Assessment of gastrointestinal symptoms in neurologically impaired children with PEG using peptide versus casein based formulae.

Autor: Tarek, Sara, Eskander, Ayman E., Younis, Alaa Mohamed, Salama, Christine G., ElNaggar, Walaa

Publikováno v: Egyptian Pediatric Association Gazette; 11/14/2024, Vol. 72 Issue 1, p1-11, 11p

Short term Neurological Complications After Surgical Correction in Children with Congenital Heart Disease: A Single Center Study

Autor: Elnaggar Walaa, Yassine Imane, Abdelwahab Mohamed, Abdelglil Ahmed, Fattouh Aya, Elkazaz Aly

Publikováno v: Pediatric Sciences Journal. 3:1-10

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1599c38fb22a18ac04aa86172707abea
https://doi.org/10.21608/cupsj.2022.140797.1053

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Clinical and Genetic Spectrum of Patients With Mitochondrial Disease in a Pediatric Egyptian Cohort: Novel Variants and Phenotypic Expansion.

Autor: Hassaan HM; Pediatric Department, Genetic Division, Faculty of Medicine, Cairo University, Cairo, Egypt., Pyle A; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK., Almenabawy N; Pediatric Department, Neurology and Metabolic Division, Faculty of Medicine Cairo University, Cairo, Egypt., Robertson FM; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK., Elkhateeb N; Department of Clinical Genetics, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK., Girgis MY; Pediatric Department, Neurology and Metabolic Division, Faculty of Medicine Cairo University, Cairo, Egypt., Mahmoud IGED; Pediatric Department, Neurology and Metabolic Division, Faculty of Medicine Cairo University, Cairo, Egypt., Amer F; Pediatric Department, Neurology and Metabolic Division, Faculty of Medicine Cairo University, Cairo, Egypt., Samaha M; Pediatric Department, Neurology and Metabolic Division, Faculty of Medicine Cairo University, Cairo, Egypt., Shaheen Y; Pediatric Department, Neurology and Metabolic Division, Faculty of Medicine Cairo University, Cairo, Egypt., ElNaggar W; Pediatric Department, Neurology and Metabolic Division, Faculty of Medicine Cairo University, Cairo, Egypt., Abdoh D; Clinical and Chemical Pathology Department, Faculty of Medicine, Cairo University, Cairo, Egypt., Mehaney DA; Clinical and Chemical Pathology Department, Faculty of Medicine, Cairo University, Cairo, Egypt., Meguid IEA; Pediatric Department, Genetic Division, Faculty of Medicine, Cairo University, Cairo, Egypt., Taylor RW; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK., McFarland R; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK., Selim L; Pediatric Department, Neurology and Metabolic Division, Faculty of Medicine Cairo University, Cairo, Egypt.

Publikováno v: American journal of medical genetics. Part A [Am J Med Genet A] 2024 Oct 14, pp. e63881. Date of Electronic Publication: 2024 Oct 14.