Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Vladimir M. Kenis"'
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
Publikováno v:
Вестник восстановительной медицины, Vol 21, Iss 4, Pp 79-87 (2023)
INTRODUCTION. Biomechanical abnormalities caused by limb length discrepancy are controversial problems of pediatric orthopedics.AIM. To assess the influence of limb length discrepancy and its compensation in children on the amplitude of pelvic motion
Externí odkaz:
https://doaj.org/article/d70febbf8b6d435fa8b74c16232c281d
Autor:
Daria A. Petrova, Vladimir M. Kenis
Publikováno v:
Travmatologiâ i Ortopediâ Rossii, Vol 28, Iss 3, Pp 97-105 (2022)
Background. Measurement of the length of the lower extremities is an important part of the assessment of the musculoskeletal system. If there is a discrepancy in the length of the legs, the accuracy of the measurement technique will determine the cho
Externí odkaz:
https://doaj.org/article/a644acdb4ea84490a3674c4a3eaac7f5
Autor:
Dmitry V. Ivanov, Anna I. Ostrun, Vladimir M. Kenis, Tatiana V. Markova, Ekaterina Yu. Zakharova
Publikováno v:
Вопросы современной педиатрии, Vol 20, Iss 6s, Pp 602-610 (2021)
Background. Mucopolysaccharidosis type VI (MPS VI, Maroteaux–Lamy syndrome) is rare autosomal-recessive multisystem disease, one of the group of lysosomal storage diseases. The MPS VI pathogenesis is determined by arylsulfatase B enzyme deficiency
Externí odkaz:
https://doaj.org/article/e6e5518aa9704b3695bb4783b93277b9
Publikováno v:
Педиатрическая фармакология, Vol 18, Iss 5, Pp 346-358 (2021)
Background. Mobile flat foot etiology and its correlations with postural imbalance remain topical issues for now, especially in children with generalized joint hypermobility. Additionally, it is poorly known that complaints prevail in children with m
Externí odkaz:
https://doaj.org/article/8a6919d582294b8697dfc69b686390dc
Autor:
Tatyana V. Markova, Vladimir M. Kenis, Evgeniy V. Melchenko, Peter A. Sparber, Marina S. Petukhova, Igor O. Bychkov, Tatyana S. Nagornova, Olga L. Shatokhina, Elena L. Dadali
Publikováno v:
Travmatologiâ i Ortopediâ Rossii, Vol 27, Iss 3, Pp 71-83 (2021)
Introduction. Desbuquois dysplasia is a rare skeletal dysplasia with an autosomal recessive inheritance, resembling to the group of multiple joint dislocations. The disease is caused by mutations in the CANT1 and XYLT1 genes, the protein products of
Externí odkaz:
https://doaj.org/article/bf1dfd3e1b1e4ddd8249e3cf94d73f95
Autor:
Tatiana V. Markova, Vladimir M. Kenis, Evgenii V. Melchenko, Dmitry A. Reshchikov, Aynur E. Alieva, Darya V. Osipova, Liudmila A. Bessonova, Tatiana S. Nagornova, Natalya N. Vasserman, Natalya Yu. Ogorodova, Olga A. Shchagina, Elena L. Dadali
Publikováno v:
Pediatric Traumatology, Orthopaedics and Reconstructive Surgery. 11:17-28
BACKGROUND: Achondroplasia and pseudoachondroplasia are hereditary systemic skeletal dysplasias characterized by a certain similarity of clinical manifestations; however, they have different etiopathogenetic mechanisms and confirmation methods for mo
Autor:
Alena Yu. Dimitrieva, Vladimir M. Kenis, Irina Yu. Klychkova, Andrey V. Sapogovskiy, Vadim V. Kozhevnikov
Publikováno v:
Pediatric Traumatology, Orthopaedics and Reconstructive Surgery. 11:49-66
BACKGROUND: To date, there is no consensus regarding the diagnostics of flatfoot in children and approaches to its classification and treatment. AIM: This study aimed to demonstrate the results of the first Russian consensus, performed according to t
Autor:
Olga E. Agranovich, Ekaterina V. Petrova, Svetlana I. Trofimova, Sergey F. Batkin, Evgeniya A. Kochenova, Vladimir M. Kenis, Andrey V. Sapogovskiy, Evgenii V. Melchenko, Konstantin A. Afonichev, Evgeniy D. Blagoveschenskiy
Publikováno v:
Pediatric Traumatology, Orthopaedics and Reconstructive Surgery. 11:29-38
BACKGROUND: The absence of active elbow flexion is the most common problem in children with amyoplasia, leading to daily living difficulties. Many variants of muscle transfer are used for the restoration of active elbow flexion. The pectoralis major
Publikováno v:
L.O. Badalyan Neurological Journal. 3:135-142
Introduction. Intraneural synovial cyst is a rare pathological condition, which can be symptomatic due to the compression of the neighboring structures, including the peroneal nerve. The purpose of this publication is to present a clinical case of in