Publications by authors named "Laila Selim"

29Publications

Implementation of ketogenic diet in children with drug-resistant epilepsy in a medium resources setting: Egyptian experience.

Epilepsy Behav Case Rep 2019 23;11:35-38. Epub 2018 Nov 23.

Department of Pediatrics, Clinical Nutrition Division, Cairo University Hospital, Cairo, Egypt.

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http://dx.doi.org/10.1016/j.ebcr.2018.11.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312833PMC
November 2018

Mitochondrial Diseases as Model of Neurodegeneration.

Adv Exp Med Biol 2017 ;1007:129-155

Kasr Al Ainy School of Medicine, Cairo University Children Hospital, Cairo, Egypt.

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http://dx.doi.org/10.1007/978-3-319-60733-7_8DOI Listing
April 2018

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.

Brain 2017 May;140(5):1316-1336

The Danish Epilepsy Centre, Dianalund, Denmark.

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http://dx.doi.org/10.1093/brain/awx054DOI Listing
May 2017

Cardiovascular Abnormalities in Egyptian Children with Mucopolysaccharidoses.

J Clin Diagn Res 2016 Nov 1;10(11):SC05-SC08. Epub 2016 Nov 1.

Researcher, Department of Paediatrics, National Research Center , Cairo, Egypt .

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http://dx.doi.org/10.7860/JCDR/2016/21135.8851DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5198412PMC
November 2016

Molybdenum cofactor and isolated sulphite oxidase deficiencies: Clinical and molecular spectrum among Egyptian patients.

Eur J Paediatr Neurol 2016 Sep 30;20(5):714-22. Epub 2016 May 30.

Medical Molecular Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo 12311, Egypt.

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http://dx.doi.org/10.1016/j.ejpn.2016.05.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993451PMC
September 2016

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

Ann Neurol 2016 07 1;80(1):59-70. Epub 2016 Jun 1.

Laboratory for Pediatric Brain Disease, Howard Hughes Medical Institute, Rockefeller University, New York, NY.

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http://dx.doi.org/10.1002/ana.24678DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4938747PMC
July 2016

Lysosomal Storage Disorders in Egyptian Children.

Indian J Pediatr 2016 Aug 2;83(8):805-13. Epub 2016 Feb 2.

Inherited Metabolic Disease Unit (IMDU), Cairo University Children's Hospital, Cairo, Egypt.

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http://dx.doi.org/10.1007/s12098-015-2014-xDOI Listing
August 2016

Inborn errors of metabolism detectable by tandem mass spectrometry in Egypt: The first newborn screening pilot study.

J Med Screen 2016 09 20;23(3):124-9. Epub 2016 Jan 20.

Clinical and Chemical Pathology Department, Faculty of Medicine, Cairo University, Cairo, Egypt Inherited Metabolic Disease Unit, Center of Social and Preventive Medicine, Cairo University, Cairo, Egypt

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http://dx.doi.org/10.1177/0969141315618229DOI Listing
September 2016

Selective screening for inborn errors of metabolism by tandem mass spectrometry in Egyptian children: a 5 year report.

Clin Biochem 2014 Jun 13;47(9):823-8. Epub 2014 Apr 13.

Inherited Metabolic Disease Unit, Cairo University Children Hospital, Cairo, Egypt; Department of Clinical and Chemical Pathology, Faculty of Medicine, Cairo University, Egypt.

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http://dx.doi.org/10.1016/j.clinbiochem.2014.04.002DOI Listing
June 2014

Clinical, neuroimaging, and genetic characteristics of megalencephalic leukoencephalopathy with subcortical cysts in Egyptian patients.

Pediatr Neurol 2014 Feb 24;50(2):140-8. Epub 2013 Oct 24.

Stem Cell Research Laboratory, Centre for Advanced Sciences-National Research Centre, Cairo, Egypt; Neurogenetics Laboratory, Weill Cornell Medical College in Qatar, Doha, Qatar; Department of Neurology, Weill Cornell Medical College, New York, New York. Electronic address:

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http://dx.doi.org/10.1016/j.pediatrneurol.2013.10.008DOI Listing
February 2014

Blood spot versus plasma chitotriosidase: a systematic clinical comparison.

Clin Biochem 2014 Jan 29;47(1-2):38-43. Epub 2013 Oct 29.

Department of Clinical and Chemical Pathology, Faculty of Medicine, Cairo University, Cairo, Egypt.

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http://dx.doi.org/10.1016/j.clinbiochem.2013.10.024DOI Listing
January 2014

ß-ureidopropionase deficiency: phenotype, genotype and protein structural consequences in 16 patients.

Biochim Biophys Acta 2012 Jul 14;1822(7):1096-108. Epub 2012 Apr 14.

Academic Medical Center, Emma Children's Hospital, Department of Clinical Chemistry, Laboratory Genetic Metabolic Diseases, 1105 AZ Amsterdam, The Netherlands.

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http://dx.doi.org/10.1016/j.bbadis.2012.04.001DOI Listing
July 2012