Results 141 to 150 of about 2,289,707 (361)

“Will you be there for me?” Social support from family and friends during cold case sexual assault prosecutions

American Journal of Community Psychology, EarlyView.
Abstract If sexual assault survivors report the assault to the criminal legal system, they often need informal support from family and friends throughout the long and frequently retraumatizing process of investigation and prosecution. This study is part of a long‐term community‐based participatory action research project in a predominately Black ...
Rebecca Campbell, Rachael Goodman‐Williams, Katie Gregory, McKenzie Javorka, Jasmine Engleton   +4 more
wiley   +1 more source

Computer Aided Modeling of Human Mastoid Cavity Biomechanics Using Finite Element Analysis

EURASIP Journal on Advances in Signal Processing, 2010
The aim of the present study was to analyze the human mastoid cavity on sound transmission using finite element method. Pressure distributions in the external ear canal and middle ear cavity at different frequencies were demonstrated. Our results showed
Chou Yuan-Fang, Chen Peir-Rong, Liu Tien-Chen, Lee Wen-Jeng, Lee Chia-Fone, Chen Jyh-Horng   +5 more
doaj  

Single origin of the epithelium of the human middle ear

, 2019
Objective: The epithelium lining the human middle ear and adjacent temporal bone cavity shows a varying morphological appearance throughout these cavities. Its embryologic origin has long been debated and recently got attention in a newly proposed theory
Oostra, Roelof-Jan, van Waegeningh, Huibert F., van Spronsen, Erik, Ebbens, Fenna A.   +3 more
core   +1 more source

Inflamed Middle Ear Epithelium.

, 2013
Figures A-C show hypertrophied mucosa with increased number of secretory cells. Immunolocalization is similar to the normal middle ear epithelium. A: Claudin 3, middle ear mucosa. B: KCNQ1, middle ear mucosa. C: ENaC, middle ear mucosa.
Frances Hausman (319206), J. Beth Kempton (319205), Jacqueline M. DeGagne (319204), Lisa M. Morris (319203), Dennis R. Trune (319207)   +4 more
core   +1 more source

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet, Sylvie A. Adams, Zoe S. Katz, Christal G. Delagrammatikas, Kosuke Izumi, Winifred Sigal, Kim Ventarola, Elaine H. Zackai, Julia E. Reid, Grant T. Liu, Jennifer M. Kalish   +10 more
wiley   +1 more source

Wideband Absorbance Pattern and its Diagnostic Value in Adults with Middle Ear Effusions and Tympanic Membrane Perforation

BACKGROUND: Middle ear effusion (MEE) and tympanic membrane perforation (TMP) are difficult to distinguish using existing immittance techniques, necessitating the use of a separate test battery.
Arunraj Karuppannan, Animesh Barman, Nerale Maraiah Mamatha   +2 more
core   +1 more source

The Critical Role of Fractionated Urine Glycosaminoglycans in the Evaluation of Mucopolysaccharidosis Type II in Four Unrelated Families

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Since 2015, Ann and Robert H. Lurie Children's Hospital has performed diagnostic testing for infants who screen positive for mucopolysaccharidosis type II (MPS II) on the Illinois newborn screen. Preliminary diagnostic testing includes measurement of plasma iduronate‐2‐sulfatase enzyme activity and urinary glycosaminoglycan analysis, followed ...
Carly A. Rasmussen, Monika Izdebski, Allison Paltzer, Rachel Hickey, Laura Pollard, Joshua Baker   +5 more
wiley   +1 more source

Hearing health outreach services to Indigenous children and young people in the Northern Territory 2012–13 and 2013–14 [PDF]

, 2015
Presents analyses on hearing health outreach services provided to Indigenous children and young people in the Northern Territory. Summary This report presents information on ear and hearing outreach services funded by the Department of Health and ...
Australian Institute of Health and Welfare
core  

The middle ear

, 2009
Structure and function of the middle ear 90 Congenital abnormalities of the middle ear 92 Acute otitis media 94 Complications of acute otitis media 96
Nicholas Steventon, Rogan Corbridge
core   +1 more source

Long‐Term Follow Up of Two Patients With Variants in the Cluster 1031‐1159 of TRRAP Gene: Expanding the Phenotype of Developmental Delay With or Without Dysmorphic Facies and Autism

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The transformation/transcription domain‐associated protein (TRRAP) gene encodes a large multidomain protein, a member of the phosphatidylinositol 3‐kinase‐related kinase (PIKK) family. TRRAP is a component of the histone acetyltransferase (HAT) complex, and it plays an important role in gene transcription, DNA repair, and cell‐cycle regulation.
Roseli Maria Zechi‐Ceide, Vinicius Contrucci Dantas Segarra, Siulan Vendramini‐Pittoli, Henrique Regonaschi Serigatto, Luiza Virmond, Heloisa Marcelina da Cunha Palhares, Fernanda Jehee, Ana Cristina Victorino Krepischi, Carla Rosenberg, Carlos Henrique Paiva Grangeiro, Nancy Mizue Kokitsu‐Nakata   +10 more
wiley   +1 more source