Search Results - "genetic testing"

Islamic perspectives on preconception, prenatal, and perinatal counseling by Abdullah Bin Shoaib, Abdullah Bin Shoaib

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The Perfect Storm: Abnormal Baseline QT With Chronic Methadone Use and Serious Hypokalemia by Oscar J. Lopez MD, Diana Othon MD, Yilen K. Ng-Wong MD, Jose Sleiman MD

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Updating the landscape of direct-to-consumer pharmacogenomic testing by Filipski KK, Murphy JD, Helzlsouer KJ

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Gray Platelet Syndrome-Unusual Presentation with Spontaneous Splenic Rupture: A Case Report and Literature Review by Duha I. Barghouthi, Lila H. Abu-Hilal, Yumna Njoum, Abeer Dar Hasan, Khaled Alshawwa, Fadi Hourani

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A pharmacogenetics approach to pain management by Kaori Yoshida, Daisuke Nishizawa, Soichiro Ide, Tatsuya Ichinohe, Ken‐ichi Fukuda, Kazutaka Ikeda

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Comparing models of delivery for cancer genetics services among patients receiving primary care who meet criteria for genetic evaluation in two healthcare systems: BRIDGE randomize... by Kimberly A. Kaphingst, Wendy Kohlmann, Rachelle Lorenz Chambers, Melody S. Goodman, Richard Bradshaw, Priscilla A. Chan, Daniel Chavez-Yenter, Sarah V. Colonna, Whitney F. Espinel, Jessica N. Everett, Amanda Gammon, Eric R. Goldberg, Javier Gonzalez, Kelsi J. Hagerty, Rachel Hess, Kelsey Kehoe, Cecilia Kessler, Kadyn E. Kimball, Shane Loomis, Tiffany R. Martinez, Rachel Monahan, Joshua D. Schiffman, Dani Temares, Katie Tobik, David W. Wetter, Devin M. Mann, Kensaku Kawamoto, Guilherme Del Fiol, Saundra S. Buys, Ophira Ginsburg, on behalf of the BRIDGE research team

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Breast Cancer Gene Research and Medical Practices Transnational Perspectives in the Time of BRCA

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Dilated Cardiomyopathy From Genetics to Clinical Management

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A case of probable non-familial early onset Alzheimer dementia in a Hispanic male by Corey Ephrussi, Richard Alweis

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A fracture, a family, legal entanglement, expensive investigation, and a familiar disease by Okpechi U, Regis K, Arcia R, Soyemi K

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Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation by Rand Murshidi, Heba Al-lala

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Case report: Prenatal diagnosis of fetal non-compaction cardiomyopathy with bradycardia accompanied by de novo CALM2 mutation by Wen Zhang, Wen Zhang, Xiaohui Dai, Xiaohui Dai, Hanmin Liu, Hanmin Liu, Lei Li, Lei Li, Shu Zhou, Shu Zhou, Qi Zhu, Qi Zhu, Jiao Chen, Jiao Chen

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Neonatal inflammatory skin and bowel disease type 2: a very rare disease associated with EGFR mutation by Mariana Lemos, Joana S. Gonçalves, Cátia R. Correia, Ana Teresa Maria

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Evaluation and Risk Assessment of Congenital Anomalies in Neonates by Rita P. Verma

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World experience on the diagnosis of interstitial diseases of the lungs in children (up-date 2017) by M.O. Gonchar, O.L. Logvinova

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Perinatal outcomes following assisted reproductive technology by Sesh Kamal Sunkara, Parimala Chinta, Mohan S Kamath

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Celiac Disease in Conjunction with Hereditary Fructose Intolerance as a Rare Cause of Liver Steatosis with Mild Hypertransaminasemia-A Case Report by Anna Bobrus-Chociej, Agnieszka Pollak, Natalia Kopiczko, Marta Flisiak-Jackiewicz, Rafał Płoski, Dariusz M. Lebensztejn

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To a question about the necessity and indications for genetic screening in obstetric and gynecological practice by K. N. Grigoreva, E. G. Demianovskaya, V. O. Bitsadze, J. Kh. Khizroeva, N. R. Gashimova, E. V. Slukhanchuk, I. S. Kalashnikova

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Problems and their solutions in genetic counseling education in Japan by Hidestugu eKohzaki

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Keratin 17 mutations in four families from India with pachyonychia congenita by Manoj Agarwala, Pankaj Salphale, Dincy Peter, Neil J Wilson, Susanne Pulimood, Mary E Schwartz, Frances J D Smith

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