Relevant bibliographies by topics / Hematologic features

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Hematologic features'

Author: Grafiati
Published: 28 May 2022
Last updated: 31 July 2025

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Journal articles on the topic "Hematologic features"

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Mody, Girish M., and Bilkish Cassim. "Rheumatologic features of hematologic disorders." Current Opinion in Rheumatology 8, no. 1 (1996): 57–61. http://dx.doi.org/10.1097/00002281-199601000-00011.

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Ehrenfeld, Michael, Hanan Gur, and Yehuda Shoenfeld. "Rheumatologic features of hematologic disorders." Current Opinion in Rheumatology 11, no. 1 (1999): 62–67. http://dx.doi.org/10.1097/00002281-199901000-00011.

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Hrycaj, Paweł, and Dorota Cieślak. "Hematologic features of systemic lupus erythematosus." Reumatologia/Rheumatology 1 (2013): 31–35. http://dx.doi.org/10.5114/reum.2013.33391.

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Zheng, J., Z. R. Dong, Y. P. Tang, et al. "AB0449 CLINICAL CHARACTERISTICS AND RISK FACTORS OF SYSTEMIC SCLEROSIS WITH HEMATOLOGIC SYSTEM DAMAGES." Annals of the Rheumatic Diseases 80, Suppl 1 (2021): 1252.1–1252. http://dx.doi.org/10.1136/annrheumdis-2021-eular.3465.

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Background:SSc characterized by varying degrees of fibrosis of the skin and internal organs, clinicians pay more attention to skin and viscera conditions, tend to ignore hematologic system damage. Studies have shown that rheumatic disease such as SLE, RA, pSS often accompanied with hematologic system damages, and hematologic system damages is multiple organ involvement and risk factor of poor prognosis[1-2].Objectives:To investigate the the clinical features, laboratory characteristics and risk factors of Systemic Sclerosis (SSc) patient with hematologic system damages.Methods:The clinical dat
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Dutta, S. K., B. E. Penney, A. C. Myrup, M. G. Robl, and R. M. Rice. "Disease features in horses with induced equine monocytic ehrlichiosis (Potomac horse fever)." American Journal of Veterinary Research 49, no. 10 (1988): 1747–51. https://doi.org/10.2460/ajvr.1988.49.10.1747.

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SUMMARY Fifty-five horses were inoculated iv and/or sc with materials containing Ehrlichia risticii, ie, infected whole blood, bufly coat cells, or cell culture, to study clinical and hematologic features of equine monocytic ehrlichiosis (Potomac horse fever). Major clinical and hematologic features of induced E risticii infection were biphasic increase in rectal temperature with peak increases of 38.9 C and 39.3 C on postinoculation days (pid) 5 and 12, respectively; depression; anorexia; decreased wbc count (maximal decrease of 47% on pid 12); and diarrhea from pid 14 to pid 18. Increased wb
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Erber, Wendy N., and Jill Finlayson. "Hematologic Features of Hepatosplenic T-Cell Lymphoma." American Journal of Clinical Pathology 137, no. 2 (2012): 334–35. http://dx.doi.org/10.1309/ajcpvbi47qpvtjow.

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Cho, Joong-Yang. "A Practical Review of Paraproteinemic Neuropathy." Korean Journal of Neuromuscular Disorders 14, no. 2 (2022): 23–29. http://dx.doi.org/10.46518/kjnmd.2022.14.2.23.

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Paraproteinemic neuropathy is a heterogeneous set of neuropathies characterized by the presence of homogeneous immunoglobulin in the serum. Most cases are associated with monoclonal gammopathy of undetermined significance. It might also occur in hematologic malignant and nonmalignant conditions. The association between neuropathy and monoclonal gammopathy requires appropriate neurological and hematological investigations. Treatment is mostly based on underlying hematologic disorders. In this review, we provide a clinically practical approach to clinical, laboratory, electrophysiological featur
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Morin, D. E., F. B. Garry, M. G. Weiser, M. J. Fettman, and L. W. Johnson. "Hematologic Features of Iron Deficiency Anemia in Llamas." Veterinary Pathology 29, no. 5 (1992): 400–404. http://dx.doi.org/10.1177/030098589202900505.

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Iron deficiency anemia was identified and characterized in three 14 to 29-month-old male llamas (llama Nos. 1–3) from separate herds in Colorado. The identification of iron deficiency anemia was based on hypoferremia (serum iron = 20–60 μg/dl), erythrocytic features, and hematologic response to iron therapy. The anemia was moderate and nonregenerative and characterized by erythrocyte hypochromia, microcytosis (mean cell volume = 15–18 fl), and decreased mean corpuscular hemoglobin concentration (36.0–41.0 g/dl). Morphologic features unique to llamas with iron deficiency anemia included irregul
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Kwon, Chang Gyu, Yoo Nee Nam, Yong Han Sun, et al. "Hematologic Features of Children with Inflammatory Bowel Disease." Korean Journal of Pediatric Gastroenterology and Nutrition 12, no. 2 (2009): 171. http://dx.doi.org/10.5223/kjpgn.2009.12.2.171.

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Balaban, Daniel Vasile, Alina Popp, Florentina Ionita Radu, and Mariana Jinga. "Hematologic Manifestations in Celiac Disease—A Practical Review." Medicina 55, no. 7 (2019): 373. http://dx.doi.org/10.3390/medicina55070373.

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Celiac disease (CD) is a systemic autoimmune disease driven by gluten-ingestion in genetically predisposed individuals. Although it primarily affects the small bowel, CD can also involve other organs and manifest as an extraintestinal disease. Among the extraintestinal features of CD, hematologic ones are rather frequent and consist of anemia, thrombocytosis (thrombocytopenia also, but rare), thrombotic or hemorrhagic events, IgA deficiency, hyposplenism, and lymphoma. These hematologic alterations can be the sole manifestation of the disease and should prompt for CD testing in a suggestive cl
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Dissertations / Theses on the topic "Hematologic features"

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Al, Tamееmi A. H., Сергій Віталійович Попов, Сергей Витальевич Попов, and Serhii Vitaliiovych Popov. "Hematological features at infants with acute respiratory infections." Thesis, Sumy State University, 2014. http://essuir.sumdu.edu.ua/handle/123456789/36157.

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Acute respiratory infections are among the most common in childhood. In Ukraine, in 2013 there were more than 5 million cases of such pathology. Most at risk of developing respiratory illnesses (ARI) at infants due to the peculiarities of formation of the immune system. This leads to greater severity of ARI and expressed a significant intoxication syndrome on a background of pronounced inflammatory reactions. When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/36157
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Ponte, MauriclÃcio Franco. "Association of HLA CLASS II alleles (DRB1 and DQB1) with clinical features and hematological parameters in sickle cell anemia." Universidade Federal do CearÃ, 2014. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=16555.

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Sickle cell anemia (SCA) is an inherited disease, often, but not exclusively, in individuals of African origin. In the black Brazilian population there is a prevalence from 0.1 to 0.3% tending to affect an ever larger portions due to miscegenation. Specific alleles of the HLA system and may influence the risk of appearance of clinical symptoms in patients with SCA, whereas their genotypes may serve as useful markers in identifying the risk for certain clinical manifestations. The study was a randomized-case control in order to evaluate the association of alleles of the HLA class II system with
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Tête, Nicolas. "Evaluation de l'exposition et des effets des éléments traces métalliques et du parasitisme chez la faune sauvage : contribution au développement d'une approche non létale." Thesis, Besançon, 2014. http://www.theses.fr/2014BESA2010/document.

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En intégrant cette étude dans un contexte d'écologie du stress, l'objectif général de cette thèse est d'une part d'évaluer l'exposition et les effets des éléments traces métalliques (ETMs)et du parasitisme chez le mulot sylvestre (apodemus sylvaticus) et d'autre part de contribuer au développement de marqueurs d'exposition et d'effets toxiques non létaux. Au cours de trois sessions de capture, des individus ont été collectés dur 30 sites localisés autour de l'ancienne fonderie de Metaleurop (Nord-Pas-de-Calais) les concentrations en Cd et Pb ont été mesurées dans les organes cibles (foie et re
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Ferreira, Daniela Filipa Cardoso. "Relevância do painel de diagnóstico fenotípico de Doenças Linfoproliferativas Crónicas de células B na identificação de rasgos fenotípicos displásicos nas linhas a neutrófilo, monocítica e eritroide." Master's thesis, 2017. http://hdl.handle.net/10316/83090.

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Dissertação de Mestrado em Bioquímica apresentada à Faculdade de Ciências e Tecnologia<br>Nas últimas décadas, tem sido cada vez mais reportado na literatura a presença de doenças múltiplas num mesmo indivíduo, nomeadamente a coexistência de mais do que uma Doença Linfoproliferativa Crónica de células B (DLPC-B), a presença simultânea de uma Gamapatia Monoclonal e/ou Mieloma Múltiplo com Síndrome Mielodisplásica (SMD) e, mais recentemente casos diagnosticados com DLPC-B concomitante a SMD. Contudo, relativamente às últimas duas doenças, não se sabe ao certo qual o impacto da presença simultâne
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Lin, Hui-Ju, and 林惠茹. "Correlation between hematological features and genetic lesions of hemoglobin gene disorders in Taiwanese patients." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/35818706948467023458.

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碩士<br>國立中興大學<br>生命科學院碩士在職專班<br>94<br>Hemoglobin (Hb) gene disorders are one of most common inherited diseases in Taiwan, which includes α-thalassemia, β-thalassemia, and associated hemoglobin variants. In this study, we collected and analyzed mutations found in 930 patients of hemoglobin gene disorders except for Hb Bart’s Hydrops and β-thalassemia major. The patients included 650 cases of α-thalassemia, 225 cases of β-thalassemia, 9 cases of α-thalassemia combined with β-thalassemia, and 46 cases of Hb variants or Hb variants combined with α-thalassemia or β-thalassemia. Our results showed th
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Books on the topic "Hematologic features"

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Cohen, Jeffrey A., Justin J. Mowchun, Victoria H. Lawson, and Nathaniel M. Robbins. A 68-Year-Old Male with Progressive Numbness and Gait Difficulties. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190491901.003.0015.

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Paraproteinemic demyelinating peripheral neuropathies require specific diagnostic and management approaches. The clinical features as well as the type of monoclonal protein and possible associated antibodies are all important considerations in evaluation and management of these complex presentations. It is important to recognize anti-myelin associated glycoproteins positive peripheral neuropathy, which is associated with IgM gammopathy, and typically presents with a sensory ataxia. Hematologic disease may mimic chronic inflammatory demyelinating polyneuropathy. This chapter also describes the
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Silberstein, Leslie E., Ronald Hoffman, Helen Heslop, Benz Edward J. Jr, and Jeffrey Weitz. Hematology E-Book: Basic Principles and Practice, Expert Consult Premium Edition - Enhanced Online Features. Elsevier - Health Sciences Division, 2013.

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Hollak, Carla E. M. Hematological Abnormalities. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0077.

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The respiratory system is frequently involved in inborn errors of metabolism, either primarily or secondary to severe systemic disease. In disorders with progressive neurological disease, recurrent chest infections are a result of aspiration. Patients with cachexia and muscle weakness can develop breathing difficulties. Metabolic acidosis causes tachypnea. These secondary problems, occurring in the context of a multisystem disease with prominent other features, are well covered elsewhere and are not discussed in this chapter. The focus of the current chapter is the adult patient who presents w
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Furie, Bruce, Philip McGlave, A. Victor Hoffbrand, Ronald Hoffman, and Benz Edward J. Jr. Hoffman, Hematology, Expert Consult Premium Edition - Enhanced Online Features and Print, 5e and Hoffbrand, Color Atlas of Clinical Hematology, Expert Consult - Online and Print, 4e Package. Elsevier - Health Sciences Division, 2009.

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Weitzman, Sheila, and R. Maarten Egeler. Histiocytic Disorders of Children and Adults: Basic Science, Clinical Features and Therapy. Cambridge University Press, 2005.

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Weitzman, Sheila, and R. Maarten Egeler. Histiocytic Disorders of Children and Adults: Basic Science, Clinical Features and Therapy. Cambridge University Press, 2009.

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Weitzman, Sheila, and R. Maarten Egeler. Histiocytic Disorders of Children and Adults: Basic Science, Clinical Features and Therapy. Cambridge University Press, 2005.

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O’Neal, M. Angela. Postpartum Left-Sided Numbness and Right-Sided Shaking. Edited by Angela O’Neal. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190609917.003.0019.

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The chapter discusses cerebral venous thrombosis (CVT) in pregnancy. The signs and symptoms of the patient depend on which venous sinus is clotted. The clinical features may include headache, bilateral symptoms, hemorrhagic stroke, and seizures. The headaches are related to elevated intracranial pressure and can mimic those of idiopathic intracranial hypertension. Hematological changes that occur in pregnancy result in a hypercoagulable state; this normal physiology can predispose in certain situations to CVT. Other factors associated with an increase in the risk of clotting include infection,
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Machtinger, Edward L., and Peter A. Nigrovic. Spanish for Pediatric Medicine. 2nd ed. Edited by Janice A. Lowe. American Academy of Pediatrics, 2005. http://dx.doi.org/10.1542/9781581104554.

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Enhance patient and parent encounters with this newly expanded and enhanced pocket guide! Here's the easy-to-use manual you need to communicate with Spanish-speaking patients and parents more efficiently and effectively. Spanish for Pediatric Medicine features a quick-reference design that enables you to rapidly identify and explore common medical problems. English and Spanish equivalents are shown side-by-side for instant, precise use. This handy resource fits right in your pocket as you travel between well-child, sick visit, and emergency department settings. Optimized for use with Bright Fu
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Book chapters on the topic "Hematologic features"

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Onida, Francesco, and Yves Chalandon. "Myelodysplastic/Myeloproliferative Neoplasms." In The EBMT Handbook. Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-44080-9_76.

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AbstractThe myelodysplastic syndrome-myeloproliferative neoplasms (MDS/MPNs) are a heterogeneous group of hematologic malignancies characterized by dysplastic and myeloproliferative clinical, laboratory, and morphological overlapping features, both in marrow and in blood. MDS/MPNs include chronic myelomonocytic leukemia (CMML), MDS/MPN with neutrophilia, MDS/MPN with SF3B1 mutation (in its absence with ringed sideroblasts) and thrombocytosis (MDS/MPN-SF3B1-T), and MDS/MPN not otherwise specified (MDS/MPN-NOS). Prognosis of MDS/MPN is highly variable, being dismal in the majority of patients wi
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Lanza, Francesco, Angela Latorraca, Sabrina Moretti, Barbara Castagnari, Luisa Ferrari, and Gianluigi Castoldi. "Acquired and Inherited Forms of Myeloperoxidase Deficiency: Clinical and Hematological Features." In The Peroxidase Multigene Family of Enzymes. Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-58314-8_21.

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Chossegros, Manon, Xavier Tannier, and Daniel Stockholm. "Improving Interpretability of Leucocyte Classification with Multimodal Network." In Studies in Health Technology and Informatics. IOS Press, 2024. http://dx.doi.org/10.3233/shti240602.

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White blood cell classification plays a key role in the diagnosis of hematologic diseases. Models can perform classification either from images or based on morphological features. Image-based classification generally yields higher performance, but feature-based classification is more interpretable for clinicians. In this study, we employed a Multimodal neural network to classify white blood cells, utilizing a combination of images and morphological features. We compared this approach with image-only and feature-only training. While the highest performance was achieved with image-only training,
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Morchi, Ravi. "Hematology." In General Surgery Board Review, edited by Ravi Morchi. Oxford University PressNew York, 2024. http://dx.doi.org/10.1093/med/9780197630525.003.0004.

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Abstract A review of clinically relevant hematologic principles for the care of surgical patients. It starts with the coagulation cascade, including the different laboratory measures of coagulative function. Then it covers features of blood product transfusion, transfusion reactions, and medical measures to augment hemostasis. Clinically relevant antiplatelets, anticoagulants, and thrombolytics are described, and commonly tested hypercoagulable states and bleeding disorders are reviewed. The chapter closes with high yield facts on dyshemoglobinemias.
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Sreedharan, Hariharan. "Chromosome Abnormalities in Hematological Malignancies and Its Clinical Significance." In Down Syndrome and Other Chromosome Abnormalities. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.101078.

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The latest version of the World Health Organization guidelines focuses mainly on the genetic and cytogenetic features of hematologic neoplasms as predictors of diagnostic, treatment decision, prognostic outcome, and for treatment monitoring in hematological malignancies. There are different techniques to identify these abnormalities. Live cells are needed for chromosome preparation. The Hematological malignancies include myeloid and lymphoid neoplasms. The myeloid neoplasms include Myelodysplastic syndromes, myeloproliferative neoplasms, and acute myeloid leukemias. The Lymphoid neoplasms incl
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Morchi, Ravi. "Anesthesia and Perioperative Care." In General Surgery Board Review, edited by Ravi Morchi. Oxford University PressNew York, 2024. http://dx.doi.org/10.1093/med/9780197630525.003.0005.

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Abstract A review of clinically relevant hematologic principles for the care of surgical patients. It starts with the coagulation cascade, including the different laboratory measures of coagulative function. Then it covers features of blood product transfusion, transfusion reactions, and medical measures to augment hemostasis. Clinically relevant antiplatelets, anticoagulants, and thrombolytics are described, and commonly tested hypercoagulable states and bleeding disorders are reviewed. The chapter closes with high yield facts on dyshemoglobinemias.
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Béné, Marie-Christine, and Anna Porwit. "Examples of Immunophenotypic Features in Various Categories of Acute Leukaemia." In Multiparameter Flow Cytometry in the Diagnosis of Hematologic Malignancies, 2nd ed. Cambridge University Press, 2025. https://doi.org/10.1017/9781009419086.006.

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Turculeanu, Adriana. "Hepatitis E: Disease in Humans." In Liver Pathology [Working Title]. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.94302.

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Hepatitis E virus (HEV) is one of the 7 viruses with mainly hepatic tropism. HEV determines 20 million new infections worldwide every year, 3.4 million acute hepatitis E and 44,000 deaths in 2015 (3.3% of the mortality due to viral hepatitis). Transmitted by the digestive tract mainly (fecal- orally, particularly by water infected with feces), the virus reaches the liver where it does not have a direct cytolytic effect, but immunological phenomena, especially cellular, activated by the replication of the virus in the hepatocytes. Clinically, over 95% of cases of HEV infection are asymptomatic
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Abdullah Saad, Ashraf. "Juvenile Myelomonocytic Leukemia (JMML): A Mimicker of KMT2A-Rearranged Acute Myeloid Leukemia (AML)." In Acute Leukemias. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.94537.

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Juvenile myelomonocytic leukemia (JMML) is the most confusing mimicker of KMT2A-rearranged acute myeloid leukemia (AML). Clinical presentation, age of susceptibility (infancy or early childhood) and abnormal monocytosis are common clinical features. To complicate matters, JMML morphologically resemble acute myelomonocytic leukemia (AML M4) and distinction must be made based on accurate blast and promonocyte counts. As treatment significantly varies, AML/JMML overlap can lead to catastrophic consequences that can be avoided by timely management. Therefore, meticulous knowledge of JMML is essent
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Kissel, John T., and Jerry R. Mendell. "Neuropathies Associated with Monoclonal Gammopathies." In Diagnosis and Management of Peripheral Nerve Disorders. Oxford University PressNew York, NY, 2001. http://dx.doi.org/10.1093/oso/9780195133011.003.0015.

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Abstract Searching for the presence of a monoclonal protein (also called paraprotein, monoclonal gammopathy, or M-protein) has become an important part of evaluating patients with chronic peripheral neuropathies of unknown cause. Approximately 10% of idiopathic neuropathy patients have an associated monoclonal gammopathy. Most of these patients do not have an identifiable underlying plasma cell disorder, instead they have a so-called monoclonal gammopathy of undetermined significance (MGUS) (Table 15-1). The pathophysiological relationship of the monoclonal protein to the neuropathy is often o
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Conference papers on the topic "Hematologic features"

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P, Sowmiya, Yogasundari S, Kaviya S, and Chandra Pritha R. "Hemo Detect Advancing Hematologic Health through Automated Leukemia Detection." In International Conference on Modern Trends in Engineering and Management (ICMTEM-24). International Journal of Advanced Trends in Engineering and Management, 2024. http://dx.doi.org/10.59544/jckd6637/icmtem24p5.

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Microscopic image analysis plays a significant role in initial leukemia screening and its efficient diagnostics. Since the present conventional methodologies partly rely on manual examination, which is time consuming and depends greatly on the experience of domain experts, automated leukemia detection opens up new possibilities to minimize human intervention and provide more accurate clinical information. This paper proposes a novel approach based on conventional digital image processing techniques and machine learning algorithms and deep learning algorithms to automatically identify acute lym
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Sultonova, Sherozakhon. "CLINICAL-HEMATOLOGICAL FEATURES OF CHRONIC MYELOID LEUKEMIA." In RICERCHE SCIENTIFICHE E METODI DELLA LORO REALIZZAZIONE: ESPERIENZA MONDIALE E REALTÀ DOMESTICHE, chair Din Mohammad, Khamid Karimov, Kodirjon Boboyev, and Khamida Kazakbayeva. European Scientific Platform, 2021. http://dx.doi.org/10.36074/logos-26.11.2021.v3.22.

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Sebezhko, O., I. Morozov, and I. Yazikov. "FEATURES OF THE HEMATOLOGICAL STATUS OF ROMANOV SHEEP IN THE CONDITIONS OF KUZBASS." In SCIENTIFIC SUPPORT FOR LIVESTOCK BREEDING IN SIBERIA. Krasnoyarsk Scientific Research Institute of Agriculture is a separate division of the Federal Research Center KSC SB RAS, 2024. https://doi.org/10.52686/conferencearticle_67597cf0dac7d5.85545563.

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The paper presents data on the hematological status of full-aged non-vegetable purebred Romanov sheep raised in the Kuzbass region. The level of leukocytes and platelets fluctuated within the normal range of 6.65 ± 0.61 x109/l and 361.8 ± 15.62 x109/l, respectively. The level of erythrocytes was lower than generally accepted values and amounted to 3.95 ± 0.06 x1012/l, which, in the absence of clinical manifestations of disease, can be considered a normal variant for the studied ewes.
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Hamdaoui, Yamina, Rania Bouneb, Abdelbaki Azouzi, et al. "Outcome and prognostic features in respiratory critically-ill patients with hematological malignancies." In Annual Congress 2015. European Respiratory Society, 2015. http://dx.doi.org/10.1183/13993003.congress-2015.pa2142.

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Vasilevich, F. I., and A. M. Vepreva. "RABBITS AS PARATENIC HOSTS OF TOXOCARA CANIS." In THEORY AND PRACTICE OF PARASITIC DISEASE CONTROL. All-Russian Scientific Research Institute for Fundamental and Applied Parasitology of Animals and Plant – a branch of the Federal State Budget Scientific Institution “Federal Scientific Centre VIEV”, 2023. http://dx.doi.org/10.31016/978-5-6048555-6-0.2023.24.123-127.

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Toxocariasis is both a veterinary and medical problem worldwide. A feature of&#x0D; Toxocara biology is that Toxocara larvae commit visceral larva migrans, damage the&#x0D; liver, lungs, and other organs and tissues in non-specific hosts, including humans.&#x0D; Constant reinvasion leads to the accumulation of stage 2–3 larvae in the body of nonspecific (paratenic) hosts. The problem of parasitological contamination of soil on the&#x0D; territory of rabbit farms and the risks of infection of rabbits were considered. Therefore,&#x0D; it became necessary to study the involvement of the rabbit as
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Ferreira, João Henrique Fregadolli, André Franzoi, Bernardo Corrêa de Almeida Teixeira, Tamires Maier Silva Ferreira, Mariana de Moura Souza, and João Cesar Beenke França. "Punctate pattern and Milky Way appearance caused by PML in a patient with AIDS." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.690.

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Introduction: Progressive multifocal leukoencephalopathy (PML) is an opportunistic infection caused by reactivation of JC virus in the central nervous system and is an important differential diagnosis in patients with subacute focal neurologic deficits. Magnetic resonance imaging (MRI) is the most sensitive tool for detection of early manifestations of the disease1 . Case Report: A 42-year-old woman with a previous diagnosis of HIV infection, without treatment for the last two years, presented with progressive headache, left hemiparesis, hypoesthesia and homonymous hemianopia in the last two m
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Kumari, Nikita, Reenu Kanwar, Bindu Bajaj, and Garima Kapoor. "Ovarian fibrothecoma: An uncommon cause of a large pelvic mass." In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685325.

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Introduction: Ovarian fibrothecomas represent an ovarian stromal neoplasm developing in a wide spectrum of clinical settings. These tumors have been described as rare ovarian neoplasm, accounting for about 4% of all ovarian tumors. We report a case whose clinical presentation was highly deceptive and was clinically and radiologically diagnosed as malignant ovarian tumor. Ascitic fluid cytology revealed absence of malignant cells. On histopathological examination, it was diagnosed as benign fibrothecoma with cystic changes. Postoperative follow-up for about six months was uneventful. Case: A 45
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Metlyaeva, Nely, Andrey Bushmanov, Irina Galstyan, Michail Konchalovsky, Anahit Davtyan, and Olga Shcherbatykh. "Features of individual psychological adaptation and periods of staged hematological syndrome in two patients with severe acute radiation sickness and moderate acute radiation sickness and acute leukemia who suffered from the Chernobyl accident (22 years and 30 years of observation)." In RAD Conference. RAD Centre, 2021. http://dx.doi.org/10.21175/rad.abstr.book.2021.32.1.

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