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PYCR2 Mutations cause a lethal syndrome of microcephaly and failure to thrive.
- Published in:
- 2016
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- Publication type:
- journal article
Biallelic loss-of-function variants in GON4L cause microcephaly and brain structure abnormalities.
- Published in:
- NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00437-5
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- Publication type:
- Article
A fast and green reversed‐phase HPLC method with fluorescence detection for simultaneous determination of amlodipine and celecoxib in their newly approved fixed‐dose combination tablets.
- Published in:
- Journal of Separation Science, 2020, v. 43, n. 16, p. 3197, doi. 10.1002/jssc.202000345
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- Publication type:
- Article
Biphasic calcium phosphate doped with zirconia nanoparticles for reconstruction of induced mandibular defects in dogs: cone-beam computed tomographic and histopathologic evaluation.
- Published in:
- Journal of Materials Science: Materials in Medicine, 2023, v. 34, n. 6, p. 1, doi. 10.1007/s10856-023-06731-5
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- Publication type:
- Article
SMILE lenticule versus amniotic membrane graft (AMG) augmented with platelet-rich plasma (PRP) for the treatment of perforated corneal ulcer.
- Published in:
- International Ophthalmology, 2023, v. 43, n. 7, p. 2341, doi. 10.1007/s10792-023-02631-3
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- Publication type:
- Article
Therapeutic Drug Monitoring of Gentamicin: Evaluation of Five Nomograms for Initial Dosing at Al-Amiri Hospital in Kuwait.
- Published in:
- Medical Principles & Practice, 2007, v. 16, n. 5, p. 348, doi. 10.1159/000104807
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- Publication type:
- Article
Trends in legal learning: The Arab-Islamic world.
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- International Social Science Journal, 1970, v. 22, n. 3, p. 367
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- Publication type:
- Article
The hip asphericity angle: a novel angle for measurement of Cam-FAI correction.
- Published in:
- Journal of Hip Preservation Surgery, 2020, v. 7, n. 3, p. 554, doi. 10.1093/jhps/hnaa060
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- Publication type:
- Article
Dandy-Walker Malformation in a Girl with DDX3X-Related Intellectual Disability.
- Published in:
- Molecular Syndromology, 2023, v. 14, n. 6, p. 523, doi. 10.1159/000531715
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- Publication type:
- Article
X-Linked Hydrocephalus with New L1CAM Pathogenic Variants: Review of the Most Prevalent Molecular and Phenotypic Features.
- Published in:
- Molecular Syndromology, 2023, v. 14, n. 4, p. 283, doi. 10.1159/000529545
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- Publication type:
- Article
Further Evidence of a Continuum in the Clinical Spectrum of Dominant PIEZO2-Related Disorders and Implications in Cerebellar Anomalies.
- Published in:
- Molecular Syndromology, 2022, v. 13, n. 5, p. 389, doi. 10.1159/000523956
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- Publication type:
- Article
First Report of Two Egyptian Patients with Desbuquois Dysplasia due to Homozygous CANT1 Mutations.
- Published in:
- Molecular Syndromology, 2021, v. 12, n. 5, p. 279, doi. 10.1159/000516607
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- Publication type:
- Article
Thymoquinone reverses nonalcoholic fatty liver disease (NAFLD) associated with experimental hypothyroidism.
- Published in:
- Romanian Journal of Morphology & Embryology, 2019, v. 60, n. 2, p. 479
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- Publication type:
- Article
Comparative Pharmacokinetic Study for Linezolid and Two Novel Antibacterial Oxazolidinone Derivatives in Rabbits: Can Differences in the Pharmacokinetic Properties Explain the Discrepancies between Their In Vivo and In Vitro Antibacterial Activities?
- Published in:
- Pharmaceutics, 2017, v. 9, n. 3, p. 34, doi. 10.3390/pharmaceutics9030034
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- Publication type:
- Article
Novel loss-of-function variants expand ABCC9-related intellectual disability and myopathy syndrome.
- Published in:
- Brain: A Journal of Neurology, 2024, v. 147, n. 5, p. 1822, doi. 10.1093/brain/awae010
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- Publication type:
- Article
Biallelic MED27 variants lead to variable ponto-cerebello-lental degeneration with movement disorders.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 12, p. 5031, doi. 10.1093/brain/awad257
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- Publication type:
- Article
Immuno-histopathologic evaluation of mineralized plasmatic matrix in the management of horizontal ridge defects in a canine model (a split-mouth comparative study).
- Published in:
- Odontology, 2022, v. 110, n. 3, p. 523, doi. 10.1007/s10266-021-00684-3
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- Publication type:
- Article
Risk factors for hepatitis C virus acquisition and predictors of persistence among Egyptian children.
- Published in:
- Liver International, 2012, v. 32, n. 3, p. 449, doi. 10.1111/j.1478-3231.2011.02643.x
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- Publication type:
- Article
Is the hepatitis C virus epidemic over in Egypt? Incidence and risk factors of new hepatitis C virus infections.
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- Liver International, 2010, v. 30, n. 4, p. 560, doi. 10.1111/j.1478-3231.2009.02204.x
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- Publication type:
- Article
Predictors of a sustained virological response in patients with genotype 4 chronic hepatitis C.
- Published in:
- Liver International, 2008, v. 28, n. 8, p. 1112, doi. 10.1111/j.1478-3231.2008.01750.x
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- Publication type:
- Article
Occult hepatitis C virus infection among Egyptian hemodialysis patients.
- Published in:
- Journal of Medical Virology, 2016, v. 88, n. 8, p. 1388, doi. 10.1002/jmv.24467
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- Publication type:
- Article
Polymorphisms at IL28B Gene as Predictors of Viral Relapse in Genotype 4 Egyptian Hepatitis C Patients.
- Published in:
- Journal of Medical Virology, 2016, v. 88, n. 3, p. 481, doi. 10.1002/jmv.24354
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- Publication type:
- Article
Response to pegylated interferon alfa-2a and ribavirin in chronic hepatitis C genotype 4.
- Published in:
- Journal of Medical Virology, 2009, v. 81, n. 9, p. 1576, doi. 10.1002/jmv.21570
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- Publication type:
- Article
Prospective cohort study of mother-to-infant infection and clearance of hepatitis C in rural Egyptian villages.
- Published in:
- Journal of Medical Virology, 2009, v. 81, n. 6, p. 1024, doi. 10.1002/jmv.21480
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- Publication type:
- Article
Surveillance of acute hepatitis C in Cairo, Egypt.
- Published in:
- Journal of Medical Virology, 2005, v. 76, n. 4, p. 520
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- Publication type:
- Article
Isolated dentinogenesis imperfecta: Novel DSPP variants and insights on genetic counselling.
- Published in:
- Clinical Oral Investigations, 2024, v. 28, n. 5, p. 1, doi. 10.1007/s00784-024-05636-z
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- Publication type:
- Article
Adaptive Frequency Control of an Isolated Microgrids Implementing Different Recent Optimization Techniques.
- Published in:
- International Journal of Robotics & Control Systems, 2024, v. 4, n. 3, p. 1000, doi. 10.31763/ijrcs.v4i3.1432
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- Publication type:
- Article
Ultrasound-Guided Genicular Nerve Block versus Intraarticular CS Injection in Chronic Knee Pain.
- Published in:
- 2023
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- Publication type:
- Abstract
The role of VEGF and BMP-2 in stimulation of bone healing with using hybrid bio-composite scaffolds coated implants in animal model.
- Published in:
- Bulletin of the National Research Centre, 2020, v. 44, n. 1, p. 1, doi. 10.1186/s42269-020-00369-x
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- Publication type:
- Article
Effective treatments of jojoba and jatropha hulls to obtain phytochemical compounds for industrial, nutritional, and pharmaceutical uses.
- Published in:
- Bulletin of the National Research Centre, 2019, v. 43, n. 1, p. N.PAG, doi. 10.1186/s42269-019-0054-5
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- Publication type:
- Article
Study of the Humoral Immune Response towards HCV Genotype 4 Using a Bead-Based Multiplex Serological Assay.
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- Microarrays (2076-3905), 2017, v. 6, n. 4, p. 15, doi. 10.3390/ht6040015
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- Publication type:
- Article
Seroprevalence and Risk Factors for Human Herpesvirus 8 Infection, Rural Egypt.
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- Emerging Infectious Diseases, 2008, v. 14, n. 4, p. 586, doi. 10.3201/eid1404.070935
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- Publication type:
- Article
APOA2 Polymorphism in Relation to Obesity and Lipid Metabolism.
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- Cholesterol, 2013, p. 1, doi. 10.1155/2013/289481
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- Publication type:
- Article
Refining the phenotypic spectrum of CCDC88A‐related PEHO‐like syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 2, p. 226, doi. 10.1002/ajmg.a.63425
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- Publication type:
- Article
A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management.
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- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 1, p. 39, doi. 10.1002/ajmg.a.63415
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- Publication type:
- Article
CHST3‐related skeletal dysplasia in 14 patients: Identification of 8 novel variants and further expansion of the phenotypic spectrum.
- Published in:
- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 8, p. 2100, doi. 10.1002/ajmg.a.63246
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- Publication type:
- Article
Bruck syndrome in 13 new patients: Identification of five novel FKBP10 and PLOD2 variants and further expansion of the phenotypic spectrum.
- Published in:
- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 6, p. 1815, doi. 10.1002/ajmg.a.62718
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- Publication type:
- Article
Expanding the phenotypic and allelic spectrum of SMG8: Clinical observations reveal overlap with SMG9‐associated disease trait.
- Published in:
- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 2, p. 648, doi. 10.1002/ajmg.a.62561
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- Publication type:
- Article
Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 6, p. 1666, doi. 10.1002/ajmg.a.62129
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- Publication type:
- Article
Blepharophimosis‐ptosis‐intellectual disability syndrome: A report of nine Egyptian patients with further expansion of phenotypic and mutational spectrum.
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- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 12, p. 2857, doi. 10.1002/ajmg.a.61857
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- Publication type:
- Article
KBG syndrome in two patients from Egypt.
- Published in:
- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 6, p. 1309, doi. 10.1002/ajmg.a.61552
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- Publication type:
- Article
Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation.
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- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 6, p. 1407, doi. 10.1002/ajmg.a.61585
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- Publication type:
- Article
Lenz–Majewski syndrome in a patient from Egypt.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 10, p. 2039, doi. 10.1002/ajmg.a.61327
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- Publication type:
- Article
Phenotypic spectrum of NDE1‐related disorders: from microlissencephaly to microhydranencephaly.
- Published in:
- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 3, p. 494, doi. 10.1002/ajmg.a.61035
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- Publication type:
- Article
GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletion.
- Published in:
- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 2, p. 237, doi. 10.1002/ajmg.a.61021
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- Publication type:
- Article
Phenotypic and molecular insights into PQBP1‐related intellectual disability.
- Published in:
- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 11, p. 2446, doi. 10.1002/ajmg.a.40479
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- Publication type:
- Article
Identification of a novel homozygous <italic>ALX4</italic> mutation in two unrelated patients with frontonasal dysplasia type‐2.
- Published in:
- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 5, p. 1190, doi. 10.1002/ajmg.a.38655
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- Publication type:
- Article
Molecular and phenotypic spectrum of ASPM-related primary microcephaly: Identification of eight novel mutations.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 8, p. 2133, doi. 10.1002/ajmg.a.37724
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- Publication type:
- Article
Long-Term Survival in Microcephalic Osteodysplastic Primordial Dwarfism Type I: Evaluation of an 18-Year-Old Male with g.55G>A Homozygous Mutation in RNU4ATAC.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 1, p. 277, doi. 10.1002/ajmg.a.37409
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- Publication type:
- Article
Clinical and Molecular Characterization of Seven Egyptian Families with Autosomal Recessive Robinow Syndrome: Identification of Four Novel ROR2 Gene Mutations.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 3054, doi. 10.1002/ajmg.a.37287
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- Publication type:
- Article