Zobrazeno 1 - 10
of 107
pro vyhledávání: '"Thouraya, Kamoun"'
Autor:
Hager barakizou, Gannouni Souha, Thouraya Kamoun, Muhammed Mehdi, Fernanda Amary, Zilla Huma, Anne-laure Todeschini, Reiner Veitia, Malcolm Donaldson
Publikováno v:
JCRPE, Vol 14, Iss 1, Pp 107-113 (2022)
Ovarian causes of precocious pseudo-puberty (PPP) include McCune-Albright syndrome (MAS) and juvenile granulosa cell tumour (JGCT). We describe a case of PPP in which bilateral ovarian enlargement with multiple cysts progressed to unilateral JGCT. A
Externí odkaz:
https://doaj.org/article/4316d518cba84646ad07adaa5729732a
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
Autor:
R. Belhadj, A. Ben Hlima, B. Maalej, Abdelmajid Mahfoudh, M. Weli, A. Elleuch, Thouraya Kamoun, Mohamed-Ridha Barbouche, Najla Mekki, Lamia Gargouri
Publikováno v:
Transfusion Clinique et Biologique. 27:61-64
Background and aim The aim of this study is to evaluate the clinical, biological and hematological profiles of autoimmune hemolytic anemia (AIHA) in children and to specify its etiologies, therapeutic modalities, and treatment responses. Methods This
Autor:
Tahia Boudaouara, Soumeya Bekri, Neji Tebib, Mongia Hachicha, Lobna Ayadi, Rim Ben Abdelaziz, Ines Maaloul, Imen Chabchoub, Thouraya Kamoun, Amel Ben Chehida, Hela Boudabbous
Publikováno v:
Journal of Pediatric Hematology/Oncology. 42:310-312
Hemophagocytic lymphohistiocytosis (HLH) is a rare and life-threatening hyperinflammatory condition that may be triggered by infections, autoimmune and immunologic disorders, malignancies, and metabolic diseases. Early and accurate diagnosis of HLH a
Autor:
Hager Barakizou, Gannouni Souha, Thouraya Kamoun, Muhammed Mehdi, Fernanda Amary, Zilla Huma, Anne-laure Todeschini, Reiner Veitia, Malcolm Donaldson
Publikováno v:
Journal of clinical research in pediatric endocrinology. 14(1)
Ovarian causes of precocious pseudo-puberty (PPP) include McCune-Albright syndrome (MAS) and juvenile granulosa cell tumour (JGCT). We describe a case of PPP in which bilateral ovarian enlargement with multiple cysts progressed to unilateral JGCT. A
Autor:
Souha Gannouni, Fernanda Amary, Reiner Veitia, Muhammed Mehdi, Hager Barakizou, Malcolm Donaldson, Zilla Huma, Anne-Laure Todeschini, Thouraya Kamoun
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology.
Ovarian causes of precocious pseudo-puberty (PPP) include McCune-Albright syndrome (MAS) and juvenile granulosa cell tumour (JGCT). We describe a case of PPP in which bilateral ovarian enlargement with multiple cysts progressed to unilateral JGCT. A
Autor:
Salma, Ben Ameur, Emna, Daoud, Amira, Bouraoui, Fedia, Khlif, Zaineb, Mnif, Abdelatif, Gargouri, Thouraya, Kamoun
Publikováno v:
La Tunisie medicale. 98(6)
Congenital lung malformations (CLM) include a complex range of developmental abnormalities. Currently, most are diagnosed prenatally or during early childhood.to investigate clinical and imaging findings of congenital lung malformations in children.R
Publikováno v:
La Presse Médicale. 47:483-486
Autor:
I. Jedidi, Ines Maaloul, L. Sfaihi, S. Kmiha, Thouraya Kamoun, O. Laaroussi, M. Hachicha, H. Aloulou
Publikováno v:
Transfusion Clinique et Biologique. 25:14-18
Resume But de l’etude Evaluer la prise en charge des patients atteints de beta-thalassemie majeure et preciser les differentes complications. Patients et methodes Une etude retrospective, colligeant 26 cas de beta-thalassemie majeure pris en charge
Autor:
Hajer Aloulou, Meriem Amouri, Thouraya Kamoun, S. Kmiha, Emna Bahloul, R. Guirat, Lamia Sfaihi, Khadija Sellami, Hamida Turki, Mongia Hachicha, Madiha Mseddi
Publikováno v:
Indian Journal of Dermatology, Vol 63, Iss 1, Pp 62-65 (2018)
Indian Journal of Dermatology
Indian Journal of Dermatology
Background: Bacillus Calmette-Guerin (BCG) vaccine is a widely used vaccine. Management of local BCG complications differs between clinicians, and the optimal approach remains unclear. Aims: We aim to describe the epidemiological, clinical and therap