Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Chaitanya Gadepalli"'
Autor:
Benjamin Cross, Karolina M. Stepien, Chaitanya Gadepalli, Ahmed Kharabish, Peter Woolfson, Govind Tol, Petra Jenkins
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
Mucopolysaccharidoses (MPS) are rare lysosomal storage diseases characterized by multiorgan involvement and shortened longevity. Due to advances in therapies such as enzyme replacement therapy and haematopoietic stem cell therapy, life expectancy has
Externí odkaz:
https://doaj.org/article/08fa6eba31394248b80e3a11dcd76d12
Autor:
Karolina M. Stepien, Andrew Bentley, Cliff Chen, M. Wahab Dhemech, Edward Gee, Peter Orton, Catherine Pringle, Jonathan Rajan, Ankur Saxena, Govind Tol, Chaitanya Gadepalli
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
Mucopolysaccharidoses (MPS) are a heterogeneous group of disorders that results in the absence or deficiency of lysosomal enzymes, leading to an inappropriate storage of glycosaminoglycans (GAGs) in various tissues of the body such as bones, cartilag
Externí odkaz:
https://doaj.org/article/6ed3828480b34d679a8a8331a1b60464
Autor:
Christian J. Hendriksz, Jane Ashworth, Ana Jovanovic, Neil J. Oxbarrow, Ankur Saxena, Chaitanya Gadepalli, Michael Rothera, Petra Jenkins, Peter Wolfson, Andrew Oldham, Govind Tol
Publikováno v:
SSRN Electronic Journal.
Autor:
Karolina M. Stepien, Jorge Menendez Lorenzo, Mairead Jones, Janet Gorton, Reena Sharma, Andrew J. Oldham, Ana Jovanovic, Chaitanya Gadepalli, Simon Jones
Publikováno v:
Molecular Genetics and Metabolism. 138:107328
Autor:
Karolina M. Stepien, Andrew Bentley, Cliff Chen, M. Wahab Dhemech, Edward Gee, Peter Orton, Catherine Pringle, Jonathan Rajan, Ankur Saxena, Govind Tol, Chaitanya Gadepalli
Publikováno v:
Frontiers in cardiovascular medicine. 9
Mucopolysaccharidoses (MPS) are a heterogeneous group of disorders that results in the absence or deficiency of lysosomal enzymes, leading to an inappropriate storage of glycosaminoglycans (GAGs) in various tissues of the body such as bones, cartilag
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 4924, p 4924 (2021)
Journal of Clinical Medicine; Volume 10; Issue 21; Pages: 4924
Journal of Clinical Medicine
Journal of Clinical Medicine; Volume 10; Issue 21; Pages: 4924
Journal of Clinical Medicine
Background: Mucopolysaccharidosis (MPS) is a rare congenital lysosomal storage disorder with complex airways. High anterior larynx is assessed by thyromental distance (TMD) nasendoscopy. A simpler method to assess this hyoid bone is described. The di
Autor:
Govind Tol, Ana Jovanovic, Chaitanya Gadepalli, Karolina M. Stepien, Andrew Bentley, Reena Sharma
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 3275, p 3275 (2021)
Journal of Clinical Medicine
Journal of Clinical Medicine
(1) Background: Mucopolysaccharidoses (MPS) are a heterogeneous group of lysosomal storage disorders caused by the absence of enzymes required for degradation of glycosaminoglycans (GAGs). GAGs deposition in tissues leads to progressive airway narrow
Publikováno v:
Rheumatology. 60:e41-e43
Publikováno v:
Clinical Otolaryngology. 44:1045-1058
OBJECTIVE To characterise the burden of voice disorders in teachers in a UK population, compare it with non-teachers and identify groups of teachers who may be particularly at risk of developing a voice problem. DESIGN Questionnaire-based survey of p