja W. Wessels,Bart Loeys +44 more
TL;DR: In this article, aneurysms affecting the aorta are a common condition associated with high mortality as a result of aortic dissection or rupture, and investigations of the pathogenic mechanisms invo...