Found: 26
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Serum apelin-12 and obesity-related markers in Egyptian children with Down syndrome.
- Published in:
- European Journal of Pediatrics, 2024, v. 183, n. 1, p. 461, doi. 10.1007/s00431-023-05315-3
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- Publication type:
- Article
Beta Thalassemia Carrier Rate: Problem Burden among High School Children.
- Published in:
- Current Pediatric Reviews, 2023, v. 19, n. 2, p. 203, doi. 10.2174/1573396318666220624142349
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- Publication type:
- Article
Prevalence and patterns of chromosomal abnormalities among Egyptian patients with infertility: a single institution's 5-year experience.
- Published in:
- Middle East Fertility Society Journal, 2022, v. 27, n. 1, p. 1, doi. 10.1186/s43043-022-00101-x
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- Publication type:
- Article
Genetic variant in the 5ʹ untranslated region of endothelin1 (EDN1) gene in children with primary nephrotic syndrome.
- Published in:
- Journal of Biochemical & Molecular Toxicology, 2022, v. 36, n. 3, p. 1, doi. 10.1002/jbt.22963
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- Publication type:
- Article
Prevalence and patterns of chromosomal abnormalities among Egyptian patients with infertility: a single institution’s 5-year experience.
- Published in:
- Middle East Fertility Society Journal, 2022, v. 27, n. 1, p. 1, doi. 10.1186/s43043-022-00101-x
- By:
- Publication type:
- Article
Serum adiponectin, body adiposity and metabolic parameters in obese Egyptian children with Down syndrome.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2021, v. 34, n. 11, p. 1401, doi. 10.1515/jpem-2021-0324
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- Publication type:
- Article
Prevalence of iron deficiency anemia and beta thalassemia carriers among relatives of beta thalassemia patients in Nile Delta region, Egypt: a multicenter study.
- Published in:
- Journal of the Egyptian Public Health Association, 2021, v. 96, n. 1, p. 1, doi. 10.1186/s42506-021-00088-9
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- Publication type:
- Article
Neurocutaneous melanosis is not always a benign disease.
- Published in:
- 2020
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- Publication type:
- case study
Oxidative stress and vitamin D receptor BsmI gene polymorphism in Egyptian children with systemic lupus erythematosus: a single center study.
- Published in:
- Lupus, 2019, v. 28, n. 6, p. 771, doi. 10.1177/0961203319846380
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- Publication type:
- Article
Angiotensin II type 1 receptor gene polymorphism and serum angiotensin-converting enzyme level in Egyptian children with systemic lupus erythematosus.
- Published in:
- Clinical Rheumatology, 2018, v. 37, n. 12, p. 3309, doi. 10.1007/s10067-018-4255-3
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- Publication type:
- Article
Prevalence of congenital heart diseases in children with Down syndrome in Mansoura, Egypt: a retrospective descriptive study.
- Published in:
- 2017
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- Publication type:
- journal article
A Novel Fibrillin–1 Mutation in an Egyptian Marfan Family: A Proband Showing Nephrotic Syndrome Due to Focal Segmental Glomerulosclerosis.
- Published in:
- Saudi Journal of Kidney Diseases & Transplantation, 2017, v. 28, n. 1, p. 141, doi. 10.4103/1319-2442.198166
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- Publication type:
- Article
Influence of hyperbilirubinemia and phototherapy on markers of genotoxicity and apoptosis in full-term infants.
- Published in:
- European Journal of Pediatrics, 2015, v. 174, n. 4, p. 459, doi. 10.1007/s00431-014-2418-z
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- Publication type:
- Article
Disruptive behavior in Down syndrome children: a cross-sectional comparative study.
- Published in:
- Annals of Saudi Medicine, 2014, v. 34, n. 6, p. 517, doi. 10.5144/0256-4947.2014.517
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- Publication type:
- Article
Prevalence of community acquired infections in down syndrome children: a single center study.
- Published in:
- Brazilian Journal of Infectious Diseases, 2013, v. 17, n. 5, p. 624, doi. 10.1016/j.bjid.2013.05.002
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- Publication type:
- Article
Predictors of anxiety and depression in Egyptian thalassemic patients: A single center study.
- Published in:
- International Journal of Hematology, 2013, v. 97, n. 5, p. 604, doi. 10.1007/s12185-013-1322-z
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- Publication type:
- Article
Low expression of glucocorticoid receptors in children with steroid-resistant nephrotic syndrome.
- Published in:
- Pediatric Nephrology, 2013, v. 28, n. 5, p. 759, doi. 10.1007/s00467-012-2385-4
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- Publication type:
- Article
Prediction of Residual Valvular Lesions in Rheumatic Heart Disease: Role of Adhesion Molecules.
- Published in:
- Pediatric Cardiology, 2013, v. 34, n. 3, p. 583, doi. 10.1007/s00246-012-0501-7
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- Publication type:
- Article
Sporadic Fiibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in ACVR1 Gene: A Case Report and Review of Literature.
- Published in:
- Case Reports in Genetics, 2013, p. 1, doi. 10.1155/2013/834605
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- Publication type:
- Article
Hidden Y Chromosome Mosaicism in 48 Egyptian Patients with Turner's Syndrome.
- Published in:
- Genetics Research International, 2013, p. 1, doi. 10.1155/2013/463529
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- Publication type:
- Article
A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 11, p. 1134, doi. 10.1038/ejhg.2012.77
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- Publication type:
- Article
Human metapneumovirus (hMPV) in acute respiratory infection: a clinic-based study in Egypt.
- Published in:
- 2012
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- Publication type:
- journal article
Leptin, insulin and thyroid hormones in a cohort of Egyptian obese Down syndrome children: a comparative study.
- Published in:
- BMC Endocrine Disorders, 2012, v. 12, n. 1, p. 22, doi. 10.1186/1472-6823-12-22
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- Publication type:
- Article
Glucosidase acid beta gene mutations in Egyptian children with Gaucher disease and relation to disease phenotypes.
- Published in:
- World Journal of Pediatrics, 2011, v. 7, n. 4, p. 326, doi. 10.1007/s12519-011-0309-1
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- Publication type:
- Article
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian family.
- Published in:
- Clinical & Experimental Nephrology, 2009, v. 13, n. 4, p. 288, doi. 10.1007/s10157-008-0126-6
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- Publication type:
- Article
Correlation of thyroid and growth hormones to chromosomal instability in Egyptian Fanconi anemia patients.
- Published in:
- Indian Journal of Pediatrics, 2008, v. 75, n. 7, p. 679, doi. 10.1007/s12098-008-0128-0
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- Publication type:
- Article