Centro de documentación: resultados de la búsqueda

Autosomal Dominant FTH1 Variant Causing Pontocerebellar Hypoplasia and Late-Onset Neuroferritinopathy: A Case Report.
Autor/es:
Hebbink JA, Niermeijer JF, Vroegindeweij E, de Vries BBA, Pegge S, Kamsteeg EJ, Willemsen MAAP.
Clinical/Scientific Notes
Año publicación:
2026
Número de revista:
Neurology® Genetics. vol. 12 n. 1
https://www.neurology.org/doi/full/10.1212/NXG.0000000000200342
Expanding the Genetic Landscape of Congenital Insensitivity to Pain.
Autor/es:
Pho-Iam T, Kulsirichawaroj P, Likasitwattanakul S, Ridchuayrod N, Sanmaneechai O, Limwongse C, Zuchner S.
Clinical/Scientific Notes
Año publicación:
2026
Número de revista:
Neurology® Genetics. vol. 12 n. 1
https://www.neurology.org/doi/full/10.1212/NXG.0000000000200346
Variant Resolution Through RNA Testing and Affected Tissue Analysis in the Neurofibromatoses: A Case Series.
Autor/es:
Schatz KS, Applegate CD, Belzberg AJ, Chen Y, Romo CG, Slobogean B, Blakeley J, Dimachkie MM.
Clinical/Scientific Notes
Año publicación:
2026
Número de revista:
Neurology® Genetics. vol. 12 n. 1
https://www.neurology.org/doi/full/10.1212/NXG.0000000000200347
Artículo
Correction
Correction for: Vigliano AP, Luce L, Pastor Rueda JM, Chaves H, Mesa L, Carcione M, Mazzanti C, Llames Massini C, Radic CP, Cejas C, Giliberto F. Whole-Body Skeletal Muscle MRI Patterns in Female Dystrophinopathy Carriers. Neurol Genet. 2025 Sep 30;11(5):e200301. doi: 10.1212/NXG.0000000000200301...
Año publicación:
2026
Número de revista:
Neurology® Genetics. vol. 12 n. 1
https://www.neurology.org/doi/full/10.1212/NXG.0000000000200349
Expanding Evidence of Leptomeningeal Involvement in MOGAD and Its Relevance to Its Pathophysiology.
Autor/es:
Cacciaguerra L, Flanagan EP.
Editorial
Año publicación:
2026
Número de revista:
Neurology Neuroimmunology & Neuroinflammation vol. 13 n. 1
https://www.neurology.org/doi/full/10.1212/NXI.0000000000200474
Correction
Correction for: Jonsson DI, Sveinsson O, Moeini N, Pivac E, Wirdefeldt K, Brundin L, Iacobaeus E. Incidence, Etiology, and Long-Term Outcome of Acute Myelitis in Stockholm County, Sweden: A Population-Based Study. Neurol Neuroimmunol Neuroinflamm. 2025 Nov;12(6):e200472. doi: 10.1212/NXI...
Año publicación:
2026
Número de revista:
Neurology Neuroimmunology & Neuroinflammation vol. 13 n. 1
https://www.neurology.org/doi/full/10.1212/NXI.0000000000200526
Correction
Correction for: Jonsson DI, Sveinsson O, Moeini N, Pivac E, Wirdefeldt K, Brundin L, Iacobaeus E. Incidence, Etiology, and Long-Term Outcome of Acute Myelitis in Stockholm County, Sweden: A Population-Based Study. Neurol Neuroimmunol Neuroinflamm. 2025 Nov;12(6):e200472. doi: 10.1212/NXI...
Año publicación:
2026
Número de revista:
Neurology Neuroimmunology & Neuroinflammation vol. 13 n. 1
https://siidon.guttmann.com/es/Correction%20for%3A%20Jonsson%20DI%2C%20Sveinsson…
Artículo
Spinal Cord Leptomeningeal Enhancement as a Marker of Extensive Spinal Cord Involvement in Children With MOGAD.
Autor/es:
Bartiromo S, Alves C, O'Mahony J, Yeh EA, Marrie RA, Narayanan S, Waters PJ, Gajofatto A, Bar-Or A, Banwell BL, Fadda G; Canadian Pediatric Demyelinating Disease Network. ...
Año publicación:
2026
Número de revista:
Neurology Neuroimmunology & Neuroinflammation vol. 13 n. 1
https://www.neurology.org/doi/full/10.1212/NXI.0000000000200449
Artículo
Bruton Tyrosine Kinase Inhibition Limits Multiple Sclerosis Disease-Driving Inflammation While Promoting Regulatory B Cells.
Autor/es:
Dybowski S, Thode J, Freier M, Saberi D, Nessler S, Geladaris A, Häusser-Kinzel S, Ringelstein M, Torke S, Weber MS.
Año publicación:
2026
Número de revista:
Neurology Neuroimmunology & Neuroinflammation vol. 13 n. 1
https://www.neurology.org/doi/full/10.1212/NXI.0000000000200510
Artículo
HTLV-1-Specific CTL Accumulation in CSF Contributes to Neuroinflammation in HTLV-1-Associated Myelopathy.
Autor/es:
Nozuma S, Dozono M, Tanaka M, Kodama D, Yoshida T, Higuchi Y, Sakiyama Y, Matsuura E, Matsuzaki T, Takashima H, Kubota R.
Año publicación:
2026
Número de revista:
Neurology Neuroimmunology & Neuroinflammation vol. 13 n. 1
https://www.neurology.org/doi/full/10.1212/NXI.0000000000200508

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Autosomal Dominant FTH1 Variant Causing Pontocerebellar Hypoplasia and Late-Onset Neuroferritinopathy: A Case Report.

Expanding the Genetic Landscape of Congenital Insensitivity to Pain.

Variant Resolution Through RNA Testing and Affected Tissue Analysis in the Neurofibromatoses: A Case Series.

Correction

Expanding Evidence of Leptomeningeal Involvement in MOGAD and Its Relevance to Its Pathophysiology.

Correction

Correction

Spinal Cord Leptomeningeal Enhancement as a Marker of Extensive Spinal Cord Involvement in Children With MOGAD.

Bruton Tyrosine Kinase Inhibition Limits Multiple Sclerosis Disease-Driving Inflammation While Promoting Regulatory B Cells.

HTLV-1-Specific CTL Accumulation in CSF Contributes to Neuroinflammation in HTLV-1-Associated Myelopathy.

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