Zobrazeno 1 - 10 of 14 pro vyhledávání: '"Kathryn K. Ostermaier"'
1
A Road Map for Academic Developmental-Behavioral Pediatric Practices to Increase Access
Autor: Dinah L, Godwin, Jennifer, Cervantes, Jennifer Y, Torres, Kathryn K, Ostermaier, Leandra N, Berry, Robert G, Voigt
Publikováno v: Journal of Developmental & Behavioral Pediatrics. 43:540-544
There are currently at least 19 million children and adolescents in the United States with disorders of development (learning disorders, attention-deficit/hyperactivity disorder, intellectual disabilities, autism, motor incoordination/cerebral palsy,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::574621902308e2c162ffae478a7f021a
https://doi.org/10.1097/dbp.0000000000001132
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2
Incidence of Celiac Disease in Down Syndrome: A Longitudinal, Population-Based Birth Cohort Study
Autor: Kathryn K. Ostermaier, Slavica K. Katusic, Amy L. Weaver, Robert G. Voigt, Ruth E. Stoeckel, Scott M. Myers
Publikováno v: Clin Pediatr (Phila)
American Academy of Pediatrics (AAP) guidelines for children with Down syndrome (DS) include assessment for celiac disease (CD), although data to support this recommendation have been inconsistent. We determined the incidence of CD among children wit
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebaeab14bbab7510bb25ca48bcb8ff9a
https://doi.org/10.1177/0009922820941247
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3
Examining genetic counselors' implicit attitudes toward disability
Autor: Jennifer Czerwinski, Helen Gould, Katie Stoll, S. Shahrukh Hashmi, Victoria F. Wagner, Kathryn K. Ostermaier
Publikováno v: Journal of genetic counselingREFERENCES. 28(6)
Genetic counselors have a unique role in healthcare that requires a balance between being a patient educator and patient advocate when discussing disability. This study aimed to determine genetic counselors' implicit attitudes toward disability, and
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::410e0bcdd0ee3bd1e17801c1c760c979
https://pubmed.ncbi.nlm.nih.gov/31442365
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4
Early postnatal bladder function in fetoscopic myelomeningocele repair patients
Autor: Duong D. Tu, Kathryn K. Ostermaier, Heidi Castillo, Chester J. Koh, Gene O. Huang, Oluyinka O. Olutoye, Michael A. Belfort, William E. Whitehead, Jonathan Castillo
Publikováno v: Journal of pediatric rehabilitation medicine. 10(3-4)
Purpose Prenatal repair of myelomeningocele (MMC) via hysterotomy has demonstrated neurosurgical and motor benefits, when compared to postnatal repairs. Urologic benefits, however, remain to be seen. The purpose of this study was to review early post
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9b3543b599a1cec8fad6205590770ca
https://pubmed.ncbi.nlm.nih.gov/29125525
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5
Urologic self-management through intermittent self-catheterization among individuals with spina bifida: A journey to self-efficacy and autonomy
Autor: Jonathan Castillo, Huirong Zhu, Gene O. Huang, Heidi Castillo, Talia Collier, Ellen Fremion, Duong D. Tu, Kathryn K. Ostermaier
Publikováno v: Journal of pediatric rehabilitation medicine. 10(3-4)
PURPOSE To describe the age of independence in intermittent self-catheterization (ISC) in a diverse patient population and identify factors associated with ISC in individuals with spina bifida. METHODS Two hundred patients with myelomeningocele or li
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e537029ac32ffeb8584f9753e5c3d8c
https://pubmed.ncbi.nlm.nih.gov/29125508
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9
Association of copper-zinc superoxide dismutase (SOD1) and manganese superoxide dismutase (SOD2) genes with nonsyndromic myelomeningocele
Autor: Kathryn K. Ostermaier, Kit Sing Au, Hope Northrup, Jack M. Fletcher, Gayle H. Tyerman, Alanna C. Morrison, Christina Davidson, Benjamin A. Kase, Amanda M. Goiffon
Publikováno v: Birth Defects Research Part A: Clinical and Molecular Teratology. 94:762-769
BACKGROUND A common and severe neural tube defect (NTD) phenotype, myelomeningocele (MM), results from the defective closure of the caudal end of the neural tube with herniation of the spinal cord and meninges through the vertebral column. The exact
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6917dbd98742059b1ad071de9767f07c
https://doi.org/10.1002/bdra.23065
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10
Association of folate receptor (folr1, folr2, folr3) and reduced folate carrier (slc19a1) genes with meningomyelocele
Autor: Sabine Doebel, Kit Sing Au, Hope Northrup, Alanna C. Morrison, Jack M. Fletcher, Michelle R. O'Byrne, Jone Ing Lin, Kathryn K. Ostermaier, Gayle H. Tyerman
Publikováno v: Birth Defects Research Part A: Clinical and Molecular Teratology. 88:689-694
Meningomyelocele (MM) results from lack of closure of the neural tube during embryologic development. Periconceptional folic acid supplementation is a modifier of MM risk in humans, leading toan interest in the folate transport genes as potential can
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91e1e83eab837eb05eea019acc032087
https://doi.org/10.1002/bdra.20706
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