Author

Elsayed Abdelkreem

Observed name: Abdelkreem, Elsayed

Institution: Sohag University

Observed institutions: Gifu University, Sohag University

ORCID: 0000-0002-8976-2989

Observed ORCID: 0000-0002-8976-2989

OpenAlex ID: A5072716007

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

2019 · Elsayed Abdelkreem, Rajesh K. Harijan, et al. · Human Mutation · 49

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Recent advances in understanding beta-ketothiolase (mitochondrial acetoacetyl-CoA thiolase, T2) deficiency

2018 · Toshiyuki Fukao, Hideo Sasai, et al. · Journal of Human Genetics · 48

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

2020 · Hiroki Otsuka, Takeshi Kimura, et al. · Journal of Inherited Metabolic Disease · 46

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

2017 · Khanh Ngoc Nguyen, Elsayed Abdelkreem, et al. · Journal of Inherited Metabolic Disease · 29

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

2021 · Seham Ahmed AboKresha, Elsayed Abdelkreem, et al. · Journal of the Egyptian Public Health Association · 24

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

2021 · Elsayed Abdelkreem, Shaimaa M. Mahmoud, et al. · The Indian Journal of Pediatrics · 24

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

2016 · Hiroki Otsuka, Hideo Sasai, et al. · Molecular Medicine Reports · 24

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Beta-Ketothiolase Deficiency

2016 · Elsayed Abdelkreem, Hiroki Otsuka, et al. · Journal of Inborn Errors of Metabolism and Screening · 24

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Clinical and Mutational Characterizations of Ten Indian Patients with Beta-Ketothiolase Deficiency

2016 · Elsayed Abdelkreem, Radha Rama Devi Akella, et al. · JIMD Reports · 23

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Intronic antisense Alu elements have a negative splicing effect on the inclusion of adjacent downstream exons

2018 · Mina Nakama, Hiroki Otsuka, et al. · Gene · 17

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

2017 · Hideo Sasai, Yuka Aoyama, et al. · Journal of Inherited Metabolic Disease · 14

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

2016 · Hiroki Otsuka, Hideo Sasai, et al. · The Tohoku Journal of Experimental Medicine · 13

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Combined Ketamine and Midazolam Versus Midazolam Alone for Initial Treatment of Pediatric Generalized Convulsive Status Epilepticus (Ket-Mid Study): A Randomized Controlled Trial

2025 · Amr A. Othman, Abdelrahim A. Sadek, et al. · Pediatric Neurology · 10

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

2020 · Yasuhiko Ago, Hiroki Otsuka, et al. · Experimental and Therapeutic Medicine · 10

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A Turkish Patient With Succinyl-CoA:3-Oxoacid CoA Transferase Deficiency Mimicking Diabetic Ketoacidosis

2016 · Sahin Erdol, Mehmet Ture, et al. · Journal of Inborn Errors of Metabolism and Screening · 10

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Needs assessment for faculty development at an Egyptian medical school: a triangulation approach

2020 · Elsayed Abdelkreem, Seham A. Abo-Kresha, et al. · International Journal of Community Medicine and Public Health · 9

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

2023 · Heba A. Ahmed, Eman M. Fahmy, et al. · Pediatric Blood & Cancer · 8

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

2019 · Yasuhiko Ago, Hideo Sugie, et al. · JIMD Reports · 8

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

2019 · Morteza Alijanpour, Hideo Sasai, et al. · JIMD Reports · 7

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

2017 · Elsayed Abdelkreem, Hanna Alobaidy, et al. · Egyptian Journal of Medical Human Genetics · 7

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

2024 · Elsayed Abdelkreem, Maha Emad Ibrahim, et al. · Journal of Empirical Research on Human Research Ethics · 6

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A novel mutation (c.121-13T>A) in the polypyrimidine tract of the splice acceptor site of intron 2 causes exon 3 skipping in mitochondrial acetoacetyl-CoA thiolase gene

2017 · Yuka Aoyama, Hideo Sasai, et al. · Molecular Medicine Reports · 6

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Single‐nucleotide substitution T to A in the polypyrimidine stretch at the splice acceptor site of intron 9 causes exon 10 skipping in the ACAT 1 gene

2017 · Hideo Sasai, Yuka Aoyama, et al. · Molecular Genetics & Genomic Medicine · 6

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Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disorders

2024 · Elisa Cali, Tania Quirin, et al. · Genetics in Medicine · 5

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Clinico-Radiological Correlation in 26 Egyptian Children with Glutaric Acidemia Type 1

2021 · Abdelrahim A. Sadek, Mohammed A. Aladawy, et al. · Neuropediatrics · 4

Works count: 79

Citation count: 448

H-index: 12

I10-index: 15