Works matching Apert syndrome

Results: 502

Arthrolysis of the shoulder in Apert syndrome.

Published in:

European Journal of Orthopaedic Surgery & Traumatology, 2008, v. 18, n. 2, p. 139, doi. 10.1007/s00590-007-0263-8

By:

Zafra, Manuel;
Carpintero, Pedro;
Moreno-Saiz, Marcos

Publication type:

Article

Monozygotic Twins With Apert Syndrome.

Published in:

Cleft Palate Craniofacial Journal, 2008, v. 45, n. 1, p. 101, doi. 10.1597/06-149.1

By:

Breugem, Corstiaan C.;
Fitzpatrick, Donald F.;
Verchere, Cynthia

Publication type:

Article

MRI characterization of the glenohumeral joint in Apert syndrome.

Published in:

2007

By:

McHugh, Tami;
Wyers, Mary;
King, Erik

Publication type:

journal article

Perioperative complications in children with Apert syndrome: a review of 509 anesthetics.

Published in:

Pediatric Anesthesia, 2011, v. 21, n. 1, p. 72, doi. 10.1111/j.1460-9592.2010.03457.x

By:

Barnett, Sarah;
Moloney, Claire;
Bingham, Robert

Publication type:

Article

Prenatal diagnosis of Apert syndrome using ultrasound, magnetic resonance imaging, and three-dimensional virtual/physical models: three case series and literature review.

Published in:

2018

By:

Werner, Heron;
Castro, Pedro;
Daltro, Pedro;
Lopes, Jorge;
Ribeiro, Gerson;
Araujo Júnior, Edward

Publication type:

Case Study

A child with Apert syndrome and Sturge-Weber syndrome: could fibronectin or the RAS/MAPK signaling pathway be the connection?

Published in:

Child's Nervous System, 2018, v. 34, n. 6, p. 1247, doi. 10.1007/s00381-018-3758-1

By:

Tan, Ai Peng;
Chong, Wui Khean

Publication type:

Article

Apert syndrome: magnetic resonance imaging (MRI) of associated intracranial anomalies.

Published in:

Child's Nervous System, 2018, v. 34, n. 2, p. 205, doi. 10.1007/s00381-017-3670-0

By:

Tan, Ai Peng;
Mankad, Kshitij

Publication type:

Article

Central nervous system and cervical spine abnormalities in Apert syndrome.

Published in:

Child's Nervous System, 2016, v. 32, n. 5, p. 833, doi. 10.1007/s00381-016-3036-z

By:

Breik, Omar;
Mahindu, Antony;
Moore, Mark;
Molloy, Cindy;
Santoreneos, Stephen;
David, David

Publication type:

Article

Atypical presentation of a newborn with Apert syndrome.

Published in:

Child's Nervous System, 2015, v. 31, n. 3, p. 481, doi. 10.1007/s00381-014-2601-6

By:

Spruijt, B.;
Rijken, B.;
Joosten, K.;
Bredero-Boelhouwer, H.;
Pullens, B.;
Lequin, M.;
Wolvius, E.;
Veelen-Vincent, M.;
Mathijssen, I.

Publication type:

Article

Apert Sendromu ve Atriyal Septal Defekt Birlikteliği.

Published in:

Journal of Academic Research in Medicine, 2016, v. 6, n. 1, p. 26, doi. 10.5152/jarem.2016.896

By:

Dervişoğlu, Pınar;
Kösecik, Mustafa;
Kumbasar, Serkan;
Salman, Süleyman;
Şık, Bulat Aytek;
Erdem, Baki;
Tekin, Bülent

Publication type:

Article

Metopic suture in fetuses with Apert syndrome at 22-27 weeks of gestation.

Published in:

2006

By:

Faro, C.;
Chaoui, R.;
Wegrzyn, P.;
Levaillant, J. M.;
Benoit, B.;
Nicolaides, K. H.

Publication type:

journal article

A 37-year-old Nigerian woman with Apert syndrome - medical and psychosocial perspectives: a case report.

Published in:

2018

By:

Kana, M. A.;
Baduku, T. S.;
Bello-Manga, H.;
Baduku, A. S.

Publication type:

journal article

A longitudinal study of dental arch morphology in children with the syndrome of Crouzon or Apert.

Published in:

European Journal of Oral Sciences, 2013, v. 121, n. 4, p. 319, doi. 10.1111/eos.12051

By:

Reitsma, Jacobus H.;
Elmi, Poejan;
Ongkosuwito, Edwin M.;
Buschang, Peter H.;
Prahl‐Andersen, Birte

Publication type:

Article

Dermal fibroblast transcriptome indicates contribution of WNT signaling pathways in the pathogenesis of Apert syndrome.

Published in:

Turkish Journal of Pediatrics, 2017, v. 59, n. 6, p. 619, doi. 10.24953/turkjped.2017.06.001

By:

Çetinkaya, Arda;
Taşkıran, Ekim;
Soyer, Tutku;
Şimşek-Kiper, Pelin Özlem;
Utine, Gülen Eda;
Tunçbilek, Gökhan;
Boduroğlu, Koray;
Alikaşifoğlu, Mehmet

Publication type:

Article

Analysis of Intracranial Volume in Apert Syndrome Genotypes.

Published in:

Pediatric Neurosurgery, 2004, v. 40, n. 4, p. 161, doi. 10.1159/000081933

By:

Anderson, Peter J.;
Netherway, David J.;
Abbott, Amanda H.;
Cox, Timothy;
Roscioli, Tony;
David, David J.

Publication type:

Article

Shape analysis of the sphenoid bone in Apert syndrome using 3D CT scans.

Published in:

Archives of Orofacial Science, 2014, v. 9, n. 1, p. 34

By:

McGlaughlin, K. L.;
Netherway, D. J.;
David, D. J.;
Anderson, P. J.

Publication type:

Article

Anesthetic management of craniosynostosis repair in patient with Apert syndrome.

Published in:

2014

By:

Kumar, Niraj;
Arora, Shubhangi;
Bindra, Ashish;
Goyal, Keshav

Publication type:

Case Study

Apert Syndrome in the Era of Prenatal Diagnosis.

Published in:

Donald School Journal of Ultrasound in Obstetrics & Gynecology, 2014, v. 8, n. 2, p. 222, doi. 10.5005/jp-journals-10009-1358

By:

Stamatian, Florin;
Kovacs, Tunde;
Militaru, Mariela;
Caracostea, Gabriela

Publication type:

Article

Apert syndrome: clinical and radiographic features and case report.

Published in:

Revista Odonto Ciencia, 2011, v. 26, n. 1, p. 96, doi. 10.1590/S1980-65232011000100021

By:

Varoli, Felipe Paes;
Santos, Karina Cecília Panelli;
Costa, Claudio;
Oliveira, Jefferson Xavier

Publication type:

Article

Clinical and radiographic presentation and preparation of the prototyping model for pre-surgical planning in Apert's syndrome.

Published in:

Dentomaxillofacial Radiology, 2006, v. 35, n. 2, p. 119, doi. 10.1259/dmfr/77056158

By:

Sannomiya, E. K.;
Reis, S. A. B.;
Asaumi, J.;
Silva, J. V. L.;
Barbara, A. S.;
Kishi, K.

Publication type:

Article

Circummaxillary Sutures in Patients With Apert, Crouzon, and Pfeiffer Syndromes Compared to Nonsyndromic Children: Growth, Orthodontic, and Surgical Implications.

Published in:

Cleft Palate Craniofacial Journal, 2021, v. 58, n. 3, p. 299, doi. 10.1177/1055665620947616

By:

Meazzini, Maria Costanza;
Corradi, Federica;
Mazzoleni, Fabio;
De Ponti, Elena;
Maccagni, Muriel;
Novelli, Giorgio;
Bozzetti, Alberto

Publication type:

Article

Social Experiences of Turkish Parents Raising a Child With Apert Syndrome: A Qualitative Study.

Published in:

Cleft Palate Craniofacial Journal, 2021, v. 58, n. 3, p. 354, doi. 10.1177/1055665620944761

By:

Saydam, Senem Zeytinoğlu;
Çüçülayef, Darina;
Doğan, Tuğçe Nur;
Crerand, Canice E.;
Özek, Memet

Publication type:

Article

Mandibular Asymmetry in Patients With the Crouzon or Apert Syndrome.

Published in:

Cleft Palate Craniofacial Journal, 2015, v. 52, n. 3, p. 327, doi. 10.1597/13-143

By:

Elmi, P.;
Reitsma, J. H.;
Buschang, P. H.;
Wolvius, E. B.;
Ongkosuwito, E. M.

Publication type:

Article

Patterns of Tooth Agenesis in Patients With Crouzon or Apert Syndrome.

Published in:

Cleft Palate Craniofacial Journal, 2014, v. 51, n. 2, p. 178, doi. 10.1597/12-180

By:

Reitsma, Jacobus H.;
Ongkosuwito, Edwin M.;
van Wijk, Arjen J.;
Prahl-Andersen, Birte

Publication type:

Article

Dysphagia and Nutrition Problems in Infants With Apert Syndrome.

Published in:

Cleft Palate Craniofacial Journal, 2009, v. 46, n. 3, p. 285, doi. 10.1597/08-010.1

By:

Pereira, Valerie;
Sacher, Paul;
Ryan, Martina;
Hayward, Richard

Publication type:

Article

Comparison of ultrasound and magnetic resonance imaging in the prenatal diagnosis of Apert syndrome: report of a case.

Published in:

Child's Nervous System, 2014, v. 30, n. 8, p. 1445, doi. 10.1007/s00381-014-2377-8

By:

Giancotti, A.;
D'Ambrosio, V.;
Filippis, A.;
Aliberti, C.;
Pasquali, G.;
Bernardo, S.;
Manganaro, L.

Publication type:

Article

Mouse models of Apert syndrome.

Published in:

Child's Nervous System, 2012, v. 28, n. 9, p. 1505, doi. 10.1007/s00381-012-1872-z

By:

Holmes, Greg

Publication type:

Article

Occipital expansion without osteotomies in Apert syndrome.

Published in:

Child's Nervous System, 2010, v. 26, n. 11, p. 1543, doi. 10.1007/s00381-010-1144-8

By:

Davis, Charles;
MacFarlane, Martin R.;
Wickremesekera, Agadha

Publication type:

Article

Anesthesia management in a patient of Apert syndrome.

Published in:

2013

By:

Patel, Kiran;
Chavan, Dilip;
Sawant, Pradnya

Publication type:

Case Study

Apert Sendromu: Olgu Sunumu.

Published in:

Medical Journal of Bakirkoy, 2013, v. 9, n. 2, p. 81, doi. 10.5350/BTDMJB201309209

By:

Karaman, Ali;
Kahveci, Hasan

Publication type:

Article

Speech and language skills and cognitive functioning in children with Apert syndrome: a pilot study.

Published in:

International Journal of Language & Communication Disorders, 2002, v. 37, n. 3, p. 325, doi. 10.1080/13682820210138816

By:

Shipster, C.;
Hearst, D.;
Dockrell, J. E.;
Kilby, E.;
Hayward, R.

Publication type:

Article

Farklı mutasyonlar taşıyan Apert sendromlu iki olgu: erken tanının önemi.

Published in:

Türk Pediatri Arşivi, 2017, v. 52, n. 4, p. 231, doi. 10.5152/TurkPediatriArs.2016.3305

By:

Işık, Esra;
Atik, Tahir;
Onay, Hüseyin;
Özkınay, Ferda

Publication type:

Article

An Exploration of the Cognitive, Physical and Psychosocial Development of Children with Apert Syndrome.

Published in:

International Journal of Disability, Development & Education, 2017, v. 64, n. 2, p. 198, doi. 10.1080/1034912X.2016.1194379

By:

Hilton, Caroline

Publication type:

Article

Apert Syndrome: Report of a Case With Emphasis on Craniofacial and Genetic Features.

Published in:

2008

By:

Martelli Jr, Hercílio;
Paranaíba, Lívia Maris Ribeiro;
De Miranda, Roseli Teixeira;
Orsi Jr, Julian;
Coletta, Ricardo D.

Publication type:

Case Study

Apert Syndrome Presenting with Omphalocele.

Published in:

Journal of Krishna Institute of Medical Sciences (JKIMSU), 2019, v. 8, n. 1, p. 95

By:

Swarnkar, Keerti;
Gaikwad, Sarika;
Uke, Punam;
Vagha, Keta;
Dalal, Yash

Publication type:

Article

Apert syndrome: A case report with discussion of craniofacial features.

Published in:

1999

By:

Paravatty, Rajesh P.;
Ahsan, Auswaf;
Sebastian, Bastian T.;
Pai, Keerthilatha M.;
Dayal, Promod K.

Publication type:

Case Study

Dynamic morphological changes in the skulls of mice mimicking human Apert syndrome resulting from gain-of-function mutation of FGFR2 (P253R).

Published in:

Journal of Anatomy, 2010, v. 217, n. 2, p. 97, doi. 10.1111/j.1469-7580.2010.01248.x

By:

Xiaolan Du;
Tujun Weng;
Qidi Sun;
Nan Su;
Zhi Chen;
Huabing Qi;
Ming Jin;
Liangjun Yin;
Qifen He;
Lin Chen

Publication type:

Article

Is the Apert foot an overlooked aspect of this rare genetic disease? Clinical findings and treatment options for foot deformities in Apert syndrome.

Published in:

2020

By:

Stauffer, Alexandra;
Farr, Sebastian

Publication type:

journal article

Case Report: Orthodontic and Dentofacial Orthopedic Considerations in Apert's Syndrome.

Published in:

2000

By:

Rynearson, R. David

Publication type:

Case Study

Prenatal Diagnosis of Apert Syndrome with Cloverleaf Skull Deformity Using Ultrasound, Fetal Magnetic Resonance Imaging and Genetic Analysis.

Published in:

Fetal Diagnosis & Therapy, 2010, v. 27, n. 1, p. 51, doi. 10.1159/000262447

By:

Weber, Benedikt;
Schwabegger, Anton H.;
Vodopiutz, Julia;
Janecke, Andreas R.;
Forstner, Rosemarie;
Steiner, Horst

Publication type:

Article

Apert Syndrome: The Current Role of Prenatal Ultrasound and Genetic Analysis in Diagnosis and Counselling.

Published in:

Fetal Diagnosis & Therapy, 2008, v. 24, n. 4, p. 495, doi. 10.1159/000181186

By:

Athanasiadis, A. P.;
Zafrakas, M.;
Polychronou, P.;
Florentin-Arar, L.;
Papasozomenou, P.;
Norbury, G.;
Bontis, J. N.

Publication type:

Article

Prenatal Diagnosis of Apert Syndrome.

Published in:

Fetal Diagnosis & Therapy, 2004, v. 19, n. 2, p. 127, doi. 10.1159/000075135

By:

Hansen, Wendy F.;
Rijhsinghani, Asha;
Grant, Stanley;
Yankowitz, Jerome

Publication type:

Article

Anaesthesia management in a child with Apert syndrome with craniosynostosis.

Published in:

2016

By:

Parate, Leena Harshad;
Nagaraj, M. C.

Publication type:

Case Study

Apert Syndrome With FGFR2 758 C > G Mutation: A Chinese Case Report.

Published in:

2018

By:

Yahong Li;
Dingyuan Ma;
Yun Sun;
Lulu Meng;
Yanyun Wang;
Tao Jiang

Publication type:

Case Study

Molecular analysis of exons 8, 9 and 10 of the fibroblast growth factor receptor 2 (FGFR2) gene in two families with index cases of Apert Syndrome.

Published in:

2015

By:

Torres, Lilian;
Hernández, Gualberto;
Barrera, Alejandro;
Ospina, Sandra;
Prada, Rolando

Publication type:

Case Study

Apert Sendromu: Olgu Sunumu.

Published in:

2009

By:

Canpolat, Mehmet;
Büyükayhan, Derya;
Güneş, Tamer;
Akçakuş, Mustafa;
Öztürk, Adnan;
Kurtoğlu, Selim

Publication type:

Case Study

Apert Syndrome with Fused Thalami.

Published in:

Fetal & Pediatric Pathology, 2012, v. 31, n. 6, p. 410, doi. 10.3109/15513815.2012.659407

By:

Ludwig, Kathrin;
Salmaso, Roberto;
Manara, Renzo;
Cosmi, Erich;
Baldi, Maurizia;
Rugge, Massimo

Publication type:

Article

Método Pilates como Tratamento de Síndrome de Apert - Efeito na Função Pulmonar: Relato de Caso.

Published in:

Revista Inspirar Movimento & Saude, 2012, v. 4, n. 3, p. 47

By:

Lima, Anne Caroline de Campos Martins de;
Valezi, Melissa Nassif;
Gimenes, Camila;
Manzano, Roberta Munhoz

Publication type:

Article

Apert sendromu: Olgu Sunumu.

Published in:

Perinatal Journal / Perinatoloji Dergisi, 2012, v. 20, n. 1, p. 30, doi. 10.2399/prn.12.0201003

By:

Alanbay, İbrahim;
Çoksüer, Hakan;
Karaşahin, Emre;
Ercan, Mutlu;
Keskin, Uğur;
Temel Ceyhan, Seyit;
Başer, İskender

Publication type:

Article

Apert 's syndrome.

Published in:

Indian Journal of Dermatology, Venereology & Leprology, 2004, v. 70, n. 2, p. 105

By:

Mukhopadhyay, Amiya Kumar;
Mukherjee, Debjani

Publication type:

Article