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1966
2025

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

Year Number of Results
1966 1
1967 1
1968 1
1969 2
1970 1
1974 2
1975 1
1976 3
1977 1
1978 1
1983 2
1984 2
1986 3
1987 3
1988 8
1989 5
1990 4
1991 6
1992 7
1993 4
1994 5
1995 10
1996 7
1997 8
1998 4
1999 6
2000 9
2001 13
2002 6
2003 6
2004 5
2005 10
2006 7
2007 7
2008 9
2009 5
2010 14
2011 8
2012 9
2013 12
2014 10
2015 7
2016 13
2017 13
2018 13
2019 9
2020 6
2021 6
2022 9
2023 7
2024 12
2025 2

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300 results

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Page 1
Mucins, Mucus, and Goblet Cells.
Ma J, Rubin BK, Voynow JA. Ma J, et al. Chest. 2018 Jul;154(1):169-176. doi: 10.1016/j.chest.2017.11.008. Epub 2017 Nov 21. Chest. 2018. PMID: 29170036 Review.
These insights into the innate immune properties of mucins and goblet cells support a shift from the current paradigm of repressing increased mucin expression to targeting regulation of specific mucins and the abnormal airway milieu....
These insights into the innate immune properties of mucins and goblet cells support a shift from the current paradigm of repressing increase …
Ptosis: causes, presentation, and management.
Finsterer J. Finsterer J. Aesthetic Plast Surg. 2003 May-Jun;27(3):193-204. doi: 10.1007/s00266-003-0127-5. Epub 2003 Aug 21. Aesthetic Plast Surg. 2003. PMID: 12925861 Review.
Treatment of ptosis depends on age, etiology, whether one or both eyelids are involved, the severity of ptosis, the levator function, and presence of additional ophthalmologic or neurologic abnormalities. ...Although improvement of the lid height is usually achieved …
Treatment of ptosis depends on age, etiology, whether one or both eyelids are involved, the severity of ptosis, the levator function, …
The Immunological Basis of Dry Eye Disease and Current Topical Treatment Options.
Periman LM, Perez VL, Saban DR, Lin MC, Neri P. Periman LM, et al. J Ocul Pharmacol Ther. 2020 Apr;36(3):137-146. doi: 10.1089/jop.2019.0060. Epub 2020 Mar 12. J Ocul Pharmacol Ther. 2020. PMID: 32175799 Free PMC article. Review.
According to the Tear Film and Ocular Surface Society Dry Eye Workshop II definition, DED is a multifactorial disorder of the ocular surface characterized by impairment and loss of tear homeostasis (hyperosmolarity), ocular discomfort or pain, and neurosensory abnormalities
According to the Tear Film and Ocular Surface Society Dry Eye Workshop II definition, DED is a multifactorial disorder of the ocular surface …
Descemetocele.
Agarwal R, Nagpal R, Todi V, Sharma N. Agarwal R, et al. Surv Ophthalmol. 2021 Jan-Feb;66(1):2-19. doi: 10.1016/j.survophthal.2020.10.004. Epub 2020 Oct 13. Surv Ophthalmol. 2021. PMID: 33058926 Review.
A corneal descemetocele, the anterior herniation of an intact Descemet membrane through an overlying stromal defect, is a rare, but serious outcome of progressive corneal ulceration and mandates urgent intervention owing to the imminent risk of perforation. Various ocular and sys …
A corneal descemetocele, the anterior herniation of an intact Descemet membrane through an overlying stromal defect, is a rare, but serious …
Ectropion, entropion, trichiasis.
Fea A, Turco D, Actis AG, De Sanctis U, Actis G, Grignolo FM. Fea A, et al. Minerva Chir. 2013 Dec;68(6 Suppl 1):27-35. Minerva Chir. 2013. PMID: 24172761 Review.
Aim of this review was to describe ectropion, entropion and trichiasis and their therapy. These eyelid pathologies are characterised by common symptoms (redness, excessive tearing and irritation of the eye) and by altered balance of the anterior and posterior lamellae of t …
Aim of this review was to describe ectropion, entropion and trichiasis and their therapy. These eyelid pathologies are characterised …
The Genetics and Biology of FOXL2.
Tucker EJ. Tucker EJ. Sex Dev. 2022;16(2-3):184-193. doi: 10.1159/000519836. Epub 2021 Nov 2. Sex Dev. 2022. PMID: 34727551 Review.
FOXL2 encodes a transcription factor that regulates a wide array of target genes including those involved in sex development, eyelid development, ovarian function and maintenance, genomic integrity as well as cellular pathways such as cell-cycle progression, proliferation, …
FOXL2 encodes a transcription factor that regulates a wide array of target genes including those involved in sex development, eyelid
Blepharoptosis.
De Sanctis U, Alovisi C, Actis AG, Vinai L, Penna R, Fea A, Actis G, Grignolo F. De Sanctis U, et al. Minerva Chir. 2013 Dec;68(6 Suppl 1):37-47. Minerva Chir. 2013. PMID: 24172762 Review.
Blepharoptosis of the upper eyelid is a common condition among patients presenting for oculoplastic surgery. Although there are many types of ptosis, the two most frequent clinical cases are simple congenital ptosis in young patients and senile ptosis in adults. ...
Blepharoptosis of the upper eyelid is a common condition among patients presenting for oculoplastic surgery. Although there are many …
Lateral canthal surgery.
Chong KK, Goldberg RA. Chong KK, et al. Facial Plast Surg. 2010 Aug;26(3):193-200. doi: 10.1055/s-0030-1254329. Epub 2010 Jun 3. Facial Plast Surg. 2010. PMID: 20524167 Review.
Reconstruction of the lateral canthus is important in the rehabilitation of the aging eyelid and an unfortunate necessity after failed lateral canthal surgery. The common methods for improving or maintaining position, tone, and shape of the lower eyelid and lateral …
Reconstruction of the lateral canthus is important in the rehabilitation of the aging eyelid and an unfortunate necessity after faile …
Ocular choristomas.
Mansour AM, Barber JC, Reinecke RD, Wang FM. Mansour AM, et al. Surv Ophthalmol. 1989 Mar-Apr;33(5):339-58. doi: 10.1016/0039-6257(89)90011-8. Surv Ophthalmol. 1989. PMID: 2655139 Review.
Choristomas are congenital lesions representing normal tissue(s) in an abnormal location. They are the most common epibulbar and orbital tumors in children. ...
Choristomas are congenital lesions representing normal tissue(s) in an abnormal location. They are the most common epibulbar a …
Fraser syndrome.
Kalpana Kumari MK, Kamath S, Mysorekar VV, Nandini G. Kalpana Kumari MK, et al. Indian J Pathol Microbiol. 2008 Apr-Jun;51(2):228-9. doi: 10.4103/0377-4929.41664. Indian J Pathol Microbiol. 2008. PMID: 18603689 Review.
Fraser syndrome or cryptophthalmos is a rare autosomal recessive disorder characterized by major features such as cryptophthalmos, syndactyly and abnormal genitalia. The diagnosis of this syndrome can be made on clinical examination and perinatal autopsy. ...
Fraser syndrome or cryptophthalmos is a rare autosomal recessive disorder characterized by major features such as cryptophthalmos, syndactyl …
300 results