Keywords: سندرم آپرت; Apert syndrome; Genetic disorder; Craniosynostosis; FGFR2;
مقالات ISI سندرم آپرت (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: سندرم آپرت; Apert syndrome; Craniosynostosis; Exome sequencing; FGFR2 gene; Parent-child trio study;
Structural characterization of recombinant human fibroblast growth factor receptor 2b kinase domain upon interaction with omega fatty acids
Keywords: سندرم آپرت; hFGFR2b; human fibroblast growth factor receptor 2b; UFAs; unsaturated fatty acids; CD; circular dichroism; FGFRs; fibroblast growth factor receptors; RTK; receptor tyrosine kinase; Ig; immunoglobulin; PLCγ; phospholipase Cγ; FRS2; fibroblast growth fac
Keywords: سندرم آپرت; Craniosynostosis; Apert syndrome; ABR; Hearing loss; Chronic otitis media;
Keywords: سندرم آپرت; Apert syndrome; Craniosynostosis; Fronto-orbital advancement; Transcranial surgery; Monobloc advancement; Posterior vault surgery
Keywords: سندرم آپرت; Apert syndrome; Craniofacial syndromes; Crouzon syndrome; FGFR mutations; Muenke syndrome; Pfeiffer syndrome; Saethre-Chotzen syndrome; Syndromic craniosynostosis;
Keywords: سندرم آپرت; Apert syndrome; Central Africa; Craniosynostosis; Syndactyly; Tandem base substitution
Keywords: سندرم آپرت; Diagnóstico prenatal; apert; vasos tortuososPrenatal diagnosis; apert syndrome; arterial tortuosity syndrome
Apert syndrome with S252W FGFR2 mutation and characterization using Phenomizer: An Indian case report
Keywords: سندرم آپرت; FGFR; fibroblast growth factor receptor; BKT; Binet Kamat intelligence test; ADHD; attention deficit hyperactivity disorder; Craniosynostosis; Apert syndrome; FGFR2; Phenomizer; Genetic diagnosis;
Apert syndrome: A consensus on the management of Apert hands
Keywords: سندرم آپرت; Apert syndrome; Apert hands; Congenital hand deformity; Craniofacial surgery;
Upper airway endoscopy to optimize obstructive sleep apnea treatment in Apert and Crouzon syndromes
Keywords: سندرم آپرت; Apert syndrome; Crouzon syndrome; Craniosynostoses; Monobloc; Obstructive sleep apnea; Respiratory system;
Fronto-facial advancement and bipartition in Crouzon-Pfeiffer and Apert syndromes: Impact of fronto-facial surgery upon orbital and airway parameters in FGFR2 syndromes
Keywords: سندرم آپرت; Monobloc-distraction; Orbit; 3D-cephalometry; Crouzon-Pfeiffer syndrome; Apert syndrome; FGFR2;
Brain overgrowth in disorders of RTK–PI3K–AKT signaling: A mosaic of malformations
Keywords: سندرم آپرت; Megalencephaly; Thanatophoric dysplasia; Apert syndrome; Balloon cells; Dysplastic neurons; Heterotopia; Polymicrogyria; Pachygyria; Tuberous sclerosis
Absceso cerebral por Haemophilus influenzae serotipo e en un paciente pediátrico con síndrome de Apert
Keywords: سندرم آپرت; Haemophilus influenzae; Absceso cerebral; Síndrome de AperHaemophilus influenzae; Brain abscess; Apert syndrome
Clinicogenetic Study of Turkish Patients With Syndromic Craniosynostosis and Literature Review
Keywords: سندرم آپرت; Apert syndrome; Crouzon syndrome; Pfeiffer syndrome; craniosynostosis; DHPLC
Morphological comparison of the craniofacial phenotypes of mouse models expressing the Apert FGFR2 S252W mutation in neural crest- or mesoderm-derived tissues
Keywords: سندرم آپرت; as; alisphenoid; bo; basioccipital; bs; basisphenoid; FGFR2; fibroblast growth factor receptor 2; Fgfr2+/S252W; ubiquitous Fgfr2 S252W mutants; fr; frontal; μCT; high resolution computed tomography; ipa; interparietal; la; lacrimal; lo; lateral occipital
Assessing the corrective effects of facial bipartition distraction in Apert syndrome using geometric morphometrics
Keywords: سندرم آپرت; Apert syndrome; Geometric morphometrics; Facial bipartition; Principal component analysis
Rapid detection of de novo P253R mutation in FGFR2 using uncultured amniocytes in a pregnancy affected by polyhydramnios, Blake's pouch cyst, and Apert syndrome
Keywords: سندرم آپرت; Apert syndrome; Blake's pouch cyst; FGFR2; P253R; prenatal diagnosis
Multiple Radiopaque Mandibular Lesions in a Patient with Apert Syndrome
Keywords: سندرم آپرت; Apert syndrome; craniosynostosis; florid osseous dysplasia;
An internal distraction device for Le Fort distraction osteogenesis: The NAVID system
Keywords: سندرم آپرت; Crouzon syndrome; Apert syndrome; Cleft lip; Midface hypoplasia; Le Fort; Distraction osteogenesis; Internal distraction device
Long-term follow-up of syndromic craniosynostosis after Le Fort III halo distraction: A cephalometric and CT evaluation
Keywords: سندرم آپرت; Craniofacialsynostyosis; Apert syndrome; Crouzon syndrome; Le fort III osteotomy; Distraction osteogenesis; Long term stability; Midfacial growth; CT scans; Cephalometry
Mesodermal expression of Fgfr2S252W is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome
Keywords: سندرم آپرت; Apert syndrome; Fgfr2S252W; Craniosynostosis; Mesoderm; Neural crest
Otolaryngologic Manifestations of Craniofacial Syndromes
Keywords: سندرم آپرت; Craniofacial; Apert syndrome; Crouzon syndrome; Treacher Collins syndrome; DiGeorge syndrome; Velocardiofacial syndrome; Opitz G/BBB syndrome; Moebius syndrome;
Textiloma of the frontal bone twenty years after craniotomy for Apert syndrome
Keywords: سندرم آپرت; Foreign body; Granuloma; Frontal bone; Apert syndrome; Neurocranium;
The primary site of the acrocephalic feature in Apert syndrome is a dwarf cranial base with accelerated chondrocytic differentiation due to aberrant activation of the FGFR2 signaling
Keywords: سندرم آپرت; AS; Apert Syndrome; Fgfr2IIIcP253R mouse; Fgfr2IIIcP253R transgenic mouse; QR-PCR; Quantitative real time polymerase chain reaction; LMD; Laser microdissection; SOS; Spheno-occipital synchondrosis; Apert syndrome; Fgfr2IIIcP253R transgenic mouse; Accelera
Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology
Keywords: سندرم آپرت; Fgfr2; Craniosynostosis; Apert syndrome; Osteoblast; Coronal suture; Calvaria; Mouse; Intramembranous ossification;
A clinical report on distraction osteogenesis applied for Apert syndrome
Keywords: سندرم آپرت; Apert syndrome; Distraction osteogenesis; Halo-type rigid external distraction device
The study of abnormal bone development in the Apert syndrome Fgfr2+/S252W mouse using a 3D hydrogel culture model
Keywords: سندرم آپرت; Tissue engineering; Apert syndrome; FGFR2; Osteoblast; Hydrogel;
A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis
Keywords: سندرم آپرت; Fibroblast growth factor receptor 2; Apert syndrome; Chondrocyte; Osteoblast; Mouse model;
Acrocephalosyndactyly, Apert type, in a newborn: Cerebral sonography
Keywords: سندرم آپرت; Apert syndrome; Acrocephalosyndactyly; Ultrasound; Intracranial morphology;
Tracheal anomalies complicating ventilation of an infant with Apert syndrome
Keywords: سندرم آپرت; Apert syndrome; Autosomal disorders; Pediatric anesthesia
Levels of mesenchymal FGFR2 signaling modulate smooth muscle progenitor cell commitment in the lung
Keywords: سندرم آپرت; FGF10; FGFR2b; Smooth muscle cells; Lung; Apert syndrome
Simultaneous multiple vector distraction for craniosynostosis syndromes
Keywords: سندرم آپرت; Apert syndrome; Pfeiffer syndrome; Osteotomy; Distraction osteogenesis;