Results 121 to 130 of about 5,507,798 (394)

Functional analysis of a novel homozygous missense IVD gene variant: a case report with dual genetic diagnoses

Frontiers in Pediatrics
BackgroundGenomic or exome sequencing is beneficial for identifying more than one pathogenic variation causing blended atypical and/or severe phenotypes.
Yuying Zhu, Ke Wu, Hanying Wen
doaj   +1 more source

Cohort Analysis of Immigrant Rhetoric on Timely and Regular Access of Prenatal Care.

Obstetrics and Gynecology, 2019
OBJECTIVE To assess whether recent anti-immigration rhetoric is significantly associated with inadequate prenatal care. METHODS This was a population-based cohort study (2011-2017).
Derrick M. Chu, Joshua Aagaard, Ryan Levitt, Megan D Whitham, J. Mastrobattista, M. Rac, C. Eppes, M. Gandhi, M. Belfort, K. Aagaard   +9 more
semanticscholar   +1 more source

Oral Health Intervention: A Multifaceted Approach to Improve Oral Health Care during Pregnancy [PDF]

, 2016
Introduction: Early Childhood Caries (ECC) is the most common chronic disease of childhood Mothers’ oral health status is a strong predictor of the oral health status of their children 2009: Vermont spends $2.7 million treating children ages 0-5 with ...
Davis, Wendy, Fontaine, Kristin, Ford, Tabitha, Frechette, Gregory, Sakamori, Sruthi, Seufert, Caleb, Shu, I-hsiang, Silveira, Patrick   +7 more
core   +1 more source

Psychiatric and Cognitive Features in Italian Women With the FMR1 Premutation: A Comprehensive Assessment Using SCID‐5 and Standardized Cognitive Measures

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Women with the FMR1 premutation (PM) are at increased risk for fragile X‐associated conditions (FXPAC), including cognitive and psychiatric features collectively termed fragile X‐associated neuropsychiatric disorders (FXAND). This study is the first to systematically investigate cognitive and psychiatric features in Italian female premutation ...
Federica Alice Maria Montanaro, Randi J. Hagerman, Giuseppina Spano, Flora Tassone, Giancarlo Logroscino, Andrea Bosco   +5 more
wiley   +1 more source

Optical Genome Mapping for Chromosomal Aberrations Detection—False-Negative Results and Contributing Factors

Diagnostics
Optical genome mapping (OGM) has been known as an all-in-one technology for chromosomal aberration detection. However, there are also aberrations beyond the detection range of OGM.
Yiyun Xu, Qinxin Zhang, Yan Wang, Ran Zhou, Xiuqing Ji, Lulu Meng, Chunyu Luo, An Liu, Jiao Jiao, Hao Chen, Huasha Zeng, Ping Hu, Zhengfeng Xu   +12 more
doaj   +1 more source

A systematic overview of the literature regarding group prenatal care for high-risk pregnant women

BMC Pregnancy and Childbirth, 2017
BackgroundGroup prenatal care (GPC) models have been gaining popularity in recent years. Studies of high-risk groups have shown improved outcomes. Our objective was to review and summarize outcomes for women in GPC for women with specific high-risk ...
Brittany Byerley, D. Haas
semanticscholar   +1 more source

Preventive Care, Care for Children and National Health Insurance [PDF]

The purpose of this paper is to examine issues related to the coverage of preventive care under national health insurance. Four specific kinds of medical care services are included under the rubric of preventive care: prenatal care; pediatric care ...
Gilbert R. Ghez, Michael Grossman
core  

Dynamics of Race, Culture and Key Indicators of Health in the Nation's 100 Largest Cities and Their Suburbs [PDF]

, 2003
Profiles the 2000 status of, and changes since 1990, in rates of health and health-related measures to identify patterns in race/ethnicity, foreign-born status, language use, poverty, income, low birth weight, teen births, prenatal care, and ...
Dennis P. Andrulis, Hailey M. Reid, Lisa M. Duchon   +2 more
core  

Rural-Based Health Promotion Model for Pregnant Women in Banyumas District [PDF]

, 2016
Previous studies show that knowledge of prenatal care in rural areas remains low that affects to bad behavior, so developing health promotion models is needed to improve prenatal care knowledge, attitude and behavior.
Anandari, D. (Dian), Gamelia, E. (Elviera), Purnamasari, D. U. (Dyah)   +2 more
core   +6 more sources

Spectrum of Congenital Anomalies in Myhre Syndrome—Insights Into Effects Brought by Altered TGF‐β Signaling via Gain‐of‐Function Variants in SMAD4

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is a rare genetic disorder characterized by progressive multisystem involvement. Gain‐of‐function missense heterozygous variants affecting the Ile500 residue and Arg496 residue of the SMAD4 gene are implicated in this condition.
Kawmadi Gunawardena, Alessandro De Falco, Deborah Osio, Eleanor Sherlock, Emma Kivuva, Erina Sasaki, Francis H. Sansbury, Nayana Lahiri, Patricia Foley, Sahar Mansour, Shane McKee, Tazeen Ashraf, Nicola Brunetti‐Pierri, Usha Kini   +13 more
wiley   +1 more source