Zobrazeno 1 - 10
of 152
pro vyhledávání: '"Rudolf, Ganger"'
Autor:
Alexandra Stauffer, Adalbert Raimann, Stefan Penzkofer, Rudolf Ganger, Christof Radler, Gabriel T. Mindler
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
BackgroundX-linked hypophosphatemia (XLH) is a rare monogenetic skeletal disorder. Lower limb deformities contribute substantially to impaired gait quality and burden of disease in patients with XLH. Standardized data regarding onset and severity of
Externí odkaz:
https://doaj.org/article/c8146e788e874b3f80154059918d2280
Autor:
Celine Akta, Florian Wenzel-Schwarz, Alexandra Stauffer, Andreas Kranzl, Adalbert Raimann, Roland Kocijan, Rudolf Ganger, Gabriel T. Mindler
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundX-linked hypophosphatemia (OMIM 307800) is a rare bone disease caused by a phosphate-wasting condition with lifelong clinical consequences. Those affected suffer from bone pain, complex skeletal deformities, impaired mobility and a reduced
Externí odkaz:
https://doaj.org/article/afd5ede4d3ce4c658bcd16853c69f5ed
Publikováno v:
Acta Orthopaedica, Vol 93 (2022)
Background and purpose: We report results and complications of gradual bone lengthening for post-traumatic lower-limb length discrepancy (LLD) with Precice intramedullary lengthening nails in 34 adults. Patients and methods: Inclusion criteria were l
Externí odkaz:
https://doaj.org/article/0be5770bab1f49d78f0c7d3d05e7e148
Autor:
Gabriel T. Mindler, Alexandra Stauffer, Andreas Kranzl, Stefan Penzkofer, Rudolf Ganger, Christof Radler, Gabriele Haeusler, Adalbert Raimann
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
BackgroundGait deviations, lower limb pain and joint stiffness represent key symptoms in patients with X-linked hypophosphatemia (XLH, OMIM 307800), a rare disorder of mineral homeostasis. While the pathomechanism for rickets is well understood, the
Externí odkaz:
https://doaj.org/article/421a326a74a542faa10669e36afd9ab7
Lower Limb Deformity and Gait Deviations Among Adolescents and Adults With X-Linked Hypophosphatemia
Autor:
Gabriel T. Mindler, Andreas Kranzl, Alexandra Stauffer, Roland Kocijan, Rudolf Ganger, Christof Radler, Gabriele Haeusler, Adalbert Raimann
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
BackgroundX-linked hypophosphatemia (XLH) is a rare genetic disorder characterized by lower limb deformity, gait and joint problems, and pain. Hence, quality of life is substantially impaired. This study aimed to assess lower limb deformity, specific
Externí odkaz:
https://doaj.org/article/699f627be92d429ea72edb33b462481e
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 MD, MSc, Vladimir Kenis MD, PhD, Mohammad Shboul PhD, Franz Grill MD, Rudolf Ganger MD, PhD, Susanne Gerit Kircher MD, MSc
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 8 (2020)
We aimed to understand the etiology behind the abnormal craniofacial contour and other clinical presentations in a number of children with Robinow syndrome. Seven children with Robinow syndrome were enrolled in this study (autosomal recessive caused
Externí odkaz:
https://doaj.org/article/6d4438a27cae4fde91e2903844915cda
Autor:
Gabriel T. Mindler, Rudolf Ganger, Alexandra Stauffer, Adalbert Raimann, Roland Kocijan, Christof Radler
Publikováno v:
Osteologie. 32:6-11
ZusammenfassungDie X-chromosomale Hypophosphatämie (XLH, OMIM 307800) ist eine seltene Knochenerkrankung, die durch Mutationen in PHEX (PHEX phosphate regulating endopeptidase X-linked) verursacht wird. Rachitis, Osteomalazie, Kleinwuchs und komplex
Publikováno v:
Foot and Ankle Surgery. 28:557-563
Background This study aimed to assess the clinical and radiographic outcomes of different surgical procedures in atraumatic osteochondrosis dissecans (OCD) of the talus in youth and adolescence. Methods 32 joints in 30 patients (mean age 14.7 ± 2.2
Publikováno v:
Die Orthopädie. 51:595-606