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Distinct TERT promoter C228T and C250T mutations in a patient with an oligodendroglioma: A case report

期刊: NEUROPATHOLOGY, 2021; 41 (3)

The majority of oligodendroglial tumors harbor mutations in the telomerase reverse transcriptase (TERT) gene (TERT) promoter and the isocitrate dehydr......

Diffuse midline glioma with H3 K27M mutation in the spinal cord: A series of 33 cases

期刊: NEUROPATHOLOGY, ; ()

We investigated the risk factors for diffuse midline gliomas of the spinal cord (DMGSCs). Seventy patients with spinal cord gliomas in two hospitals w......

Supratentorial ependymoma with YAP1:FAM118B fusion: A case report

期刊: NEUROPATHOLOGY, ; ()

We report a case of a 26-year-old Chinese man who had experienced three grand mal seizures in the past two months. Magnetic resonance imaging revealed......

Formation of new lymphatic vessels in glioma: An immunohistochemical analysis

期刊: NEUROPATHOLOGY, 2020; 40 (3)

We investigated the distribution and formation of new lymphatic vessels in gliomas. Specimens from seven glioma cases were analyzed by immunohistochem......

Phosphatase and tensin homolog deletion enhances neurite outgrowth during neural stem cell differentiation

期刊: NEUROPATHOLOGY, 2020; 40 (3)

Neural stem cell (NSC) transplantation has emerged as a promising approach for the treatment of neurological disorders such as cerebral ischemia. As t......

Red nucleus IL-6 mediates the maintenance of neuropathic pain by inducing the productions of TNF-alpha and IL-1 beta through the JAK2/STAT3 and ERK signaling pathways

期刊: NEUROPATHOLOGY, 2020; 40 (4)

We previously reported that interleukin (IL)-6 in the red nucleus (RN) is involved in the maintenance of neuropathic pain induced by spared nerve inju......

Investigation of adult-onset multipleAcyl-CoAdehydrogenase deficiency associated with peripheral neuropathy

期刊: NEUROPATHOLOGY, 2020; 40 (6)

Multiple Acyl-CoA dehydrogenase deficiency (MADD), one of the most common lipid storage myopathies (LSMs), is a heterogeneous inherited muscular disor......

High-grade gliomas with isocitrate dehydrogenase wild-type and 1p/19q codeleted: Atypical molecular phenotype and current challenges in molecular diagnosis

期刊: NEUROPATHOLOGY, 2020; 40 (6)

Glioma is the most common intracranial malignant tumor, with poor prognosis. The new World Health Organization (WHO) integrated classification (2016) ......

An adult case of diffuse midline glioma withH3K27M mutation

期刊: NEUROPATHOLOGY, 2020; 40 (6)

Cartilaginous metaplasia is rare in primary central nervous system (CNS) neoplasms and has not been described in the histone 3 (H3) gene (H3) with a s......

Dexmedetomidine protects rats from postoperative cognitive dysfunction via regulating the GABA(B)R-mediated cAMP-PKA-CREB signaling pathway

期刊: NEUROPATHOLOGY, 2019; 39 (1)

This work attempts to discuss whether dexmedetomidine (Dex) can protect rats from postoperative cognitive dysfunction (POCD) through regulating the ga......

JIF:2.16

A case of solitary fibrous tumor/hemangiopericytoma in the central nervous system with papillary morphology

期刊: NEUROPATHOLOGY, 2019; 39 (2)

This report describes the clinicopathological findings of a solitary fibrous tumor (SFT)/hemangiopericytoma (HPC) of the central nervous system in a 5......

JIF:2.16

Modified Xiaoyaosan reverses aberrant brain regional homogeneity to exert antidepressive effects in mice

期刊: NEUROPATHOLOGY, 2019; 39 (2)

The aim of this study is to explore the macroscale neural mechanisms of the antidepressant effects of Xiaoyaosan, a traditional Chinese herbal formula......

JIF:2.16

A family with nemaline myopathy type 6 caused by hseterozygous mutation (c.1222C>T) in the KBTBD13 gene in China: A case report

期刊: NEUROPATHOLOGY, 2020; 40 (1)

Nemaline myopathy (NEM) is a congenital myopathy that typically presents with proximal muscle weakness and hypotonia. To date, 13 genes have been asso......

Identification of a novel SGCA missense mutation in a case of limb-girdle muscular dystrophy 2D with the absence of four sarcoglycan proteins

期刊: NEUROPATHOLOGY, 2019; 39 (3)

Limb-girdle muscular dystrophy 2D (LGMD2D) is caused by mutations in the alpha-sarcoglycan gene (SGCA). Due to lack of specificity, it is impossible t......

JIF:2.16

Sural nerve pathology in TFG-associated motor neuron disease with sensory neuropathy

期刊: NEUROPATHOLOGY, 2019; 39 (3)

The tropomyosin-receptor kinase fused gene (TFG) functions in vesicles formation and egress at the endoplasmic reticulum (ER). A heterozygous missense......

JIF:2.16

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