Found: 9
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CYP2C9 (*2&*3) and CYP2C19 (*2&*3) polymorphisms among children with nonlesional epilepsy: a single-center study.
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- Acta Neurologica Belgica, 2021, v. 121, n. 6, p. 1623, doi. 10.1007/s13760-020-01442-y
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- Article
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian family.
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- Clinical & Experimental Nephrology, 2009, v. 13, n. 4, p. 288, doi. 10.1007/s10157-008-0126-6
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- Article
Novel truncating mutation in the CTNS gene in an Egyptian family with cases of infantile nephropathic cystinosis and congenital heart malformations.
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- Middle East Journal of Medical Genetics, 2012, v. 1, n. 2, p. 71, doi. 10.1097/01.MXE.0000414810.01450.3c
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- Article
Numerically efficient full-vectorial rational Chebyshev pseudo-spectral modal analysis for optical Waveguides.
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- Optical & Quantum Electronics, 2023, v. 55, n. 11, p. 1, doi. 10.1007/s11082-023-05279-6
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- Article
Efficient analysis of electron waveguides with multiple discontinuities.
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- Optical & Quantum Electronics, 2015, v. 47, n. 6, p. 1333, doi. 10.1007/s11082-014-0055-4
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- Article
Rs-10889677 variant in interleukin-23 receptor may contribute to creating an inflammatory milieu more susceptible to bladder tumourigenesis: report and meta-analysis.
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- Immunogenetics, 2021, v. 73, n. 3, p. 207, doi. 10.1007/s00251-021-01205-w
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- Article
LES DÉNOMINATIONS BILINGUES PORTEUSES D'IDÉOLOGIE : LE CAS DES LIEUX SAINTS EN TERRE SAINTE.
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- Atelier de Traduction, 2019, n. 31/32, p. 151
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- Article
The Fate of Oxidative Strand Breaks in Mitochondrial DNA.
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- Antioxidants, 2023, v. 12, n. 5, p. 1087, doi. 10.3390/antiox12051087
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- Article
Impact of gene polymorphism of glutathione S-transferase and ghrelin as a risk factor in Egyptian women with gestational diabetes mellitus.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00228-6
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- Article