Zobrazeno 1 - 10
of 156
pro vyhledávání: '"H, Jemni"'
Autor:
Jalel Chemli, Nadia Mama, S. Abroug, N. Arifa, Nesrine Jammeli, N. Zouari, H. Jemni, H. Ajmi, Sameh Mabrouk, S. Hassayoun
Publikováno v:
Archives de Pédiatrie. 28:638-646
Background Acute disseminated encephalomyelitis (ADEM) is an inflammatory demyelinating disorder of the central nervous system. Little information is available about the clinical and neuroradiological profile or the follow-up of this disease in Tunis
Akademický článek
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Autor:
I Hasni Bouraoui, N Arifa, M Gaha, W Kermani, K Mrad Dali, H Jemni, H Hmouda, K Tlili Graiess
Publikováno v:
Journal of the Belgian Society of Radiology, Vol 95, Iss 1, Pp 6-9 (2012)
Sternocleidomastoid tumor of infancy (SCMTI) is a rare cause of benign neck masses in neonates and infants. It has to be differentiated from other congenital space-occupying lesions in the cervical region. 'Patients and methods: 'The files of 13 infa
Externí odkaz:
https://doaj.org/article/ae6b241084154098a9023c2633c26316
Autor:
Saoussen Abroug, Nadia Mama, Miniar Tfifha, T. Kamoun, N. Zouari, Sarra Mestiri, H. Jemni, S. Hassayoun
Publikováno v:
The Turkish journal of pediatrics. 61(6)
Tfifha M, Kamoun T, Mama N, Mestiri S, Hassayoun S, Zouari N, Jemni H, Abroug S. Childhood sclerosing cholangitis associations in a Tunisian tertiary care hospital: a many-faceted disease. Turk J Pediatr 2019; 61: 905-914. Sclerosing cholangitis (SC)
Autor:
Kaouther Chatti, R. Sfar, Y. Ben Cheikh, M. Ben Fradj, Z. Jemni, T. Dardouri, H. Jemni, M. Taktak, A. Yaacoub, H. Charfi
Publikováno v:
Médecine Nucléaire. 45:220
Les tumeurs neuroendocrines thymiques (TNET) sont des tumeurs rares, decrites aussi sous le terme de carcinoide thymique. Elles representent 0,4 a 2 % de l’ensemble des tumeurs neuroendocrines (TNE). Nous presentons, a travers un cas, l’aspect sc
Autor:
Z. Jemni, A. Yaacoub, S. Mensi, T. Dardouri, H. Jemni, A. Bettaieb, Kaouther Chatti, N. Arifa, W. Touila, H. Boudrigua
Publikováno v:
Médecine Nucléaire. 45:201
Autor:
Manel Nouira, H. Jemni, T. Dardouri, I. Dhieb, H. Charfi, Z. Jemni, G. Baazoug, I. Hasni, Kaouther Chatti, A. Mustapha
Publikováno v:
Médecine Nucléaire. 45:230
Introduction L’histiocytose langerhansienne (HL) est une maladie rare qui touche principalement l’enfant et l’adulte jeune. L’atteinte osseuse peut etre uni- ou multifocale. Nous rapportons les aspects en scintigraphie osseuse, SPECT-CT et IR
Pilocytic astrocytoma mimicking cavernous angioma: Imaging features and histological characteristics
Publikováno v:
Neurochirurgie. 63:330-333
Pilocytic astrocytoma (PA) commonly occurs during the first two decades of life. Typical locations include cerebellum, optic nerve, optic chiasm/hypothalamus and brainstem. PA should be considered in the differential diagnosis of patients with brain
Autor:
N. Zouari, Jalel Chemli, S. Hassayoun, Wided Gamaoun, Mehdi Gaha, H. Jemni, Sameh Mabrouk, Miniar Tfifha, Saoussen Abroug
Publikováno v:
The Turkish journal of pediatrics. 59(4)
Tfifha M, Gaha M, Gamaoun W, Chemli J, Mabrouk S, Hassayoun S, Zouari N, Jemni H, Abroug S. Clinical and imaging features of malignant infantile osteopetrosis. Turk J Pediatr 2017; 59: 452-457. Human osteopetrosis is a rare genetic disorder caused by
Autor:
Nada Garrouche, N. Arifa, H. Jemni, Amel Ben Abdallah, I. Hasni, Waad Ben Farhat, Sana Ben Amor, Yasser Ben Cheikh
Publikováno v:
Insights into Imaging
Insights into Imaging, Vol 9, Iss 5, Pp 661-671 (2018)
Insights into Imaging, Vol 9, Iss 5, Pp 661-671 (2018)
Neurofibromatosis type 1 (NF1) is one of the most common genetic disorders. Gastrointestinal manifestations of NF-1 are seldom thought of in routine clinical practice and might thus be significantly under-recognised. Their heterogeneous spectrum rang