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Vanden Brande Laura

Département des sciences cliniques > Médecine générale

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Main Referenced Co-authors
Servais, Laurent  (6)
Daron, Aurore  (4)
Dangouloff, Tamara  (3)
Mackels, Laurane (3)
Delstanche, Stéphanie  (2)
Main Referenced Keywords
Humans (3); Child (2); Female (2); Genetic testing (2); Infant (2);
Main Referenced Disciplines
Neurology (7)
Pediatrics (5)
Genetics & genetic processes (1)

Publications (total 9)

The most downloaded
2008 downloads
Vanden Brande, L., ALKAN, S., BARREA, C., & LEROY, P. (January 2022). Comment j’explore. Une macrocéphalie. Revue Médicale de Liège, 77 (1), 56-62. https://hdl.handle.net/2268/267422

The most cited

46 citations (OpenAlex)

Aragon-Gawinska, K., DARON, A., Ulinici, A., Vanden Brande, L., Seferian, A., Gidaro, T., Scoto, M., Deconinck, N., & Servais, L. (March 2020). Sitting in patients with spinal muscular atrophy type 1 treated with nusinersen. Developmental Medicine and Child Neurology, 62 (3), 310-314. doi:10.1111/dmcn.14412 https://hdl.handle.net/2268/244023

Dangouloff, T., Chantraine, F., Hennuy, N., Rigo, V., Tribolet, S., Vanden Brande, L., & Servais, L. (2026). Elective Preterm Birth for Earlier Spinal Muscular Atrophy Treatment. Molecular Therapy: Methods and Clinical Development, 201673. doi:10.1016/j.omta.2026.201673
Peer Reviewed verified by ORBi

Mouraux, C., Dangouloff, T., Poleur, M., Mackels, L., Vanden Brande, L., Daron, A., Servais, L., Maertens de Noordhout, A., & DELSTANCHE, S. (29 August 2025). Epidemiological report and diagnostic approach used in the neuromuscular population of Liege, Belgium. Orphanet Journal of Rare Diseases, 20 (1), 464. doi:10.1186/s13023-025-03963-2
Peer Reviewed verified by ORBi

Finkel, R. S., Servais, L., Vlodavets, D., Zanoteli, E., Mazurkiewicz-Bełdzińska, M., Jong, Y.-J., Navas-Nazario, A., Al-Muhaizea, M., Araujo, A. P. Q. C., Nelson, L., Wang, Y., Jaber, B., Gorni, K., Kletzl, H., Palfreeman, L., Rabbia, M., Summers, D., Gaki, E., Wagner, K. R., ... Wells, J. (Other coll.). (14 August 2025). Risdiplam in Presymptomatic Spinal Muscular Atrophy. New England Journal of Medicine, 393 (7), 671-682. doi:10.1056/NEJMoa2410120
Peer Reviewed verified by ORBi

De Leeuw, S., Delens, G., Vanden Brande, L., Henrion, E., & Legros, L. (March 2024). Socio-familial environment influence on cognitive and language development in very preterm children. Child: Care, Health and Development, 50 (2), 13239. doi:10.1111/cch.13239
Peer Reviewed verified by ORBi

Mouraux, C., Dangouloff, T., Poleur, M., Mackels, L., Vanden Brande, L., Daron, A., Servais, L., Maertens de Noordhout, A., & DELSTANCHE, S. (2024). Epidemiological study and diagnostic approach analysis of Neuromuscular population of Neuromuscular Reference Center of Liege, Belgium [Poster presentation]. BeSHG annual symposium 2024, Belgium.
Peer reviewed

Vanden Brande, L., Bauché, S., Pérez-Guàrdia, L., Sternberg, D., Seferian, A. M., Malfatti, E., Silva-Rojas, R., Labasse, C., Chevessier, F., Carlier, P., Eymard, B., Romero, N. B., Laporte, J., Servais, L., Gidaro, T., & Böhm, J. (2024). Pathogenic DPAGT1 variants in limb-girdle congenital myasthenic syndrome (LG-CMS) associated with tubular aggregates and ORAI1 hypoglycosylation. Neuropathology and Applied Neurobiology, 50 (1), 12952. doi:10.1111/nan.12952
Peer Reviewed verified by ORBi

Vanden Brande, L., ALKAN, S., BARREA, C., & LEROY, P. (January 2022). Comment j’explore. Une macrocéphalie. Revue Médicale de Liège, 77 (1), 56-62.
Peer reviewed

Aragon-Gawinska, K., DARON, A., Ulinici, A., Vanden Brande, L., Seferian, A., Gidaro, T., Scoto, M., Deconinck, N., & Servais, L. (March 2020). Sitting in patients with spinal muscular atrophy type 1 treated with nusinersen. Developmental Medicine and Child Neurology, 62 (3), 310-314. doi:10.1111/dmcn.14412
Peer Reviewed verified by ORBi

GERNAY, C., Vanden Brande, L., & De Bilderling, G. (10 March 2016). Acute pancreatitis as initial presentation for hereditary spherocytosis: A case report [Poster presentation]. 44th Annual Congress BVK-SBP, Bruxelles, Belgium.

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