Works matching AU Abdelkreem, Elsayed

Results: 28

Urinary stones as the initial presentation in a child with late-onset molybdenum cofactor deficiency type B: a case report and review of literature.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00720-9

By:

Sadek, Abdelrahim A.;
Aladawy, Mohammed A.;
Magdy, Rofaida M.;
Fouad, Mohammed Fawzy;
Mansour, Tarek M. M.;
Gad, Eman Fathalla;
Abdelkreem, Elsayed

Publication type:

Article

Mutation update on ACAT1 variants associated with mitochondrial acetoacetyl‐CoA thiolase (T2) deficiency.

Published in:

Human Mutation, 2019, v. 40, n. 10, p. 1641, doi. 10.1002/humu.23831

By:

Abdelkreem, Elsayed;
Harijan, Rajesh K.;
Yamaguchi, Seiji;
Wierenga, Rikkert K.;
Fukao, Toshiyuki

Publication type:

Article

Impact of COVID-19 pandemic and related isolation measures on violence against children in Egypt.

Published in:

Journal of the Egyptian Public Health Association, 2021, v. 96, n. 1, p. 1, doi. 10.1186/s42506-021-00071-4

By:

AboKresha, Seham Ahmed;
Abdelkreem, Elsayed;
Ali, Rasha Abd Elhameed

Publication type:

Article

Genetic variants in NHEJ1 and related DNA repair disorders: insights into phenotypic heterogeneity and links to hypoplastic myelodysplastic syndromes and familial hematological malignancies susceptibility.

Published in:

Annals of Hematology, 2025, v. 104, n. 3, p. 1633, doi. 10.1007/s00277-025-06257-6

By:

Elbadry, Mahmoud I.;
Abdelkreem, Elsayed;
Tawfeek, Ahmed;
Seo, Go Hun;
Aziz, Shereen Philip

Publication type:

Article

Levetiracetam and Midazolam vs Midazolam Alone for First-Line Treatment of Children With Generalized Convulsive Status Epilepticus (Lev-Mid Study): A Randomized Controlled Trial.

Published in:

Indian Pediatrics, 2023, v. 60, n. 8, p. 630, doi. 10.1007/s13312-023-2960-8

By:

Elshater, Ahmed A.;
Sadek, Abdelrahim A.;
Abdelkreem, Elsayed

Publication type:

Article

Japanese patients with mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: In vitro functional analysis of five novel HMGCS2 mutations.

Published in:

Experimental & Therapeutic Medicine, 2020, v. 20, n. 5, p. N.PAG, doi. 10.3892/etm.2020.9166

By:

Ago, Yasuhiko;
Otsuka, Hiroki;
Sasai, Hideo;
Abdelkreem, Elsayed;
Nakama, Mina;
Aoyama, Yuka;
Matsumoto, Hideki;
Fujiki, Ryoji;
Ohara, Osamu;
Akiyama, Kazumasa;
Fukui, Kaori;
Watanabe, Yoriko;
Nakajima, Yoko;
Ohnishi, Hidenori;
Ito, Tetsuya;
Fukao, Toshiyuki

Publication type:

Article

Two Libyan siblings with beta-ketothiolase deficiency: A case report and review of literature.

Published in:

2017

By:

Abdelkreem, Elsayed;
Alobaidy, Hanna;
Yuka Aoyama;
Mahmoud, Shaimaa;
Abd El Aal, Mohamed;
Toshiyuki Fukao

Publication type:

Case Study

Perceptions of the Research Integrity Climate in Egyptian Universities: A Survey Among Academic Researchers.

Published in:

Journal of Empirical Research on Human Research Ethics, 2024, v. 19, n. 4/5, p. 250, doi. 10.1177/15562646241273097

By:

Abdelkreem, Elsayed;
Ibrahim, Maha Emad;
Elateek, Sawsan;
Abdelgawad, Fatma;
Silverman, Henry J.

Publication type:

Article

Association between SARS-CoV-2 seropositivity and disease activity in children with systemic lupus erythematosus.

Published in:

Microbes & Infectious Diseases, 2025, v. 6, n. 1, p. 32, doi. 10.21608/MID.2024.321382.2231

By:

Mahmoud, Ekram Abdel-Rahman;
Abdelkreem, Elsayed;
Fayez, Ebtesam;
Fahmy, Eman Mohamed;
Mohamed, Nesma A.

Publication type:

Article

Frequency of CD40‐1C>T polymorphism (rs1883832) and association with response to treatment in children with primary immune thrombocytopenia.

Published in:

Pediatric Blood & Cancer, 2024, v. 71, n. 12, p. 1, doi. 10.1002/pbc.31356

By:

Ahmed, Heba A.;
Abdelkreem, Elsayed;
Hamed, Elham O.;
Abo Elmahassen, Nagwa M.;
Younis, Mustafa Adel A.

Publication type:

Article

Frequency of toll‐like receptor 4 variants and association with treatment response in children with primary immune thrombocytopenia.

Published in:

Pediatric Blood & Cancer, 2023, v. 70, n. 11, p. 1, doi. 10.1002/pbc.30646

By:

Ahmed, Heba A.;
Fahmy, Eman M.;
Abdelkreem, Elsayed;
Mahmoud, Ekram A.;
Nafady, Asmaa;
Ahmed, Eman H.

Publication type:

Article

Pattern of hereditary renal tubular disorders in Egyptian children.

Published in:

Turkish Journal of Pediatrics, 2023, v. 65, n. 4, p. 611, doi. 10.24953/turkjped.2022.688

By:

Osman, Mohamed A. M.;
Abd-Elrehim, Ghada A. B.;
Abdelkreem, Elsayed;
Abosdera, Mostafa M.;
Kassem, Mohamed A.

Publication type:

Article

Deficiency of 3‐hydroxybutyrate dehydrogenase (BDH1) in mice causes low ketone body levels and fatty liver during fasting.

Published in:

Journal of Inherited Metabolic Disease, 2020, v. 43, n. 5, p. 960, doi. 10.1002/jimd.12243

By:

Otsuka, Hiroki;
Kimura, Takeshi;
Ago, Yasuhiko;
Nakama, Mina;
Aoyama, Yuka;
Abdelkreem, Elsayed;
Matsumoto, Hideki;
Ohnishi, Hidenori;
Sasai, Hideo;
Osawa, Masatake;
Yamaguchi, Seiji;
Mitchell, Grant A.;
Fukao, Toshiyuki

Publication type:

Article

Heterozygous carriers of succinyl-CoA:3-oxoacid CoA transferase deficiency can develop severe ketoacidosis.

Published in:

Journal of Inherited Metabolic Disease, 2017, v. 40, n. 6, p. 845, doi. 10.1007/s10545-017-0065-z

By:

Sasai, Hideo;
Aoyama, Yuka;
Otsuka, Hiroki;
Abdelkreem, Elsayed;
Naiki, Yasuhiro;
Kubota, Mitsuru;
Sekine, Yuji;
Itoh, Masatsune;
Nakama, Mina;
Ohnishi, Hidenori;
Fujiki, Ryoji;
Ohara, Osamu;
Fukao, Toshiyuki

Publication type:

Article

Characterization and outcome of 41 patients with beta-ketothiolase deficiency: 10 years' experience of a medical center in northern Vietnam.

Published in:

Journal of Inherited Metabolic Disease, 2017, v. 40, n. 3, p. 395, doi. 10.1007/s10545-017-0026-6

By:

Nguyen, Khanh;
Abdelkreem, Elsayed;
Colombo, Roberto;
Hasegawa, Yuki;
Can, Ngoc;
Bui, Thao;
Le, Hai;
Tran, Mai;
Nguyen, Hoan;
Trinh, Hung;
Aoyama, Yuka;
Sasai, Hideo;
Yamaguchi, Seiji;
Fukao, Toshiyuki;
Vu, Dung

Publication type:

Article

A rare PHKA2 variant (p.G991A) identified in a patient with ketotic hypoglycemia.

Published in:

Journal of Inherited Metabolic Disease Reports, 2019, v. 48, n. 1, p. 15, doi. 10.1002/jmd2.12041

By:

Yasuhiko Ago;
Hideo Sugie;
Tokiko Fukuda;
Hiroki Otsuka;
Hideo Sasai;
Mina Nakama;
Elsayed Abdelkreem;
Toshiyuki Fukao

Publication type:

Article

Beta‐ketothiolase deficiency: A case with unusual presentation of nonketotic hypoglycemic episodes due to coexistent probable secondary carnitine deficiency.

Published in:

Journal of Inherited Metabolic Disease Reports, 2019, v. 46, n. 1, p. 23, doi. 10.1002/jmd2.12022

By:

Alijanpour, Morteza;
Sasai, Hideo;
Abdelkreem, Elsayed;
Ago, Yasuhiko;
Soleimani, Shima;
Moslemi, Leila;
Yamaguchi, Seiji;
Rezapour, Masomeh;
Hakimi, Mohammad T.;
Matsumoto, Hideki;
Fukao, Toshiyuki

Publication type:

Article

Single-nucleotide substitution T to A in the polypyrimidine stretch at the splice acceptor site of intron 9 causes exon 10 skipping in the ACAT1 gene.

Published in:

Molecular Genetics & Genomic Medicine, 2017, v. 5, n. 2, p. 177, doi. 10.1002/mgg3.275

By:

Sasai, Hideo;
Aoyama, Yuka;
Otsuka, Hiroki;
Abdelkreem, Elsayed;
Nakama, Mina;
Hori, Tomohiro;
Ohnishi, Hidenori;
Turner, Lesley;
Fukao, Toshiyuki

Publication type:

Article

Characterization and outcome of 11 children with non-diabetic ketoacidosis.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2021, v. 34, n. 1, p. 95, doi. 10.1515/jpem-2020-0324

By:

Abdelkreem, Elsayed;
Magdy, Rofaida M.;
Sadek, Abdelrahim A.

Publication type:

Article

Exon 10 skipping in ACAT1 caused by a novel c.949G>A mutation located at an exonic splice enhancer site.

Published in:

Molecular Medicine Reports, 2016, v. 14, n. 5, p. 4906, doi. 10.3892/mmr.2016.5819

By:

HIROKI OTSUKA;
HIDEO SASAI;
MINA NAKAMA;
YUKA AOYAMA;
ABDELKREEM, ELSAYED;
HIDENORI OHNISHI;
KONSTANTOPOULOU, VASSILIKI;
SASS, JÖRN OLIVER;
TOSHIYUKI FUKAO

Publication type:

Article

Clinicoradiologic Correlation in 22 Egyptian Children With Megalencephalic Leukoencephalopathy With Subcortical Cysts.

Published in:

Journal of Child Neurology, 2022, v. 37, n. 5, p. 380, doi. 10.1177/08830738221078683

By:

Sadek, Abdelrahim A.;
Aladawy, Mohammed A.;
Mansour, Tarek M. M.;
Ibrahim, Mohamed F.;
Mohamed, Montaser M.;
Gad, Eman F.;
Othman, Amr A.;
Ahmed, Hosny A.;
Kasim, Abdin K.;
Wagdy, Wael M.;
Hasan, Mohamed H. T.;
Abdelkreem, Elsayed

Publication type:

Article

Serum Levels of Interleukins 6 And 8 In Malnourished Children with Acute Diarrhea: A Case-Control Study.

Published in:

Egyptian Journal of Hospital Medicine, 2024, v. 94, n. 1, p. 305, doi. 10.21608/ejhm.2024.337169

By:

Abou-Taleb, Ashraf;
Bakry, Rania;
Hassan, Moataz M.;
Shaker, John S.;
Abdelkreem, Elsayed;
Kassem, Mohamed

Publication type:

Article

Serum Levels of Leptin and Adiponectin in Children with Febrile Seizures: A Case-Control Study.

Published in:

Egyptian Journal of Hospital Medicine, 2023, v. 90, n. 1, p. 1494, doi. 10.21608/ejhm.2023.282376

By:

Abdelkreem, Elsayed;
Mohamed, Hager A.;
Sadek, Abdelrahim A.;
Abdel-Gawad, Abdelhady R.;
Othman, Amr A.

Publication type:

Article

Characterization of 42 Egyptian Children with Lysosomal Storage Disorders.

Published in:

Egyptian Journal of Hospital Medicine, 2022, v. 88, p. 3069, doi. 10.21608/ejhm.2022.244542

By:

Fahmy, Eman M.;
Abdelkreem, Elsayed;
Mohamed, Osama E.;
Abosdera, Mostafa M.;
Sadek, Abdelrahim A.

Publication type:

Article

Nebulized Magnesium Sulfate for Treatment of Persistent Pulmonary Hypertension of Newborn: A Pilot Randomized Controlled Trial.

Published in:

Indian Journal of Pediatrics, 2021, v. 88, n. 8, p. 771, doi. 10.1007/s12098-020-03643-y

By:

Abdelkreem, Elsayed;
Mahmoud, Shaimaa M.;
Aboelez, Moustafa O.;
Abd El Aal, Mohamed

Publication type:

Article

Evaluation of Neutrophil Gelatinase-Associated Lipocalin Levels in Children With Febrile Seizures: A Case-Control Study.

Published in:

Clinical Pediatrics, 2025, v. 64, n. 6, p. 771, doi. 10.1177/00099228241292948

By:

Kassem, Mohamed A.;
Abbass, Amany;
Ahmed, Heba A.;
Othman, Amr A.;
Fahim, Bishoy;
Sadek, Abdelrahim A.;
Abdelkreem, Elsayed

Publication type:

Article

The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report.

Published in:

Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00579-2

By:

Sadek, Abdelrahim A.;
Aladawy, Mohammed A.;
Mansour, Tarek M. M.;
Sayed, Khulood M.;
Khang, Rin;
Abdelkreem, Elsayed

Publication type:

Article

Effectiveness of Medium-Chain Triglyceride Oil Therapy in Two Japanese Citrin-Deficient Siblings: Evaluation Using Oral Glucose Tolerance Tests.

Published in:

Tohoku Journal of Experimental Medicine, 2016, v. 240, n. 4, p. 323, doi. 10.1620/tjem.240.323

By:

Hiroki Otsuka;
Hideo Sasai;
Abdelkreem, Elsayed;
Norio Kawamoto;
Minako Kawamoto;
Toshiya Kamiya;
Yasuo Tanimoto;
Atsuo Kikuchi;
Shigeo Kure;
Chikahiko Numakura;
Kiyoshi Hayasaka;
Toshiyuki Fukao

Publication type:

Article