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892 results

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Page 1
Defining the typical characteristics of orthostatic headache in patients with spontaneous intracranial hypotension.
Mehta D, Cheema S, Glover S, Qureshi AM, Davagnanam I, Kamourieh S, Sayal P, Toma A, Lagrata S, Joy C, Duncan C, Anderson J, Davies B, Dorman PJ, Angus-Leppan H, Walkden J, Rohrer J, Matharu MS. Mehta D, et al. Among authors: rohrer j. Cephalalgia. 2025 Jan;45(1):3331024241308154. doi: 10.1177/03331024241308154. Cephalalgia. 2025. PMID: 39781568
Primary Progressive Aphasia in Italian and English: A Cross-Linguistic Cohort Study.
Mazzeo S, Hardy CJD, Jiang J, Morinelli C, Moschini V, Brooks E, Johnson JCS, Chokesuwattanaskul A, Giacomucci G, Volkmer A, Rohrer JD, Ingannato A, Bagnoli S, Padiglioni S, Nacmias B, Sorbi S, Bessi V, Warren JD. Mazzeo S, et al. Among authors: rohrer jd. Neurology. 2024 Dec 24;103(12):e210058. doi: 10.1212/WNL.0000000000210058. Epub 2024 Nov 21. Neurology. 2024. PMID: 39571120 Free PMC article.
Association of Changes in Cerebral and Hypothalamic Structure With Sleep Dysfunction in Patients With Genetic Frontotemporal Dementia.
Best PT, Van Swieten JC, Jiskoot LC, Moreno F, Sánchez-Valle R, Laforce R Jr, Graff C, Masellis M, Tartaglia C, Rowe JB, Borroni B, Finger E, Synofzik M, Galimberti D, Vandenberghe R, de Mendonça A, Butler C, Gerhard A, Le Ber I, Tiraboschi P, Santana I, Pasquier F, Levin J, Otto M, Sorbi S, Seelaar H, Bouzigues A, Cash DM, Russell LL, Bocchetta M, Rohrer JD, Devenyi GA, Chakravarty M, Ducharme S; Genetic Frontotemporal Dementia Initiative (GENFI). Best PT, et al. Among authors: rohrer jd. Neurology. 2024 Dec 10;103(11):e209829. doi: 10.1212/WNL.0000000000209829. Epub 2024 Nov 11. Neurology. 2024. PMID: 39527773 Free article.
Association of Initial Side of Brain Atrophy With Clinical Features and Disease Progression in Patients With GRN Frontotemporal Dementia.
Borrego-Ecija S, Juncà-Parella J, Vandebergh M, Pérez Millan A, Balasa M, Llado A, Bouzigues A, Russell LL, Foster PH, Ferry-Bolder E, Van Swieten JC, Jiskoot LC, Seelaar H, Laforce R Jr, Graff C, Galimberti D, Vandenberghe R, de Mendonça A, Tiraboschi P, Santana I, Gerhard A, Levin J, Sorbi S, Otto M, Pasquier F, Ducharme S, Butler C, Le Ber I, Finger E, Tartaglia MC, Masellis M, Rowe JB, Synofzik M, Moreno F, Borroni B, Rademakers R, Rohrer JD, Sánchez-Valle R; Genetic Frontotemporal Initiative (GENFI). Borrego-Ecija S, et al. Among authors: rohrer jd. Neurology. 2024 Dec 10;103(11):e209944. doi: 10.1212/WNL.0000000000209944. Epub 2024 Nov 11. Neurology. 2024. PMID: 39527772 Free PMC article.
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses.
Demidov G, Yaldiz B, Garcia-Pelaez J, de Boer E, Schuermans N, Van de Vondel L, Paramonov I, Johansson LF, Musacchia F, Benetti E, Bullich G, Sablauskas K, Beltran S, Gilissen C, Hoischen A, Ossowski S, de Voer R, Lohmann K, Oliveira C, Topf A, Vissers LELM; Solve-RD Consortium; Laurie S. Demidov G, et al. NPJ Genom Med. 2024 Oct 26;9(1):49. doi: 10.1038/s41525-024-00436-6. NPJ Genom Med. 2024. PMID: 39461972 Free PMC article.
892 results