Zobrazeno 1 - 10
of 155
pro vyhledávání: '"Ali Al Kaissi"'
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:
V. M. Kenis, E. V. Melchenko, T. V. Markova, Ali Al Kaissi, A. V. Sapogovskiy, O. V. Agranovich, E. V. Petrova
Publikováno v:
Travmatologiâ i Ortopediâ Rossii, Vol 27, Iss 2, Pp 34-43 (2021)
Background. Despite the success in the treatment of children with mucopolysaccharidoses (MPS) as a result of the widespread of enzyme replacement therapy and hematopoietic stem cells transplantation, orthopedic manifestations continue to be a signifi
Externí odkaz:
https://doaj.org/article/e243b276f82b48b381df0a7fdafacee4
Autor:
Mohammad Shboul, Hela Sassi, Houweyda Jilani, Imen Rejeb, Yasmina Elaribi, Syrine Hizem, Lamia Ben Jemaa, Marwa Hilmi, Susanna Gerit Kircher, Ali Al Kaissi
Publikováno v:
AIMS Molecular Science, Vol 8, Iss 1, Pp 76-85 (2021)
Objective: Osteochondrodysplasias are a heterogeneous group of genetic skeletal dysplasias. Mutations in the COL2A1 gene cause a spectrum of rare autosomal-dominant type II collagenopathies characterized by skeletal dysplasia, short stature, and wit
Externí odkaz:
https://doaj.org/article/9c3c872dcc524ba59cff224ed5df0062
Autor:
Ali Al Kaissi, Marwa Hilmi, Zulfiya Betadolova, Sami Bouchoucha, Svetlana Trofimova, Mohammad Shboul, Guseyn Rustamov, Wiam Dwera, Katharina Sigl, Vladimir Kenis, Susanne Gerit Kircher
Publikováno v:
African Journal of Paediatric Surgery, Vol 18, Iss 4, Pp 224-230 (2021)
Background: Infantile systemic hyalinosis (ISH) is an autosomal recessively inherited disorder. The classical natural history of the disease is characterised by hypotonia, multiple contractures, skin lesions, osteopenia, joint pain, bone fractures, p
Externí odkaz:
https://doaj.org/article/11666cef287646cda2cd50ae5c176c17
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, Maher Ben Ghachem, Vladimir Kenis, Eugene Melchenko, Franz Grill, Rudolf Ganger, Susanne Gerit Kircher
Publikováno v:
African Journal of Paediatric Surgery, Vol 16, Iss 1, Pp 23-28 (2019)
Background: Trendelenburg's gait can be observed in Legg-Calvé-Perthes disease, antalgic gait observed in osteoarthropathy and waddling gait is usually seen in genu varum and circumduction gait in patients with genu valgum. Disabling pain was a prim
Externí odkaz:
https://doaj.org/article/21945b2a3c7b423ea2527201d5b95339
Autor:
Ali Al Kaissi, Nabil Nassib, Sami Bouchoucha, Mohammad Shboul, Franz Grill, Susanne Gerit Kircher, Polina Ochirova, Sergey Ryabykh
Publikováno v:
Diagnostics, Vol 12, Iss 7, p 1672 (2022)
Purpose: Torticollis is not of uncommon occurrence in orthopaedic departments. Various theories and studies concerning the pathogenesis of the deformity have been suggested. We aimed to highlight and discuss the underlying cervical and spine malforma
Externí odkaz:
https://doaj.org/article/584d604510c24b56beadf1866f7ef415