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Removal of heavy metal ions from aqueous solutions with multi-walled carbon nanotubes: Kinetic and thermodynamic studies

International journal of environmental science and technology (Tehran), 2013-07, Vol.10 (4), p.677-688

Abdel Salam, M.

2013

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Delineating the phenotype of PNPLA8‐related mitochondriopathies

Clinical genetics, 2024-01, Vol.105 (1), p.92-98

2024

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A founder PPIL1 variant underlies a recognizable form of microlissencephaly with pontocerebellar hypoplasia

Clinical genetics, 2023-09, Vol.104 (3), p.356-364

2023

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PUS7 mutations impair pseudouridylation in humans and cause intellectual disability and microcephaly

Human genetics, 2019-03, Vol.138 (3), p.231-239

2019

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CHST3‐related skeletal dysplasia in 14 patients: Identification of 8 novel variants and further expansion of the phenotypic spectrum

American journal of medical genetics. Part A, 2023-08, Vol.191 (8), p.2100-2112

2023

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Novel CoQ10 antidiabetic mechanisms underlie its positive effect: modulation of insulin and adiponectine receptors, Tyrosine kinase, PI3K, glucose transporters, sRAGE and visfatin in insulin resistant/diabetic rats

PloS one, 2014-02, Vol.9 (2), p.e89169

2014

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Mutations in CIT, encoding citron rho-interacting serine/threonine kinase, cause severe primary microcephaly in humans

Human genetics, 2016-10, Vol.135 (10), p.1191-1197

2016

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Liraglutide mends cognitive impairment by averting Notch signaling pathway overexpression in a rat model of polycystic ovary syndrome

Life sciences (1973), 2021-01, Vol.265, p.118731, Article 118731

2021

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Expanding the phenotypic and allelic spectrum of SMG8: Clinical observations reveal overlap with SMG9‐associated disease trait

American journal of medical genetics. Part A, 2022-02, Vol.188 (2), p.648-657

2022

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New Approach for Using of Mentha longifolia L. and Citrus reticulata L. Essential Oils as Wood-Biofungicides: GC-MS, SEM, and MNDO Quantum Chemical Studies

Materials, 2021-03, Vol.14 (6), p.1361

2021

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Molecular and phenotypic spectrum of ASPM-related primary microcephaly: Identification of eight novel mutations

American journal of medical genetics. Part A, 2016-08, Vol.170A (8), p.2133-2140

2016

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Raine syndrome: Prenatal diagnosis based on recognizable fetal facial features and characteristic intracranial calcification

Prenatal diagnosis, 2020-12, Vol.40 (12), p.1578-1597

2020

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Biallelic novel missense HHAT variant causes syndromic microcephaly and cerebellar‐vermis hypoplasia

American journal of medical genetics. Part A, 2019-06, Vol.179 (6), p.1053-1057

2019

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MWCNTs decorated with Mn0.8Zn0.2Fe2O4 nanoparticles for removal of crystal-violet dye from aqueous solutions

Chemical engineering journal (Lausanne, Switzerland : 1996), 2014-11, Vol.255, p.156-164

2014

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Expanding the KIF4A‐associated phenotype

American journal of medical genetics. Part A, 2021-12, Vol.185 (12), p.3728-3739

2021

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El‐Hattab‐Alkuraya syndrome caused by biallelic WDR45B pathogenic variants: Further delineation of the phenotype and genotype

Clinical genetics, 2022-05, Vol.101 (5-6), p.530-540

2022

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Quantitative dissection of multilocus pathogenic variation in an Egyptian infant with severe neurodevelopmental disorder resulting from multiple molecular diagnoses

American journal of medical genetics. Part A, 2022-03, Vol.188 (3), p.735-750

2022

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Spatial Prediction and Optimized Sampling Design for Sodium Concentration in Groundwater

PloS one, 2016-09, Vol.11 (9), p.e0161810-e0161810

2016

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Thermal Performance Analysis of an Indirect Solar Cooker Using a Graphene Oxide Nanofluid

Sustainability, 2024-03, Vol.16 (6), p.2539

2024

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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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Influence of nitrogen excited species on the destruction of naphthalene in nitrogen and air using surface dielectric barrier discharge

Journal of hazardous materials, 2013-02, Vol.246-247, p.26-33

2013

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Lenz–Majewski syndrome in a patient from Egypt

American journal of medical genetics. Part A, 2019-10, Vol.179 (10), p.2039-2042

2019

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Chemical Composition of Aqueous Ethanol Extract of Luffa cylindrica Leaves and Its Effect on Representation of Caspase‐8, Caspase‐3, and the Proliferation Marker Ki67 in Intrinsic Molecular Subtypes of Breast Cancer in Vitro

Chemistry & biodiversity, 2018-08, Vol.15 (8), p.e1800045-n/a

2018

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Effect of transition metal (M: Fe, Co or Mn) for the oxygen reduction reaction with non-precious metal catalysts in acid medium

International journal of hydrogen energy, 2014-03, Vol.39 (10), p.5309-5318

2014

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Production of Plant Secondary Metabolites: Examples, Tips and Suggestions for Biotechnologists

Genes, 2018-06, Vol.9 (6), p.309

2018

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Removal of heavy metal ions from aqueous solutions with multi-walled carbon nanotubes: Kinetic and thermodynamic studies

Delineating the phenotype of PNPLA8‐related mitochondriopathies

A founder PPIL1 variant underlies a recognizable form of microlissencephaly with pontocerebellar hypoplasia

PUS7 mutations impair pseudouridylation in humans and cause intellectual disability and microcephaly

CHST3‐related skeletal dysplasia in 14 patients: Identification of 8 novel variants and further expansion of the phenotypic spectrum

Novel CoQ10 antidiabetic mechanisms underlie its positive effect: modulation of insulin and adiponectine receptors, Tyrosine kinase, PI3K, glucose transporters, sRAGE and visfatin in insulin resistant/diabetic rats

Mutations in CIT, encoding citron rho-interacting serine/threonine kinase, cause severe primary microcephaly in humans

Liraglutide mends cognitive impairment by averting Notch signaling pathway overexpression in a rat model of polycystic ovary syndrome

Expanding the phenotypic and allelic spectrum of SMG8: Clinical observations reveal overlap with SMG9‐associated disease trait

New Approach for Using of Mentha longifolia L. and Citrus reticulata L. Essential Oils as Wood-Biofungicides: GC-MS, SEM, and MNDO Quantum Chemical Studies

Molecular and phenotypic spectrum of ASPM-related primary microcephaly: Identification of eight novel mutations

Raine syndrome: Prenatal diagnosis based on recognizable fetal facial features and characteristic intracranial calcification

Biallelic novel missense HHAT variant causes syndromic microcephaly and cerebellar‐vermis hypoplasia

MWCNTs decorated with Mn0.8Zn0.2Fe2O4 nanoparticles for removal of crystal-violet dye from aqueous solutions

Expanding the KIF4A‐associated phenotype

El‐Hattab‐Alkuraya syndrome caused by biallelic WDR45B pathogenic variants: Further delineation of the phenotype and genotype

Quantitative dissection of multilocus pathogenic variation in an Egyptian infant with severe neurodevelopmental disorder resulting from multiple molecular diagnoses

Spatial Prediction and Optimized Sampling Design for Sodium Concentration in Groundwater

Thermal Performance Analysis of an Indirect Solar Cooker Using a Graphene Oxide Nanofluid

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

Influence of nitrogen excited species on the destruction of naphthalene in nitrogen and air using surface dielectric barrier discharge

Lenz–Majewski syndrome in a patient from Egypt

Chemical Composition of Aqueous Ethanol Extract of Luffa cylindrica Leaves and Its Effect on Representation of Caspase‐8, Caspase‐3, and the Proliferation Marker Ki67 in Intrinsic Molecular Subtypes of Breast Cancer in Vitro

Effect of transition metal (M: Fe, Co or Mn) for the oxygen reduction reaction with non-precious metal catalysts in acid medium

Production of Plant Secondary Metabolites: Examples, Tips and Suggestions for Biotechnologists

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