Publicaciones científicas

Wetzel NS, Kulsvehagen L, Lecourt AC, Filipek B, Lipps P, Rieder L, Berve K, Krishnamoorthy G, 't Hart BA, Schirmer L, Yandamuri SS, O'Connor KC, Pröbstel AK. ...

Año publicación:

2026

Número de revista:

Neurology Neuroimmunology & Neuroinflammation vol. 13 n. 1

https://www.neurology.org/doi/full/10.1212/NXI.0000000000200520

Artículo

Patterns and Trajectories of Behavioral and Neuropsychiatric Symptoms in Frontotemporal Dementia and Primary Progressive Aphasia.

Autor/es:

Marth L, Martinez-Murcia FJ, Górriz-Sáez JM, Denecke J, Ewers M, Prix C, Stockbauer AC, Bernhardt AM, Wagemann O, Wlasich E, Kustermann J, Peters O, Hellmann-Regen J, Droste Zu Senden L, Priller J, Spruth EJ, Spottke A, Asperger H, Schroeck F, Gamez A, Schneider A, Fliessbach K, Dinter E, Linn J,...

Año publicación:

2026

Número de revista:

Neurology vol. 106 n. 4

https://www.neurology.org/doi/full/10.1212/WNL.0000000000214510

Pearls & Oy-sters: Hereditary Spastic Paraplegia Type 15 Presenting as Juvenile Onset Levodopa-Responsive Parkinsonism.

Autor/es:

Thatikala A, Boddu AV, Nayar D, Virmani T.

Resident & Fellow Section

Año publicación:

2026

Número de revista:

Neurology vol. 106 n. 3

https://www.neurology.org/doi/full/10.1212/WNL.0000000000214514

Pearls & Oy-sters: Reversible Leukoencephalopathy and Parkinsonism Due to CNS Involvement in Cryoglobulinemia.

Autor/es:

German A, Grotemeyer A, Rothhammer V, Doerfler A, Winkler J, Regensburger M.

Resident & Fellow Section

Año publicación:

2026

Número de revista:

Neurology vol. 106 n. 3

https://www.neurology.org/doi/full/10.1212/WNL.0000000000214622

Pearls & Oy-sters: SCA27B as an Elusive Genetic Cause of Episodic Neurologic Symptoms in Later Adulthood.

Autor/es:

Yomtoob J, Morse L, Keller Sarmiento IJ, Kinsley L, Gomez CM, Opal P, Mencacci NE.

Resident & Fellow Section

Año publicación:

2026

Número de revista:

Neurology vol. 106 n. 6

https://www.neurology.org/doi/full/10.1212/WNL.0000000000214754

Pearls & Oy-sters: Use of Short-Acting B-Agonist in DOK7-Related Congenital Myasthenic Syndrome Treatment.

Autor/es:

Gill H, Van Slooten R, Wilson A, Bromberg MB, Butterfield RJ.

Resident & Fellow Section

Año publicación:

2026

Número de revista:

Neurology vol. 106 n. 7

https://www.neurology.org/doi/full/10.1212/WNL.0000000000214797

Pearls & Oy-sters: Using Susceptibility-Based Imaging in Highly Active Late-Onset Multiple Sclerosis.

Autor/es:

Martinez Sosa S, Tisavipat N, Betting T, Guo Y, Pillai JJ, Stitt D, Flanagan EP, Paz Soldán MM, Aboseif A.

Resident & Fellow Section

Año publicación:

2026

Número de revista:

Neurology vol. 106 n. 7

https://www.neurology.org/doi/full/10.1212/WNL.0000000000214794

Artículo

Pediatric Cohort of Charcot-Marie-Tooth Disease: Clinical Features and Genetic Distribution.

Autor/es:

Alawneh I, Alemán A, Nigro E, Bouchard M, Gonorazky HD.

Año publicación:

2026

Número de revista:

Neurology® Genetics. vol. 12 n. 1

https://www.neurology.org/doi/full/10.1212/NXG.0000000000200339

Una iniciativa de:

Buscador

Patient Perspective: Closing the Gap: Personal and Clinical Reflections on Functional Neurologic Disorder.

Patient Perspective: Words That Matter: Reflections on a Patient's Experiences With Guillain-Barré Syndrome.

Patient-Derived Monoclonal Myelin Oligodendrocyte Glycoprotein Autoantibodies Mediate Cytotoxicity.

Patterns and Trajectories of Behavioral and Neuropsychiatric Symptoms in Frontotemporal Dementia and Primary Progressive Aphasia.

Pearls & Oy-sters: Hereditary Spastic Paraplegia Type 15 Presenting as Juvenile Onset Levodopa-Responsive Parkinsonism.

Pearls & Oy-sters: Reversible Leukoencephalopathy and Parkinsonism Due to CNS Involvement in Cryoglobulinemia.

Pearls & Oy-sters: SCA27B as an Elusive Genetic Cause of Episodic Neurologic Symptoms in Later Adulthood.

Pearls & Oy-sters: Use of Short-Acting B-Agonist in DOK7-Related Congenital Myasthenic Syndrome Treatment.

Pearls & Oy-sters: Using Susceptibility-Based Imaging in Highly Active Late-Onset Multiple Sclerosis.

Pediatric Cohort of Charcot-Marie-Tooth Disease: Clinical Features and Genetic Distribution.

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