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pro vyhledávání: '"Souha Gannouni"'
Autor:
Hager Barakizou, Souha Gannouni, Khalil Messaoui, Mathilde Difilippo, Agnès Sassolas, Fethi Bayoudh
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 17, Iss 3, Pp 251-254 (2016)
Abetalipoproteinemia (ABL), or Bassen–Kornzweig syndrome, is a rare autosomal recessive disorder of lipoprotein metabolism, characterized by fat malabsorption, hypocholesterolemia, retinitis pigmentosa, progressive neuropathy and acanthocytosis. We
Externí odkaz:
https://doaj.org/article/83b96c1b23fb43e494b888e7d7061a5b
Publikováno v:
Iranian Journal of Toxicology, Vol 10, Iss 3, Pp 1-5 (2016)
Background: Acute drug poisoning remains an important public health problem and represents the second most frequent accidental disease in children. In this study, we identified epidemiological and clinical features of children admitted for acute drug
Externí odkaz:
https://doaj.org/article/c250bed2fb4c4f608e647d5ed44fbb35
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff625537a0ea164bc279baa080621ccb
https://doi.org/10.4274/jcrpe.galenos.2021.2020.0039
https://doi.org/10.4274/jcrpe.galenos.2021.2020.0039
Autor:
Samir, Boukthir, Leila, Essaddam, Sonia, Mazigh Mrad, Lamia, Ben Hassine, Souha, Gannouni, Fayrouz, Nessib, Asma, Bouaziz, Ines, Brini, Azza, Sammoud, Olfa, Bouyahia, Bechir, Zouari
Publikováno v:
La Tunisie medicale. 89(1)
Local data about prevalence of obesity in emerging countries are rather scarce. Risk factors for obesity, well known in most industrialized countries, are poorly understood in Tunisia.To assess prevalence of overweight and obesity and to investigate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0dd71be0b0de7cec7ab0570eab632b42
https://pubmed.ncbi.nlm.nih.gov/21267829
https://pubmed.ncbi.nlm.nih.gov/21267829
Akademický článek
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Autor:
Khalil Messaoui, Hager Barakizou, Agnès Sassolas, Mathilde Difilippo, Souha Gannouni, Fethi Bayoudh
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 17, No 3 (2016); 251–254
Egyptian Journal of Medical Human Genetics, Vol 17, Iss 3, Pp 251-254 (2016)
Egyptian Journal of Medical Human Genetics, Vol 17, Iss 3, Pp 251-254 (2016)
Abetalipoproteinemia (ABL), or Bassen–Kornzweig syndrome, is a rare autosomal recessive disorder of lipoprotein metabolism, characterized by fat malabsorption, hypocholesterolemia, retinitis pigmentosa, progressive neuropathy and acanthocytosis. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ef061bfe8a1da57a3c6bb361d7b2ff3