Profil

Dangouloff Tamara

Département des sciences cliniques

See author's contact details
ORCID
0000-0002-5435-4774
Main Referenced Co-authors
Servais, Laurent  (36)
Boemer, François  (21)
Caberg, Jean-Hubert  (9)
Bours, Vincent  (7)
Daron, Aurore  (7)
Main Referenced Keywords
Spinal muscular atrophy (10); Newborn screening (9); Humans (7); Infant, Newborn (7); Neonatal Screening/methods (6);
Main Referenced Disciplines
Neurology (15)
Pediatrics (15)
Genetics & genetic processes (4)
Laboratory medicine & medical technology (3)
Public health, health care sciences & services (3)

Publications (total 38)

The most downloaded
911 downloads
Daron, A., DELSTANCHE, S., Dangouloff, T., & Servais, L. (February 2019). Amyotrophie spinale infantile (R)évolution thérapeutique. Revue Médicale de Liège, 74 (2), 82-85. https://hdl.handle.net/2268/244951

The most cited

191 citations (OpenAlex)

Dangouloff, T., & Servais, L. (2019). Clinical Evidence Supporting Early Treatment Of Patients With Spinal Muscular Atrophy: Current Perspectives. Therapeutics and Clinical Risk Management, 15, 1153-1161. doi:10.2147/TCRM.S172291 https://hdl.handle.net/2268/240476

Boemer, F., Hovhannesyan, K., JACQUEMIN, V., Mni, M., Flohimont, C., Mashhadizadeh, D., HELOU, L., Palmeira, L., Dangouloff, T., & Servais, L. (October 2025). Population-based 1st-tier Genomic Newborn Screening : Results of BabyDetect Study [Poster presentation]. ICoNS 2025, Londres, United Kingdom.
Peer reviewed

Bartoszek, P., Boemer, F., Hovhannesyan, K., JACQUEMIN, V., Piazzon, F., Mashhadizadeh, D., Bours, V., HELOU, L., Rigo, V., HENNUY, N., Dangouloff, T., & Servais, L. (01 October 2025). Genetic Newborn Screening for Retinoblastoma: A Belgian Initiative Baby Detect. International Ophthalmology Clinics, 65 (4), 47 - 50. doi:10.1097/IIO.0000000000000593
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

Dangouloff, T., Hovhannesyan, K., JACQUEMIN, V., Mashhadizadeh, D., Mni, M., Flohimont, C., HELOU, L., PALMEIRA, L., Pieltain, C., Grandfils, S., Rigo, V., HENNUY, N., Boemer, F., & Servais, L. (June 2025). Dépistage néonatal génomique : vers une identification précoce et ciblée des maladies rares. Percentile, 30 (3), 15-18.
Editorial reviewed

Minten, T., Bick, S., Adelson, S., Gehlenborg, N., Amendola, L. M., Boemer, F., Coffey, A. J., Encina, N., Ferlini, A., Kirschner, J., Russell, B. E., Servais, L., Sund, K. L., Taft, R. J., Tsipouras, P., Zouk, H., ICoNS Gene List Contributors, Green, R. C., Gold, N. B., ... Nusair, A. (2025). Data-driven consideration of genetic disorders for global genomic newborn screening programs. Genetics in Medicine, 101443. doi:10.1016/j.gim.2025.101443
Peer Reviewed verified by ORBi

Servais, L., Dangouloff, T., Muntoni, F., Scoto, M., & Baranello, G. (22 February 2025). Spinal muscular atrophy in the UK: the human toll of slow decisions. The Lancet, 405 (10479), 619 - 620. doi:10.1016/S0140-6736(25)00048-0
Peer Reviewed verified by ORBi

Boemer, F., Hovhannesyan, K., Piazzon, F., MINNER, F., Mni, M., Jacquemin, V., Mashhadizadeh, D., BENMHAMMED, N., Bours, V., Jacquinet, A., Harvengt, J., Bulk, S., Dideberg, V., Helou, L., Palmeira, L., Dangouloff, T., BabyDetect Expert Panel, Servais, L., Alkan, S. (Other coll.), ... Vaessen, S. (Other coll.). (28 January 2025). Population-based, first-tier genomic newborn screening in the maternity ward. Nature Medicine, 31 (4), 1339-1350. doi:10.1038/s41591-024-03465-x
Peer Reviewed verified by ORBi

Dangouloff, T., Lang, H., BENMHAMMED, N., & Servais, L. (2025). Newborn screening and rapid genomic diagnosis of neuromuscular diseases. Journal of Neuromuscular Diseases, 22143602241296286. doi:10.1177/22143602241296286
Peer Reviewed verified by ORBi

Vrščaj, E., Dangouloff, T., Osredkar, D., Servais, L., & SMA NBS World Study Group. (November 2024). Newborn screening programs for spinal muscular atrophy worldwide in 2023. Journal of Neuromuscular Diseases, 11 (6), 1180 - 1189. doi:10.1177/22143602241288095
Peer Reviewed verified by ORBi

Becker, M. M., Nardes, F., Dangouloff, T., Servais, L., Araujo, A. P. D. Q. C., & Gurgel-Giannetti, J. (October 2024). Why should a 5q spinal muscular atrophy neonatal screening program be started? Arquivos de Neuro-Psiquiatria, 82 (10), 1 - 9. doi:10.1055/s-0044-1791201
Peer Reviewed verified by ORBi

Dangouloff, T., Hovhannesyan, K., Mashhadizadeh, D., MINNER, F., Mni, M., Helou, L., Piazzon, F., Palmeira, L., Boemer, F., & Servais, L. (30 July 2024). Feasibility and Acceptability of a Newborn Screening Program Using Targeted Next-Generation Sequencing in One Maternity Hospital in Southern Belgium. Children, 11 (8), 926. doi:10.3390/children11080926
Peer Reviewed verified by ORBi

Oskoui, M., Dangouloff, T., & Servais, L. (01 June 2024). Universal Newborn Screening for Spinal Muscular Atrophy. JAMA Pediatrics, 178 (6), 520 - 521. doi:10.1001/jamapediatrics.2024.0489
Peer Reviewed verified by ORBi

Dangouloff, T., Thokala, P., Stevenson, M. D., Deconinck, N., D'Amico, A., Daron, A., DELSTANCHE, S., Servais, L., & Hiligsmann, M. (02 January 2024). Cost-effectiveness of spinal muscular atrophy newborn screening based on real-world data in Belgium. Neuromuscular Disorders, 34, 61-67. doi:10.1016/j.nmd.2023.11.013
Editorial reviewed

Tychon, C., BENMHAMMED, N., Daron, A., Deconinck, N., Dontaine, P., Boemer, F., Servais, L., & Dangouloff, T. (2024). Follow-up of SMA children identified by newborn screening in southern Belgium [Paper presentation]. 52nd Congress of the BVK-SBP, Anvers, Belgium.
Editorial reviewed

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

Abiusi, E., Costa-Roger, M., Bertini, E. S., Tiziano, F. D., Tizzano, E. F., SMN2 Study group, Abiusi, E., Baranello, G., Bertini, E., Boemer, F., Burghes, A., Codina-Solà, M., Costa-Roger, M., Dangouloff, T., Groen, E., Gos, M., Jędrzejowska, M., Kirschner, J., Lemmink, H. H., ... Wirth, B. (January 2024). 270th ENMC International Workshop: Consensus for SMN2 genetic analysis in SMA patients 10-12 March, 2023, Hoofddorp, the Netherlands. Neuromuscular Disorders, 34, 114 - 122. doi:10.1016/j.nmd.2023.12.008
Peer Reviewed verified by ORBi

Aragon-Gawinska, K., Mouraux, C., Dangouloff, T., & Servais, L. (29 June 2023). Spinal Muscular Atrophy Treatment in Patients Identified by Newborn Screening-A Systematic Review. Genes, 14 (7), 1377. doi:10.3390/genes14071377
Peer Reviewed verified by ORBi

Dangouloff, T., MOURAUX, C., Piazzon, F., Mashhadizadeh, D., Hovhannesyan, K., Helou, L., Palmeira, L., Boemer, F., & Servais, L. (2023). Dépistage génétique néonatal universel de 126 maladies précoces et traitables : premiers résultats du projet Babydetect [Poster presentation]. 33e Séminaire de Génétique Clinique, Angers, France.
Peer reviewed

Dangouloff, T. (2022). Analyse médico-économique du dépistage néonatal de l’amyotrophie spinale en Fédération Wallonie-Bruxelles [Doctoral thesis, ULiège - Université de Liège]. ORBi-University of Liège. https://orbi.uliege.be/handle/2268/296328

Dangouloff, T., Hiligsmann, M., Deconinck, N., D'Amico, A., Seferian, A. M., Boemer, F., & Servais, L. (2022). Financial cost and quality of life of patients with spinal muscular atrophy identified by symptoms or newborn screening. Developmental Medicine and Child Neurology. doi:10.1111/dmcn.15286
Peer Reviewed verified by ORBi

Dangouloff, T., & Servais, L. (2022). Dépistage et traitement de l’amyotrophie spinale. Percentile.
Editorial reviewed

BECKERS, P., CABERG, J.-H., DIDEBERG, V., Dangouloff, T., den Dunnen, J. T., BOURS, V., Servais, L., & BOEMER, F. (04 February 2021). Newborn screening of duchenne muscular dystrophy specifically targeting deletions amenable to exon‑skipping therapy. Scientific Reports, 11, 3011. doi:10.1038/s41598-021-82725-z
Peer Reviewed verified by ORBi

BECKERS, P., CABERG, J.-H., DIDEBERG, V., Dangouloff, T., den Dunnen, J. T., BOURS, V., Servais, L., & BOEMER, F. (2021). Newborn Screening of Duchenne Muscular Dystrophy Specifically Targeting Deletions Amenable to Exon-skipping Therapy [Poster presentation]. European Human Genetics Conference - ESHG.

Dangouloff, T., Botty, C., Beaudart, C., Servais, L., & Hiligsmann, M. (January 2021). Systematic literature review of the economic burden of spinal muscular atrophy and economic evaluations of treatments. Orphanet Journal of Rare Diseases, 16 (1), 47. doi:10.1186/s13023-021-01695-7
Peer Reviewed verified by ORBi

BOEMER, F., Caberg, J.-H., Beckers, P., Dideberg, V., di Fiore, S., Bours, V., Marie, S., Dewulf, J., Marcelis, L., Deconinck, N., Daron, A., Blasco-Perez, L., Tizzano, E., Hiligsmann, M., Lombet, J., Pereira, T., Lopez-Granados, L., Shalchian-Tehran, S., van Assche, V., ... Servais, L. (2021). Three years pilot of spinal muscular atrophy newborn screening turned into official program in Southern Belgium. Scientific Reports, 11 (1), 19922. doi:10.1038/s41598-021-99496-2
Peer Reviewed verified by ORBi

Dangouloff, T., Vrščaj, E., Servais, L., & Osredkar, D. (2021). Newborn screening programs for spinal muscular atrophy worldwide: where we stand and where to go. Neuromuscular Disorders, 31 (6), 574 - 582. doi:10.1016/j.nmd.2021.03.007
Peer Reviewed verified by ORBi

Dangouloff, T., Boemer, F., & Servais, L. (2021). Newborn screening of neuromuscular diseases. Neuromuscular Disorders. doi:10.1016/j.nmd.2021.07.008
Peer Reviewed verified by ORBi

Dangouloff, T., Servais, L., & Hiligsmann, M. (2020). SMA: REGISTRIES, BIOMARKERS & OUTCOME MEASURES: P.187 Systematic literature review of the economic burden and economic evaluations in spinal muscular atrophy. Neuromuscular Disorders. doi:10.1016/j.nmd.2020.08.189
Peer Reviewed verified by ORBi

Dangouloff, T., Servais, L., & Hiligsmann, M. (2020). SMA: REGISTRIES, BIOMARKERS & OUTCOME MEASURES: P.191 Preliminary data for the cost-effectiveness assessment of the newborn screening for SMA in Belgium. Neuromuscular Disorders. doi:10.1016/j.nmd.2020.08.193
Peer Reviewed verified by ORBi

Dangouloff, T., BOEMER, F., CABERG, J.-H., & Servais, L. (2020). Correspondence on: “Discrepancy in Spinal Muscular Atrophy Incidence findings in newborn screening programs: the influence of carrier screening?” by Kay et al. Genetics in Medicine. doi:10.1038/s41436-020-0887-1
Peer Reviewed verified by ORBi

Dangouloff, T., BOEMER, F., DIDEBERG, V., CABERG, J.-H., & Servais, L. (2020). Reader response: Discrepancy in redetermination of SMN2 copy numbers in children with SMA [letter to the editor]. Neurology. doi:10.1212/WNL.0000000000009907
Peer Reviewed verified by ORBi

Dangouloff, T., Burghes, A., Bertini, E., BOEMER, F., Hiligsmann, M., Mueller-Felber, W., Tiziano, F. D., Young, P., Germanenko, O., De Lemus, M., Ouillade, L., Rucinski, K., Stephenson, K., Farwell, W., Gorni, K., Hjort, M., Kausar, I., Tizzano, E. F., & Servais, L. (January 2020). 244th ENMC International Workshop: Newborn screening in Spinal Muscular Atrophy May 10-12, 2019, Hoofdorp, The Netherlands. Neuromuscular Disorders, 30 (1), 93-103. doi:10.1016/j.nmd.2019.11.002
Peer Reviewed verified by ORBi

BOEMER, F., CABERG, J.-H., DIDEBERG, V., BECKERS, P., Marie, S., Marcelis, L., Bours, V., Dangouloff, T., & Servais, L. (September 2019). (S)un (M)ay (A)rise on SMA : l'espoir d'une region sans amyotrophie spinale. Revue Médicale de Liège, 74 (9), 461-464.
Peer reviewed

Daron, A., DELSTANCHE, S., Dangouloff, T., & Servais, L. (February 2019). Amyotrophie spinale infantile (R)évolution thérapeutique. Revue Médicale de Liège, 74 (2), 82-85.

Boemer, F., CABERG, J.-H., Dideberg, V., DARDENNE, D., Bours, V., Hiligsmann, M., Dangouloff, T., & Servais, L. (2019). Newborn screening for SMA in Southern Belgium. Neuromuscular Disorders. doi:10.1016/j.nmd.2019.02.003
Peer Reviewed verified by ORBi

Dangouloff, T., BOEMER, F., CABERG, J.-H., DIFIORE, S., BECKERS, P., MARIE, S., MARCELIS, L., & Servais, L. (2019). Reducing the diagnosis time of neonatal screening by optimizing the screening process: the southern Belgian experience. Neuromuscular Disorders, 29, 132. doi:10.1016/j.nmd.2019.06.339
Peer Reviewed verified by ORBi

Dangouloff, T., & Servais, L. (2019). Clinical Evidence Supporting Early Treatment Of Patients With Spinal Muscular Atrophy: Current Perspectives. Therapeutics and Clinical Risk Management, 15, 1153-1161. doi:10.2147/TCRM.S172291
Peer Reviewed verified by ORBi

Dangouloff, T., Hiligsmann, M., CABERG, J.-H., BOEMER, F., & Servais, L. (2018). Development of a decision-analytic model for the economic evaluation of newborn screening for spinal muscular atrophy. Neuromuscular Disorders, 28 (S29–S146), 59. doi:10.1016/j.nmd.2018.06.125
Peer Reviewed verified by ORBi

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