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期刊名:Iranian journal of pathology

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ISSN:1735-5303

e-ISSN:2345-3656

IF/分区:0.0/

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共收录本刊相关文章索引692
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Malihe Ram,Ali Najafi,Mohammad Taghi Shakeri Malihe Ram
Background & objective: Microarray and next generation sequencing (NGS) data are the important sources to find helpful molecular patterns. Also, the great number of gene expression data increases the challenge of how to i...
Mehrdad Gholami,Mohammadreza Haghshenas,Mona Moshiri et al. Mehrdad Gholami et al.
Background & objective: Multidrug-resistant Acinetobacter baumannii (MDR-AB) is an important nosocomial pathogen which is associated with significant morbidity and mortality, particularly in high-risk populations. Aminogl...
Maliheh Khoddami,Seyed Alireza Nadji,Paria Dehghanian Maliheh Khoddami
Background and objective: Langerhans cell histiocytosis (LCH) is a rare histiocytic proliferative disorder of unknown etiology and mainly affects young children. The histological feature is granuloma-like proliferation of...
Fatemeh Khatami,Seyed Mohammad Tavangar Fatemeh Khatami
Pheochromocytomas (PCCs) are rare neuroendocrine tumors. The current diagnostic tools are based on biochemistry and histopathology results, but heterogeneity of diagnostic markers, signs and symptoms of PCCs bring a lot of difficulties for ...
Martina Montagnana,Elisa Danese,Gabriel Lima-Oliveira et al. Martina Montagnana et al.
Beside the well-established impact on decreasing the risk of cardiovascular diseases (1), recent attention has been paid to the relationship between cocoa-containing foods and the immune system (2), showing that dark chocolate consumption e...
Subrata Pal,Kingshuk Bose,Prabhat Ch Mondal et al. Subrata Pal et al.
Placental mesenchymal dysplasia (PMD) is a rare benign placental abnormality. It is characterized by hydropic degeneration of stem villi, placentomegaly, and increased maternal serum alpha-fetoprotein (AFP). It can be associated with differ...
Rupam Sinha,Soumyabrata Sarkar,Tanya Khaitan et al. Rupam Sinha et al.
Gorham's disease is a rare and atypical disorder epitomized by progressive osteolysis of bone with eventual total disappearance of bone. The etiology is poorly understood with variable clinical presentation. Most times it is initially misdi...
Chandan Kumar,Pragya Jain,Neelam Wadhwa et al. Chandan Kumar et al.
Mucormycosis is a rare but highly invasive opportunistic fungal infection. Gastrointestinal disease although uncommon is highly fatal. We report a case of jejunal mucormycosis in a 24 year old undernourished female with preceding surgical i...
Indranil Chakrabarti,Priyanka Agarwala,Pranati Bera et al. Indranil Chakrabarti et al.
Background: Phyllodes tumors (PTs) are uncommon biphasic fibroepithelial neoplasms of the breast occurring in elderly females with a peak incidence between 45 and 49 years. Depending on various histological criteria, they...
Alireza Sadeghipour,Navid Abdi,Pegah Babaheidarian Alireza Sadeghipour
Background: Tuberous sclerosis (TSC) is inherited as an autosomal dominant disease, characterized by skin lesion and tubers in vital organs, especially brain in three categories including subependymal nodules, cortical tu...