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Early application of haemostatic powder added to standard management for oesophagogastric variceal bleeding: a randomised trial

Gut, 2019-05, Vol.68 (5), p.844-853

2019

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Cost optimization of sewage pipelines inspection

Ain Shams Engineering Journal, 2023-05, Vol.14 (5), p.101960, Article 101960

2023

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Evaluation of Pesticide Residues in Vegetables from the Asir Region, Saudi Arabia

Molecules (Basel, Switzerland), 2020-01, Vol.25 (1), p.205

2020

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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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Biphasic calcium phosphate doped with zirconia nanoparticles for reconstruction of induced mandibular defects in dogs: cone-beam computed tomographic and histopathologic evaluation

Journal of materials science. Materials in medicine, 2023-05, Vol.34 (6), p.27-27, Article 27

2023

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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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Clinical and molecular spectrum of a large Egyptian cohort with ALS2‐related disorders of infantile‐onset of clinical continuum IAHSP/JPLS

Clinical genetics, 2023-08, Vol.104 (2), p.238-244

2023

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A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management

American journal of medical genetics. Part A, 2024-01, Vol.194 (1), p.39-45

2024

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Refining the phenotypic spectrum of CCDC88A‐related PEHO‐like syndrome

American journal of medical genetics. Part A, 2024-02, Vol.194 (2), p.226-232

2024

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Bruck syndrome in 13 new patients: Identification of five novel FKBP10 and PLOD2 variants and further expansion of the phenotypic spectrum

American journal of medical genetics. Part A, 2022-06, Vol.188 (6), p.1815-1825

2022

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The clinical and genetic landscape of developmental and epileptic encephalopathies in Egyptian children

Clinical genetics, 2024-05, Vol.105 (5), p.510-522

2024

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Micro and Martsolf syndromes in 34 new patients: Refining the phenotypic spectrum and further molecular insights

Clinical genetics, 2020-11, Vol.98 (5), p.445-456

2020

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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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A Homozygous Missense Variant in Hedgehog Acyltransferase (HHAT) Gene Associated with 46,XY Gonadal Dysgenesis

Sexual development, 2023-02, Vol.16 (4), p.261-265

2023

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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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Papillon-Lefevre syndrome in twelve Egyptian patients: Five novel CTSC variants and functional characterization of a missense variant and its effect on splicing

Archives of oral biology, 2024-02, Vol.158, p.105869-105869, Article 105869

2024

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Two new patients with focal dermal hypoplasia: A novel PORCN variant and insights on the diagnostic considerations

Congenital anomalies, 2022-03, Vol.62 (2), p.68-77

2022

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KBG syndrome in two patients from Egypt

American journal of medical genetics. Part A, 2020-06, Vol.182 (6), p.1309-1312

2020

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Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development

American journal of medical genetics. Part A, 2021-06, Vol.185 (6), p.1666-1677

2021

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PYCR2 Mutations cause a lethal syndrome of microcephaly and failure to thrive

Annals of neurology, 2016-07, Vol.80 (1), p.59-70

2016

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OTUD6B-associated intellectual disability: novel variants and genetic exclusion of retinal degeneration as part of a refined phenotype

Journal of human genetics, 2022-01, Vol.67 (1), p.55-64

2022

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Retraction Note: Rectal vs. sublingual misoprostol before cesarean section: double-blind, three-arm, randomized clinical trial

Archives of gynecology and obstetrics, 2024-05, Vol.309 (5), p.2265-2265

2024

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Immuno-histopathologic evaluation of mineralized plasmatic matrix in the management of horizontal ridge defects in a canine model (a split-mouth comparative study)

Odontology, 2022-07, Vol.110 (3), p.523-534

2022

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ASAH1‐related disorders: Description of 15 novel pediatric patients and expansion of the clinical phenotype

Clinical genetics, 2020-12, Vol.98 (6), p.598-605

2020

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Blepharophimosis‐ptosis‐intellectual disability syndrome: A report of nine Egyptian patients with further expansion of phenotypic and mutational spectrum

American journal of medical genetics. Part A, 2020-12, Vol.182 (12), p.2857-2866

2020

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Early application of haemostatic powder added to standard management for oesophagogastric variceal bleeding: a randomised trial

Cost optimization of sewage pipelines inspection

Evaluation of Pesticide Residues in Vegetables from the Asir Region, Saudi Arabia

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

Biphasic calcium phosphate doped with zirconia nanoparticles for reconstruction of induced mandibular defects in dogs: cone-beam computed tomographic and histopathologic evaluation

Delineating the phenotype of PNPLA8‐related mitochondriopathies

Clinical and molecular spectrum of a large Egyptian cohort with ALS2‐related disorders of infantile‐onset of clinical continuum IAHSP/JPLS

A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management

Refining the phenotypic spectrum of CCDC88A‐related PEHO‐like syndrome

Bruck syndrome in 13 new patients: Identification of five novel FKBP10 and PLOD2 variants and further expansion of the phenotypic spectrum

The clinical and genetic landscape of developmental and epileptic encephalopathies in Egyptian children

Micro and Martsolf syndromes in 34 new patients: Refining the phenotypic spectrum and further molecular insights

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

A Homozygous Missense Variant in Hedgehog Acyltransferase (HHAT) Gene Associated with 46,XY Gonadal Dysgenesis

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

Papillon-Lefevre syndrome in twelve Egyptian patients: Five novel CTSC variants and functional characterization of a missense variant and its effect on splicing

Two new patients with focal dermal hypoplasia: A novel PORCN variant and insights on the diagnostic considerations

KBG syndrome in two patients from Egypt

Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development

PYCR2 Mutations cause a lethal syndrome of microcephaly and failure to thrive

OTUD6B-associated intellectual disability: novel variants and genetic exclusion of retinal degeneration as part of a refined phenotype

Retraction Note: Rectal vs. sublingual misoprostol before cesarean section: double-blind, three-arm, randomized clinical trial

Immuno-histopathologic evaluation of mineralized plasmatic matrix in the management of horizontal ridge defects in a canine model (a split-mouth comparative study)

ASAH1‐related disorders: Description of 15 novel pediatric patients and expansion of the clinical phenotype

Blepharophimosis‐ptosis‐intellectual disability syndrome: A report of nine Egyptian patients with further expansion of phenotypic and mutational spectrum

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