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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1974 1
1975 1
1984 1
1987 4
1988 1
1989 1
1990 4
1991 5
1992 5
1993 5
1994 4
1995 1
1996 5
1997 3
1998 1
1999 5
2000 5
2001 5
2002 3
2003 11
2004 10
2005 2
2006 5
2007 3
2008 5
2009 5
2010 2
2011 5
2012 8
2013 5
2014 7
2015 5
2016 8
2017 8
2018 5
2019 1
2020 2
2021 3
2022 2
2023 5
2024 3

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158 results

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Page 1
Congenital Anomalies of the Kidney and the Urinary Tract (CAKUT).
Rodriguez MM. Rodriguez MM. Fetal Pediatr Pathol. 2014 Oct-Dec;33(5-6):293-320. doi: 10.3109/15513815.2014.959678. Epub 2014 Oct 14. Fetal Pediatr Pathol. 2014. PMID: 25313840 Free PMC article. Review.
This article reviews the majority of Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) with emphasis in Pediatric Pathology describing and illustrating lesions as varied as ureteral duplications, ureteropelvic junction obstruction, horseshoe kidney, posterior ur …
This article reviews the majority of Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) with emphasis in Pediatric Patholog …
Intrathoracic rib: rare rib anomaly, review of the literature and proposal for classification.
Xue X, Zhao S, Li K, Zhao B. Xue X, et al. Int J Med Sci. 2021 Oct 16;18(16):3800-3807. doi: 10.7150/ijms.63828. eCollection 2021. Int J Med Sci. 2021. PMID: 34790056 Free PMC article. Review.
Background: Intrathoracic ribs are very rare congenital anomalies, and often discovered incidentally on chest X-ray. ...Methods: All relevant literatures were searched and reviewed. The terms include intrathoracic rib, intrathoracic bifid rib, trans-thoracic …
Background: Intrathoracic ribs are very rare congenital anomalies, and often discovered incidentally on chest X-ray. ...Methods: All …
Complex lymphatic anomalies.
Trenor CC 3rd, Chaudry G. Trenor CC 3rd, et al. Semin Pediatr Surg. 2014 Aug;23(4):186-90. doi: 10.1053/j.sempedsurg.2014.07.006. Epub 2014 Jul 22. Semin Pediatr Surg. 2014. PMID: 25241096 Review.
Biopsy may be needed for diagnosis, though avoidance of rib biopsy is advised to prevent iatrogenic chronic pleural effusion. Lymphangiography can visualize the anatomy and function of the lymphatic system and may identify dysfunction of the thoracic duct in central …
Biopsy may be needed for diagnosis, though avoidance of rib biopsy is advised to prevent iatrogenic chronic pleural effusion. Lymphan …
Disordered vertebral and rib morphology in pudgy mice. Structural relationships to human scoliosis.
Shapiro F. Shapiro F. Adv Anat Embryol Cell Biol. 2016;221:1-123. doi: 10.1007/978-3-319-43151-2_1. Adv Anat Embryol Cell Biol. 2016. PMID: 27655002 Review.
This work will detail our studies on the structural deformities of the vertebral column and adjacent ribs in the pudgy mouse [1] caused by mutations in the delta-like 3 (Dll3) gene of the Notch family [2]. While gene abnormalities in the pudgy mouse have been outlined, the …
This work will detail our studies on the structural deformities of the vertebral column and adjacent ribs in the pudgy mouse [1] caused by m …
The etiology, clinical features, and treatment options of hemifacial microsomia.
Luo S, Sun H, Bian Q, Liu Z, Wang X. Luo S, et al. Oral Dis. 2023 Sep;29(6):2449-2462. doi: 10.1111/odi.14508. Epub 2023 Mar 13. Oral Dis. 2023. PMID: 36648381 Review.
The second most frequent craniomaxillofacial congenital deformity is hemifacial microsomia (HFM). Patients often accompany short mandible, ear dysplasia, facial nerve, and soft tissue dysplasia. ...Reviewing the potential causes, exploring the clinical features of HFM and …
The second most frequent craniomaxillofacial congenital deformity is hemifacial microsomia (HFM). Patients often accompany short mand …
Skeletal ciliopathies: a pattern recognition approach.
Handa A, Voss U, Hammarsjö A, Grigelioniene G, Nishimura G. Handa A, et al. Jpn J Radiol. 2020 Mar;38(3):193-206. doi: 10.1007/s11604-020-00920-w. Epub 2020 Jan 21. Jpn J Radiol. 2020. PMID: 31965514 Review.
Common skeletal ciliopathies include Jeune asphyxiating thoracic dysplasia, Ellis-van Creveld syndrome, Sensenbrenner syndrome, and short-rib polydactyly syndromes. These disorders share common clinical and radiological features. ...Skeletal ciliopathies are commonly assoc …
Common skeletal ciliopathies include Jeune asphyxiating thoracic dysplasia, Ellis-van Creveld syndrome, Sensenbrenner syndrome, and short- …
Sacrococcygeal dysgenesis association.
Duncan PA, Shapiro LR, Klein RM. Duncan PA, et al. Am J Med Genet. 1991 Nov 1;41(2):153-61. doi: 10.1002/ajmg.1320410203. Am J Med Genet. 1991. PMID: 1785625 Review.
SDA patients have a relatively small average number (3.3) of anomalies per patient as compared with 9.3 in sirenomelia and 6.2 in VATER patients. SDA abnormalities occurred to a significant degree only in 6 of 20 designated malformation categories (vertebral, rib, p …
SDA patients have a relatively small average number (3.3) of anomalies per patient as compared with 9.3 in sirenomelia and 6.2 in VATER pati …
Ciliary Dyneins and Dynein Related Ciliopathies.
Antony D, Brunner HG, Schmidts M. Antony D, et al. Cells. 2021 Jul 25;10(8):1885. doi: 10.3390/cells10081885. Cells. 2021. PMID: 34440654 Free PMC article. Review.
Autologous Rib Microtia Construction: Nagata Technique.
Yamada A. Yamada A. Facial Plast Surg Clin North Am. 2018 Feb;26(1):41-55. doi: 10.1016/j.fsc.2017.09.006. Facial Plast Surg Clin North Am. 2018. PMID: 29153188 Review.
Nagata technique becomes most popular method of autologous rib microtia construction. To achieve successful outcome, 3 keys must be perfect: skin envelope, 3D cartilage framework, and proper location of the construct. ...Relationship between the auricular rectangle and the …
Nagata technique becomes most popular method of autologous rib microtia construction. To achieve successful outcome, 3 keys must be p …
Controversies surrounding Jarcho-Levin syndrome.
Cornier AS, Ramirez N, Carlo S, Reiss A. Cornier AS, et al. Curr Opin Pediatr. 2003 Dec;15(6):614-20. doi: 10.1097/00008480-200312000-00012. Curr Opin Pediatr. 2003. PMID: 14631208 Review.
PURPOSE OF THE REVIEW: Jarcho-Levin syndrome is an eponym that has been used to describe a variety of clinical phenotypes consisting of short-trunk dwarfism associated with rib and vertebral anomalies. This admixture of phenotypes under Jarcho-Levin syndrome has allowed so …
PURPOSE OF THE REVIEW: Jarcho-Levin syndrome is an eponym that has been used to describe a variety of clinical phenotypes consisting of shor …
158 results