Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Farhana Suleman"'
Publikováno v:
South African Journal of Radiology, Vol 28, Iss 1, Pp e1-e5 (2024)
Fibrous dysplasia (FD) is a rare, non-inherited, congenital bone disorder which may be monostotic or polyostotic. The polyostotic form may rarely present in syndromic forms when associated with extra-skeletal manifestations. Mazabraud syndrome is a r
Externí odkaz:
https://doaj.org/article/e044fb925caa419896089954a56a6ad0
Publikováno v:
South African Journal of Radiology, Vol 26, Iss 1, Pp e1-e6 (2022)
Background: Pulmonary thromboembolism is one of the leading causes of maternal death worldwide. Globally there has been increasing physician reliance on CT pulmonary angiogram for definitive diagnoses and exclusion of pulmonary thromboembolism. The p
Externí odkaz:
https://doaj.org/article/51749504b4a1465baf614a0bd92a5946
Publikováno v:
Journal of the Pakistan Medical Association, Vol 72, Iss 01 (2022)
Objective: To study the effects of delta-tocotrienol on glycaemic control parameters in individuals with pre-diabetes. Method: The randomised control trial was conducted at the Armed Forces Institute of Pathology, Rawalpindi, Pakistan, from July 15
Externí odkaz:
https://doaj.org/article/9e8667c942654571adb8a9e58c81ad3c
Autor:
null Farhana Suleman, null Dilshad Ahmed Khan, null Muhammad Amjad Pervez, null Mohammad Aamir
Publikováno v:
JPMA. The Journal of the Pakistan Medical Association. 72(1)
Objective: To study the effects of delta-tocotrienol on glycaemic control parameters in individuals with pre-diabetes. Method: The randomised control trial was conducted at the Armed Forces Institute of Pathology, Rawalpindi, Pakistan, from July 15 t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f169491bf59db78c621c6acb5600436
https://pubmed.ncbi.nlm.nih.gov/35099428
https://pubmed.ncbi.nlm.nih.gov/35099428
Publikováno v:
South African Journal of Radiology, Vol 19, Iss 2, Pp e1-e5 (2015)
Heterotaxy syndrome is a rare and complex disorder of the chest and abdominal organ arrangements, and presents a diagnostic challenge to the radiologist. This article describes the morphological characteristics of heterotaxy and situs abnormalities,
Externí odkaz:
https://doaj.org/article/764432ecda23409b99af1faed0ed30ff
Autor:
Vicci du Plessis, Farhana Suleman
Publikováno v:
South African Journal of Radiology, Vol 19, Iss 2, Pp e1-e2 (2015)
The South African Society of Paediatric Imaging (SASPI) is honoured to guest edit this special issue of the SA Journal of Radiology (SAJR) in celebration of the International Day of Radiology (IDoR) on 08 November, which is dedicated to paediatrics t
Externí odkaz:
https://doaj.org/article/e75de898b7d74538a652e834316a1406
Autor:
Katarzyna A. Piróg, Paul Holden, Benedetta Gualeni, Hannah J Gregson, Farhana Suleman, Matthew Leighton, Sarah M. Edwards, Raymond P. Boot-Handford, Michael D. Briggs
Publikováno v:
Human Mutation
Pseudoachondroplasia (PSACH) results from mutations in cartilage oligomeric matrix protein (COMP) and the p.D469del mutation within the type III repeats of COMP accounts for approximately 30% of PSACH. To determine disease mechanisms of PSACH in vivo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52cbb09ef75e20f747cbf6b79a5a38f7
https://doi.org/10.1002/humu.21631
https://doi.org/10.1002/humu.21631
Autor:
Veronique Siegler, Suzanne M. Mithieux, Thomas C. Irving, John Y.H. Chow, Farhana Suleman, Tim J Wess, Anthonoy S. Weiss, Liang Ma, Liang Guo, Andres F. Oberhauser, Donna Lammie, Sarah E. Rogers, Clair Baldock, Marc Malfois, Yidong Tu
Publikováno v:
Proceedings of the National Academy of Sciences. 108:4322-4327
Elastin enables the reversible deformation of elastic tissues and can withstand decades of repetitive forces. Tropoelastin is the soluble precursor to elastin, the main elastic protein found in mammals. Little is known of the shape and mechanism of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::107905197c942f2f7de5ed678e8f1e75
https://doi.org/10.1073/pnas.1014280108
https://doi.org/10.1073/pnas.1014280108
Autor:
Raimund Wagener, Matthew Leighton, Michael D. Briggs, Tobias Starborg, Roger S. Meadows, Farhana Suleman, Lynnette Knowles, David J. Thornton, Karl E. Kadler, Seema Nundlall, Raymond P. Boot-Handford
Publikováno v:
Human Molecular Genetics. 16:1728-1741
Disruption to endochondral ossification leads to delayed and irregular bone formation and can result in a heterogeneous group of genetic disorders known as the chondrodysplasias. One such disorder, multiple epiphyseal dysplasia (MED), is characterize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9726aa3d1a2c50bebbf8ba6ff2499639
https://doi.org/10.1093/hmg/ddm121
https://doi.org/10.1093/hmg/ddm121
Autor:
Yi Wen, John LaFrancois, Mark P. Burns, Boris Feinstein, Wendy Noble, Karen Duff, Vicki Olm, Lili Wang, Kate Gaynor, Pavan Krishnamurthy, Ratan Bhat, Jada Lewis, Dennis W. Dickson, Farhana Suleman, Cindy Zehr, Jordana L Meyerson, Emmanuel Planel
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 102(19)
Neurofibrillary tangles composed of hyperphosphorylated, aggregated tau are a common pathological feature of tauopathies, including Alzheimer's disease. Abnormal phosphorylation of tau by kinases or phosphatases has been proposed as a pathogenic mech
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25842cdc9062a3d460c811e97b22364b
https://pubmed.ncbi.nlm.nih.gov/15867159
https://pubmed.ncbi.nlm.nih.gov/15867159