Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Michèl Willemsen"'
Publikováno v:
Case Reports in Ophthalmology, Vol 13, Iss 2, Pp 341-349 (2022)
Sjögren-Larsson syndrome (SLS) is a neurometabolic disease with a peculiar crystalline maculopathy. It is yet unclear if vascular abnormalities play a role in SLS maculopathy pathogenesis. We used optical coherence tomography angiography (OCT-A) to
Externí odkaz:
https://doaj.org/article/14b351100f424a9198520aa802d4ea7d
Autor:
Hans J. ten Donkelaar, Bart van de Warrenburg, Michèl Willemsen, Benno Küsters, Yoshio Hashizume, Akira Hori
Publikováno v:
Clinical Neuroanatomy ISBN: 9783030418779
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d01bd54b6d63f9d793db3d5b0024a553
https://doi.org/10.1007/978-3-030-41878-6_11
https://doi.org/10.1007/978-3-030-41878-6_11
Autor:
Michèl Willemsen
Publikováno v:
Neuropediatrics, 50, 1
Neuropediatrics, 50, 1, pp. 1
Neuropediatrics, 50, 1, pp. 1
Item does not contain fulltext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe730d4ed84e1ab64854ce01eeaf4e9b
http://hdl.handle.net/2066/202655
http://hdl.handle.net/2066/202655
Publikováno v:
Pediatric Nephrology, 32, 1171-1174
Pediatric Nephrology (Berlin, Germany)
Pediatric Nephrology, 32, 7, pp. 1171-1174
Pediatric Nephrology (Berlin, Germany)
Pediatric Nephrology, 32, 7, pp. 1171-1174
Contains fulltext : 174487.pdf (Publisher’s version ) (Open Access) 01 juli 2017
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcb14810271cba70a15d2c1b10ec192c
https://biblio.vub.ac.be/vubir/(743361ad-ffe2-48fb-bd25-64ce6cfa449f).html
https://biblio.vub.ac.be/vubir/(743361ad-ffe2-48fb-bd25-64ce6cfa449f).html
Autor:
Martin Lammens, Hans J. ten Donkelaar, John M. G. van Vugt, Gerard van Noort, Michèl Willemsen, Ben Hamel
Publikováno v:
Clinical Neuroembryology ISBN: 9783540291404
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2361c163f8a653728072a3d73b2a889
https://doi.org/10.1007/3-540-34659-7_3
https://doi.org/10.1007/3-540-34659-7_3
Autor:
Joerg Klepper, Cigdem Akman, Marisa Armeno, Stéphane Auvin, Mackenzie Cervenka, Helen J. Cross, Valentina De Giorgis, Adela Della Marina, Kristin Engelstad, Nicole Heussinger, Eric H. Kossoff, Wilhelmina G. Leen, Baerbel Leiendecker, Umrao R. Monani, Hirokazu Oguni, Elizabeth Neal, Juan M. Pascual, Toni S. Pearson, Roser Pons, Ingrid E. Scheffer, Pierangelo Veggiotti, Michél Willemsen, Sameer M. Zuberi, Darryl C. De Vivo
Publikováno v:
Epilepsia Open, Vol 5, Iss 3, Pp 354-365 (2020)
Abstract Glut1 deficiency syndrome (Glut1DS) is a brain energy failure syndrome caused by impaired glucose transport across brain tissue barriers. Glucose diffusion across tissue barriers is facilitated by a family of proteins including glucose trans
Externí odkaz:
https://doaj.org/article/2fa0007690e94933a2416d2145d27364