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The efficacy of cefuroxime in the treatment of bacterial meningitis in infants and children

Clinical therapeutics, 1983, Vol.5 (6), p.644

1983

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Viral etiology of obscure splenomegaly in Egyptian children

Journal of the Egyptian Public Health Association, 1990, Vol.65 (1-2), p.177-189

1990

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Analysis of BRAF V600E mutation in 1,320 nervous system tumors reveals high mutation frequencies in pleomorphic xanthoastrocytoma, ganglioglioma and extra-cerebellar pilocytic astrocytoma

Acta neuropathologica, 2011-03, Vol.121 (3), p.397-405

2011

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Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndrome

Nature genetics, 2015-07, Vol.47 (7), p.809-813

2015

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Biallelic mutations in valyl-tRNA synthetase gene VARS are associated with a progressive neurodevelopmental epileptic encephalopathy

Nature communications, 2019-02, Vol.10 (1), p.707-10, Article 707

2019

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An international registry for primary ciliary dyskinesia

The European respiratory journal, 2016-03, Vol.47 (3), p.849-859

2016

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Homozygous nonsense mutation in SCHIP1/IQCJ‐SCHIP1 causes a neurodevelopmental brain malformation syndrome

Clinical genetics, 2018-02, Vol.93 (2), p.387-391

2018

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Circulating spexins in children with obesity: relation to cardiometabolic risk

European journal of clinical nutrition, 2022-01, Vol.76 (1), p.119-125

2022

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Early effective treatment may protect from cognitive decline in paediatric multiple sclerosis

European journal of paediatric neurology, 2019-11, Vol.23 (6), p.783-791

2019

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DNAI2 Mutations Cause Primary Ciliary Dyskinesia with Defects in the Outer Dynein Arm

American journal of human genetics, 2008-11, Vol.83 (5), p.547-558

2008

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Deep immune profiling of MIS-C demonstrates marked but transient immune activation compared to adult and pediatric COVID-19

Science immunology, 2021-03, Vol.6 (57)

2021

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Interleukin-1β and microRNA-146a in an immature rat model and children with mesial temporal lobe epilepsy

Epilepsia (Copenhagen), 2012-07, Vol.53 (7), p.1215-1224

2012

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Effect of nusinersen on motor, respiratory and bulbar function in early-onset spinal muscular atrophy

Brain (London, England : 1878), 2023-02, Vol.146 (2), p.668-677

2023

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Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure

Thorax, 2012-05, Vol.67 (5), p.433-441

2012

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Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome

Genetics in medicine, 2019-09, Vol.21 (9), p.2025-2035

2019

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Lung cancer in Basrah, Iraq during 2005-2012. Incidence and time trend

Saudi medical journal, 2016-11, Vol.37 (11), p.1214-1219

2016

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Mutations in a novel gene, NPHP3 , cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis

Nature genetics, 2003-08, Vol.34 (4), p.455-459

2003

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Mutations in ACY1, the Gene Encoding Aminoacylase 1, Cause a Novel Inborn Error of Metabolism

American journal of human genetics, 2006-03, Vol.78 (3), p.401-409

2006

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INTESTINAL PARASITES IN PATIENTS WITH CHRONIC ABDOMINAL PAIN

Journal of the Egyptian Society of Parasitology, 2015-08, Vol.45 (2), p.389-396

2015

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Mutations in SPAG1 Cause Primary Ciliary Dyskinesia Associated with Defective Outer and Inner Dynein Arms

American journal of human genetics, 2013-10, Vol.93 (4), p.711-720

2013

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Overexpression of Orphan Receptor Tyrosine Kinase Ror1 as a Putative Tumor-Associated Antigen in Iranian Patients with Acute Lymphoblastic Leukemia

Tumor biology, 2007-01, Vol.28 (6), p.318-326

2007

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Loss of Nephrocystin-3 Function Can Cause Embryonic Lethality, Meckel-Gruber-like Syndrome, Situs Inversus, and Renal-Hepatic-Pancreatic Dysplasia

American journal of human genetics, 2008-04, Vol.82 (4), p.959-970

2008

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Buccal versus lingual mucosal graft urethroplasty for complex hypospadias repair

Journal of pediatric urology, 2013-12, Vol.9 (6), p.754-758

2013

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Relationship between bacteriology of the adenoid core and middle meatus in children with sinusitis

Journal of laryngology and otology, 2011-03, Vol.125 (3), p.279-281

2011

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The efficacy of cefuroxime in the treatment of bacterial meningitis in infants and children

Viral etiology of obscure splenomegaly in Egyptian children

Analysis of BRAF V600E mutation in 1,320 nervous system tumors reveals high mutation frequencies in pleomorphic xanthoastrocytoma, ganglioglioma and extra-cerebellar pilocytic astrocytoma

Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndrome

Biallelic mutations in valyl-tRNA synthetase gene VARS are associated with a progressive neurodevelopmental epileptic encephalopathy

An international registry for primary ciliary dyskinesia

Homozygous nonsense mutation in SCHIP1/IQCJ‐SCHIP1 causes a neurodevelopmental brain malformation syndrome

Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield

Circulating spexins in children with obesity: relation to cardiometabolic risk

Early effective treatment may protect from cognitive decline in paediatric multiple sclerosis

DNAI2 Mutations Cause Primary Ciliary Dyskinesia with Defects in the Outer Dynein Arm

Deep immune profiling of MIS-C demonstrates marked but transient immune activation compared to adult and pediatric COVID-19

Interleukin-1β and microRNA-146a in an immature rat model and children with mesial temporal lobe epilepsy

Effect of nusinersen on motor, respiratory and bulbar function in early-onset spinal muscular atrophy

Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure

Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome

Lung cancer in Basrah, Iraq during 2005-2012. Incidence and time trend

Mutations in a novel gene, NPHP3 , cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis

Mutations in ACY1, the Gene Encoding Aminoacylase 1, Cause a Novel Inborn Error of Metabolism

INTESTINAL PARASITES IN PATIENTS WITH CHRONIC ABDOMINAL PAIN

Mutations in SPAG1 Cause Primary Ciliary Dyskinesia Associated with Defective Outer and Inner Dynein Arms

Overexpression of Orphan Receptor Tyrosine Kinase Ror1 as a Putative Tumor-Associated Antigen in Iranian Patients with Acute Lymphoblastic Leukemia

Loss of Nephrocystin-3 Function Can Cause Embryonic Lethality, Meckel-Gruber-like Syndrome, Situs Inversus, and Renal-Hepatic-Pancreatic Dysplasia

Buccal versus lingual mucosal graft urethroplasty for complex hypospadias repair

Relationship between bacteriology of the adenoid core and middle meatus in children with sinusitis

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