Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Doug Biggar"'
Autor:
Audrey Abad, Tim Takken, Brian W. McCrindle, Samantha K. Stephens, Jane E. Schneiderman, Joseph Beyene, Dale W. Esliger, Dan Ignas, Pat Longmuir, Janjaap van der Net, Brian M. Feldman, Eleanor Pullenayegum, Doug Biggar, Mark S. Tremblay
Publikováno v:
Pediatric exercise science, 28(1), 117. Human Kinetics Publishers Inc.
The purpose of this study was to assess the criterion validity of existing accelerometer-based energy expenditure (EE) prediction equations among children with chronic conditions, and to develop new prediction equations. Children with congenital hear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98e746456091d2b50673d49a87c89271
https://dspace.library.uu.nl/handle/1874/333825
https://dspace.library.uu.nl/handle/1874/333825
Autor:
Doug Biggar, Hanna Kolski, Sharan Goobie, Grace Yoon, Laura McAdam, Kathy Selby, Craig Campbell, Natashia Seemann
Publikováno v:
Neuromuscular Disorders. 21:172-177
Although manifesting female carriers of dystrophinopathies have been documented in adults, there are few reports of females presenting with symptomatic dystrophinopathies during childhood. The Canadian Pediatric Neuromuscular Group identified and cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85dca617c34e173514a67fbb434840f7
https://doi.org/10.1016/j.nmd.2010.11.001
https://doi.org/10.1016/j.nmd.2010.11.001
Autor:
Jiri Vajsar, Cynthia Hawkins, Ben Alman, Mayana Zatz, Flavia de Paula, Doug Biggar, Hanna Kolski
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
The Western blot technique is currently the standard detection method for suspected limb girdle muscular dystrophy (LGMD) 2A (calpainopathy). This is the first report in the English literature of the successful application of immunohistochemical tech
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c805abb178959a13b446b033dfc33bb
https://doi.org/10.1111/j.1440-1789.2007.00871.x
https://doi.org/10.1111/j.1440-1789.2007.00871.x
Publikováno v:
Neuromuscular Disorders. 20:238-240
Cap myopathy is a congenital myopathy with cap-like structures under the sarcolemma. Mutations in TPM2 and TPM3 genes have been reported in cap myopathy so far. We report a newborn boy with persistent profound weakness who required gastro-jejunal tub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dc7c5d82b014d8bba88908c5b3ad69c
https://doi.org/10.1016/j.nmd.2010.01.011
https://doi.org/10.1016/j.nmd.2010.01.011
Autor:
Doug Biggar, Jean K. Mah
Publikováno v:
Neuromuscular Disorders
Duchenne muscular dystrophy (DMD, OMIM #310200) is the most common form of muscular dystrophy in childhood, with an incidence of approximately 1 per 3,500 live-born males [Emery, 1991]. It is caused by mutations of the DMD gene located on Xp21 which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f904c6091e2efac93937011d8065f5b0
https://doi.org/10.5772/34647
https://doi.org/10.5772/34647
Autor:
James J. Dowling, Doug Biggar, T. Moraes, R. Cohn, Willliam Halliday, K. Amburgey, N. Chrestian, Jiri Vajsar, Laura McAdam, Cynthia Hawkins
Publikováno v:
Neuromuscular Disorders. 24:808-809
Congenital myopathies with centrally placed nuclei are a heterogenous group of diseases and mutations in the genes associated with centronuclear or myotobular myoapthy and even myotonia dystrophica congenita have been all well described. Recently, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf53e0c1149abf69a4026896e553a20e
https://doi.org/10.1016/j.nmd.2014.06.061
https://doi.org/10.1016/j.nmd.2014.06.061
Autor:
Mark S. Tremblay, M Hendricks, Brian W. McCrindle, Joseph Beyene, Astrid C. J. Balemans, Tim Takken, Doug Biggar, J. van der Net, Dale W. Esliger, Jane E. Schneiderman, S Stephens, A Abad, Patricia E. Longmuir, Virginia Wright, Brian M. Feldman
Publikováno v:
European journal of clinical nutrition. 64(12)
The purpose of this study was to develop an activity energy expenditure (AEE) prediction equation for the Actiheart activity monitor for use in children with chronic disease.In total, 63 children, aged 8-18 years with different types of chronic disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e95783a8b34dad200c7c739087caad6
https://pubmed.ncbi.nlm.nih.gov/20877392
https://pubmed.ncbi.nlm.nih.gov/20877392
Publikováno v:
Neuromuscular disorders : NMD. 18(8)
Walker-Warburg Syndrome (WWS) is an alpha-dystroglycan deficient congenital muscular dystrophy that is associated with brain and eye abnormalities. Patients present with hypotonia, weakness, developmental delay, mental retardation and occasional seiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25a71417e4f73f91b50cbda8a82d67e4
https://pubmed.ncbi.nlm.nih.gov/18640039
https://pubmed.ncbi.nlm.nih.gov/18640039
Autor:
Wenli Zhang, Ann Haskins Olney, Catherine M. Burson, Harry Schachter, Doug Biggar, Cynthia Hawkins, Jiri Vajsar, William B. Dobyns, Kenton R. Holden, Anand Srivastava, Peter N. Ray
Publikováno v:
Neuromuscular disorders : NMD. 16(2)
We report a new fibroblast and lymphoblast based protein O -mannosyl β-1,2- N -acetylglucosaminyltransferase 1 enzymatic assay, which allows rapid and accurate diagnosis of carriers and patients with muscle–eye–brain type of congenital muscular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::687b4425f18dd32793c11c42fae3e7d0
https://pubmed.ncbi.nlm.nih.gov/16427280
https://pubmed.ncbi.nlm.nih.gov/16427280
Autor:
James G. Wright, Derek Stephen, Benjamin A. Alman, K. Kellie Leitch, Naweed Raza, Doug Biggar
Publikováno v:
Journal of pediatric orthopedics. 25(1)
The authors conducted a retrospective study to determine the outcome of foot surgery in full-time wheelchair users with Duchenne muscular dystrophy. Medical records on all 88 teenaged boys with Duchenne muscular dystrophy treated at the authors' inst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83cda3ff85eaf537bb701e253bae4a3f
https://pubmed.ncbi.nlm.nih.gov/15614068
https://pubmed.ncbi.nlm.nih.gov/15614068