Clinical outcomes in an adult patient with mannose phosphate isomerase-congenital disorder of glycosylation who discontinued mannose therapy

Autor: Kinza Noman, Christian J. Hendriksz, Graham Radcliffe, Federico Roncaroli, Sulleman Moreea, Afifah Hussain, Karolina M. Stepien

Publikováno v: Molecular Genetics and Metabolism Reports, Vol 25, Iss , Pp 100646- (2020)

The mannose phosphate isomerase-congenital disorder of glycosylation (MPI-CDG) is caused by phosphomannose isomerase deficiency. Clinical features include hyperinsulinaemic hypoglycaemia, protein losing enteropathy, hepatomegaly and hepatic fibrosis,

Externí odkaz: https://doaj.org/article/0693708412b94132acfceb32145e99f7

Osteochondral Avulsion Fracture of the Femoral Origin of the Anterior Cruciate Ligament in an 11-Year-Old Child

Autor: Sunil Kumar Pai, Nayef Aslam Pervez, Graham Radcliffe

Publikováno v: Case Reports in Medicine, Vol 2012 (2012)

Although tibial end avulsions of the anterior cruciate ligament are relatively common in clinical practice, avulsions of the femoral end of this ligament are by comparison rare. We present the case of an 11-year-old boy with a bony avulsion injury, w

Externí odkaz: https://doaj.org/article/9ab87703c9464880922ac9dd870db923

Clinical outcomes in an adult patient with mannose phosphate isomerase-congenital disorder of glycosylation who discontinued mannose therapy

Autor: Federico Roncaroli, Christian J. Hendriksz, Graham Radcliffe, Kinza Noman, Sulleman Moreea, Karolina M. Stepien, Afifah Hussain

Publikováno v: Molecular Genetics and Metabolism Reports
Noman, K, Hendriksz, C J, Radcliffe, G, Roncaroli, F, Moreea, S, Hussain, A & Stepien, K M 2020, ' Clinical outcomes in an adult patient with mannose phosphate isomerase-congenital disorder of glycosylation who discontinued mannose therapy ', Molecular Genetics and Metabolism Reports, vol. 25, pp. 100646 . https://doi.org/10.1016/j.ymgmr.2020.100646
Molecular Genetics and Metabolism Reports, Vol 25, Iss, Pp 100646-(2020)

The mannose phosphate isomerase-congenital disorder of glycosylation (MPI-CDG) is caused by phosphomannose isomerase deficiency. Clinical features include hyperinsulinaemic hypoglycaemia, protein losing enteropathy, hepatomegaly and hepatic fibrosis,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29e89da12b76a43da3a98b15233df6bb
http://europepmc.org/articles/PMC7490551

Epsilon-aminocaproic acid versus tranexamic acid in total knee arthroplasty: a meta-analysis study

Autor: Raees Vanker, Graham Radcliffe, Richard Grogan, Osman Riaz, Samir Asmar, Christopher Brew, James Hahnel, Adeel Aqil

Publikováno v: Journal of Orthopaedics and Traumatology : Official Journal of the Italian Society of Orthopaedics and Traumatology
Journal of Orthopaedics and Traumatology, Vol 20, Iss 1, Pp 1-8 (2019)

Introduction Total knee arthroplasty (TKA) surgery can be associated with significant blood loss. Among the problems associated with such blood loss is the need for transfusions of banked blood [1]. Transfusions not only have a financial consequence

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cc17bf87f7c1e26185a0895fbf2d48c
https://doi.org/10.1186/s10195-019-0534-2

Quadriceps Tendon-Bone or Patellar Tendon-Bone Autografts When Reconstructing the Anterior Cruciate Ligament: A Meta-analysis

Autor: Osman Riaz, Mubusher Ali, Fahad Hossain, Ashim Mannan, Gautam Chakrabarty, Adeel Aqil, Graham Radcliffe

Publikováno v: Clinical journal of sport medicine : official journal of the Canadian Academy of Sport Medicine. 28(3)

OBJECTIVE We aimed to quantitatively assess the outcomes of studies, comparing the use of Bone-patellar tendon-bone (BPTB) and the quadriceps tendon-bone (QTB) autografts when reconstructing the anterior cruciate ligament (ACL). DATA SOURCES MEDLINE,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60e34ca3de4108c7680b3007dbefea6c
https://pubmed.ncbi.nlm.nih.gov/28654440