Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Amel Tej"'
Autor:
Mohamed Amine El Ghali, Ons Kaabia, Zaineb Ben Mefteh, Maha Jgham, Amel Tej, Asma Sghayer, Amine Gouidar, Afra Brahim, Rafik Ghrissi, Rached Letaief
Publikováno v:
The Pan African Medical Journal, Vol 30, Iss 212 (2018)
The occurrence of acute appendicitis during pregnancy may pose diagnostic and therapeutic difficulties. In fact pregnancy can make the clinical diagnosis delicate and the use of morphological examinations is still subject to controversy. The debates
Externí odkaz:
https://doaj.org/article/377ba0876fa040268dbba93b282967bb
Autor:
Sameh Ghorbel, Samia Tilouche, Saima Khenis, Manel Marzouk, Nejla Soyah, Amel Tej, Raoudha Kebaili, Maroua abdelbari, Hajer Benbelgacem, Jihene Bouguila, Houneida Zaghouani, Neila Hannachi, Abassi Bakir Dejla, Asma Ammar, Mansour Njah, Jalel Boukadida, Lamia Boughamoura
Publikováno v:
F1000Research. 11:1215
Background: Data reported from several countries show that both children and adolescents accounted for less than 2% of symptomatic cases of Coronavirus disease 2019 (COVID-19). The study objective was to describe the clinical characteristics of child
Publikováno v:
Endocrine Abstracts.
Autor:
Faiza Fakhfakh, Emna Mkaouar-Rebai, Leila Keskes, Marwa Ammar, Amel Tej, Rahma Felhi, Jihene Bouguila, Senda Majdoub, Mouna Tabbebi, Samia Tilouche, Marwa Maalej, Boudour Khabou, Lamia Boughamoura
Publikováno v:
Biochemical and Biophysical Research Communications. 495:1730-1737
Deficiency of the mitochondrial enzyme succinyl COA ligase (SUCL) is associated with encephalomyopathic mtDNA depletion syndrome and methylmalonic aciduria. This disorder is caused by mutations in both SUCL subunits genes: SUCLG1 (α subnit) and SUCL
Autor:
Hajer Ben Belgacem, Lamia Boughamoura, Raoudha Kebaili, Samia Ben Hassan, Koussay Eleuch, Abdelatif Nouri, Sana Alilech, Amel Tej, Yosra Hasni
Publikováno v:
Endocrine Abstracts.
Autor:
Najla Soyah, Bernd Dworniczak, Jihene Bouguila, Samia Tilouche, Asma Marzouk, Amel Tej, Moez Gribaa, Lamia Boughamoura
Publikováno v:
Open Journal of Pediatrics. :290-294
Hypomagnesemia with secondary hypocalcemia (HSH) is a rare inherited disorder, characterized by extremely low levels of serum magesium associated with symptomatic hypocalcemia. HSH manifests in the new born period with neurological symptoms, includin