Disease: Dysgnathia complex
- 3-D COSMOS: a new 3-D model based computerised operation simulation and navigation system
- 3-D imaging of the facial surface by topometry using projected white light strips
- A case of rare isolated agnathia and literature review
- A familial PLCB4 mutation causing auriculocondylar syndrome 2 with variable severity
- A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome
- A novel missense variant of the GNAI3 gene and recognisable morphological characteristics of the mandibula in ARCND1
- Agnathia-otocephaly complex: a case report and examination of the OTX2 and PRRX1 genes
- Airway management during an EXIT procedure for a fetus with dysgnathia complex
- Attitudes Toward Domestic Violence and Corporal Punishment Among Former Soviet Union Immigrants in Israel
- Auriculo-condylar syndrome
- Auriculo-condylar syndrome is associated with highly variable ear and mandibular defects in multiple kindreds
- Auriculo-condylar syndrome or new syndrome?
- Auriculo-condylar syndrome: additional patients
- Auriculo-condylar syndrome: further evidence for a new disorder
- Auriculo-condylar syndrome: mapping of a first locus and evidence for genetic heterogeneity
- Auriculo-condylar syndrome. Confronting a diagnostic challenge
- Auriculocondylar syndrome 2 results from the dominant-negative action of PLCB4 variants
- Auriculocondylar syndrome: Pathogenesis, clinical manifestations and surgical therapies
- Autosomal dominant isolated question mark ear
- Bilateral choanal stenosis in auriculocondylar syndrome caused by a PLCB4 variant
- Clinical and magnetic resonance findings in the temporomandibular joints of patients before and after orthognathic surgery
- Clinical evidence for a mandibular to maxillary transformation in Auriculocondylar syndrome
- Complete mouth rehabilitation after transposition osteotomy based on intraoral scanning: an experimental approach
- Computed tomographic reconstruction of a fetus with the dysgnathia complex (agnathia-otocephaly)
- Dominant-negative Gα subunits are a mechanism of dysregulated heterotrimeric G protein signaling in human disease
- Dysgnathia complex sine holoprosencephaly nor synotia: a case report and discussion of its nosology
- Dysgnathia complex, a rare deviation
- Early childhood temperament predicts substance use in young adults
- Focus Issue: New insights in GPCR to G protein signaling
- Further characterization of atypical features in auriculocondylar syndrome caused by recessive PLCB4 mutations
- Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases
- Further phenotypic delineation of the auriculocondylar syndrome type 2 with literature review
- Genetic factors in isolated and syndromic laryngeal cleft
- Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome
- Holoprosencephaly at prenatal diagnosis: analysis of 28 cases regarding etiopathogenic diagnoses
- Loss-of-function of Endothelin receptor type A results in Oro-Oto-Cardiac syndrome
- Mandibular distraction osteogenesis as first step in the early treatment of severe dysgnathia in childhood
- Microtia, severe micrognathia and absent ossicles: auriculo-condylar syndrome or new entity?
- Muscle function therapy of the orofacial area
- Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears
- Mutations in Hedgehog acyltransferase (Hhat) perturb Hedgehog signaling, resulting in severe acrania-holoprosencephaly-agnathia craniofacial defects
- New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving <em>TWIST1</em> regulatory elements
- Novel features in auriculo-condylar syndrome
- Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect
- Ossicular fusion and cholesteatoma in auriculo-condylar syndrome: in vivo evidence of arrest of embryogenesis
- Otocephaly-Dysgnathia Complex: Description of Four Cases and Confirmation of the Role of OTX2
- OTX2 mutations contribute to the otocephaly-dysgnathia complex
- PAN-AMPK activator O304 improves glucose homeostasis and microvascular perfusion in mice and type 2 diabetes patients
- Preferences for treatment among adolescents with Type 1 diabetes: a national study using a discrete choice experiment model
- Prenatal diagnosis of auriculocondylar syndrome with a novel missense variant of GNAI3: a case report
- Public Knowledge and Attitudes Regarding the Use of Antibiotics and Resistance: Findings from a Cross-Sectional Study Among Palestinian Adults
- Question mark ears and post-auricular tags
- Question mark ears, temporo-mandibular joint malformation and hypotonia: auriculo-condylar syndrome or a distinct entity?
- Respiratory and gastrointestinal dysfunctions associated with auriculo-condylar syndrome and a homozygous PLCB4 loss-of-function mutation
- Sibling number and prevalence of allergic disorders in pregnant Japanese women: baseline data from the Kyushu Okinawa Maternal and Child Health Study
- Subjective evaluation of the accuracy of video imaging prediction following orthognathic surgery in Chinese patients
- Surgical Approach in a Patient With Agnathia-Otocephaly Complex: Three-Stage Mandibular Distraction Protocol
- Surgical options for treatment of snoring and sleep apnea
- Surgical visual treatment objective: cephalometric planning in the treatment of dysgnathia of facial complex
- Syndromes of the first and second branchial arches, part 2: syndromes
- Syndromes of the first and second pharyngeal arches: A review
- Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome
- The association between Helicobacter pylori and laryngopharyngeal reflux in laryngeal pathologies
- The association of severe encephalopathy and question mark ear is highly suggestive of loss of MEF2C function
- The correction of auricular and mandibular deformities in auriculo-condylar syndrome
- The Partnership of Medical Genetics and Oral and Maxillofacial Surgery When Evaluating Craniofacial Anomalies
- Three-dimensional registration of the facial surface using projected white light stripes (TRICOLITE - triangulation with coded light technique)
- Transmission of the dysgnathia complex from mother to daughter
- Understanding the basis of auriculocondylar syndrome: Insights from human, mouse and zebrafish genetic studies