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2006 1
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Revision Functional Endoscopic Sinus Surgery.
Levine CG, Casiano RR. Levine CG, et al. Otolaryngol Clin North Am. 2017 Feb;50(1):143-164. doi: 10.1016/j.otc.2016.08.012. Otolaryngol Clin North Am. 2017. PMID: 27888911 Review.
Preoperative imaging and sinonasal endoscopy are systematically reviewed; areas of disease and "danger" zones are identified. Traditional anatomic landmarks are often obscured or absent; thus, a set of consistent landmarks (unchanged despite prior surgery) are used to navi …
Preoperative imaging and sinonasal endoscopy are systematically reviewed; areas of disease and "danger" zones are identified. Traditional an …
Oxycephaly-systematic review, case presentation, and diagnostic clarification.
Pontell ME, Barrero CE, Wagner CS, Salinero LK, Swanson JW, Taylor JA, Bartlett SP. Pontell ME, et al. Childs Nerv Syst. 2023 Nov;39(11):3041-3049. doi: 10.1007/s00381-023-06048-2. Epub 2023 Jul 26. Childs Nerv Syst. 2023. PMID: 37493719 Review.
One patient also had a direct intracranial pressure (ICP) measurement of 25 mmHg, and the other had a Chiari I malformation. Both were treated with posterior vault distraction osteogenesis (PVDO) to alleviate the cephalo-cranial disproportion while simultaneously allowing …
One patient also had a direct intracranial pressure (ICP) measurement of 25 mmHg, and the other had a Chiari I malformation. Both were treat …
Radiology of Osteogenesis Imperfecta, Rickets and Other Bony Fragility States.
Calder AD. Calder AD. Endocr Dev. 2015;28:56-71. doi: 10.1159/000380992. Epub 2015 Jun 12. Endocr Dev. 2015. PMID: 26138835 Review.
Radiological diagnosis of severe forms is usually straightforward, but that of milder disease may be challenging because specific features are often absent. However, a multidisciplinary approach is usually successful. Features of OI, including Wormian bones, skull b …
Radiological diagnosis of severe forms is usually straightforward, but that of milder disease may be challenging because specific features a …
Three-dimensional ultrasound in the prenatal diagnosis of cleidocranial dysplasia associated with B-cell immunodeficiency.
Soto E, Richani K, Gonçalves LF, Devers P, Espinoza J, Lee W, Treadwell MC, Romero R. Soto E, et al. Ultrasound Obstet Gynecol. 2006 May;27(5):574-9. doi: 10.1002/uog.2770. Ultrasound Obstet Gynecol. 2006. PMID: 16619383 Free article. Review.
A patient with a singleton pregnancy was referred for three-dimensional ultrasonography (3DUS) at 18 + 3 weeks for suspected hypomineralization of the skull bones and absence of the nasal bones. Three-dimensional rendered images of the fetal skull revealed widening …
A patient with a singleton pregnancy was referred for three-dimensional ultrasonography (3DUS) at 18 + 3 weeks for suspected hypomineralizat …
Fetal acrania diagnosed at 17 weeks of gestation by 2D∕3D ultrasound: a case report and literature review.
Ştefănescu BI, Mihalache TI, Constantin GB, Ţocu G, Ştefănescu MM, Bogdan Goroftei RE. Ştefănescu BI, et al. Rom J Morphol Embryol. 2024 Jan-Mar;65(1):125-129. doi: 10.47162/RJME.65.1.16. Rom J Morphol Embryol. 2024. PMID: 38527993 Free article. Review.
Acrania is a fetal malformation characterized by complete or partial absence of the calvaria above the orbits and supraciliary ridge. No exact mechanism is demonstrated for this anomaly but disturbances in mesenchymal migration during the fourth week of development are the …
Acrania is a fetal malformation characterized by complete or partial absence of the calvaria above the orbits and supraciliary ridge. …
[Mutations in renin-angiotensin system genes and kidney developmental anomalies].
Gubler MC, Gribouval O, Morinière V, Pawtowski A, Antignac C. Gubler MC, et al. J Soc Biol. 2009;203(4):311-8. doi: 10.1051/jbio/2009035. Epub 2010 Feb 1. J Soc Biol. 2009. PMID: 20122389 Review. French.
Autosomal recessive renal tubular dysgenesis (RTD) is a clinical disorder observed in fetuses, characterized by absence or poor development of proximal tubules and early onset and persistent oligohydramnios leading to the Potter sequence, associated with skull ossificat
Autosomal recessive renal tubular dysgenesis (RTD) is a clinical disorder observed in fetuses, characterized by absence or poor development …