Search Results - "MACRI, Charles J"
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Dynamically decreased miR-671-5p expression is associated with oncogenic transformation and radiochemoresistance in breast cancer
Published in Breast cancer research : BCR (07-08-2019)“…Understanding the molecular alterations associated with breast cancer (BC) progression may lead to more effective strategies for both prevention and…”
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Prenatal Genetic Screening and Diagnostic Testing: Assessing Patients' Knowledge, Clinical Experiences, and Utilized Resources in Comparison to Provider's Perceptions
Published in American journal of perinatology reports (01-01-2022)“…This survey study aimed to assess patient knowledge, clinical resources, and utilized resources about genetic screening and diagnostic testing. A one-time…”
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Leprosy in pregnant woman, United States
Published in Emerging infectious diseases (01-10-2013)Get full text
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4
Differentially Regulated miRNAs and Their Related Molecular Pathways in Lichen Sclerosus
Published in Cells (Basel, Switzerland) (02-09-2021)“…Lichen sclerosus (LS) is a chronic inflammatory skin disorder with unknown pathogenesis. The aberrant expression of microRNAs (miRNAs) is considered to exert a…”
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Lichen Sclerosus: An autoimmunopathogenic and genomic enigma with emerging genetic and immune targets
Published in International journal of biological sciences (01-01-2019)“…Lichen sclerosus (LS) is an inflammatory dermatosis with a predilection for anogenital skin. Developing lesions lead to vulvar pain and sexual dysfunction,…”
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Improving teaching skills in obstetrics and gynecology residents: evaluation of a residents-as-teachers program
Published in American journal of obstetrics and gynecology (2007)“…Objective The purpose of this study was to determine if a residents-as-teachers program improves residents’ teaching skills. Study design Twenty-four residents…”
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Expression of Adrenomedullin and Its Receptor in Normal and Malignant Human Skin: A Potential Pluripotent Role in the Integument
Published in Endocrinology (Philadelphia) (01-12-1997)“…Adrenomedullin (AM) is a multifunctional peptide involved in a variety of physiological functions, including growth regulation and antimicrobial activity. We…”
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Provider and Patient Knowledge and Views of Office Practices on Weight Gain and Exercise during Pregnancy
Published in American journal of perinatology (01-01-2018)“…This study sought to assess provider and patient knowledge and beliefs on gestational weight gain (GWG) and exercise during pregnancy, outline current clinical…”
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Genetics Education in US Dermatology Residency Programs: A Survey-Based Study
Published in Journal of graduate medical education (01-08-2017)Get full text
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10
In utero copper treatment for Menkes disease associated with a severe ATP7A mutation
Published in Molecular genetics and metabolism (01-09-2012)“…Menkes disease is a lethal X-linked recessive neurodegenerative disorder of copper transport caused by mutations in ATP7A, which encodes a copper-transporting…”
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Maternal healthcare needs assessment survey at Rabia Balkhi Hospital in Kabul, Afghanistan
Published in International journal of gynecology and obstetrics (01-06-2008)“…Abstract Objective Since the Department of Health and Human Services chose Rabia Balkhi Hospital (RBH) in Kabul, Afghanistan, as a site for intervention in…”
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Maternal asthma, race and low birth weight deliveries
Published in Early human development (01-07-2011)“…Abstract Background Asthma during pregnancy may compromise the well-being of the fetus and potentially impact an infant's birth weight via different…”
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Use of a Doula for Labor Coaching in a Patient With Indolent Systemic Mastocytosis in Pregnancy
Published in Obstetrics and gynecology (New York. 1953) (01-02-2006)“…BACKGROUND:Few cases of pregnancy in women with systemic mastocytosis have been reported. The effects of this disease on pregnancy have not been well…”
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Arrhythmogenic right ventricular dysplasia in pregnancy : A case report
Published in Journal of reproductive medicine (01-09-2006)“…Arrhythmogenic right ventricular dysplasia (ARVD) is characterized by progressive fibrous or fibrofatty tissue replacement of the right ventricular myocardium…”
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Assessment of genetics knowledge and skills in medical students: Insight for a clinical neurogenetics curriculum
Published in Biochemistry and molecular biology education (01-05-2011)“…The pace of discovery in biochemistry and genetics and its effect on clinical medicine places new curricular challenges in medical school education. We sought…”
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Implementation and evaluation of a genetics curriculum to improve obstetrician-gynecologist residents' knowledge and skills in genetic diagnosis and counseling
Published in American journal of obstetrics and gynecology (01-11-2005)“…This study was undertaken to develop, implement, and evaluate a genetics curriculum for obstetrician-gynecologist residents. We prospectively evaluated the…”
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Pregnancy in a woman with a continent appendicovesicostomy : A case report
Published in Journal of reproductive medicine (01-09-2006)“…Few cases of pregnancy following the Mitrofanoff procedure (continent appendicovesicostomy) have been reported, but in those cases there was an increased rate…”
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Erythropoietin use in a pregnant Jehovah's Witness with anemia and β-thalassemia: A case report
Published in Journal of reproductive medicine (01-02-2005)“…Anemia in pregnancy is seen often because of iron deficiency and the "physiologic dilution" that occurs in the third trimester. Other causes include genetic…”
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Differences in Patient and Provider Views on Gestational Weight Gain and Exercise Counseling During Pregnancy [10E]
Published in Obstetrics and gynecology (New York. 1953) (01-05-2017)“…INTRODUCTION: Appropriate gestational weight gain (GWG) during pregnancy impacts the health of a mother and child long after birth, yet reports show only one…”
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Autosomal dominant polycystic kidney disease in pregnancy complicated by twin gestation and severe preeclampsia : A case report
Published in Journal of reproductive medicine (01-05-2005)“…Autosomal dominant polycystic kidney disease (ADPKD), an autosomal dominant genetic disorder with a reported prevalence of 1 in 1,000, may be associated with…”
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