نتایج جستجو برای: plexiform

تعداد نتایج: 2398  

Journal: :Revista Española de Enfermedades Digestivas 2020

Journal: :Journal of Oral and Maxillofacial Pathology 2014

Journal: :IP International Journal of Maxillofacial Imaging 2019

Journal: :Medical Journal of Dr. D.Y. Patil Vidyapeeth 2021

Journal: :Neurology 2021

Optical coherence tomography (OCT) is considered a key research tool to monitor neurodegenerative processes in CNS disorders. This particularly applicable multiple sclerosis (MS), which retinal changes (peripapillary nerve fiber layer and ganglion cell–inner plexiform [GCIPL] thicknesses) tend reflect MRI markers of damage atrophy, especially eyes not affected by previous optic neuritis.1

Journal: :International Journal of Medical and Biomedical Studies 2022

Introduction Ameloblastoma is common benign epithelial tumor of odontogenic origin. The presentation ameloblastoma unique as it locally aggressive with high recurrence rate if not treated adequately. This study aimed to conduct retrospective analyze the characteristics and management in patient Oral Maxillofacial Surgery at Hasan Sadikin General Hospital between periods January 2020 – December ...

2012
Yujuan Wang Mones S Abu-Asab Wei Li Mary E Aronow Arun D Singh Chi-Chao Chan

BACKGROUND Paraneoplastic retinopathy is caused by the cross-reaction of neoplasm-directed autoantibodies against retinal antigens and results in retinal damage. Paraneoplastic vitelliform retinopathy, a presumed paraneoplastic retinopathy with features of atypical melanoma-associated retinopathy, has recently been reported in patients with metastatic melanoma. Ocular ultrastructure and its aut...

2018
Fan Yang Song Xu Renwang Liu Tao Shi Xiongfei Li Xuebing Li Gang Chen Hongyu Liu Qinghua Zhou Jun Chen

Introduction Neurofibromatosis type 1 (NF1) is a common Mendelian multi-system disorder that is characterized by café-au-lait spots (CLS), axillary freckling, optic glioma and plexiform neurofibroma. Various mutations of the NF1 gene are widely accepted to be the main cause of this disease, while whether there are still certain other modifier genes that could influence the phenotypes of NF1 is ...

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