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

Year Number of Results
1986 1
1988 2
1989 1
1990 3
1992 1
1995 1
1996 2
1998 1
1999 1
2000 1
2001 1
2002 1
2003 1
2008 2
2011 1
2012 1
2013 1
2014 2
2015 1
2016 1
2017 1
2018 1
2019 2
2020 1
2022 2
2023 1
2024 0

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32 results

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Page 1
Pai syndrome: a review.
Olivero F, Foiadelli T, Luzzi S, Marseglia GL, Savasta S. Olivero F, et al. Childs Nerv Syst. 2020 Nov;36(11):2635-2640. doi: 10.1007/s00381-020-04788-z. Epub 2020 Jul 10. Childs Nerv Syst. 2020. PMID: 32651596 Free PMC article. Review.
METHODS: We analyzed the PubMed database using the words "Pai syndrome", "frontonasal dysplasia", "cleft lip", "nasal polyp", "facial polyp", and "corpus callosum lipoma", including reviews, case reports and case series. ...
METHODS: We analyzed the PubMed database using the words "Pai syndrome", "frontonasal dysplasia", "cleft lip", "nasal polyp", …
Addressing hypertelorism: Indications and techniques.
Laure B, Batut C, Benouhagrem A, Joly A, Travers N, Listrat A, Pare A. Laure B, et al. Neurochirurgie. 2019 Nov;65(5):286-294. doi: 10.1016/j.neuchi.2019.09.007. Epub 2019 Sep 23. Neurochirurgie. 2019. PMID: 31557491 Review.
Oculoauriculovertebral spectrum: an updated critique.
Cohen MM Jr, Rollnick BR, Kaye CI. Cohen MM Jr, et al. Cleft Palate J. 1989 Oct;26(4):276-86. Cleft Palate J. 1989. PMID: 2680167 Review.
A number of conditions are discussed that are commonly differentiated from oculoauriculovertebral spectrum but have overlapping relationships, in some instances, with frontonasal dysplasia, branchio-oto-renal (BOR) syndrome, Townes-Brocks syndrome, Wildervanck syndr …
A number of conditions are discussed that are commonly differentiated from oculoauriculovertebral spectrum but have overlapping relationship …
Marfan syndrome: from gene to therapy.
Bolar N, Van Laer L, Loeys BL. Bolar N, et al. Curr Opin Pediatr. 2012 Aug;24(4):498-504. doi: 10.1097/MOP.0b013e3283557d4c. Curr Opin Pediatr. 2012. PMID: 22705998 Review.
Oculoauriculofrontonasal syndrome: Refining the phenotype through a new case series and literature review.
Serigatto HR, Kokitsu-Nakata NM, Vendramini-Pittoli S, Tonello C, Moura PP, Peixoto AP, Gomes LP, Zechi-Ceide RM. Serigatto HR, et al. Am J Med Genet A. 2023 Oct;191(10):2493-2507. doi: 10.1002/ajmg.a.63319. Epub 2023 Jun 7. Am J Med Genet A. 2023. PMID: 37282829 Review.
The oculoauriculofrontonasal syndrome (OAFNS) is a rare condition, with unknown etiology, characterized by the association of frontonasal dysplasia (FND) and oculoauriculovertebral spectrum (OAVS). ...
The oculoauriculofrontonasal syndrome (OAFNS) is a rare condition, with unknown etiology, characterized by the association of frontonasal …
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.
This article provides a comprehensive review of the syndromes and disorders associated with NTDs, including Pallister-Hall syndrome, Walker-Warburg syndrome and Fukuyama congenital muscular dystrophy, MURCS association, Roberts syndrome, cerebro-costo-mandibular syndrome, lateral …
This article provides a comprehensive review of the syndromes and disorders associated with NTDs, including Pallister-Hall syndrome, Walker- …
Acromelic frontonasal dysostosis.
Slaney SF, Goodman FR, Eilers-Walsman BL, Hall BD, Williams DK, Young ID, Hayward RD, Jones BM, Christianson AL, Winter RM. Slaney SF, et al. Am J Med Genet. 1999 Mar 12;83(2):109-16. Am J Med Genet. 1999. PMID: 10190481 Review.
In contrast, the upper limbs were normal. This rare variant of frontonasal dysplasia may represent a distinct autosomal-recessive disorder. ...
In contrast, the upper limbs were normal. This rare variant of frontonasal dysplasia may represent a distinct autosomal-recess …
Frontonasal dysplasia: analysis of 21 cases and literature review.
Guion-Almeida ML, Richieri-Costa A, Saavedra D, Cohen MM Jr. Guion-Almeida ML, et al. Int J Oral Maxillofac Surg. 1996 Apr;25(2):91-7. doi: 10.1016/s0901-5027(96)80048-8. Int J Oral Maxillofac Surg. 1996. PMID: 8727576 Review.
Twenty-one patients with frontonasal dysplasia were studied. A 2:1 male-to-female sex ratio and increased paternal and maternal ages at the time of conception were found. ...Three patients had the combination of agenesis of the corpus callosum, mental deficiency, an …
Twenty-one patients with frontonasal dysplasia were studied. A 2:1 male-to-female sex ratio and increased paternal and materna …
32 results