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Showing 1 to 20 of 28 for “"Birth defect"”.

  1. Birth Defect Amelioration and Placental Cytokine Expression in Mnu-Exposed Dams Treated With Ifn-Gamma

    Each year, 7.9 million babies are born with birth defects. Seventy percent of those could be prevented, ameliorated, or repaired; yet 3.2 million children still die by the age of three (March of Dimes Global Report 2006). We have found that non-specific maternal immune stimulation with the cytokine …

    vt Repository record for Birth Defect Amelioration and Placental Cytokine Expression in Mnu-Exposed Dams Treated With Ifn-Gamma (opens in a new tab)

  2. Congenital Palatopharyngeal Incompetence (Cpi): The Natural History of a Late Appearing Birth Defect Manifest by Hypernasality

    Made available in DSpace on 2014-12-14T05:26:40Z (GMT). No. of bitstreams: 1 7616086.pdf: 5558059 bytes, checksum: 14011dfb420af2d2ee49d9ece959f761 (MD5) Previous issue date: 1976

    uiuc Repository record for Congenital Palatopharyngeal Incompetence (Cpi): The Natural History of a Late Appearing Birth Defect Manifest by Hypernasality (opens in a new tab)

  3. Systematic review of speech and language intervention for young children with cochlear implants : a guide for speech language pathologists

    … 3 newborns in 1,000 making it the most common birth defect. Current widespread use of universal newborn hearing screening has resulted in an average age of identification of hearing loss of 2-3 months. As the population of children who are identified early in life and fitted with cochlear …

    texas Repository record for Systematic review of speech and language intervention for young children with cochlear implants : a guide for speech language pathologists (opens in a new tab)

  4. Fluid Flow Forces Regulate Fibrous Extracellular Matrix Protein Expression and Deposition Via A Rhoa/Rho Kinase Dependent Pathway During Atrioventricular Valve Development

    <p> Today, congenital heart defects are collectively the most common birth defect as well as the leading cause of birth defect related deaths, which often require surgical procedures, a lifetime of medications and preventative measures on the patient to maintain a working heart and a healthy body. …

    south-carolina Repository record for Fluid Flow Forces Regulate Fibrous Extracellular Matrix Protein Expression and Deposition Via A Rhoa/Rho Kinase Dependent Pathway During Atrioventricular Valve Development (opens in a new tab)

  5. Ethnic Identity and Teratogenic Risk Perceptions

    … estimated an elevated baseline risk of 25% for birth defects among the general population. In addition, participants overestimated birth defect risks for specific exposures, such as alcohol and marijuana. Based on the MEIM scores, ethnic identity was not significantly associated with teratogenic …

    uthsc Repository record for Ethnic Identity and Teratogenic Risk Perceptions (opens in a new tab)

  6. Identifying Genetic Variants and Characterizing Their Role In Clubfoot

    <p>Clubfoot is a common, complex birth defect affecting 4,000 newborns in the United States and 135,000 world-wide each year. The clubfoot deformity is characterized by inward and rigid downward displacement of one or both feet, along with persistent calf muscle hypoplasia. Despite strong evidence …

    uthsc Repository record for Identifying Genetic Variants and Characterizing Their Role In Clubfoot (opens in a new tab)

  7. AN URBAN BIOETHICS APPROACH TO UNDERSTANDING DISPARITIES IN NEURODEVELOPMENTAL OUTCOMES FOR CHILDREN WITH CONGENITAL HEART DISEASE

    Congenital heart disease (CHD) is the most common birth defect and often resultsin neurodevelopmental impairments and psychological problems which impede educational and occupational attainment and decrease overall quality of life into adulthood. While morbidity and mortality outcomes have improved …

    temple Repository record for AN URBAN BIOETHICS APPROACH TO UNDERSTANDING DISPARITIES IN NEURODEVELOPMENTAL OUTCOMES FOR CHILDREN WITH CONGENITAL HEART DISEASE (opens in a new tab)

  8. Fzd6, Matn2 and Slc25A32, Possible Candidate Genes In Nonsyndromic Cleft Lip and Palate

    … with or without cleft palate (NSCLP) is a common birth defect with a multifactorial etiology. Despite decades of research, the genetic underpinnings of NSCLP still remain largely unexplained. A genome wide association study (GWAS) of a large NSCLP African American family with seven affected …

    uthsc Repository record for Fzd6, Matn2 and Slc25A32, Possible Candidate Genes In Nonsyndromic Cleft Lip and Palate (opens in a new tab)

  9. Contractile Properties of Striated Muscle in Development and In Disease

    … time for muscle formation, and muscle-related birth defects are sometimes linked to mutations in muscle contractile proteins expressed in utero. Even in heart disease, the development of the disease pre-dates the clinical symptoms; however, studying the developing muscle before it presents in …

    washington Repository record for Contractile Properties of Striated Muscle in Development and In Disease (opens in a new tab)

  10. Analysis of Human Face Shape Abnormalities Using Machine Learning

    … with cleft lip and/or palate. Cleft lip is a birth defect that results in deformity of the upper lip and nose. Its severity is widely variable and the results of treatment are influenced by the initial deformity. Objective assessment of severity would help to guide prognosis and treatment. …

    washington Repository record for Analysis of Human Face Shape Abnormalities Using Machine Learning (opens in a new tab)

  11. Analysis of Variation In Clubfoot Candidate Genes

    Isolated clubfoot, a common birth defect occurring in more than 135,000 livebirths worldwide each year, is associated with significant health care and financial burdens. Clubfoot is defined by forefoot adduction, hindfoot varus, midfoot cavus and hindfoot equinus. Isolated clubfoot, which is the …

    uthsc Repository record for Analysis of Variation In Clubfoot Candidate Genes (opens in a new tab)

  12. Yap and Taz Are Required For Neural Crest-Derived Cardiovascular Development

    <p>Congenital heart defects (CHDs) are the most common human birth defect, occurring in ~1/100 newborns, and are a leading cause of early infant death. Cardiac neural crest cells (NCCs) are a migratory and multipotent cell population known to aid in the development of the cardiac outflow tract …

    uthsc Repository record for Yap and Taz Are Required For Neural Crest-Derived Cardiovascular Development (opens in a new tab)

  13. Long Term Follow-Up of Morbidity and Quality of Life Associated With Isolated Gastroschisis

    <p>Gastroschisis is a birth defect in which an opening in the abdominal wall allows herniation of the viscera. Prenatal counseling regarding gastroschisis typically discusses that, although these infants often endure a difficult neonatal course, they experience few long-term complications. However, …

    uthsc Repository record for Long Term Follow-Up of Morbidity and Quality of Life Associated With Isolated Gastroschisis (opens in a new tab)

  14. Gene Discovery In Nonsyndromic Cleft Lip With Or Without Cleft Palate

    … palate (NSCLP), a common, complex orofacial birth defect that affects approximately 4,000 newborns each year in the United States, is caused by both genetic and environmental factors. Orofacial clefts affect the mouth and nose, causing severe deformity of the face, which require medical, …

    uthsc Repository record for Gene Discovery In Nonsyndromic Cleft Lip With Or Without Cleft Palate (opens in a new tab)

  15. Assessment of fetoscopic tracheal occlusion using ultrasound images in phantom study

    Congenital Diaphragmatic Hernia (CDH) is a birth defect that affects approximately 1 in 2000-5000 neonates. Most of the CDH cases are isolated, which means that affected individuals have no other major malformations. The diaphragm is a muscle that separates the chest from the abdomen. Incomplete …

    strathclyde Repository record for Assessment of fetoscopic tracheal occlusion using ultrasound images in phantom study (opens in a new tab)

  16. The Misexpression of Sonic Hedgehog Leads to Digit Duplication

    … Shh results in polydactyly. Polydactyly is a birth defect characterized by the presence of more than the normal number of fingers or toes. This defect with or without associated malformation(s) is found to be 5 to 19 in every 10000 births. To further understand the etiology of abnormal limb …

    creighton Repository record for The Misexpression of Sonic Hedgehog Leads to Digit Duplication (opens in a new tab)

  17. Univariate and Multivariate Surveillance Methods for Detecting Increases in Incidence Rates

    … the incidence of a given disease, infection or birth defect. Observations are regularly taken in which either an incidence occurs or one does not. This dissertation contains the result of an investigation of prospective monitoring techniques in two distinct surveillance situations. In the first …

    vt Repository record for Univariate and Multivariate Surveillance Methods for Detecting Increases in Incidence Rates (opens in a new tab)

  18. Molecular genetic investigation of autosomal dominant hemifacial microsomia

    … to one side of the face and is a common birth defect with an estimated incidence of 1 in 1,000 to 1 in 5.600 births. Most HFM cases are sporadic, but there are rare familial cases that exhibit autosomal dominant inheritance. These families present the best opportunity for locating and …

    edithcowan Repository record for Molecular genetic investigation of autosomal dominant hemifacial microsomia (opens in a new tab)

  19. Xenobiotic Metabolism Genes and Clubfoot

    … or isolated clubfoot is a common orthopedic birth defect that affects approximately 135,000 children worldwide. It is characterized by equinus, varus and adductus deformities of the ankle and foot. Correction of clubfoot involves months of serial manipulations, castings and bracing, with …

    uthsc Repository record for Xenobiotic Metabolism Genes and Clubfoot (opens in a new tab)

  20. Effect of Anchoring On Perceived Amniocentesis Related Miscarriage Risk Within A Latina Population

    … a 3-5% background risk to have a child with a birth defect. Amniocentesis, the most common type of prenatal diagnostic test, is used to detect chromosomal abnormalities, such as Down syndrome. Amniocentesis is associated with a risk of complications that can lead to a miscarriage, which is …

    uthsc Repository record for Effect of Anchoring On Perceived Amniocentesis Related Miscarriage Risk Within A Latina Population (opens in a new tab)

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