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Genetic and Epigenetic Regulation of MEFV Gene and Their Impact on Clinical Outcome in Auto-Inflammatory Familial Mediterranean Fever Patients

Current issues in molecular biology, 2023-01, Vol.45 (1), p.721-737

2023

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Impact of heat shock protein and tumour necrosis factor on klinefelter syndrome

New Zealand journal of medical laboratory science, 2023-07, Vol.77 (2), p.71-74

2023

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Chemerin: An exploitable biomarker for familial Mediterranean fever in Egyptian patients

New Zealand journal of medical laboratory science, 2023-11, Vol.77 (3), p.114-118

2023

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Serum levels of chemokines MCP-1, GRO-alpha and E-selectin correlates with familial Mediterranean fever

New Zealand journal of medical laboratory science, 2021-04, Vol.75 (1), p.21-25

2021

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Brain derived neurotrophic factor, oxidative stress status and vitamin D levels in patients with autism spectrum disorder

New Zealand journal of medical laboratory science, 2022-03, Vol.76 (1), p.10-13

2022

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Effect of obesity on serum IL-10 concentrations and messenger RNA expression in women with metabolic syndrome

New Zealand journal of medical laboratory science, 2022-07, Vol.76 (2), p.69-73

2022

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Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants

Brain (London, England : 1878), 2020-08, Vol.143 (8), p.2388-2397

2020

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Sialic acid and anti-ganglioside M1 antibodies are invaluable biomarkers correlated with the severity of autism spectrum disorder

Brain & development (Tokyo. 1979), 2023-04, Vol.45 (4), p.212-219

2023

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Emanuel syndrome due to unusual pattern

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.21, Article 21

2024

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Correction: Emanuel syndrome due to unusual pattern

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.75, Article 75

2024

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Inflammatory and endothelial dysfunction indices among Egyptian females with obesity classes I-III

Bioscience reports, 2020-09, Vol.40 (9)

2020

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New diagnostic biomarkers for celiac disease in Egyptian children: Cyclophilin a and netrin-1

New Zealand journal of medical laboratory science, 2021-11, Vol.75 (3), p.189-191

2021

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Evaluation of adropin, fibroblast growth factor-1 (FGF-1), and Toll-like receptor-1 (TLR1) biomarkers in patients with inflammatory bowel disease: gene expression of TNF-α as a marker of disease severity

The Egyptian journal of medical human genetics, 2024-06, Vol.25 (1), p.63

2024

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Evaluation of DNA damage profile in obese women and its association to risk of metabolic syndrome, polycystic ovary syndrome and recurrent preeclampsia

Genes & diseases, 2018-12, Vol.5 (4), p.367-373

2018

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Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation

American journal of medical genetics. Part A, 2020-06, Vol.182 (6), p.1407-1420

2020

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Broadening the clinical spectrum of ALGS: an Egyptian cohort with five novel mutations in JAG1 gene

Egyptian Journal of Medical Human Genetics, 2022-03, Vol.23 (1), p.28, Article 28

2022

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Dynamic disequilibrium-based pathogenicity model in mutated pyrin’s B30.2 domain—Casp1/p20 complex

Journal of Genetic Engineering and Biotechnology, 2022-02, Vol.20 (1), p.31, Article 31

2022

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IGF1R, IGFALS, and IGFBP3 gene copy number variations in a group of non-syndromic Egyptian short children

Journal of Genetic Engineering and Biotechnology, 2021-07, Vol.19 (1), p.109, Article 109

2021

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Coenzyme Q10 and pro-inflammatory markers in children with Down syndrome: clinical and biochemical aspects

Jornal de pediatria, 2017-01, Vol.93 (1), p.100-104

2017

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Screening of the SHOX/PAR1 region using MLPA and miRNA expression profiling in a group of Egyptian children with non-syndromic short stature

Egyptian Journal of Medical Human Genetics, 2020-09, Vol.21 (1), p.47, Article 47

2020

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Altered expression of miR-17 and miR-148b in pediatric familial mediterranean fever patients

Clinical rheumatology, 2024-08, Vol.43 (8), p.2661-2667

2024

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Molecular and Clinical Characterization of a Cohort of Autosomal Recessive Sensorineural Hearing Loss in Egyptian Patients

Journal of molecular neuroscience, 2024-10, Vol.74 (4), p.102, Article 102

2024

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Growth curves of Egyptian patients with Turner syndrome

American journal of medical genetics. Part A, 2012-11, Vol.158A (11), p.2687-2691

2012

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The role of the deficiency of vitamin B12 and folic acid on homocysteinemia in children with Turner syndrome

Journal of Pediatric Endocrinology and Metabolism, 2023-02, Vol.36 (2), p.147

2023

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The correlation of estrogen receptor 1 and progesterone receptor genes polymorphisms with recurrent pregnancy loss in a cohort of Egyptian women

Molecular biology reports, 2021-05, Vol.48 (5), p.4413-4420

2021

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Genetic and Epigenetic Regulation of MEFV Gene and Their Impact on Clinical Outcome in Auto-Inflammatory Familial Mediterranean Fever Patients

Impact of heat shock protein and tumour necrosis factor on klinefelter syndrome

Chemerin: An exploitable biomarker for familial Mediterranean fever in Egyptian patients

Serum levels of chemokines MCP-1, GRO-alpha and E-selectin correlates with familial Mediterranean fever

Brain derived neurotrophic factor, oxidative stress status and vitamin D levels in patients with autism spectrum disorder

Effect of obesity on serum IL-10 concentrations and messenger RNA expression in women with metabolic syndrome

Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants

Sialic acid and anti-ganglioside M1 antibodies are invaluable biomarkers correlated with the severity of autism spectrum disorder

Emanuel syndrome due to unusual pattern

Correction: Emanuel syndrome due to unusual pattern

Inflammatory and endothelial dysfunction indices among Egyptian females with obesity classes I-III

New diagnostic biomarkers for celiac disease in Egyptian children: Cyclophilin a and netrin-1

Evaluation of adropin, fibroblast growth factor-1 (FGF-1), and Toll-like receptor-1 (TLR1) biomarkers in patients with inflammatory bowel disease: gene expression of TNF-α as a marker of disease severity

Evaluation of DNA damage profile in obese women and its association to risk of metabolic syndrome, polycystic ovary syndrome and recurrent preeclampsia

Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation

Broadening the clinical spectrum of ALGS: an Egyptian cohort with five novel mutations in JAG1 gene

Dynamic disequilibrium-based pathogenicity model in mutated pyrin’s B30.2 domain—Casp1/p20 complex

IGF1R, IGFALS, and IGFBP3 gene copy number variations in a group of non-syndromic Egyptian short children

Coenzyme Q10 and pro-inflammatory markers in children with Down syndrome: clinical and biochemical aspects

Screening of the SHOX/PAR1 region using MLPA and miRNA expression profiling in a group of Egyptian children with non-syndromic short stature

Altered expression of miR-17 and miR-148b in pediatric familial mediterranean fever patients

Molecular and Clinical Characterization of a Cohort of Autosomal Recessive Sensorineural Hearing Loss in Egyptian Patients

Growth curves of Egyptian patients with Turner syndrome

The role of the deficiency of vitamin B12 and folic acid on homocysteinemia in children with Turner syndrome

The correlation of estrogen receptor 1 and progesterone receptor genes polymorphisms with recurrent pregnancy loss in a cohort of Egyptian women

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