Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Saayda Ben Becher"'
Publikováno v:
Clinical Case Reports, Vol 9, Iss 7, Pp n/a-n/a (2021)
Abstract Congenital Methemoglobinemia is a rare condition that may mimic congenital heart diseases. There are two types of congenital Methemoglobinemia. The type I is usually benign. The enzyme deficiency is limited to red blood cells. Clinically, th
Externí odkaz:
https://doaj.org/article/f05505bac675487b84d437197d65fc63
Autor:
Leïla Essaddam, Asma Ben Mansour, Arwa Ben Amor, Ulribe Ravens-Sieberer, Toni Maria Klein, Saayda Ben Becher
Publikováno v:
Libyan Journal of Medicine, Vol 14, Iss 1 (2019)
Aim: We aimed to validate the Arabic and Tunisian Arabic versions of diabetes- specific quality of life (QOL) instrument KINDL-R Diabetes Module for Tunisian children population with type 1 diabetes. Patients and methods: This a cross-sectional study
Externí odkaz:
https://doaj.org/article/c11a754d0e804c9e9036bbe57770a144
Autor:
Leila Essaddam, Ons Zitouni, Lilia Kraoua, Madiha Trabelsi, Hella Sassi, Sana Kmiha, Fatma Charfi, Dorra El Guiche, Raoudha Kebaïli, Nesrine Jaballah, Maroua Rjeb, Noura Zouari, Yasmina El Aribi, Syrine Hizem, Salmen Wannes, Ibtihel Fkih Romdhane, Mohamed Tahar Sfar, Hechmi Ben Hamouda, Radhia Hadj Salem, Zied Khlayfia, Tarek Khmiss, Kamel Monastiri, Nadia Siala, Slaheddine Chouchane, Habib Souaa, Inès Khochtali, Bahri Mahjoub, Habib Sfar, Lamia Ben Jemâa, Saoussen Abroug, Lamia Boughamoura, Inès Kamoun, Thouraya Kamoun, Ridha Mrad, Saayda Ben Becher
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism.
Objectives Early diagnosis in Turner syndrome is desirable to optimize growth and puberty and yet, it is often made late. Here, we aim to identify age at diagnosis, clinical features at presentation and potential strategies to improve the care of TS
Publikováno v:
Rheumatology. 60
Background Multisystem inflammatory syndrome in children (MIS-C) is a severe immune-mediated syndrome that occurs after COVID-19 infection. It mainly affects children and presents several clinical aspects. The cutaneous and mucous signs are very much
Publikováno v:
Clinical Case Reports, Vol 9, Iss 7, Pp n/a-n/a (2021)
Clinical Case Reports
Clinical Case Reports
Congenital Methemoglobinemia is a rare condition that may mimic congenital heart diseases. There are two types of congenital Methemoglobinemia. The type I is usually benign. The enzyme deficiency is limited to red blood cells. Clinically, the patient
Autor:
Mohamed Hsairi, Saayda Ben Becher, Hager Kandara, Leïla Ben Salem, Manel Jemel, Wafa Kallali, Inès Kammoun, L. Essaddam
Publikováno v:
Acta Diabetologica. 55:1163-1169
Type 1 diabetes is increasing in children leading more T1D young adults to adult healthcare settings. This change is experienced as a tear and results in a disengagement from specialist services. This study reports on an implementation of an effectiv
Autor:
Leïla, Essaddam, Saayda Ben, Becher
Publikováno v:
Indian pediatrics. 56(9)
Autor:
Emna Cherifi, L. Essaddam, Wafa Kallali, R. Guedri, Z. Fitouri, Saayda Ben Becher, Nadia Mattoussi
Publikováno v:
International Journal of Pediatrics & Adolescent Medicine
International Journal of Pediatrics and Adolescent Medicine, Vol 7, Iss 2, Pp 74-77 (2020)
International Journal of Pediatrics and Adolescent Medicine, Vol 7, Iss 2, Pp 74-77 (2020)
Background Short stature is a common reason for referral to pediatric endocrinology clinics. It may be a manifestation of a pathological condition requiring early treatment. The aim of this study was to describe the characteristics and etiologies of
Autor:
Toni Maria Klein, Saayda Ben Becher, Asma Mansour, Arwa Ben Amor, Ulrike Ravens-Sieberer, L. Essaddam
Publikováno v:
Libyan Journal of Medicine; Vol 14, No 1 (2019); 1-7
The Libyan Journal of Medicine
Libyan Journal of Medicine, Vol 14, Iss 1 (2019)
The Libyan Journal of Medicine
Libyan Journal of Medicine, Vol 14, Iss 1 (2019)
Aim : We aimed to validate the Arabic and Tunisian Arabic versions of diabetes- specific quality of life (QOL) instrument KINDL-R Diabetes Module for Tunisian children population with type 1 diabetes. Patients and methods : This a cross-sectional stu
Autor:
Najla Mekki, Mohamed Bejaoui, Mohamed-Ridha Barbouche, Meriem Ben-Ali, S. Hassayoun, Saayda Ben-Becher, Karen Rouault, Fethi Mellouli, Lamia Boughamoura, Imen Ben-Mustapha, Monia Khemiri, Leila Ben-Khemis, Leila Essaddam
Publikováno v:
Molecular immunology. 90
Phosphoglucomutase 3 (PGM3) protein catalyzes the conversion of N-acetyl-d-glucosamine-6-phosphate (GlcNAc-6-P) to N-acetyl-d-glucosamine-1-phosphate (GlcNAc-1-P), which is required for the synthesis of uridine diphosphate N-acetylglucosamine (UDP-Gl