Results 171 to 180 of about 13,295,690 (363)

Expert System to Diagnose Skin Diseases What Caused by Virus or Bacteria [PDF]

, 2009
Expert system for diagnosing skin diseases caused by viruses or bacteria is an expert system that can diagnose skin disease suffered by the patient without having to deal directly with doctors or specialists skin diseases.
Willyadi, R. K. (Rahmat), Yudi Irawan Chandra, SKom, MMSI   +1 more
core  

Evidence of Iron Accumulation in Cerebral Adrenoleukodystrophy: A Potential Novel Disease Mechanism

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT In this first application of Quantitative Susceptibility Mapping Source Separation to cerebral adrenoleukodystrophy, we uncovered alterations in iron and myelin within lesions and normal appearing white matter. As validation, we demonstrate abnormal iron accumulation in those same compartments within primary brain tissue.
Christina L. Nemeth, Mert Sisman, Jinwei Zhang, Hyeong‐geol Shin, Xu Li, Bela Turk, Ali Fatemi, Thanh Nguyen, Eric Mallack   +8 more
wiley   +1 more source

Factors associated with a better treatment efficacy among psoriasis patients: a study based on decision tree model and logistic regression in Shanghai, China

BMC Public Health
Background Many effective therapies for psoriasis are being applied in clinical practice in recent years, however, some patients still can’t achieve satisfied effect even with biologics.
Fanlingzi Shen, Zhen Duan, Siyuan Li, Zhongzhi Gao, Rui Zhang, Xiangjin Gao, Bin Li, Ruiping Wang   +7 more
doaj   +1 more source

Systemic comparison of molecular characteristics in different skin fibroblast senescent models

Chinese Medical Journal
. Background:. Senescent human skin primary fibroblast (FB) models have been established for studying aging-related, proliferative, and inflammatory skin diseases.
Xiaokai Fang, Shan Zhang, Mingyang Wu, Yang Luo, Xingyu Chen, Yuan Zhou, Yu Zhang, Xiaochun Liu, Xu Yao, Lishao Guo   +9 more
doaj   +1 more source

Minimally Clinically Important Difference of the Clinical Assessment Scale in Autoimmune Encephalitis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT The Clinical Assessment Scale in Autoimmune Encephalitis (CASE) tracks disease severity in autoimmune encephalitis (AE), but no threshold for significant change exists. We aimed to determine the minimally clinically important difference (MCID) for CASE.
Yihui Goh, Yoon Hee Shin, Soo Hyun Ahn, Su Yee Mon, Soo Jean Shin, Woo‐Jin Lee, Yoonhyuk Jang, Myoung‐Jin Jang, Soon‐Tae Lee   +8 more
wiley   +1 more source

The Efficacy of an Innovative Method of Melanocytes-Keratinocytes Suspension for the Treatment of Stable Vitiligo (A Report of 20 Cases)

مجله دانشکده پزشکی اصفهان, 2016
Background: Vitiligo is the most common chronic depigmentation disorder caused by melanocyte loss in the basal epidermis. Drug therapy and surgical procedures are two main modalities for its treatment and one of the most effective surgical procedures is ...
Fariba Jaffary, Mohammad Ali Nilforoushzadeh, Elaheh Haftbaradaran, Azadeh Zolfaghari-Baghbaderani, Zahra Mollabashi   +4 more
doaj  

Meta-Analysis of Gene Expression Reveals the Core Transcriptomic Profile of Lesional Scalp in Alopecia Areata

Dermatology and Therapy
Introduction Alopecia areata (AA) is an immune-mediated inflammatory skin disease that targets hair follicles. Current research yields varied lists of differentially expressed genes (DEGs).
Irene Rivera-Ruiz, Jesús Gay-Mimbrera, Pedro J. Gómez-Arias, Macarena Aguilar-Luque, Miguel Juan-Cencerrado, Carmen Mochón-Jiménez, Esmeralda Parra-Peralbo, Beatriz Isla-Tejera, Francisco Gómez-García, Juan Ruano   +9 more
doaj   +1 more source

SPG4 and Dementia: Expanding the Clinical Spectrum

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza, Arun Meyyazhagan, Eliseo Picchi, Gustavo Ribas, Ingrid Faber, Ryosuke Miyamoto, Preethi Basavaraju, Paolo Eusebi, Haripriya Kuchi Bhotla, Mario Stasi, Fabrizio Gaudiello, Francesco Patti, Filippo Maria Santorelli, Marcondes Cavalcante França Jr, José Luiz Pedroso, Orlando Graziani Povoas Barsottini, Hélio Afonso Ghizoni Teive, Peter Henry St George‐Hyslop, Toshitaka Kawarai, Antonio Orlacchio   +19 more
wiley   +1 more source

تأثیر سودوكاتالاز/سوپراکسید دیسموتاز در درمان ویتیلیگو: یک مطالعه‌ی مقدماتی

مجله دانشکده پزشکی اصفهان, 2014
مقدمه: سودوكاتالاز/سوپراکسید دیسموتاز (PSD یا Pseudocatalase/superoxide dismutase) یک ژل موضعی است که به خاطر داشتن اثرات درمانی، در درمان ویتیلیگو مورد استفاده قرار می‌گیرد. این مطالعه به منظور بررسی اثر این ترکیب در ویتیلیگو طراحی شد.
Farahnaz Fatemi-Naeini, Alireza Vaez-Shooshtari, Bahareh Ebrahimi, Mohammad Ali Nilforoushzadeh, Razieh Molaei   +4 more
doaj  

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu, Xin Duan, Fatemeh Peymani, Jia Wang, Chengjia Bao, Chaolong Xu, Ying Zou, Zixuan Zhang, Yunxi Zhang, Tongyue Li, Martin Pavlov, Junling Wang, Minhan Song, Tianyu Song, Xiaodi Han, Mingxi Sun, Danmin Shen, Ruoyu Duan, Huafang Jiang, Manting Xu, Holger Prokisch, Fang Fang   +21 more
wiley   +1 more source