Results 111 to 120 of about 23,761 (351)
Nasal obstruction as a drug side effect
Nasal obstruction is a common symptom of various diseases, allergies, and structural deformities and a ‘stuffy nose’ is one of the most common reasons that patients seek a physician’s aid.
Cemal Cingi +2 more
doaj +1 more source
بازسازی کامل بینی پس از تخریب به علت گرانولوماتوز وگنر [PDF]
تغییر شکل بینی یکی از عوارض ضایع در گرانولوماتوز وگنر است که علت آن درگیری عروق سایز متوسط می¬باشد. این بیماری می¬تواند منجر به نکروز و تخریب مخاط بینی و اسکلت استخوانی غضروفی شود.
حافظی, فرهاد +4 more
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Degree theory for 4‐dimensional asymptotically conical gradient expanding solitons
Abstract We develop a new degree theory for 4‐dimensional, asymptotically conical gradient expanding solitons. Our theory implies the existence of gradient expanding solitons that are asymptotic to any given cone over S3$S^3$ with non‐negative scalar curvature. We also obtain a similar existence result for cones whose link is diffeomorphic to S3/Γ$S^3/\
Richard H. Bamler, Eric Chen
wiley +1 more source
Achieving midvault symmetry in unilateral cleft nose deformity rhinoplasty [PDF]
Brajendra Baser +2 more
openalex +1 more source
Abstract Background Gene transcription is crucial for embryo and postnatal development and is regulated by the Mediator complex. Mediator is comprised of four submodules, including the kinase submodule (CKM). The CKM consists of MED13, MED12, CDK8, and CCNC.
Anna K. Leinheiser +5 more
wiley +1 more source
Rhinoplasty Using Autologous Costal Cartilage in a Patient with Acrodysostosis
Summary:. Acrodysostosis, a rare congenital syndrome, is characterized by peripheral dysostosis, nasal hypoplasia, mental retardation, and other skeletal deformities.
Lilia Kase, MD +4 more
doaj +1 more source
Abstract Trichorhinophalangeal syndrome (TRPS) is a rare genetic disease inherited in an autosomal dominant manner. It occurs in 1 in 100,000 people globally and is caused by several types of mutations of the TRPS1 gene. Since the first human patient was reported in 1966, typical and atypical pathologies, disease courses, and treatment case ...
Naoya Saeki +6 more
wiley +1 more source
The role of Rho GTPases in facial morphogenesis
The role of small GTPases, RHOA, RAC1, and CDC42 and pathway mediators is reviewed in the context of embryonic facial development. Lip fusion requires cytoskeletal remodeling during morphogenesis of the facial processes and during lip fusion. Fnm, frontonasal mass; lnp, lateral nasal process; mnp, medial nasal process; mxp, maxillary process; np, nasal
Isra Ibrahim, Joy M. Richman
wiley +1 more source
CASE OF CONGENITAL DEFORMITY OF THE NOSE ASSOCIATED WITH A DEGREE OF MEDIAN HARELIP [PDF]
Alex MacLennan
openalex +1 more source
'Bochanan modhail foghlaimte': Tiree Gaelic, lexicology and Glasgow's historical dictionary of Scottish Gaelic [PDF]
The present paper is intended as a modest contribution towards the study of Tiree Gaelic, particularly its lexicon, drawing on a small part of the archives of the Historical Dictionary of Scottish Gaelic (HDSG) held in the Department of Celtic ...
Ó Maolalaigh, R.
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