Publicacions científiques

Nakamura K, Kishita Y, Sugiura A, Ozaki K, Yatsuka Y, Matsumoto N, Okazaki A, Prokisch H, Maruyama K, Iwasa H, Murayama K, Matsumoto H, Ohtake A, Shiraishi Y, Okazaki Y.

Any publicació:

2026

Número de revista:

Neurology® Genetics. vol. 12 n. 1

https://www.neurology.org/doi/full/10.1212/NXG.0000000000200330

Article

Identification of Novel Genetic Risk Variants Associated With Early-Onset Ischemic Stroke in Taiwan.

Autor/s:

Wang YC, Liu KM, Gan YL, Chi NF, Lu LS, Chou CY, Wang LY, Chang LH, Hou MC, Fu YC, Chiou JF, Wu MS, Yang SF, Pang ST, Wang JY, Tsai YT, Huang CY, Chiu KM, Chen M, Chiang FT, Wang CH, Yao WJ, Lee SL, Huang CH, Liu YT, Wang SJ, Ko WY, Chen CH, Lee IH.

Any publicació:

2026

Número de revista:

Neurology vol. 106 n. 12

https://www.neurology.org/doi/full/10.1212/WNL.0000000000218126

Article

Identification of Nuclear Genetic Loci Linked to Clinical Features of the m.3243A>G Mitochondrial DNA Variant.

Autor/s:

Boggan RM, Michalettou TD, Ng YS, Franklin IG, Cortés LT, Alston CL, Blakely EL, Büchner B, Bugiardini E, Colclough K, Feeney C, Hanna MG, Hattersley AT, Klopstock T, Kornblum C, Mancuso M, Patel KA, Pitceathly RDS, Pizzamiglio C, Prokisch H, Schäfer J, Schaefer AM, Shepherd MH, Thaele A, Thomas RH...

Any publicació:

2026

Número de revista:

Neurology® Genetics. vol. 12 n. 4

https://www.neurology.org/doi/full/10.1212/NXG.0000000000200411

Identifying a High-Risk Hemorrhagic Phenotype in Children With Moyamoya Disease.

Autor/s:

Sun LR, Jordan LC.

Editorial

Any publicació:

2026

Número de revista:

Neurology vol. 106 n. 4

https://www.neurology.org/doi/full/10.1212/WNL.0000000000214718

Article

Identifying MicroRNA Biomarkers in Idiopathic Intracranial Hypertension: A Pilot Study.

Autor/s:

Hill LJ, Begum G, Thomas CN, Hubbard JC, Mugo C, Alimajstorovic Z, Botfield HF, Lyons HS, Thaller M, Yiangou A, Ludwig C, Grech O, Mitchell JL, Mollan SP, Sinclair AJ.

Any publicació:

2026

Número de revista:

Neurology vol. 107 n. 1

https://www.neurology.org/doi/full/10.1212/WNL.0000000000218162

Una iniciativa de:

Cercador

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

Human IgLON5 Antibodies Reduce Neuronal IgLON5 Clusters and Cause Motor Dysfunction in Mice.

Hyperbaric Oxygen Therapy Combined with Polarized Light Therapy on Neuropathic Foot Ulcer: A Randomized Controlled Study.

Hypnotic Cognitive Therapy for Chronic Pain in Spinal Cord Injury: A Randomized Controlled Trial.

Iatrogenic and Sporadic Cerebral Amyloid Angiopathy: Same Amyloid, Different Pathways?

Identification of Intronic Variants in NDUFA3 as a Cause of Leigh Syndrome by Whole Genome Sequencing and RNA Sequencing.

Identification of Novel Genetic Risk Variants Associated With Early-Onset Ischemic Stroke in Taiwan.

Identification of Nuclear Genetic Loci Linked to Clinical Features of the m.3243A>G Mitochondrial DNA Variant.

Identifying a High-Risk Hemorrhagic Phenotype in Children With Moyamoya Disease.

Identifying MicroRNA Biomarkers in Idiopathic Intracranial Hypertension: A Pilot Study.

Trobes a faltar informació? Fes-nos arribar els teus suggeriments!