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Hacohen, Yael

https://orcid.org/0000-0001-8490-9657

Mayo Clinic

Great Ormond Street Hospital

Citations 10

Outcomes After Acute Plasma Exchange for Myelin Oligodendrocyte Glycoprotein Antibody–Associated Disease
Thakolwiboon, Smathorn , Redenbaugh, Vyanka , Chen, Bo , Hewitt, S., Shah, Shailee , Lotan, Itay , Levy, Michael , Forcadela, Mirasol , Huda, Saif , Pique, Julie , Marignier, Romain , Audoin, Bertrand , Poullin, Pascale , Champsas, Dimitrios , Choi, David, Danesh‐Meyer, Helen V. , Vasileiou, Eleni S. , Sotirchos, Elias S. , Davis, James , Wilf‐Yarkoni, Adi , Bonelli, Laura , Arnold, Anthony C. , Motte, Marine Boudot de la , Deschamps, Romain , Jitprapaikulsan, Jiraporn , Moss, Heather E. , Navarro, Sylvia E. Villarreal , Mao‐Draayer, Yang , Mishra, Murli , Tisavipat, Nanthaya , Tajfirouz, Deena , Tillema, Jan-Mendelt , López‐Chiriboga, A. Sebastian , Palace, Jacqueline , Chen, John J. , Boutiere, Clemence , Audoin, Bertrand , Champsas, Dimitrios , Vasileiou, Eleni , Sotirchos, Elias S , Henderson, Amanda D , Wilf-Yarkoni, Adi , Stiebel-Kalish, Hadas , Maillart, Elisabeth , Bonelli, Laura , Deschamps, Romain , Jitprapaikulsan, Jiraporn , Moss, Heather E , Villarreal Navarro, Sylvia E , Mao-Draayer, Yang , Mishra, Murli , Vorasoot, Nisa , Cacciaguerra, Laura , Tisavipat, Nanthaya , Tajfirouz, Deena , Tillema, Jan‐Mendelt , Lopez-Chiriboga, A Sebastian , Palace, Jacqueline , Hacohen, Yael , Pittock, S J , Flanagan, E P , Chen, John J , Levy, Michael , Shah, Shailee , Lotan, Itay , Thakolwiboon, Smathorn , Hewitt, Sage, Henderson, Amanda D. , Stiebel‐Kalish, Hadas , Vorasoot, Nisa , Cacciaguerra, Laura , Hacohen, Yael , Pittock, Sean J. , Flanagan, Eoin P.

Neurology | August 29, 2025 | Volume: 105 | Issue: 6 | Pages: No page available

10.1212/wnl.0000000000213903 Get It

Meningitis as an Attack Phenotype of Myelin Oligodendrocyte Glycoprotein Antibody–Associated Disease
Aboseif, Albert , Kim, Nee Na , Bou, Gabriela , Nathoo, Nabeela , Guo, Yong , Pique, Julie , Kerbrat, Anne, Audoin, Bertrand, Demortière, Sarah , Bourre, Bertrand , Ciron, Jonathan , Chen, John J. , Tolédano, Michel B. , Quek, Amy May Lin, Marignier, Romain , Chen, John J , Ciron, Jonathan , Nathoo, Nabeela , Aboseif, Albert , Kerbrat, Anne , Audoin, Bertrand , Bourre, Bertrand , Cacciaguerra, Laura , Toledano, Michel, Gombolay, Grace , Hacohen, Yael , Flanagan, Eoin P.

JAMA Neurology | June 16, 2025 | Volume: 82 | Issue: 8 | Pages: 871

10.1001/jamaneurol.2025.1774 Get It

This international multicenter study seeks to determine the frequency and characteristics of meningitis in myelin oligodendrocyte glycoprotein antibody (MOGAD)–associated disease and highlight its pathology.
Investigating Radiological Lag and the Temporal Evolution of MRI Lesions Within the Same Attack in MOGAD (S32.008)
Mankad, Kshitij , Krecke, Karl N. , Chen, John , Redenbaugh, Vyanka , Lopez, Alfonso, Sánchez, Cristina Valencia, Tillema, Jan‐Mendelt , Cacciaguerra, Laura , Abdel‐Mannan, Omar , Champsas, Dimitrios , Syc‐Mazurek, Stephanie B. , Hemingway, Cheryl , Ciccarelli, Olga , Pittock, Sean J. , Hacohen, Yael , Flanagan, Eoin P.

Neurology | April 9, 2024 | Volume: 102 | Issue: 7_supplement_1 | Pages: No page available

10.1212/wnl.0000000000205834 Get It

Intravenous immunoglobulin treatment for acute attacks in myelin oligodendrocyte glycoprotein antibody disease
Lotan, Itay , Chen, John J. , Huda, Saif , Gibbons, Emily , Wilf‐Yarkoni, Adi , Hellmann, Mark A. , Pittock, Sean J, Molazadeh, Negar , Anderson, Monique , Salky, Rebecca, Romanow, Gabriela , Schindler, Patrick , Paul, Friedemann , Levy, Michael , Pittock, Sean J. , Pittock, S J , Pittock, Sean J , Flanagan, E P , Molazadeh, Negar , Levy, Michael , Chen, John J , Paul, Friedemann , Lotan, Itay , Schindler, Patrick , Hacohen, Yael , Abdel‐Mannan, Omar , Mariotto, Sara , Stiebel‐Kalish, Hadas , Flanagan, Eoin P. , Duchow, Ankelien Solveig

Multiple Sclerosis Journal | July 11, 2023 | Volume: 29 | Issue: 9 | Pages: 1080-1089

10.1177/13524585231184738 Get It

Background: The potential therapeutic benefit of intravenous immunoglobulins (IVIGs) for acute attacks of myelin oligodendrocyte glycoprotein antibody disease (MOGAD) is unknown. Objective: The objective was to describe the outcomes of IVIG treatment for acute MOGAD attacks. Methods: A retrospective observational study involving seven tertiary neuroimmunology centers. Data collection included patients’ demographics, Expanded Disability Status Scale (EDSS), and visual acuity (VA) before the attack, at the nadir of the attack before IVIG treatment, and at follow-up visits ⩾3 months after treatment. Results: Thirty-nine patients were included, of which 21 (53.8%) were female. The median age was 23 years (range 5–74 years), and the median disease duration was 4 months (range 0–93 months). The most common type of attack treated with IVIG was isolated optic neuritis (ON) (unilateral n = 14, bilateral n = 5, associated with transverse myelitis (TM), n = 1), followed by acute disseminated encephalomyelitis (ADEM) ( n = 8), multifocal ( n = 7), TM ( n = 3), brainstem ( n = 1), and other encephalitis ( n = 1). A significant improvement in both the EDSS and VA measures was observed at follow-up compared to the time of IVIG treatment initiation ( p < 0.0001 for both outcome measures). Conclusion: IVIG may be an effective treatment option for acute MOGAD attacks. Further prospective studies are warranted to validate our results.
Comparison of MRI T2-lesion evolution in pediatric MOGAD, NMOSD, and MS
Redenbaugh, Vyanka , McCombe, Jennifer A. , Tillema, Jan‐Mendelt , Chen, John J. , López‐Chiriboga, A. Sebastian , Sechi, Elia , Pittock, Sean J, Pittock, Sean J. , Kunchok, Amy , Pittock, S J , Chia, Nicholas H , Lopez-Chiriboga, A Sebastian , Sechi, Elia , Pittock, Sean J , Flanagan, E P , Chen, John J , Redenbaugh, Vyanka , Chia, Nicholas , Cacciaguerra, Laura , Hacohen, Yael , Flanagan, Eoin P.

Multiple Sclerosis Journal | May 23, 2023 | Volume: 29 | Issue: 7 | Pages: 799-808

10.1177/13524585231166834 Get It

Background: Magnetic resonance imaging (MRI) T2-lesions resolve more often in myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD) than aquaporin-4 IgG-positive neuromyelitis optica spectrum disorder (AQP4 + NMOSD) and multiple sclerosis (MS) in adults but few studies analyzed children. Objective: The main objective of this study is to investigate MRI T2-lesion evolution in pediatric MOGAD, AQP4 + NMOSD, and MS. Methods: Inclusion criteria were as follows: (1) first clinical attack; (2) abnormal MRI (⩽6 weeks); (3) follow-up MRI beyond 6 months without relapses in that region; and (4) age < 18 years. An index T2-lesion (symptomatic/largest) was identified, and T2-lesion resolution or persistence on follow-up MRI was determined. Results: We included 56 patients (MOGAD, 21; AQP4 + NMOSD, 8; MS, 27) with 69 attacks. Index T2-lesion resolution was more frequent in MOGAD (brain 9 of 15 [60%]; spine 8 of 12 [67%]) than AQP4 + NMOSD (brain 1 of 4 [25%]; spine 0 of 7 [0%]) and MS (brain 0 of 18 [0%]; spine 1 of 13 [8%]), p < 0.01. Resolution of all T2-lesions occurred more often in MOGAD (brain 6 of 15 [40%]; spine 7 of 12 [58%]) than AQP4 + NMOSD (brain 1 of 4 [25%]; spine 0 of 7 [0%]), and MS (brain 0 of 18 [0%]; spine 1 of 13 [8%]), p < 0.01. Reductions in median index T2-lesion area were greater in MOGAD (brain, 305 mm; spine, 23 mm) than MS (brain, 42 mm [ p<0.001]; spine, 10 mm [ p<0.001]) without differing from AQP4 + NMOSD (brain, 133 mm [ p=0.42]; spine, 19.5 mm [ p=0.69]). Conclusion: In children, MRI T2-lesions resolved more often in MOGAD than AQP4 + NMOSD and MS which is similar to adults suggesting these differences are related to pathogenesis rather than age.
The risk of infections for multiple sclerosis and neuromyelitis optica spectrum disorder disease-modifying treatments: Eighth European Committee for Treatment and Research in Multiple Sclerosis Focused Workshop Review. April 2021
Tur, Carmen , Otero‐Romero, Susana , Amato, Maria Pia , Derfuss, Tobias , Pauli, Franziska Di , Abboud, Hesham , Achiron, Anat , Casanova, Jean‐Laurent , Clifford, David B. , Fonderico, Mattia , Gouider, Riadh , Hacohen, Yael , Kappos, Ludwig , Ladeira, Filipa , Louapre, Céline , Magyari, Melinda , Papeix, Caroline , Piehl, Fredrik , Ruíz-Camps, Isabel , Selmaj, Krzysztof , Simpson, Steve , Sıva, Aksel , Vaknin‐Dembinsky, Adi , Weinshenker, Brian G. , Winkelmann, Alexander, Rodas, María Isabel Zuluaga , Tintoré, Mar , Amato, Maria Pia , Derfuss, Tobias , Abboud, Hesham , Achiron, Anat , Dobson, Ruth , Filippi, Massimo , Fitzgerald, Kathryn C , Fonderico, Mattia , Hellwig, Kerstin , Hemmer, Bernhard , Ladeira, Filipa , Lebrun‐Frénay, Christine , Magyari, Melinda , Oreja-Guevara, Celia , Pandit, Lekha , Papeix, Caroline , Portaccio, Emilio , Simpson-Yap, Steve , Siva, Aksel , Sormani, Maria P , Vukusic, Sandra , Wiendl, Heinz , Tintoré, Mar , Weinshenker, Brian G , Casanova, Jean Laurent , Hacohen, Yael , Dubessy, Anne‐Laure , Iacobaeus, Ellen , Mycko, Marcin P. , Bellinvia, Angelo , Boyко, Alexey , Farez, Mauricio , Filippi, Massimo , Mehling, Matthias , Oreja‐Guevara, Celia , Pandit, Lekha , Sørensen, Per Soelberg , Sormani, Maria Pia , Trojano, María , Wiendl, Heinz , Stankoff, Bruno

Multiple Sclerosis Journal | February 24, 2022 | Volume: 28 | Issue: 9 | Pages: 1424-1456

10.1177/13524585211069068 Get It

Over the recent years, the treatment of multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD) has evolved very rapidly and a large number of disease-modifying treatments (DMTs) are now available. However, most DMTs are associated with adverse events, the most frequent of which being infections. Consideration of all DMT-associated risks facilitates development of risk mitigation strategies. An international focused workshop with expert-led discussions was sponsored by the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) and was held in April 2021 to review our current knowledge about the risk of infections associated with the use of DMTs for people with MS and NMOSD and corresponding risk mitigation strategies. The workshop addressed DMT-associated infections in specific populations, such as children and pregnant women with MS, or people with MS who have other comorbidities or live in regions with an exceptionally high infection burden. Finally, we reviewed the topic of DMT-associated infectious risks in the context of the current SARS-CoV-2 pandemic. Herein, we summarize available evidence and identify gaps in knowledge which justify further research.