Search Results - "genetic testing"

Clinical Knowledge, Attitude, and Perceptions of Community Pharmacists Towards Pharmacogenomics - A Cross-Sectional Study from Saudi Arabia by Alrabiah Z, Syed W, Babelghaith SD, Al Arifi MN

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The rs5918 polymorphism in the <i>ITGB3</i> gene increases the risk for preeclampsia in pregnant women with fetal growth retardation by Oleg V. Golovchenko, Irina V. Ponomarenko, Mikhail I. Churnosov

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Clinical Value of Magnetic Resonance Spectroscopy in the Initial Evaluation of Patients with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes by Hyunjoo Lee, Je Hee Shin, Ji-Hoon Na, Young-Mock Lee

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Gene Mutations Related to Glucocorticoid Resistance in Pediatric Acute Lymphoblastic Leukemia by JinFang Zhang, LingJi Zeng, YuLian Wang, JianWei Pan, XingDong Li, Bei Feng, Quan Yang

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Practice patterns and results of tumor and germline genetic evaluation of women with endometrial cancer in south Louisiana by Morgan McDougal, Pallavi Nair-Fairless, Tova Weiss, Elizabeth Dao, Andrew G. Chapple, Amelia Jernigan

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Prader-Willi syndrome: a single center's experience in Korea by Yea Ji Kim, Chong Kun Cheon

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International Atherosclerosis Society Roadmap for Familial Hypercholesterolaemia by Gerald F. Watts, Laney K. Jones, Mitchell N. Sarkies, Jing Pang, Samuel S. Gidding, Peter Libby, Raul D. Santos

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Clinical pharmacists' knowledge, attitude, perception, and beliefs about the role of pharmacogenetic testing for genes polymorphisms when prescribing mercaptopurine by Norah O. Abanmy, Sara A. Alghamdi, Raneem K. Aljudaie, Omar A. Almohammed

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Clinical and Genetic Characteristics of Young Children with Fragile X Syndrome by So-Hee Lee, Ji-Eun Jeong, Yoon-Young Jang, Jin-Kyung Kim

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Atypical preeclampsia before 20 weeks of gestation with multicystic placenta, hyperreactio luteinalis, and elevated sFlt-1/PlGF ratio as manifestations of fetal triploidy: A case r... by Harue Hayashida, Koji Nakamura, Koto Ukon, Kazuaki Sato, Kazuya Mimura, Mamoru Kakuda, Aska Toda, Tatsuya Miyake, Kosuke Hiramatsu, Toshihiro Kimura, Masayuki Endo, Tadashi Kimura

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Compound heterozygosity for a whole gene deletion and p.R124C mutation in causing nonclassic congenital adrenal hyperplasia by Hamza Nasir, Syed Ibaad Ali, Naeem Haque, Stefan K. Grebe, Salman Kirmani

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Relevance of Fluorodopa PET Scan in Dopamine Responsive Dystonia and Juvenile Parkinsonism: A Systematic Review by Juan A. Moncayo, Maite Vargas, Juan F. Ortiz, Pablo Granda, Alex S. Aguirre, Jennifer Argudo, Willians Tambo, Gabriela Garofalo, Christian John Capirig, Melisa German-Montenegro, Luis G. Rueda

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Phenotypic and genetic characterization of children with Wilson Disease from Northeast China by Tianhe Zhang, Wenliang Song, Zhiqin Mao

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Ovarian metastases from ileum cancer in a patient with germline EPCAM gene deletion successfully treated with surgical resection and CAPOX chemotherapy: a case report by Narushi Iwata, Ayumi Shikama, Wataru Takao, Yoshihiko Hosokawa, Hiroya Itagaki, Nobutaka Tasaka, Azusa Akiyama, Hiroyuki Ochi, Takeo Minaguchi, Miwa Arita, Emiko Noguchi, Toshikazu Moriwaki, Toyomi Satoh

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Initially categorized 46,XY embryo transfer ending with 45,X products of conception-a case report and a review of discordant result management by Prapti Singh, D.O., M.S, Alyssa Snider, M.S., Ph.D, Refik Kayali, Ph.D, Abigail Mancuso, M.D

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New approaches to pediatric dilated cardiomyopathy in current practice by Amalia Fagarasan, Maria Oana Sasaran

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Successful Sirolimus Treatment for Recurrent Pericardial Effusion in a Large Cervicomediastinal Provisionally Unclassified Vascular Anomaly: A Case Report by Moreno-Alfonso, San Basilio Berenguer San Basilio Berenguer, Sarmiento Caldas Sarmiento Caldas, González Cayón González Cayón, de la Puente de la Puente, Triana Triana, López-Gutiérrez

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Fructose 1,6 bisphosphatase deficiency mimicking glycogen storage disease as recurrent hypoglycemia by Manoj Madhusudan, Janani Sankar, Venkateswari Ramesh

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Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in <it>GNE</it> by Mahoney Lane J, Lidov Hart GW, Estrella Elicia A, Duncan Anna R, Boyden Steven E, Katz Jonathan S, Kunkel Louis M, Kang Peter B

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Effects of chromosomal translocation characteristics on fertilization and blastocyst development - a retrospective cohort study by Shanshan Wu, Jianrui Zhang, Yichun Guan, Bingnan Ren, Yuchao Zhang, Xinmi Liu, Kexin Wang, Mingmei Zhang, Zhen Li

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