Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sayda, Ben Becher"'
Autor:
Sonia, Halioui-Louhaichi, Ons, Azzabi, Nadia, Mattoussi, Hasna, Labiadh, Khadija, Bousseta, Neji, Tebib, Taher, Gargah, Sayda, Ben Becher, Mohamed Ridha, Barbouch, Mohamed, Bejaoui, Ahmed, Maherzi
Publikováno v:
La Tunisie medicale. 94(4)
Background Primary immunodeficiencies (PID) are a group of heterogeneous and relatively rare diseases. Aim to determine the clinical characteristics, outcome and genetic data of primary immunodeficiencies in pediatrics patients. Methods A retrospecti
Publikováno v:
Journal of Cosmetology & Trichology.
Objective: Cradle cap is a multifactorial pediatric skin condition characterized by inflammation, irritation, and scalp flaking. The aim of this international, phase III, open-labeled, randomized, parallel-group study was to demonstrate the efficacy
Publikováno v:
La Tunisie medicale. 86(10)
The chronic primary adrenal insufficiency or Addison's disease is uncommon in children and belongs generally to a complex syndrome.Study of the clinical and aetiological features of primary adrenal insufficiencies in children.In a retrospective study
Autor:
Olfa, Bouyahia, Ibtissem, Khelifi, Sonia Mrad, Mazigh, Lamia, Gharsallah, Beji, Chaouachi, Mourad, Hamzaoui, Sihem, Barsaoui, Sayda, Ben Becher, Souad, Bousnina, Samir, Boukthir, Azza Sammoud, El Gharbi
Publikováno v:
La Tunisie medicale. 86(2)
Cholestasis in infant constitutes an heterogeneous group of disease; diagnosis and management are often difficult. THE AIM of the study is to describe clinical, paraclinical characteristics and outcome of infants hospitalized for cholestasis in child
Publikováno v:
La Tunisie medicale. 84(10)
Severe hyperlipidaemia in presenting diabetic ketoacidosis was rarely reported in child. We report the case of a three-year-old girl with presenting diabetic ketoacidosis. Family history was negative for hyperlipidaemia. Serum was creamy pink in gros