Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Farid Ben Chehida"'
Autor:
Ali Al Kaissi, Sergey Ryabykh, Farid Ben Chehida, Hamza Al Kaissi, Vasileios Dougales, Vladimir M. Kenis, Franz Grill
Publikováno v:
Pediatric Reports, Vol 16, Iss 2, Pp 410-419 (2024)
Background: Neither radiological phenotypic characteristics nor reconstruction CT scan has been used to study the early anatomical disruption of the cranial bone in children with the so-called idiopathic type of West syndrome. Material and Methods: T
Externí odkaz:
https://doaj.org/article/43259bbec7e54a17a7f5750213975033
Autor:
Ali Al Kaissi, Sergey Ryabykh, Vladimir Kenis, Farid Ben Chehida, Hamza Al Kaissi, Susanne Gerit Kircher, Franz Grill
Publikováno v:
Children, Vol 10, Iss 10, p 1715 (2023)
Background: The diagnostic process for children and adults manifesting a constellation of ectodermal abnormalities requires a conscientious and highly structured process. Material and Methods: Six girls (aged 6-month–8 years) and two older girls (a
Externí odkaz:
https://doaj.org/article/6571236cff734a31aed06819965da515
Autor:
Ali Al Kaissi, Sergey Ryabykh, Farid Ben Chehida, Hamza Al Kaissi, Susanne Gerit Kircher, Franz Grill, Alexander Guben
Publikováno v:
Children, Vol 10, Iss 7, p 1240 (2023)
Background: Omitting the early closure of the cranial sutures in newly born children is not an uncommon practice. We describe the natural history of several unrelated children and adults from two unrelated families. These children were born with vari
Externí odkaz:
https://doaj.org/article/d505a89f735d4fa186857cc1446d1e0a
Autor:
Ali Al Kaissi, Sergey Ryabykh, Farid Ben Chehida, Hamza Al Kaissi, Susanne Gerit Kircher, Martin J. Stransky, Franz Grill
Publikováno v:
Diagnostics, Vol 13, Iss 5, p 874 (2023)
Background: We describe patients who were recognized via conventional radiographs of the skull as manifesting wormian bones. Wormian bones are not a specific diagnostic entity and can be seen in variable forms of syndromic disorders. Materials and Me
Externí odkaz:
https://doaj.org/article/811f50d861684385b4c9c4f7dd58a5a4
Autor:
Ali Al Kaissi, Sergey Ryabykh, Nabil Nassib, Sami Bouchoucha, Lamia Benjemaa, Imen Rejeb, Syrine Hizem, Vladimir Kenis, Franz Grill, Susanne Gerit Kircher, Mohammad Shboul, Farid Ben Chehida
Publikováno v:
Diagnostics, Vol 12, Iss 10, p 2375 (2022)
Background: A long list of syndromic entities can be diagnosed immediately through scrutinizing the clinical phenotype of the craniofacial features. The latter should be assisted via proper radiological interpretations. Patients and Methods: Differen
Externí odkaz:
https://doaj.org/article/c050500642434ea7bb8e3acc6ebb24b5
Autor:
Ali Al Kaissi, Vladimir Kenis, Farid Ben Chehida, Jochen Hofstaetter, Franz Grill, Rudolf Ganger
Publikováno v:
African Journal of Paediatric Surgery, Vol 13, Iss 3, Pp 125-130 (2016)
Background: The skeletal changes in McCune-Albright disease are usually severe because of the polyostotic form of the disease. Trendelenberg gait and limited mobility are the most common presenting features. The constellation of Café-au lait spots a
Externí odkaz:
https://doaj.org/article/5244bc35aed243829f0e11de616c772a
Autor:
Ali Al Kaissi, Farid Ben Chehida, Hassan Gharbi, Mourad Jinziri, Hatem Safi, Maher Ben Ghachem, Franz Grill, Franz Varga, Klaus Klaushofer
Publikováno v:
Jornal de Pediatria, Vol 82, Iss 3, Pp 236-239 (2006)
OBJETIVO: O arqueamento das pernas geralmente é atribuído ao raquitismo causado pela carência de vitamina D; portanto, várias crianças afetadas acabam sendo classificadas erroneamente e tratadas inadequadamente. Este caso ilustra como uma avalia
Externí odkaz:
https://doaj.org/article/03e2b9beb5f54597b4c222364c4dd2d9
Autor:
Sudipto Roy, Noémi van Hul, Janine Altmüller, Hyungwon Choi, Nur'Ain Binte Ali, Xavier Bisteau, Shuhui Lim, Christian Windpassinger, Stéphane Blouin, Verena Rupp, Carine Bonnard, Franz Grill, Byrappa Venkatesh, Bruno Reversade, Rudolf Ganger, Vincenzo Coppola, S. Zakiah A. Talib, Klaus Klaushofer, Majid Alfadhel, Gökhan Yigit, Farid Ben Chehida, Paul Roschger, Ali Al Kaissi, Matias J. Caldez, Umut Altunoglu, Bernd Wollnik, Hülya Kayserili, Lionel Van Maldergem, Alvin Yu Jin Ng, Sameh A. Youssef, Lino Tessarollo, Katharina M. Roetzer, Hao Lu, Philipp Kaldis, Juliette Piard, Alain de Bruin, Sumanty Tohari
Publikováno v:
American Journal of Human Genetics
American journal of human genetics, 101(3), 391-403. Cell Press
American Journal of Human Genetics, 101(3), 391. Cell Press
American journal of human genetics, 101(3), 391-403. Cell Press
American Journal of Human Genetics, 101(3), 391. Cell Press
In five separate families, we identified nine individuals affected by a previously unidentified syndrome characterized by growth retardation, spine malformation, facial dysmorphisms, and developmental delays. Using homozygosity mapping, array CGH, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f40dd9590bfaaffdcbe2fe81c6b9ab32
https://doi.org/10.1016/j.ajhg.2017.08.003
https://doi.org/10.1016/j.ajhg.2017.08.003
Autor:
Ali Al Kaissi, Franz Grill, Eugeniy Melchenko, Klaus Klaushofer, Farid Ben Chehida, Vladimir Kenis, Rudolf Ganger
Publikováno v:
Orthopaedic Surgery. 6:274-279
Objective Accurate understanding of the cause of the underlying pathology in children with diastrophic dysplasia would help in designing targeted management of their locomotion. Methods Diastrophic dysplasia was diagnosed in twelve patients (nine gir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bcbfa4913740b336b92a34984c818f1
https://doi.org/10.1111/os.12146
https://doi.org/10.1111/os.12146
Publikováno v:
European Spine Journal. 24:594-599
Goldenhar syndrome consists of a combination of unilateral auricular appendages, auricular fistulas, and ocular epibulbar dermoids combined with a unilateral underdevelopment of the craniofacial structures and vertebral abnormalities. We aimed to eli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::464656f3b98a1b8aa977cd1152017a45
https://doi.org/10.1007/s00586-014-3204-3
https://doi.org/10.1007/s00586-014-3204-3