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

Year Number of Results
1973 1
1975 1
1977 1
1980 1
1982 1
1985 3
1986 2
1987 1
1988 1
1990 1
1991 2
1993 1
1994 4
1995 1
1997 2
1998 1
1999 2
2000 1
2001 2
2002 1
2003 5
2004 3
2005 1
2006 3
2007 4
2008 5
2009 8
2010 2
2011 11
2012 4
2013 1
2014 1
2015 3
2016 2
2017 8
2018 2
2019 4
2020 6
2021 7
2022 6
2023 10
2024 2

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115 results

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Page 1
Tracheostomy.
Freezer NJ, Beasley SW, Robertson CF. Freezer NJ, et al. Arch Dis Child. 1990 Jan;65(1):123-6. doi: 10.1136/adc.65.1.123. Arch Dis Child. 1990. PMID: 2301974 Free PMC article.
The conditions necessitating tracheostomy were trauma (n = 21), acquired subglottic stenosis (n = 21), subglottic haemangioma (n = 16), Guillain-Barre syndrome (n = 14), Pierre Robin syndrome (n = 9), craniofacial disorders (n = 9), micrognathia (n = 5), and others in 47. …
The conditions necessitating tracheostomy were trauma (n = 21), acquired subglottic stenosis (n = 21), subglottic haemangioma (n = 16), Guil …
Pycnodysostosis at otorhinolaryngology.
Baglam T, Binnetoglu A, Fatih Topuz M, Baş Ikizoglu N, Ersu R, Turan S, Sarı M. Baglam T, et al. Int J Pediatr Otorhinolaryngol. 2017 Apr;95:91-96. doi: 10.1016/j.ijporl.2017.02.009. Epub 2017 Feb 11. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28576543
Our aim was to describe the otorhinolaryngologic findings, differential diagnoses, various treatment options, and followup in eight cases of pycnodysostosis. METHOD: This retrospective clinical study used data from eight patients diagnosed with pycnodysostosis by a single …
Our aim was to describe the otorhinolaryngologic findings, differential diagnoses, various treatment options, and followup in eight cases of …
Robin Sequence: Neonatal Mandibular Distraction.
Morrison KA, Collares MV, Flores RL. Morrison KA, et al. Clin Plast Surg. 2021 Jul;48(3):363-373. doi: 10.1016/j.cps.2021.03.005. Epub 2021 May 8. Clin Plast Surg. 2021. PMID: 34051891 Review.
Pierre Robin sequence is defined by the clinical triad: mandibular hypoplasia, glossoptosis, and airway obstruction. ...
Pierre Robin sequence is defined by the clinical triad: mandibular hypoplasia, glossoptosis, and airway obstruction. ...
Hallermann-Streiff syndrome: a review.
Cohen MM Jr. Cohen MM Jr. Am J Med Genet. 1991 Dec 15;41(4):488-99. doi: 10.1002/ajmg.1320410423. Am J Med Genet. 1991. PMID: 1776643 Review.
The Hallermann-Streiff syndrome is characterized by dyscephaly, hypotrichosis, microphthalmia, cataracts, beaked nose, micrognathia, and proportionate short stature. Cause is unknown; sporadic occurrence is the rule. ...
The Hallermann-Streiff syndrome is characterized by dyscephaly, hypotrichosis, microphthalmia, cataracts, beaked nose, micrognathia, …
Fetal valproate syndrome: the Irish experience.
Mohd Yunos H, Green A. Mohd Yunos H, et al. Ir J Med Sci. 2018 Nov;187(4):965-968. doi: 10.1007/s11845-018-1757-6. Epub 2018 Feb 3. Ir J Med Sci. 2018. PMID: 29396778
Features commonly described are prominent metopic ridge, midface hypoplasia, epicanthic folds, micrognathia and broad and flat nasal bridge. Four (13.7%) had cleft palate, three (10%) had neural tube defect, four (13.7%) with cardiac malformation, 15 (52%) experienced deve …
Features commonly described are prominent metopic ridge, midface hypoplasia, epicanthic folds, micrognathia and broad and flat nasal …
Congenital Malformations Attributed to Prenatal Exposure to Cyclophosphamide.
Rengasamy P. Rengasamy P. Anticancer Agents Med Chem. 2017;17(9):1211-1227. doi: 10.2174/1871520616666161206150421. Anticancer Agents Med Chem. 2017. PMID: 27924730 Review.
Both sporadic case reports and larger case series have demonstrated that babies with cyclophosphamide embryopathy are afflicted with intrauterine growth restriction, small for gestational age, and craniofacial malformations including eye anomalies, cleft/arched palate, hydrocepha …
Both sporadic case reports and larger case series have demonstrated that babies with cyclophosphamide embryopathy are afflicted with intraut …
Managing infants with craniofacial malformations - Where to go next?
Poets CF, Abadie V, Breugem C, Wallis C, Abel F, Chalouhi C, Kruisinga F, Sorg AL, Wiechers C. Poets CF, et al. Semin Fetal Neonatal Med. 2021 Dec;26(6):101289. doi: 10.1016/j.siny.2021.101289. Epub 2021 Sep 17. Semin Fetal Neonatal Med. 2021. PMID: 34548245 Review.
Robin sequence, is characterized by considerable heterogeneity and a lack of randomized trials to identify an optimal approach. We propose to establish an international register using a common minimal dataset that will better allow for a comparison between key determinants …
Robin sequence, is characterized by considerable heterogeneity and a lack of randomized trials to identify an optimal approach. We pr …
Possible valproate teratogenicity.
Tein I, MacGregor DL. Tein I, et al. Arch Neurol. 1985 Mar;42(3):291-3. doi: 10.1001/archneur.1985.04060030113019. Arch Neurol. 1985. PMID: 3919693
We present a patient whose defects in morphogenesis appear to be associated with valproic acid exposure only, and suggest a clinical phenotype that our patient shares with other children exposed to prenatal valproic acid therapy. Features described previously include dysmo …
We present a patient whose defects in morphogenesis appear to be associated with valproic acid exposure only, and suggest a clinical
Study protocol for a multicenter, multinational, observational registry of epidemiology, treatment and outcome of patients with Robin sequence.
Oechsle AL, Wiechers C, Abadie V, Abel F, Breugem C, Poets CF. Oechsle AL, et al. Head Face Med. 2023 May 20;19(1):20. doi: 10.1186/s13005-023-00364-3. Head Face Med. 2023. PMID: 37210548 Free PMC article.
BACKGROUND: Robin sequence (RS) is a congenital condition characterized by micrognathia, glossoptosis and upper airway obstruction. Diagnosis and treatment are characterized by heterogeneity, resulting in a lack of uniformly collected data. ...These data, urgently demanded …
BACKGROUND: Robin sequence (RS) is a congenital condition characterized by micrognathia, glossoptosis and upper airway obstruction. D …
Total facial nerve injury during mandibular distraction osteogenesis.
Belcher RH, Phillips JD. Belcher RH, et al. Int J Pediatr Otorhinolaryngol. 2020 Sep;136:110182. doi: 10.1016/j.ijporl.2020.110182. Epub 2020 Jun 13. Int J Pediatr Otorhinolaryngol. 2020. PMID: 32563840 Review.
Pubmed was queried for terms singularly and in combination including "mandibular distraction osteogenesis", "facial nerve", "cranial nerve", "complications", "micrognathia", "retrognathia". After reviewing the results, studies discussing complications of MDO that involved …
Pubmed was queried for terms singularly and in combination including "mandibular distraction osteogenesis", "facial nerve", "cranial nerve", …
115 results