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

Year Number of Results
2005 1
2008 2
2010 1
2011 1
2012 1
2013 2
2014 2
2015 3
2016 1
2017 4
2018 3
2019 2
2020 2
2021 5
2022 2
2023 3
2024 2

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32 results

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Page 1
[Diffuse retinal epitheliopathy].
Abaloun Y, Omari A. Abaloun Y, et al. Pan Afr Med J. 2017 Oct 27;28:182. doi: 10.11604/pamj.2017.28.182.11355. eCollection 2017. Pan Afr Med J. 2017. PMID: 29541328 Free PMC article. French.
Fundus examination showed alteration of the pigment epithelium (APE) in the RE associated with osteoblast-like pigment migrations involving the macula and a wide area due to gravitational descent of the superior temporal arcade onto the lower temporal quadrant. ...
Fundus examination showed alteration of the pigment epithelium (APE) in the RE associated with osteoblast-like pigment migrations involving …
Monoclonal Antibodies Application in Lateral Flow Immunochromatographic Assays for Drugs of Abuse Detection.
Qriouet Z, Cherrah Y, Sefrioui H, Qmichou Z. Qriouet Z, et al. Molecules. 2021 Feb 18;26(4):1058. doi: 10.3390/molecules26041058. Molecules. 2021. PMID: 33670468 Free PMC article. Review.
Lateral flow assays (lateral flow immunoassays and nucleic acid lateral flow assays) have experienced a great boom in a wide variety of early diagnostic and screening applications. As opposed to conventional examinations (High Performance Liquid Chromatography, Polymerase …
Lateral flow assays (lateral flow immunoassays and nucleic acid lateral flow assays) have experienced a great boom in a wide variety …
A new case with the recurrent PURA p.(Phe233del) pathogenic variant: Expansion of the phenotype and review of the literature.
Ben Issa A, Ben Ayed I, Jallouli O, Souissi A, Bouchaalla W, Ben Said M, Mallouli S, Masmoudi S, Charfi Triki C, Hadj Kacem H, Kammoun F. Ben Issa A, et al. Int J Dev Neurosci. 2023 Jun;83(4):383-395. doi: 10.1002/jdn.10266. Epub 2023 May 19. Int J Dev Neurosci. 2023. PMID: 37204304 Review.
Our finding defines and expands the phenotypic and genotypic spectrum of the PURA syndrome supporting the absence of reliable genotype-phenotype correlations and the existence of a highly variable, wide-ranging clinical spectrum....
Our finding defines and expands the phenotypic and genotypic spectrum of the PURA syndrome supporting the absence of reliable genotype-pheno …
Psychiatric Symptoms in Stiff-Person Syndrome: A Systematic Review and a Report of Two Cases.
Nasri A, Gharbi A, Ouali U, Mrabet S, Souissi A, Jomli R, Gargouri A, Bendjebara M, Kacem I, Gouider R. Nasri A, et al. J Acad Consult Liaison Psychiatry. 2023 Mar-Apr;64(2):183-191. doi: 10.1016/j.jaclp.2022.07.005. Epub 2022 Aug 5. J Acad Consult Liaison Psychiatry. 2023. PMID: 35940576 Review.
BACKGROUND: The clinical spectrum of stiff-person syndrome (SPS) encompasses a wide range of signs including psychiatric symptoms (PS). OBJECTIVE: Our objective was to provide an overview of the spectrum of PS in SPS through a systematic literature search and 2 illustrativ …
BACKGROUND: The clinical spectrum of stiff-person syndrome (SPS) encompasses a wide range of signs including psychiatric symptoms (PS …
An intramuscular hemangioma of the semispinalis muscle: A case report.
Sellami M, Ayadi S, Sellami N, Triki M, Souissi B, Boudaouara T, Ben Mahfoudh K, Charfeddine I. Sellami M, et al. SAGE Open Med Case Rep. 2023 Oct 16;11:2050313X231205800. doi: 10.1177/2050313X231205800. eCollection 2023. SAGE Open Med Case Rep. 2023. PMID: 37860284 Free PMC article.
Intramuscular hemangiomas in the posterior neck muscles are rare, with only a few reported cases. Wide surgical resection with control of feeding vessels is the optimal treatment, and follow-up is recommended to monitor for local recurrence. ...
Intramuscular hemangiomas in the posterior neck muscles are rare, with only a few reported cases. Wide surgical resection with contro …
The genome of the European estuarine calanoid copepod Eurytemora affinis: Potential use in molecular ecotoxicology.
Choi BS, Kim DH, Kim MS, Park JC, Lee YH, Kim HJ, Jeong CB, Hagiwara A, Souissi S, Lee JS. Choi BS, et al. Mar Pollut Bull. 2021 May;166:112190. doi: 10.1016/j.marpolbul.2021.112190. Epub 2021 Mar 9. Mar Pollut Bull. 2021. PMID: 33711609
A total of 18,014 genes were annotated and orthologous gene clusters were analyzed in comparison to other copepods. In addition, genome-wide identification of cytochrome P450s, glutathione S-transferases, and ATP-binding cassette transporters in E. affinis was performed to …
A total of 18,014 genes were annotated and orthologous gene clusters were analyzed in comparison to other copepods. In addition, genome-w
Characteristics, onset, and evolution of neurological symptoms in patients with COVID-19.
Kacem I, Gharbi A, Harizi C, Souissi E, Safer M, Nasri A, Letaief H, Akkari M, Hechaichi A, Mrabet S, Dhaouadi S, Ben Djebara M, Derouiche S, Gargouri A, Chahed M, Ben Alaya N, Gouider R. Kacem I, et al. Neurol Sci. 2021 Jan;42(1):39-46. doi: 10.1007/s10072-020-04866-9. Epub 2020 Nov 17. Neurol Sci. 2021. PMID: 33201360 Free PMC article.
BACKGROUND: A wide range of neurological manifestations has been described in COVID-19. ...
BACKGROUND: A wide range of neurological manifestations has been described in COVID-19. ...
SRD5A3-CDG: 3D structure modeling, clinical spectrum, and computer-based dysmorphic facial recognition.
Ben Ayed I, Ouarda W, Frikha F, Kammoun F, Souissi A, Ben Said M, Bouzid A, Elloumi I, Hamdani TM, Gharbi N, Baklouti N, Guirat M, Mejdoub F, Kharrat N, Boujelbene I, Abdelhedi F, Belguith N, Keskes L, Gibriel AA, Kamoun H, Triki C, Alimi AM, Masmoudi S. Ben Ayed I, et al. Am J Med Genet A. 2021 Apr;185(4):1081-1090. doi: 10.1002/ajmg.a.62065. Epub 2021 Jan 6. Am J Med Genet A. 2021. PMID: 33403770
Based on phenotypes of our patients and all published SRD5A3-CDG cases, we identified the most common clinical features as well as some recurrent dysmorphic features such as arched eyebrows, wide eyes, shallow nasal bridge, short nose, and large mouth. Based on facial digi …
Based on phenotypes of our patients and all published SRD5A3-CDG cases, we identified the most common clinical features as well as some recu …
32 results