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

Year Number of Results
1977 1
1990 1
1991 1
1997 1
1998 1
2005 1
2007 1
2010 1
2016 1
2017 2
2018 2
2021 1
2022 3
2024 0

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15 results

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Page 1
PDGF-C and PDGF-D in ocular diseases.
Kumar A, Li X. Kumar A, et al. Mol Aspects Med. 2018 Aug;62:33-43. doi: 10.1016/j.mam.2017.10.002. Epub 2017 Oct 27. Mol Aspects Med. 2018. PMID: 29079201 Review.
In addition, PDGFs and PDGFRs are also important players in ocular diseases involving the degeneration of retinal neuronal and vascular cells, such as glaucoma and retinitis pigmentosa. Due to their critical roles in the pathogenesis of many blinding ocular diseases …
In addition, PDGFs and PDGFRs are also important players in ocular diseases involving the degeneration of retinal neuronal and vascular cell …
Wide-Field Fundus Autofluorescence for Retinitis Pigmentosa and Cone/Cone-Rod Dystrophy.
Oishi A, Oishi M, Ogino K, Morooka S, Yoshimura N. Oishi A, et al. Adv Exp Med Biol. 2016;854:307-13. doi: 10.1007/978-3-319-17121-0_41. Adv Exp Med Biol. 2016. PMID: 26427426 Review.
Retinitis pigmentosa and cone/cone-rod dystrophy are inherited retinal diseases characterized by the progressive loss of rod and/or cone photoreceptors. ...With wide-field analysis, an association between abnormal FAF areas and visual function was demonstrated in …
Retinitis pigmentosa and cone/cone-rod dystrophy are inherited retinal diseases characterized by the progressive loss of rod a …
Hearing loss in Africa: current genetic profile.
Adadey SM, Wonkam-Tingang E, Aboagye ET, Quaye O, Awandare GA, Wonkam A. Adadey SM, et al. Hum Genet. 2022 Apr;141(3-4):505-517. doi: 10.1007/s00439-021-02376-y. Epub 2021 Oct 5. Hum Genet. 2022. PMID: 34609590 Free PMC article. Review.
A total of 89 full-text records was selected and retrieved for data extraction and analyses. We found reports from only 17/54 (31.5%) African countries. The majority (61/89; 68.5%) of articles were from North Africa, with few reports found from sub-Saharan Africa. ...
A total of 89 full-text records was selected and retrieved for data extraction and analyses. We found reports from only 17/54 (31.5%) …
[The relationship between necroptosis and blinding eye diseases].
Xie LL, Jiang B. Xie LL, et al. Zhonghua Yan Ke Za Zhi. 2018 Mar 11;54(3):234-240. doi: 10.3760/cma.j.issn.0412-4081.2018.03.018. Zhonghua Yan Ke Za Zhi. 2018. PMID: 29518884 Review. Chinese.
In this review, the related mechanism of necroptosis, the relationship between necroptosis and multiple blinding eye diseases, such as age-related macular degeneration, retinitis pigmentosa and glaucoma, and the potential therapeutic targets of necroptosis are discu …
In this review, the related mechanism of necroptosis, the relationship between necroptosis and multiple blinding eye diseases, such as age-r …
Critical review of bariatric surgical outcomes in patients with Prader-Willi syndrome and other hyperphagic disorders.
Gantz MG, Driscoll DJ, Miller JL, Duis JB, Butler MG, Gourash L, Forster J, Scheimann AO. Gantz MG, et al. Obesity (Silver Spring). 2022 May;30(5):973-981. doi: 10.1002/oby.23385. Epub 2022 Apr 13. Obesity (Silver Spring). 2022. PMID: 35416416 Review.
For PWS, postoperative weight-change percentage and BMI up to 14 years following surgery were analyzed using general linear mixed models, with descriptive outcomes for other conditions. RESULTS: A total of 54 publications were identified, with variable follow-up periods fo …
For PWS, postoperative weight-change percentage and BMI up to 14 years following surgery were analyzed using general linear mixed models, wi …
[Genetics of retinitis pigmentosa: metabolic classification and phenotype/genotype correlations].
Maubaret C, Hamel C. Maubaret C, et al. J Fr Ophtalmol. 2005 Jan;28(1):71-92. doi: 10.1016/s0181-5512(05)81029-0. J Fr Ophtalmol. 2005. PMID: 15767903 Review. French.
Retinitis pigmentosa (RP, prevalence 1/4000) is a set of hereditary retinal dystrophies characterized by pigment deposits in fundus and progressive death of photoreceptors, always associated with the alteration of retinal pigment epithelium. ...A survey of mutation …
Retinitis pigmentosa (RP, prevalence 1/4000) is a set of hereditary retinal dystrophies characterized by pigment deposits in f …
Apoptosis: clinical relevance and pharmacological manipulation.
Thatte U, Dahanukar S. Thatte U, et al. Drugs. 1997 Oct;54(4):511-32. doi: 10.2165/00003495-199754040-00002. Drugs. 1997. PMID: 9339959 Review.
AIDS and neurodegenerative disorders like Alzheimer's or Parkinson's disease represent the most widely studied group of disorders where an excess of apoptosis has been implicated. Amyotrophic lateral sclerosis, retinitis pigmentosa, epilepsy and alcoholic brain dama …
AIDS and neurodegenerative disorders like Alzheimer's or Parkinson's disease represent the most widely studied group of disorders where an e …
Visual pigment: G-protein-coupled receptor for light signals.
Shichida Y, Imai H. Shichida Y, et al. Cell Mol Life Sci. 1998 Dec;54(12):1299-315. doi: 10.1007/s000180050256. Cell Mol Life Sci. 1998. PMID: 9893707 Free PMC article. Review.
In addition to the recent findings on dysfunctional mutations in patients with retinitis pigmentosa or congenital night blindness, the mechanism of intramolecular signal transduction in visual pigments and their evolutionary relationship are discussed....
In addition to the recent findings on dysfunctional mutations in patients with retinitis pigmentosa or congenital night blindn …
Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes.
Bruel AL, Franco B, Duffourd Y, Thevenon J, Jego L, Lopez E, Deleuze JF, Doummar D, Giles RH, Johnson CA, Huynen MA, Chevrier V, Burglen L, Morleo M, Desguerres I, Pierquin G, Doray B, Gilbert-Dussardier B, Reversade B, Steichen-Gersdorf E, Baumann C, Panigrahi I, Fargeot-Espaliat A, Dieux A, David A, Goldenberg A, Bongers E, Gaillard D, Argente J, Aral B, Gigot N, St-Onge J, Birnbaum D, Phadke SR, Cormier-Daire V, Eguether T, Pazour GJ, Herranz-Pérez V, Goldstein JS, Pasquier L, Loget P, Saunier S, Mégarbané A, Rosnet O, Leroux MR, Wallingford JB, Blacque OE, Nachury MV, Attie-Bitach T, Rivière JB, Faivre L, Thauvin-Robinet C. Bruel AL, et al. J Med Genet. 2017 Jun;54(6):371-380. doi: 10.1136/jmedgenet-2016-104436. Epub 2017 Mar 13. J Med Genet. 2017. PMID: 28289185 Free PMC article. Review.
15 results