[The pathogenesis of INH-neuropathy. I. Fine structural similarities and differences to wallerian degeneration]

Pustular diseases and keratinocyte-myeloid synergy.

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Novel SBF2 mutations and clinical spectrum of Charcot-Marie-Tooth neuropathy type 4B2.

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Neuromuscular disorders : NMD·2013

Immunohistological pointers to a possible role for excessive cathelicidin (LL-37) expression by apocrine sweat glands in the pathogenesis of hidradenitis suppurativa/acne inversa.

The British journal of dermatology·2011

Oculopharyngeal muscle dystrophy: fine structure and mRNA expression levels of PABPN1.

Clinical neuropathology·2011

Incontinetia pigmenti-related myopathy or unsolved "double trouble"?

Neuromuscular disorders : NMD·2010

Deletion or immunotherapeutic blockade of FcγRIIb (CD32b) impairs α-Syn propagation in vivo.

Acta neuropathologica·2026

Functional proteomic and phosphoproteomic profiling of routine FFPE CNS tumor tissue complements genomic and epigenomic characterization.

Acta neuropathologica·2026

Integrative synaptosome multi-omics reveals disrupted synapse organization and localized cryptic transcripts in C9ORF72-frontotemporal dementia.

Acta neuropathologica·2026

Integrated multi-omics identifies lineage-dependent myeloid cells recruitment and the APP-CD74 axis as an immunoregulatory target in pediatric high-grade glioma.

Acta neuropathologica·2026

Life at the interface: Byron Caughey's search for prion disease inhibitors through chemistry, structure, and cell physiology.

Acta neuropathologica·2026

Peripheral TDP-43 pathology in amyotrophic lateral sclerosis: toward a systemic proteinopathy.

Acta neuropathologica·2026

When the Electromyography (EMG) and the Patient Disagree: Unraveling a Motor Neuron Disease Mimic With Small-Fiber Dysfunction.

Cureus·2026

Human iPSC-Derived Tissue-Engineered Nigrostriatal Pathway for Chronic Restoration of Dopaminergic Axon Tracts in a Rat Parkinson's Model.

Advanced healthcare materials·2026

Increased CCR2-immunopositive myeloid cells in the putamen and cerebellar white matter with blood-brain barrier disruption in multiple system atrophy.

Neuroscience letters·2026

Loss of Cotl1 disrupts mitochondrial fission and impairs learning and memory in mice.

Life sciences·2026

Polydatin Encapsulated in Human Serum Albumin Nanoparticles Attenuates Oxidative Damage and Protects Rotenone-Induced Neuroblastoma cells.

European journal of pharmacology·2026

Comparative quantitative analysis of choroidal abnormalities in patients with type 1 neurofibromatosis using multimodal retinal imaging.

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie·2026

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[The pathogenesis of INH-neuropathy. I. Fine structural similarities and differences to wallerian degeneration]

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Pustular diseases and keratinocyte-myeloid synergy.

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Immunohistological pointers to a possible role for excessive cathelicidin (LL-37) expression by apocrine sweat glands in the pathogenesis of hidradenitis suppurativa/acne inversa.

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