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

por AboKresha, Seham Ahmed, Abdelkreem, Elsayed, Ali, Rasha Abd Elhameed
Publicado 2021

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

por Abdelkreem, Elsayed, Harijan, Rajesh K., Yamaguchi, Seiji, Wierenga, Rikkert K., Fukao, Toshiyuki
Publicado 2019

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

por Abdelkreem, Elsayed, Mahmoud, Shaimaa M., Aboelez, Moustafa O., Abd El Aal, Mohamed
Publicado 2021

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

por Ago, Yasuhiko, Sugie, Hideo, Fukuda, Tokiko, Otsuka, Hiroki, Sasai, Hideo, Nakama, Mina, Abdelkreem, Elsayed, Fukao, Toshiyuki
Publicado 2019

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

por Sasai, Hideo, Aoyama, Yuka, Otsuka, Hiroki, Abdelkreem, Elsayed, Nakama, Mina, Hori, Tomohiro, Ohnishi, Hidenori, Turner, Lesley, Fukao, Toshiyuki
Publicado 2017

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

por Alijanpour, Morteza, Sasai, Hideo, Abdelkreem, Elsayed, Ago, Yasuhiko, Soleimani, Shima, Moslemi, Leila, Yamaguchi, Seiji, Rezapour, Masomeh, Hakimi, Mohammad T., Matsumoto, Hideki, Fukao, Toshiyuki
Publicado 2019

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

por 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
Publicado 2020