3M Syndrome: A Rare Cause of Short Stature von Essaddam, Leïla, Becher, Saayda Ben

Volltext

Vitamin D status and VDR gene polymorphisms in patients with growth hormone deficiency: A case control Tunisian study von Tombari, Sarra, Amri, Yessine, Hasni, Yosra, Hadj Fredj, Sondess, Salem, Yesmine, Ferchichi, Salima, Essaddam, Leila, Messaoud, Taieb, Dabboubi, Rym

Volltext

Retrospective Analysis of Clinical Characteristics and Disease Outcomes in Children and Adolescents Hospitalized Due to COVID-19 Infection in Tunisia von Borgi, Aida, Meftah, Khaoula, Trabelsi, Ines, Kyaw, Moe H, Zaghden, Hela, Bouafsoun, Aida, Mezghani, Fatma, Missaoui, Nada, Abdel Ali, Alya, Essaddam, Leila, Khemiri, Haifa, Haddad-Boubaker, Sondes, Boussetta, Khedija, Khemiri, Monia, Ben Becher, Saida, Boukthir, Samir, Triki, Henda, Menif, Khaled, Smaoui, Hanen

Volltext

A rare cause of cyanosis: Congenital methemoglobinemia von Guedri, Rahma, Missaoui, Nada, Essaddam, Leila, Ben Becher, Saayda

Volltext

Validation of the Arabic and Tunisian Arabic version of the KINDL questionnaires for children with diabetes type 1 von Essaddam, Leïla, Ben Mansour, Asma, Ben Amor, Arwa, Ravens-Sieberer, Ulribe, Klein, Toni Maria, Ben Becher, Saayda

Volltext

Congenital hypothyroidism presenting with reversible renal impairment: an under-recognised problem? von Essaddam, Leïla, Ben Mansour, Asma, Missaoui, Nada, Guedri, Rahma, Mattoussi, Nadia, Fitouri, Zohra, Ben Becher, Saayda

Volltext

Central System Nervous Tuberculosis in Infants von Tinsa, Faten, Essaddam, Leila, Fitouri, Zohra, Boussetta, Khadija, Ben Becher, Saida, Bousnina, Souad

Volltext

Implementation of effective transition from pediatric to adult diabetes care: epidemiological and clinical characteristics—a pioneering experience in North Africa von Essaddam, Leïla, Kallali, Wafa, Jemel, Manel, Kandara, Hager, Kammoun, Inès, Hsairi, Mohamed, Ben Salem, Leïla, Ben Becher, Saayda

Volltext

SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype von Motta, Marialetizia, Fasano, Giulia, Gredy, Sina, Brinkmann, Julia, Bonnard, Adeline Alice, Simsek-Kiper, Pelin Ozlem, Gulec, Elif Yilmaz, Essaddam, Leila, Utine, Gulen Eda, Guarnetti Prandi, Ingrid, Venditti, Martina, Pantaleoni, Francesca, Radio, Francesca Clementina, Ciolfi, Andrea, Petrini, Stefania, Consoli, Federica, Vignal, Cédric, Hepbasli, Denis, Ullrich, Melanie, de Boer, Elke, Vissers, Lisenka E.L.M., Gritli, Sami, Rossi, Cesare, De Luca, Alessandro, Ben Becher, Saayda, Gelb, Bruce D., Dallapiccola, Bruno, Lauri, Antonella, Chillemi, Giovanni, Schuh, Kai, Cavé, Hélène, Zenker, Martin, Tartaglia, Marco

Volltext

A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients von Ben-Khemis, Leila, Mekki, Najla, Ben-Mustapha, Imen, Rouault, Karen, Mellouli, Fethi, Khemiri, Monia, Bejaoui, Mohamed, Essaddam, Leila, Ben-Becher, Saayda, Boughamoura, Lamia, Hassayoun, Saida, Ben-Ali, Meriem, Barbouche, Mohamed-Ridha

Volltext

Inherited bisalbuminemia with growth hormone deficiency von Dabboubi, Rym, Amri, Yessine, Sahli, Chaima, Fredj, Sondess Hadj, Essaddam, Leila, Zoghlami, Ala, Ben Becher, Saida, Messaoud, Taieb

Volltext

Abdominal Tuberculosis in Children von Tinsa, Faten, Essaddam, Leila, Fitouri, Zohra, Brini, Ines, Douira, Wiem, Becher, Saida Ben, Boussetta, Khadija, Bousnina, Souad

Volltext

Validation of the Arabic and Tunisian Arabic version of the KINDL questionnaires for children with diabetes type 1 von Essaddam, Leila, Mansour, Asma, Amor, Arwa, Ravens-Sieberer, Ulrike, Klein, Toni, Becher, Saayda

Volltext

Characteristics and etiologies of short stature in children: Experience of an endocrine clinic in a Tunisian tertiary care hospital von Essaddam, Leïla, Kallali, Wafa, Cherifi, Emna, Guedri, Rahma, Mattoussi, Nadia, Fitouri, Zohra, Ben Becher, Saayda

Volltext

Prevalence and risk factors of overweight and obesity in elementary schoolchildren in the metropolitan region of Tunis, Tunisia von BOUKTHIR, Samir, ESSADDAM, Leila, ZOUARI, Bechir, SONIA MAZIGH MRAD, LAMIA BEN HASSINE, GANNOUNI, Souha, NESSIB, Fayrouz, BOUAZIZ, Asma, BRINI, Ines, SAMMOUD, Azza, BOUYAHYA, Olfa

Volltext

EXTRA-PULMONARY TUBERCULOSIS IN CHILDREN: A STUDY OF 41 CASES von TINSA, Faten, ESSADDAM, Leila, FITOURI, Zohra, NOUIRA, Faouzi, DOUIRA, Wiem, SAIDA BEN BECHER, BOUSSETTA, Khadija, BOUSNINA, Souad

Volltext

A rare cause of cyanosis: Congenital methemoglobinemia von Guedri, Rahma, Missaoui, Nada, Essaddam, Leila, Ben Becher, Saayda

Volltext

Inherited bisalbuminemia with growth hormone deficiency von Dabboubi, Rym, Amri, Yessine, Sahli, Chaima, Fredj, Sondess Hadj, Essaddam, Leila, Zoghlami, Ala, Ben Becher, Saida, Messaoud, Taieb

Volltext

Congenital hypothyroidism presenting with reversible renal impairment: an under-recognised problem? von Essaddam, Leïla, Ben Mansour, Asma, Missaoui, Nada, Guedri, Rahma, Mattoussi, Nadia, Fitouri, Zohra, Ben Becher, Saayda

Volltext