Results 101 to 110 of about 13,861 (294)

The Crescent Student Newspaper, January 20, 2006

, 2006
Student newspaper of George Fox University.https://digitalcommons.georgefox.edu/the_crescent/2294/thumbnail ...
George Fox University Archives
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Crisp and Sanders\u27 Locating atonement: Explorations in constructive dogmatics (Book Review)

, 2017
A review of Crisp, O., & Sanders, F. (Eds.). (2015). Locating atonement: Explorations in constructive dogmatics. Grand Rapids, MI: Zondervan. 256 pp. $26.99.
Rosauer, Greg
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Remote Language Assessment in School‐Age Children With Phelan–McDermid Syndrome and Genotype–Phenotype Correlation

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT People with Phelan–McDermid syndrome (PMS) have reduced speech and language abilities, yet little research has profiled the communication abilities in this population. The purpose of this study was threefold: identifying the language and communication profiles of school‐aged children with PMS, identifying genetic contributions to language and ...
Sarah Quadri‐Valverde, Jessica Klusek, Linda D. Ward, Diana Ivankovic, Nancy Powers, Vijay Shankar, Rachel A. Lyman, Trudy F. C. Mackay, William Bridges, Katy Phelan, Curtis Rogers, Luigi Boccuto, Sara M. Sarasua   +12 more
wiley   +1 more source

Hallowe'en, October 31, 1994 [PDF]

, 1994
This is the concert program of the Hallowe'en performance on Monday, October 31, 1994 at 8:00 p.m., at the Tsai Performance Center, 685 Commonwealth Avenue, Boston, Massachusetts.
School of Music, Boston University
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Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12‐Related Developmental Disorders

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

Management of hypotrichosis of the eyelashes: Focus on bimatoprost

Clinical, Cosmetic and Investigational Dermatology, 2010
Steven FagienAesthetic Eyelid Plastic Surgery, Boca Raton, FL, USAAbstract: Prominent eyelashes are generally recognized as enhancing beauty and are often desired by women. Until recently, the options available to augment the prominence of eyelashes were
Steven Fagien
doaj  

Atypical Clinical Course of Griscelli Syndrome Type 2 With Primarily Neurologic Presentation and Adult‐Onset in a 46‐Year‐Old Male

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Griscelli Syndrome Type 2 (GS2) is a rare autosomal recessive disorder caused by pathogenic mutations in the RAB27A gene. Typically, it is characterized by cutaneous hypopigmentation, immunodeficiency, with or without neurological abnormalities secondary to hemophagocytic lymphohistiocytosis (HLH). Without treatment, GS2 often results in fatal
Dzhoy Papingi, Michael Kutsche, Helena Lichtenfeld, Fanny Kortüm, Angela Abicht, Laura Herrmann, Theresia Herget   +6 more
wiley   +1 more source

Biofilm Exoproteins From Staphylococcus Species Impede Re‐Epithelialization of Nasal Epithelial Cells During Wound Healing and Cease Ciliary Beat Frequency

International Forum of Allergy &Rhinology, EarlyView.
ABSTRACT Introduction Chronic rhinosinusitis (CRS) is an inflammatory disease with many different contributing factors, including bacterial infection. CRS patients are typically managed with medical therapies; however, these treatments frequently fail, leaving surgery as the only viable option.
Sintayehu Ambachew, Mahnaz Ramezanpour, Clare M. Cooksley, Emma F. Barry, Lindsay Durr, Kevin Aaron Fenix, P. J. Wormald, Alkis J. Psaltis, Sarah Vreugde   +8 more
wiley   +1 more source

Fungi and eyelashes [PDF]

Australian and New Zealand Journal of Ophthalmology, 1991
F P, English, W, Barnes, G W, Zhang, D P, McManus, P, Campbell   +4 more
openaire   +2 more sources

Summary proposal to encode characters for Vedic in the BMP of the UCS [PDF]

, 2008
This is a proposal to encode Vedic characters in the international character encoding standard Unicode. This set of characters was published in Unicode Standard version 5.2 in October 2009.
Everson, Michael, Scharf, Peter
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