Search Results - "Hens, Greet"

Pregnancy Termination in the Case of an Orofacial Cleft: An Investigation of the Concept of Reproductive Autonomy by Hens, Kristien, Hens, Greet

“…Objective: To describe ethical approaches to the issue of pregnancy termination after prenatal detection of cleft lip ± palate. Results: Gynecologists and…”
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Oral steroids and doxycycline: Two different approaches to treat nasal polyps by Van Zele, Thibaut, MD, PhD, Gevaert, Philippe, MD, PhD, Holtappels, Gabriele, Beule, Achim, MD, Wormald, Peter John, MD, Mayr, Susanne, MD, Hens, Greet, MD, PhD, Hellings, Peter, MD, PhD, Ebbens, Fenna A., MD, PhD, Fokkens, Wytske, MD, PhD, Van Cauwenberge, Paul, MD, PhD, Bachert, Claus, MD, PhD

“…Background There is little scientific evidence to support the current practice of using oral glucocorticosteroids and antibiotics to treat patients with…”
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Endoscopic Treatment of Idiopathic Subglottic Stenosis: A Systematic Review by Lavrysen, Emilie, Hens, Greet, Delaere, Pierre, Meulemans, Jeroen

“…To identify different endoscopic techniques for treatment of idiopathic subglottic stenosis (iSGS) and evaluate treatment results. Embase and Cochrane Library…”
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A Case Report of Nasal Glial Heterotopia by Annelien Huygen, Joren Waumans, Greet Hens, Jan Vranckx, Philippe De Vloo

“…Nasal glial heterotopia (NGH), also known as nasal glioma, is a rare congenital malformation in which a mature glial cell mass is found in a location other…”
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Exploring the Underlying Genetics of Craniofacial Morphology through Various Sources of Knowledge by Shriver, Mark D., Mattern, Brooke C., Hens, G., Roosenboom, J., Claes, Peter

“…The craniofacial complex is the billboard of sorts containing information about sex, health, ancestry, kinship, genes, and environment. A thorough knowledge of…”
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3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies by Hoskens, Hanne, Liu, Dongjing, Naqvi, Sahin, Lee, Myoung Keun, Eller, Ryan J, Indencleef, Karlijne, White, Julie D, Li, Jiarui, Larmuseau, Maarten H D, Hens, Greet, Wysocka, Joanna, Walsh, Susan, Richmond, Stephen, Shriver, Mark D, Shaffer, John R, Peeters, Hilde, Weinberg, Seth M, Claes, Peter

“…The analysis of contemporary genomic data typically operates on one-dimensional phenotypic measurements (e.g. standing height). Here we report on a…”
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MEIS2 involvement in cardiac development, cleft palate, and intellectual disability by Louw, Jacoba J., Corveleyn, Anniek, Jia, Yaojuan, Hens, Greet, Gewillig, Marc, Devriendt, Koenraad

“…MEIS2 has been associated with cleft palate and cardiac septal defects as well as varying degrees of intellectual disability. We present a female patient with…”
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Histological analysis of the medial gastrocnemius muscle in young healthy children by Andries, Anke, Deschrevel, Jorieke, Maes, Karen, De Beukelaer, Nathalie, Corvelyn, Marlies, Staut, Lauraine, De Houwer, Hannah, Costamagna, Domiziana, Nijs, Stefaan, Metsemakers, Willem-Jan, Nijs, Elga, Hens, Greet, De Wachter, Eva, Prinsen, Sandra, Desloovere, Kaat, Van Campenhout, Anja, Gayan-Ramirez, Ghislaine

“…Histological data on muscle fiber size and proportion in (very) young typically developing (TD) children is not well documented and data on capillarization and…”
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Malformations of the middle and inner ear on CT imaging in 22q11 deletion syndrome by Loos, Elke, Verhaert, Nicolas, Willaert, Annelore, Devriendt, Koenraad, Swillen, Ann, Hermans, Robert, Op de Beeck, Katya, Hens, Greet

“…The 22q11 deletion syndrome (22q11DS), the most frequent microdeletion syndrome in humans, presents with a large variety of abnormalities. A common abnormality…”
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Deletions and loss-of-function variants in TP63 associated with orofacial clefting by Khandelwal, Kriti D, van den Boogaard, Marie-José H, Mehrem, Sarah L, Gebel, Jakob, Fagerberg, Christina, van Beusekom, Ellen, van Binsbergen, Ellen, Topaloglu, Ozan, Steehouwer, Marloes, Gilissen, Christian, Ishorst, Nina, van Rooij, Iris A L M, Roeleveld, Nel, Christensen, Kaare, Schoenaers, Joseph, Bergé, Stefaan, Murray, Jeffrey C, Hens, Greet, Devriendt, Koen, Ludwig, Kerstin U, Mangold, Elisabeth, Hoischen, Alexander, Zhou, Huiqing, Dötsch, Volker, Carels, Carine E L, van Bokhoven, Hans

“…We aimed to identify novel deletions and variants of TP63 associated with orofacial clefting (OFC). Copy number variants were assessed in three OFC families…”
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Prevalence and Nature of Hearing Loss in 22q11.2 Deletion Syndrome by Van Eynde, Charlotte, Swillen, Ann, Lambeens, Elien, Verhaert, Nicolas, Desloovere, Christian, Luts, Heleen, Vander Poorten, Vincent, Devriendt, Koenraad, Hens, Greet

“…Purpose: The purpose of this study was to clarify the prevalence, type, severity, and age-dependency of hearing loss in 22q11.2 deletion syndrome. Method:…”
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Fourth Branchial Anomalies: Diagnosis, Treatment, and Long-Term Outcome by Boonen, Annelien, Hens, Greet, Meulemans, Jeroen, Hermans, Robert, Delaere, Pierre, Vander Poorten, Vincent

“…Introduction: Fourth branchial anomalies, the rarest among anomalies of the branchial apparatus, often present diagnostic and therapeutic challenges. We…”
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Three-dimensional Morphing and Its Added Value in the Rhinoplasty Consult by Lekakis, Garyfalia, Hens, Greet, Claes, Peter, Hellings, Peter W.

“…BACKGROUND:The evolving literature on 3D surface imaging demonstrates that this technology is becoming the preferred simulation technique in hospitals and…”
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Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation by Indencleef, Karlijne, Roosenboom, Jasmien, Hoskens, Hanne, White, Julie D, Shriver, Mark D, Richmond, Stephen, Peeters, Hilde, Feingold, Eleanor, Marazita, Mary L, Shaffer, John R, Weinberg, Seth M, Hens, Greet, Claes, Peter

“…Orofacial clefting is one of the most prevalent craniofacial malformations. Previous research has demonstrated that unaffected relatives of patients with…”
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The Intersection of the Genetic Architectures of Orofacial Clefts and Normal Facial Variation by Indencleef, Karlijne, Hoskens, Hanne, Lee, Myoung Keun, White, Julie D, Liu, Chenxing, Eller, Ryan J, Naqvi, Sahin, Wehby, George L, Moreno Uribe, Lina M, Hecht, Jacqueline T, Long, Jr, Ross E, Christensen, Kaare, Deleyiannis, Frederic W, Walsh, Susan, Shriver, Mark D, Richmond, Stephen, Wysocka, Joanna, Peeters, Hilde, Shaffer, John R, Marazita, Mary L, Hens, Greet, Weinberg, Seth M, Claes, Peter

“…Unaffected relatives of individuals with non-syndromic cleft lip with or without cleft palate (NSCL/P) show distinctive facial features. The presence of this…”
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In search of the optimal surgical treatment for velopharyngeal dysfunction in 22q11.2 deletion syndrome: a systematic review by Spruijt, Nicole E, Reijmanhinze, Judith, Hens, Greet, Vander Poorten, Vincent, Mink van der Molen, Aebele B

“…Patients with the 22q11.2 deletion syndrome (22qDS) and velopharyngeal dysfunction (VPD) tend to have residual VPD following surgery. This systematic review…”
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Spatially Dense 3D Facial Heritability and Modules of Co-heritability in a Father-Offspring Design by Hoskens, Hanne, Li, Jiarui, Indencleef, Karlijne, Gors, Dorothy, Larmuseau, Maarten H D, Richmond, Stephen, Zhurov, Alexei I, Hens, Greet, Peeters, Hilde, Claes, Peter

“…The human face is a complex trait displaying a strong genetic component as illustrated by various studies on facial heritability. Most of these start from…”
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Testing the face shape hypothesis in twins discordant for nonsyndromic orofacial clefting by Roosenboom, Jasmien, Indencleef, Karlijne, Hens, Greet, Peeters, Hilde, Christensen, Kaare, Marazita, Mary L., Claes, Peter, Leslie, Elizabeth J., Weinberg, Seth M.

“…Nonsyndromic orofacial clefts (OFCs) are complex traits characterized by multifactorial inheritance and wide phenotypic variability. Numerous studies have…”
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Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate by Breckpot, Jeroen, Anderlid, Britt-Marie, Alanay, Yasemin, Blyth, Moira, Brahimi, Afane, Duban-Bedu, Bénédicte, Gozé, Odile, Firth, Helen, Yakicier, Mustafa Cengiz, Hens, Greet, Rayyan, Maissa, Legius, Eric, Vermeesch, Joris Robert, Devriendt, Koen

“…We report on seven novel patients with a submicroscopic 22q12 deletion. The common phenotype constitutes a contiguous gene deletion syndrome on chromosome…”
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Selective nasal allergen provocation induces substance P-mediated bronchial hyperresponsiveness by Hens, Greet, Raap, Ulrike, Vanoirbeek, Jeroen, Meyts, Isabelle, Callebaut, Ina, Verbinnen, Bert, Vanaudenaerde, Bart M, Cadot, Pascal, Nemery, Benoit, Bullens, Dominique M A, Ceuppens, Jan L, Hellings, Peter W

“…Although the concept of "global airway allergy" has become widely accepted during recent years, nasobronchial interaction and its mechanisms remain…”
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