Management of progressive genu varum in a patient with Dyggve-Melchior-Clausen syndrome

por Kenis, Vladimir, Baindurashvili, Alexey, Melchenko, Evgeniy, Grill, Franz, Al Kaissi, Ali
Publicado 2011

Spinal and extraspinal deformities in a patient with dysspondyloenchondromatosis

por Kenis, Vladimir, Baindurashvili, Alexey, Melchenko, Evgeniy, Ganger, Rudolf, Grill, Franz, Al Kaissi, Ali
Publicado 2013

Leri-Weill Dyschondrosteosis Syndrome: Analysis via 3DCT Scan

por Al Kaissi, Ali, Shboul, Mohammad, Kenis, Vladimir, Grill, Franz, Ganger, Rudolf, Kircher, Susanne Gerit
Publicado 2019

Tomographic Study of the Malformation Complex in Correlation With the Genotype in Patients With Robinow Syndrome: Review Article

por Kaissi, Ali Al, Kenis, Vladimir, Shboul, Mohammad, Grill, Franz, Ganger, Rudolf, Kircher, Susanne Gerit
Publicado 2020

Progressive Deformity of the Lower Limbs in a Patient with KID (Keratitis-Ichthyosis-Deafness) Syndrome

por Kozhevnikov, Oleg, Kralina, Svetlana, Yurasova, Yulia, Kenis, Vladimir, Kircher, Susanne Gerit, Al Kaissi, Ali
Publicado 2020

Corrections of diverse forms of lower limb deformities in patients with mucopolysaccharidosis type IVA (Morquio syndrome)

por Al Kaissi, Ali, Kenis, Vladimir, Melchenko, Eugeniy, Ghachem, Maher Ben, Csepan, Robert, Grill, Franz, Ganger, Rudolf
Publicado 2016

Massive Axial and Appendicular Skeletal Deformities in Connection with Gorham-Stout Syndrome

por Al Kaissi, Ali, Bouchoucha, Sami, Shboul, Mohammad, Kenis, Vladimir, Grill, Franz, Ganger, Rudolf, Kircher, Susanne Gerit
Publicado 2019

The Diversity of the Clinical Phenotypes in Patients With Fibrodysplasia Ossificans Progressiva

por Al Kaissi, Ali, Kenis, Vladimir, Ben Ghachem, Maher, Hofstaetter, Jochen, Grill, Franz, Ganger, Rudolf, Kircher, Susanne Gerit
Publicado 2016

A Constellation of Orthopaedic Deformities in Connection with Cartilage Oligomeric Matrix Protein Mutation

por Al Kaissi, Ali, Ghachem, Maher Ben, Kenis, Vladimir, Melchenko, Eugene, Grill, Franz, Ganger, Rudolf, Kircher, Susanne Gerit
Publicado 2019

Addressing the need for patient-friendly medical communications: adaptation of the 2019 recommendations for the management of MPS VI and MPS IVA

por Bruce, Iain A., Ezgü, Fatih S., Kampmann, Christoph, Kenis, Vladimir, Mackenzie, William, Stevens, Bob, Walker, Robert, Hendriksz, Christian
Publicado 2022

Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia

por Al Kaissi, Ali, Ryabykh, Sergey, Kenis, Vladimir, Ben Chehida, Farid, Al Kaissi, Hamza, Kircher, Susanne Gerit, Grill, Franz
Publicado 2023

Clinical and Genetic Characteristics of COL2A1-Associated Skeletal Dysplasias in 60 Russian Patients: Part I

por Markova, Tatyana, Kenis, Vladimir, Melchenko, Evgeniy, Osipova, Darya, Nagornova, Tatyana, Orlova, Anna, Zakharova, Ekaterina, Dadali, Elena, Kutsev, Sergey
Publicado 2022

Clinical and genetic characterization of three Russian patients with pycnodysostosis due to pathogenic variants in the CTSK gene

por Markova, Tatiana Vladimirovna, Kenis, Vladimir, Melchenko, Evgeniy, Guseva, Darya, Osipova, Darya, Galeeva, Nailya, Nagornova, Tatiana, Dadali, Elena Leonidovna
Publicado 2022

Radiographic and Tomographic Analysis in Patients with Stickler Syndrome Type I

por Al Kaissi, Ali, Chehida, Farid Ben, Ganger, Rudolf, Kenis, Vladimir, Zandieh, Shahin, Hofstaetter, Jochen G, Klaushofer, Klaus, Grill, Franz
Publicado 2013

Broad Spectrum of Skeletal Malformation Complex in Patients with Cleidocranial Dysplasia Syndrome: Radiographic and Tomographic Study

por Al Kaissi, Ali, Ben Chehida, Farid, Kenis, Vladimir, Ganger, Rudolf, Radler, Christof, Hofstaetter, Jochen G., Klaushofer, Klaus, Grill, Franz
Publicado 2013

Muscle Weakness: A Misleading Presentation in Children With Distinctive Syndromic Entities (Clinical Case Reports)

por Al Kaissi, Ali, Ryabykh, Sergey, Ochirova, Polina, Kenis, Vladimir, Hofstätter, Jochen G., Grill, Franz, Ganger, Rudolf, Kircher, Susanne Gerit
Publicado 2017

Are parents of children with Cockayne syndrome manifesting features of the disorder?: Case reports

por Al Kaissi, Ali, Kuranova, Mirya, Pleskach, Nadezhda, Kenis, Vladimir, Nassib, Nabil M., Grill, Franz, Ganger, Rudolf, Gerit Kircher, Susanne
Publicado 2017

Processed pseudogene insertion in GLB1 causes Morquio B disease by altering intronic splicing regulatory landscape

por Bychkov, Igor, Kuznetsova, Antonina, Baydakova, Galina, Gorobets, Leonid, Kenis, Vladimir, Dimitrieva, Alena, Filatova, Alexandra, Tabakov, Vyacheslav, Skoblov, Mikhail, Zakharova, Ekaterina
Publicado 2022

Publisher Correction: Processed pseudogene insertion in GLB1 causes Morquio B disease by altering intronic splicing regulatory landscape

por Bychkov, Igor, Kuznetsova, Antonina, Baydakova, Galina, Gorobets, Leonid, Kenis, Vladimir, Dimitrieva, Alena, Filatova, Alexandra, Tabakov, Vyacheslav, Skoblov, Mikhail, Zakharova, Ekaterina
Publicado 2022

The Managment of cervical spine abnormalities in children with spondyloepiphyseal dysplasia congenita: Observational study

por Al Kaissi, Ali, Ryabykh, Sergey, Pavlova, Olga M., Ochirova, Polina, Kenis, Vladimir, Chehida, Farid Ben, Ganger, Rudolf, Grill, Franz, Kircher, Susanne Gerit
Publicado 2019