Works matching DE "VAN der Woude syndrome"

Results: 49

Maxillary Rehabilitation Using a Removable Partial Denture with Attachments in a Cleft Lip and Palate Patient: A Clinical Report.

Published in:

Journal of Prosthodontics (John Wiley & Sons, Inc.), 2015, v. 24, n. 3, p. 250, doi. 10.1111/jopr.12188

By:

Palmeiro, Marina Rechden Lobato;
Piffer, Caroline Scheeren;
Brunetto, Vivian Martins;
Maccari, Paulo César;
Shinkai, Rosemary Sadami Arai

Publication type:

Article

Novel IRF6 mutations in families with Van Der Woude syndrome and popliteal pterygium syndrome from sub-Saharan Africa.

Published in:

Molecular Genetics & Genomic Medicine, 2014, v. 2, n. 3, p. 254, doi. 10.1002/mgg3.66

By:

Butali, Azeez;
Mossey, Peter A.;
Adeyemo, Wasiu L.;
Eshete, Mekonen A.;
Gaines, LauRen A.;
Even, Dee;
Braimah, Ramat O.;
Aregbesola, Babatunde S.;
Rigdon, Jennifer V.;
Emeka, Christian I.;
James, Olutayo;
Ogunlewe, Mobolanle O.;
Ladeinde, Akinola L.;
Abate, Fikre;
Hailu, Taye;
Mohammed, Ibrahim;
Gravem, Paul E.;
Deribew, Milliard;
Gesses, Mulualem;
Adeyemo, Adebowale A.

Publication type:

Article

PEDIATRIC DENTAL CARE FOR CLEFT LIP AND PALATE CHILD-PART 2.

Published in:

Journal of Ahmedabad Dental College & Hospital (JADCH), 2012, v. 3, n. 1, p. 7

By:

GANESH, M.;
PARIKH, DHAVAL;
BHASKAR, VIJAY

Publication type:

Article

Unsettling the fistula narrative: cultural pathology, biomedical redemption, and inequities of health access in Niger and Ethiopia.

Published in:

Anthropology & Medicine, 2017, v. 24, n. 1, p. 81, doi. 10.1080/13648470.2016.1249252

By:

Heller, Alison;
Hannig, Anita

Publication type:

Article

Síndrome de Van der Woude. Presentación de un caso.

Published in:

Revista de la Academia Mexicana de Odontología Pediátrica (2594-1798), 2021, v. 33, n. 1, p. 38

By:

Tiol-Carrillo, Agustín;
Martín Núñez-Martínez, José;
Enzaldo-de la Cruz, Patricia;
Cenoz-Urbina, Erika

Publication type:

Article

Epidemiological Study of Orofacial Clefts among Population of Eastern Slovakia during the Period 1996-2013.

Published in:

2016

By:

Pacáková, Diana;
Zábavníková, Marianna;
Miklošová, Mária;
Kúkeľová, Diana;
Dankovčík, Róbert

Publication type:

journal article

Causal Variations at IRF6 Gene Identified in Van der Woude Syndrome Pedigrees.

Published in:

Cleft Palate Craniofacial Journal, 2024, v. 61, n. 7, p. 1134, doi. 10.1177/10556656231157575

By:

Yang, Cheng-Wei;
Yin, Bin;
Shi, Jia-Yu;
Shi, Bing;
Jia, Zhong-Lin

Publication type:

Article

Rare and Multiple Hypodontia in Van der Woude Syndrome: Case Report.

Published in:

Cleft Palate Craniofacial Journal, 2023, v. 60, n. 2, p. 243, doi. 10.1177/10556656211058265

By:

Trevizan, Aline Cristina da Silva;
Gonçales, Andréa Guedes Barreto;
Centurion Pagin, Bruna Stuchi;
Pagin, Otávio;
Neves, Lucimara Teixeira das

Publication type:

Article

A Novel IRF6 Frameshift Mutation in a Large Chinese Pedigree With Van der Woude syndrome.

Published in:

Cleft Palate Craniofacial Journal, 2022, v. 59, n. 4, p. 548, doi. 10.1177/10556656211010909

By:

Peng, Qi;
Qin, Wenyan;
Li, Siping;
Huang, Meihua;
Rao, Chunbao;
Lu, Xiaomei

Publication type:

Article

Screening of IRF6 Variants in Patients Subjected to Genetic Association Studies for Nonsyndromic Cleft Lip/Palate.

Published in:

Cleft Palate Craniofacial Journal, 2021, v. 58, n. 9, p. 1128, doi. 10.1177/1055665620980238

By:

Velázquez-Aragón, José A.;
Angel, Ariadna González-del;
Alcántara-Ortigoza, Miguel A.;
Reyna-Fabián, Miriam E.;
Estandia-Ortega, Bernardette

Publication type:

Article

Patients With Cleft Lip and Palate Associated With Intraoral Fibrous Bands: A Report of 3 Cases and Review of Literature.

Published in:

Cleft Palate Craniofacial Journal, 2020, v. 57, n. 3, p. 389, doi. 10.1177/1055665619867233

By:

Vamvanij, Natthacha;
Chen, Zung-Chung;
Lo, Lun-Jou

Publication type:

Article

Combined Tongue-Palate Fusion With Alveolar Bands in a Patient With Pierre Robin Sequence and Van der Woude Syndrome.

Published in:

2019

By:

Robbins, Alexa;
Zarate, Yuri A.;
Hartzell, Larry D.

Publication type:

Case Study

A Novel Interferon Regulatory Factor 6 Mutation in an Asian Family With Van der Woude Syndrome.

Published in:

Cleft Palate Craniofacial Journal, 2017, v. 54, n. 4, p. 442, doi. 10.1597/15-327

By:

Ene-Choo Tan;
Hwee-Woon Lim;
Lim, Eileen C. P.;
Seng-Teik Lee

Publication type:

Article

Interferon Regulatory Factor 6 Controls Proliferation of Keratinocytes From Children With Van der Woude Syndrome.

Published in:

Cleft Palate Craniofacial Journal, 2017, v. 54, n. 3, p. 281, doi. 10.1597/15-275

By:

Hixon, Katherine;
Rhea, Lindsey;
Standley, Jennifer;
Canady, Frank J.;
Canady, John W.;
Dunnwald, Martine

Publication type:

Article

Anatomic Severity, Midfacial Growth, and Speech Outcomes in Van der Woude/Popliteal Pterygium Syndromes Compared to Nonsyndromic Cleft Lip/Palate.

Published in:

Cleft Palate Craniofacial Journal, 2015, v. 52, n. 6, p. 676, doi. 10.1597/14-132

By:

Reardon, Jeffrey B.;
Brustowicz, Katherine A.;
Marrinan, Eileen M.;
Mulliken, John B.;
Padwa, Bonnie L.

Publication type:

Article

Lower Lip Pits: Van der Woude or Kabuki Syndrome?

Published in:

Cleft Palate Craniofacial Journal, 2014, v. 51, n. 6, p. 729, doi. 10.1597/12-258

By:

David-Paloyo, Ferri P.;
Xuecai Yang;
Ju-Li Lin;
Fen-Hwa Wong;
Yah-Huei Wu-Chou;
Lun-Jou Lo

Publication type:

Article

Lack of Association between Missense Variants in GRHL3 (rs2486668 and rs545809) and Susceptibility to Non-Syndromic Orofacial Clefts in a Han Chinese Population.

Published in:

PLoS ONE, 2016, v. 11, n. 7, p. 1, doi. 10.1371/journal.pone.0159940

By:

He, Miao;
Bian, Zhuan

Publication type:

Article

Diagnosing rashes, part 12: lip lesions.

Published in:

Practice Nursing, 2014, v. 25, n. 11, p. 557, doi. 10.12968/pnur.2014.25.11.557

By:

Watkins, Jean

Publication type:

Article

Van der Woude Syndrome with Short Review of the Literature.

Published in:

2014

By:

Deshmukh, Pallavi K.;
Deshmukh, Kiran;
Mangalgi, Anand;
Patil, Subhash;
Hugar, Deepa;
Fakirappa Kodangal, Saraswathi

Publication type:

Case Study

Van der Woude Syndrome Associated with Hypodontia: A Rare Clinical Entity.

Published in:

Case Reports in Dentistry, 2012, p. 1, doi. 10.1155/2012/283946

By:

Soni, Romesh;
Vivek, Rajul;
Srivastava, Adit;
Singh, Ankita;
Srivastava, Shalabh;
Chaturvedi, T. P.

Publication type:

Article

Craniofacial morphology in children with van der Woude syndrome and isolated cleft palate.

Published in:

Journal of Plastic Surgery & Hand Surgery (Taylor & Francis Ltd), 2015, v. 49, n. 4, p. 209, doi. 10.3109/2000656X.2014.992904

By:

Heliövaara, Arja;
Karhulahti, Rekina;
Rautio, Jorma

Publication type:

Article

Van der Woude syndrome: A review of 11 cases seen at the Lagos University Teaching Hospital.

Published in:

African Journal of Paediatric Surgery, 2014, v. 11, n. 1, p. 52, doi. 10.4103/0189-6725.129235

By:

James, Olutayo;
Adeyemo, Wasiu L.;
Emeka, Christian I.;
Ogunlewe, Mobolanle O.;
Ladeinde, Akinola L.;
Butali, Azeez

Publication type:

Article

Parental age is related to the occurrence of cleft lip and palate in Brazilian populations.

Published in:

Brazilian Journal of Oral Sciences, 2016, v. 15, n. 2, p. 167, doi. 10.20396/bjos.v15i2.8648758

By:

de Carvalho, Paulo Henrique Pimenta;
Machado, Renato Assis;
de Almeida Reis, Silvia Regina;
Barbosa Martelli, Daniella Reis;
Dias, Verônica Oliveira;
Martelli-Júnior, Hercílio

Publication type:

Article

A combined targeted mutation analysis of IRF6 gene would be useful in the first screening of oral facial clefts.

Published in:

BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-37

By:

Wu-Chou, Yah-Huei;
Lo, Lun-Jou;
Philip Chen, Kuo-Ting;
Frank Chang, Chun-Shin;
Chen, Yu-Ray

Publication type:

Article

Cheiloscopy and dermatoglyphics as genetic markers in the transmission of cleft lip and palate: A case-control study.

Published in:

2016

By:

K., Saujanya;
M., Ghanashyam Prasad;
B., Sushma;
J., Raghavendra Kumar;
Y. S. N., Reddy;
K., Niranjani;
Saujanya, K;
Prasad, M Ghanashyam;
Sushma, B;
Kumar, J Raghavendra;
Reddy, Y S N;
Niranjani, K

Publication type:

journal article

Congenital Lower Lip Pits (van der Woude Syndrome): What Pathologists Need to Know.

Published in:

Pediatric & Developmental Pathology, 2013, v. 16, n. 5, p. 343, doi. 10.2350/13-02-1302-OA.1

By:

RONG FAN;
FLORES, ROBERTO L.;
FAUGHT, PHILIP R.;
JINGMEI LIN

Publication type:

Article

MIDLINE CLEFT OF LOWER LIP: REVIEW AND CASE REPORTS.

Published in:

2016

By:

ADESINA, O. A.;
EFUNKOYA, A. A.;
OMEJE, K. U.;
SULEIMAN, A. R.

Publication type:

Case Study

Nonsyndromic palate Synechia with floor of mouth.

Published in:

2015

By:

Naidoo, Sharan;
Bütow, Kurt W.

Publication type:

Case Study

Rare health conditions 15: long QT syndrome, Wernicke-Korsakoff syndrome, Zellweger syndrome and Van der Woude syndrome.

Published in:

British Journal of Healthcare Assistants, 2018, v. 12, n. 8, p. 386, doi. 10.12968/bjha.2018.12.8.386

By:

Barber, Chris

Publication type:

Article

The syndrome of pit of the lower lip and its association with cleft palate.

Published in:

Contemporary Clinical Dentistry, 2014, v. 5, n. 3, p. 383, doi. 10.4103/0976-237X.137961

By:

KAUL, BHAVNA;
MAHAJAN, NANIKA;
GUPTA, RAKESH;
KOTWAL, BHANU

Publication type:

Article

Van der Woude syndrome: Management in the mixed dentition.

Published in:

2013

By:

AGARWAL, SONAHITA;
DINESH, M. R.;
DHARMA, R. M.;
AMARNATH, B. C.

Publication type:

Case Study

Prevalence of commissural lip pits in population of central Gujarat: A hospital-based study.

Published in:

Journal of Oral & Maxillofacial Pathology (0973029X), 2018, v. 22, n. 1, p. 144, doi. 10.4103/jomfp.JOMFP_126_15

By:

Tailor, Mansi;
Joshi, Manjiri

Publication type:

Article

IRF6 and SPRY4 Signaling Interact in Periderm Development.

Published in:

2017

By:

Kousa, Y. A.;
Roushangar, R.;
Patel, N.;
Walter, A.;
Marangoni, P.;
Krumlauf, R.;
Klein, O. D.;
Schutte, B. C.

Publication type:

journal article

Novel IRF6 Mutations Detected in Orofacial Cleft Patients by Targeted Massively Parallel Sequencing.

Published in:

2017

By:

Khandelwal, K. D.;
Ishorst, N.;
Zhou, H.;
Ludwig, K. U.;
Venselaar, H.;
Gilissen, C.;
Thonissen, M.;
van Rooij, I. A. L. M.;
Dreesen, K.;
Steehouwer, M.;
van de Vorst, M.;
Bloemen, M.;
van Beusekom, E.;
Roosenboom, J.;
Borstlap, W.;
Admiraal, R.;
Dormaar, T.;
Schoenaers, J.;
Vander Poorten, V.;
Hens, G.

Publication type:

journal article

Isolated Congenital Midline Upper Lip Sinus in A 5-year Old Child: A Rarity.

Published in:

2017

By:

Alam, Mehtab;
Hasan, Syed;
Hashmi, Shahab;
Singh, Piyush

Publication type:

Report

Craniofacial characteristics in Van der Woude syndrome.

Published in:

Oral Diseases, 2023, v. 29, n. 4, p. 1680, doi. 10.1111/odi.14187

By:

Estévez‐Arroyo, Blanca;
Gómez‐Mendo, Ignacio;
Romero‐Maroto, Martín;
Solano‐Reina, Enrique;
Iglesias‐Linares, Alejandro

Publication type:

Article

Novel de novo missense mutation in the interferon regulatory factor 6 gene in an Italian infant with IRF6-related disorder.

Published in:

Italian Journal of Pediatrics, 2022, v. 48, n. 1, p. 1, doi. 10.1186/s13052-022-01330-6

By:

Schierz, Ingrid Anne Mandy;
Amoroso, Salvatore;
Antona, Vincenzo;
Giuffrè, Mario;
Piro, Ettore;
Serra, Gregorio;
Corsello, Giovanni

Publication type:

Article

BASICS OF DERMATOGLYPHIC IN MEDICINE.

Published in:

European Science Review, 2018, v. 1, n. 9/10, p. 80

By:

A. T., Kurbanov

Publication type:

Article

Congenital Symmetrical Lower Lip Pits: Van der Woude Syndrome.

Published in:

Oman Medical Journal, 2015, v. 30, n. 1, p. 69, doi. 10.5001/omj.2015.16

By:

Ibrahim, Abdulrasheed;
Ajike, Sunday

Publication type:

Article

IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families.

Published in:

Clinical Genetics, 2016, v. 90, n. 1, p. 28, doi. 10.1111/cge.12675

By:

Leslie, E.J.;
Koboldt, D.C.;
Kang, C.J.;
Ma, L.;
Hecht, J.T.;
Wehby, G.L.;
Christensen, K.;
Czeizel, A.E.;
Deleyiannis, F.W.‐B.;
Fulton, R.S.;
Wilson, R.K.;
Beaty, T.H.;
Schutte, B.C.;
Murray, J.C.;
Marazita, M.L.

Publication type:

Article

Novel lip pit phenotypes and mutations of IRF6 in Van der Woude syndrome patients from Pakistan.

Published in:

Clinical Genetics, 2014, v. 85, n. 5, p. 487, doi. 10.1111/cge.12207

By:

Malik, S.;
Wilcox, E.R.;
Naz, S.

Publication type:

Article

Cell-Autonomous and Non-Cell-Autonomous Roles for <i>Irf6</i> during Development of the Tongue.

Published in:

PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0056270

By:

Goudy, Steven;
Angel, Peggi;
Jacobs, Britni;
Hill, Cynthia;
Mainini, Veronica;
Smith, Arianna L.;
Kousa, Youssef A.;
Caprioli, Richard;
Prince, Lawrence S.;
Baldwin, Scott;
Schutte, Brian C.

Publication type:

Article

Global health issues related to cleft lip and palate: Prevention and treatment need to team together.

Published in:

2016

By:

Tolarová, Marie M.;
Tolarova, Marie M

Publication type:

Editorial

A rare nonsyndromic presentation of bilateral doughnut shaped lip pits in an Indian child.

Published in:

2016

By:

Senthil Balasubramani;
Sudhakar Sankaran;
Abhishek Madhavan;
Selvakumar Jayaraman

Publication type:

Case Study

Van der Woude syndrome: Report of two cases with supplementary findings.

Published in:

Indian Journal of Dental Research, 2013, v. 24, n. 3, p. 387, doi. 10.4103/0970-9290.118015

By:

More, Chandramani B.;
Varma, Saurabh;
Tailor, Mansi;
Bhavsar, Khushbu

Publication type:

Article

Genetic heterogeneity in Van der Woude syndrome: identification of <bold><italic>NOL4</italic></bold> and <bold><italic>IRF6</italic></bold> haplotype from the noncoding region as candidates in two families.

Published in:

Journal of Genetics, 2018, v. 97, n. 1, p. 275, doi. 10.1007/s12041-018-0903-2

By:

Kumari, Priyanka;
Ali, Akhtar;
Singh, Subodh Kumar;
Chaurasia, Amit;
Raman, Rajiva

Publication type:

Article

A Bilateral Tessier Number 4 and 5 Facial Cleft and Surgical Strategy: A Case Report.

Published in:

2013

By:

AbdollahiFakhim, Shahin;
Shahidi, Nikzad;
Bayazian, Gholamreza

Publication type:

Case Study

Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex.

Published in:

2016

By:

Rincic, Martina;
Rados, Milan;
Krsnik, Zeljka;
Gotovac, Kristina;
Borovecki, Fran;
Liehr, Thomas;
Brecevic, Lukrecija

Publication type:

Case Study

De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus.

Published in:

2013

By:

Ene-Choo Tan;
Lim, Eileen C. P.;
Seng-Teik Lee

Publication type:

Case Study