Results 61 to 70 of about 2,948,023 (230)

Population-Based Study of Epilepsy in Infants

Pediatric Neurology Briefs, 2013
Investigators at the Paediatric Neurology Department, Great Ormond Street Hospital for Children, London, and other centers in the UK and USA carried out a population-based study of children, 1-24 months of age, with new-onset epilepsy, ascertained over ...
J Gordon Millichap
doaj   +1 more source

Hypoxia-Induced Reactive Oxygen Species Cause Chromosomal Abnormalities in Endothelial Cells in the Tumor Microenvironment

PLoS ONE, 2013
There is much evidence that hypoxia in the tumor microenvironment enhances tumor progression. In an earlier study, we reported abnormal phenotypes of tumor-associated endothelial cells such as those resistant to chemotherapy and chromosomal instability ...
Miyako Kondoh, N. Ohga, K. Akiyama, Y. Hida, N. Maishi, A. Towfik, N. Inoue, M. Shindoh, K. Hida   +8 more
semanticscholar   +1 more source

Chromosome abnormalities in erythroleukemia [PDF]

Cancer, 1987
Erythroleukemia (EL) is a heterogeneous disease in terms of cell type affected, chromosome abnormalities found in the malignant clone, and clinical course. In this article, cases of erythroid EL from the recent medical literature are reviewed using cytogenetic criteria to distinguish such cases from those of myeloid EL.
openaire   +2 more sources

Maternal age-specific rates of fetal chromosomal abnormalities in Korean pregnant women of advanced maternal age

Obstetrics & Gynecology Science, 2013
Objective To evaluate the association of maternal age with occurrence of fetal chromosomal abnormalities in Korean pregnant women of advanced maternal age (AMA).
Young Joo Kim, J. Lee, S. Kim, S. Shim, D. Cha   +4 more
semanticscholar   +1 more source

Prevalence of chromosomal abnormalities identified by copy number variation sequencing in high-risk pregnancies, spontaneous abortions, and suspected genetic disorders

Journal of International Medical Research, 2019
Objective High-throughput sequencing based on copy number variation (CNV-seq) is commonly used to detect chromosomal abnormalities including aneuploidy.
Rui Zhang, Xiangbin Chen, Dong Wang, Xuan Chen, Chao Wang, Yuhong Zhang, Mengnan Xu, Jingcui Yu   +7 more
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Risk of Chromosomal Abnormalities in Early Spontaneous Abortion after Assisted Reproductive Technology: A Meta-Analysis

PLoS ONE, 2013
Background Studies on the risk of chromosomal abnormalities in early spontaneous abortion after assisted reproductive technology (ART) are relatively controversial and insufficient.
Jun-Zhen Qin, Li-Hong Pang, Min-Qing Li, Jing Xu, Xing Zhou   +4 more
semanticscholar   +1 more source

Chromosomal Abnormalities

This book highlights the importance of various types of chromosomal aberrations and their profound impact on genomic stability, disease development, evolutionary processes, and clinical practice.

core   +1 more source

Chromosomal in situ suppression hybridization of immunologically classified mitotic cells in hematologic malignancies [PDF]

, 1992
Chromosomal in situ suppression (CISS) hybridization was performed with library DNA from sorted human chromosomes 8, 9, 15, 17, 21, and 22 on immunologically stained bone marrow cells of four patients with a hematologic neoplasm, including two patients ...
Knuutila, Sakari, Jotterand Bellomo, Martine, Marianne Tiainen, Tiainen, Marianne, Sakari Knuutila, Tapani Ruutu, Emmerich, Patricia, Cremer, Thomas, Susanne Popp, Martine Jotterand Bellomo, Ruutu, Tapani, Parlier, Valerie, Patricia Emmerich, Popp, Susanne, Thomas Cremer, Valerie Parlier   +15 more
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Chronic lymphocytic leukemia-associated chromosomal abnormalities and miRNA deregulation

, 2012
Yvonne Kiefer1, Christoph Schulte2, Markus Tiemann2, Joern Bullerdiek11Center for Human Genetics, University of Bremen, Bremen, Germany; 2Hematopathology Hamburg, Hamburg, GermanyAbstract: Chronic lymphocytic leukemia is the most common leukemia in ...
Bullerdiek J, Schulte C, Kiefer Y, Tiemann M   +3 more
core  

Evaluation of the cytogenetical results of 4707 cases diagnosed with amniocentesis.

Çukurova Üniversitesi Tıp Fakültesi Dergisi, 2011
PURPOSE: Amniocentesis is a very crucial diagnostic procedure for preventing the birth of genetically defective fetuses in order to decrease the prevalence of genetic diseases in populations.
Ayfer Pazarbasi, Osman Demirhan, Deniz Tasdemir, Erdal Tunc, Fatma Tuncay Ozgunen, Davut Alptekin, Cuneyt Evruke, Cansun Demir, Mulkiye Kasap, Zeynep Karakan Karakas, Nihal Inandikoglu, Lutfiye Ozpak   +11 more
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