Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1963 1
1971 2
1972 3
1973 3
1974 1
1975 1
1976 5
1977 4
1978 6
1979 2
1980 7
1981 6
1982 1
1983 3
1984 7
1985 7
1986 6
1987 5
1988 6
1989 6
1990 10
1991 9
1992 8
1993 14
1994 9
1995 17
1996 22
1997 18
1998 16
1999 17
2000 24
2001 25
2002 16
2003 14
2004 21
2005 28
2006 30
2007 22
2008 39
2009 42
2010 54
2011 53
2012 69
2013 68
2014 65
2015 54
2016 38
2017 33
2018 37
2019 33
2020 37
2021 35
2022 23
2023 22
2024 12

Text availability

Article attribute

Article type

Publication date

Search Results

988 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Mandibular hypoplasia-deafness-progeroid syndrome"
Page 1
Hypodontia: An Update on Its Etiology, Classification, and Clinical Management.
Al-Ani AH, Antoun JS, Thomson WM, Merriman TR, Farella M. Al-Ani AH, et al. Biomed Res Int. 2017;2017:9378325. doi: 10.1155/2017/9378325. Epub 2017 Mar 19. Biomed Res Int. 2017. PMID: 28401166 Free PMC article. Review.
Hypodontia, or tooth agenesis, is the most prevalent craniofacial malformation in humans. It may occur as part of a recognised genetic syndrome or as a nonsyndromic isolated trait. Excluding third molars, the reported prevalence of hypodontia ranges from 1.6 to 6.9%, depen …
Hypodontia, or tooth agenesis, is the most prevalent craniofacial malformation in humans. It may occur as part of a recognised genetic sy …
Glossoptosis.
Schweiger C, Manica D, Kuhl G. Schweiger C, et al. Semin Pediatr Surg. 2016 Jun;25(3):123-7. doi: 10.1053/j.sempedsurg.2016.02.002. Epub 2016 Feb 18. Semin Pediatr Surg. 2016. PMID: 27301596 Review.
Despite several attempts to classify severity in Robin Sequence patients, taking into account symptoms, presence of concomitant syndromes or malformations, and even endoscopic findings, there is still no general consensus. ...The present article provides an overview of cli …
Despite several attempts to classify severity in Robin Sequence patients, taking into account symptoms, presence of concomitant syndromes …
Numb Chin Syndrome.
Smith RM, Hassan A, Robertson CE. Smith RM, et al. Curr Pain Headache Rep. 2015 Sep;19(9):44. doi: 10.1007/s11916-015-0515-y. Curr Pain Headache Rep. 2015. PMID: 26210355 Review.
"Numb chin syndrome" (NCS) refers to new-onset numbness of the lower lip and chin within the distribution of the mental or inferior alveolar nerves. ...This paper will discuss the differential, recommended evaluations, and the prognosis, for a patient presenting wit …
"Numb chin syndrome" (NCS) refers to new-onset numbness of the lower lip and chin within the distribution of the mental or inferior a …
The ontogeny of Robin sequence.
Logjes RJH, Breugem CC, Van Haaften G, Paes EC, Sperber GH, van den Boogaard MH, Farlie PG. Logjes RJH, et al. Am J Med Genet A. 2018 Jun;176(6):1349-1368. doi: 10.1002/ajmg.a.38718. Epub 2018 Apr 25. Am J Med Genet A. 2018. PMID: 29696787 Review.
RS is heterogeneous and many different etiologies have been described including syndromic, RS-plus, and isolated forms. For an optimal diagnosis, subsequent treatment and prognosis, a thorough understanding of the embryology and pathogenesis is necessary. This manus …
RS is heterogeneous and many different etiologies have been described including syndromic, RS-plus, and isolated forms. For an optima …
Numb chin syndrome.
Maillefert JF, Gazet-Maillefert MP, Tavernier C, Farge P. Maillefert JF, et al. Joint Bone Spine. 2000;67(2):86-93. Joint Bone Spine. 2000. PMID: 10769099 Review.
Numb chin syndrome reflects an abnormality in the mental nerve or inferior alveolar nerve, or occasionally in a nervous structure located higher up in the body. ...This article provides background information on numb chin syndrome, discusses its causes (including th …
Numb chin syndrome reflects an abnormality in the mental nerve or inferior alveolar nerve, or occasionally in a nervous structure loc …
Cerebro-costo-mandibular syndrome.
Silverman FN, Strefling AM, Stevenson DK, Lazarus J. Silverman FN, et al. J Pediatr. 1980 Sep;97(3):406-16. doi: 10.1016/s0022-3476(80)80190-9. J Pediatr. 1980. PMID: 7411303
The cerebro-costo-mandibular syndrome is characterized by cerebral maldevelopment or malfunction or both, costal deficiencies, and micrognathia. ...Pulmonary complications incident to lack of thoracic cage support result in poor prognosis for survival....
The cerebro-costo-mandibular syndrome is characterized by cerebral maldevelopment or malfunction or both, costal deficiencies, …
New therapeutics in promoting and modulating mandibular growth in cases with mandibular hypoplasia.
El-Bialy T, Alhadlaq A. El-Bialy T, et al. Biomed Res Int. 2013;2013:789679. doi: 10.1155/2013/789679. Epub 2013 May 29. Biomed Res Int. 2013. PMID: 23819121 Free PMC article. Review.
Mandibular distraction osteogenesis has been proposed in neonates with mandibular deficiency as a treatment option to avoid tracheostomy procedure later in life. ...Forward jaw positioning appliances have been also used to enhance mandible growth. However, th …
Mandibular distraction osteogenesis has been proposed in neonates with mandibular deficiency as a treatment option to avoid tr …
Treacher Collins Syndrome and Tracheostomy: Decannulation Using Mandibular Distraction Osteogenesis.
Ali-Khan S, Runyan C, Nardini G, Shetye P, Staffenberg D, McCarthy JG, Flores RL. Ali-Khan S, et al. Ann Plast Surg. 2018 Sep;81(3):305-310. doi: 10.1097/SAP.0000000000001514. Ann Plast Surg. 2018. PMID: 29905603
INTRODUCTION: Treacher Collins syndrome (TC) and Pierre Robin sequence (RS) are associated with hypoplastic mandible, glossoptosis, and consequent airway obstruction. Although TC and RS are often grouped together, airway outcomes of bilateral mandibular distr …
INTRODUCTION: Treacher Collins syndrome (TC) and Pierre Robin sequence (RS) are associated with hypoplastic mandible, glossopt …
Syndromes, disorders and maternal risk factors associated with neural tube defects (V).
Chen CP. Chen CP. Taiwan J Obstet Gynecol. 2008 Sep;47(3):259-66. doi: 10.1016/S1028-4559(08)60122-9. Taiwan J Obstet Gynecol. 2008. PMID: 18935987 Free article. Review.
Fetuses with neural tube defects (NTDs) may suffer from associated syndromes and disorders. This article provides a comprehensive review of the syndromes and disorders associated with NTDs, including Pallister-Hall syndrome, Walker-Warburg syndrome and …
Fetuses with neural tube defects (NTDs) may suffer from associated syndromes and disorders. This article provides a comprehensive rev …
Current perspectives on the etiology of agnathia-otocephaly.
Gekas J, Li B, Kamnasaran D. Gekas J, et al. Eur J Med Genet. 2010 Nov-Dec;53(6):358-66. doi: 10.1016/j.ejmg.2010.09.002. Epub 2010 Sep 16. Eur J Med Genet. 2010. PMID: 20849990 Review.
It is a principal anomaly derived from the first pharyngeal arch as a consequence of failed mesenchymal migration of the maxillary prominence and atrophy in the development of the mandibular prominences. Unfortunately, these patients have poor prognoses and may succ …
It is a principal anomaly derived from the first pharyngeal arch as a consequence of failed mesenchymal migration of the maxillary prominenc …
988 results