Zobrazeno 1 - 10
of 16
pro vyhledávání: '"D D, Kilmer"'
Autor:
L E, Paulson, D D, Kilmer
Publikováno v:
Physical medicine and rehabilitation clinics of North America. 12(2)
An appropriate orthosis can improve the function of a patient with peripheral neuropathy. It is crucial to be cognizant of the patient's goals, concomitant medical conditions, cosmesis, comfort, and functional deficits. In addition, a close working r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::90fd9ddc047826a7f0e4c00daf799c43
https://pubmed.ncbi.nlm.nih.gov/11345016
https://pubmed.ncbi.nlm.nih.gov/11345016
Publikováno v:
Musclenerve. 23(9)
The purpose of the study is to further assess the usefulness of short TI (time to inversion) recovery (STIR) magnetic resonance imaging (MRI) in detecting denervation of skeletal muscle compared to needle electromyography (EMG). Ninety subjects with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5e6e5b170b77bb7f7b93fd66702da7ee
https://pubmed.ncbi.nlm.nih.gov/10951448
https://pubmed.ncbi.nlm.nih.gov/10951448
Publikováno v:
Physical medicine and rehabilitation clinics of North America. 9(1)
Evidence suggests that individuals with DMD have reduced skeletal development, including decreased linear growth and bone mineral density, compared to normal subjects. Despite their reduced muscle mass, a high percentage of DMD patients are overweigh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2d5e093c40e991fec722b04ad5eb3c30
https://pubmed.ncbi.nlm.nih.gov/9894137
https://pubmed.ncbi.nlm.nih.gov/9894137
Autor:
D D, Kilmer
Publikováno v:
Physical medicine and rehabilitation clinics of North America. 9(1)
Persons with hereditary neuromuscular diseases generally lead a sedentary lifestyle, placing them at risk for diseases associated with inactivity and causing weakness, which compounds their primary disease. Although research is lacking in this area,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9c22f88c6e98d9e115138beb01f42b42
https://pubmed.ncbi.nlm.nih.gov/9894136
https://pubmed.ncbi.nlm.nih.gov/9894136
Publikováno v:
Musclenerve. 19(5)
A 30-year-old male with hereditary motor and sensory neuropathy, type I (HMSN I), presented with asymmetric weakness of finger extension and radial deviation with left wrist extension, previously felt to be a manifestation of the peripheral neuropath
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9e4f9cb02afa96602a7f3592dc25a311
https://pubmed.ncbi.nlm.nih.gov/8618563
https://pubmed.ncbi.nlm.nih.gov/8618563
Autor:
D D, Kilmer, R T, Abresch, M A, McCrory, G T, Carter, W M, Fowler, E R, Johnson, C M, McDonald
Publikováno v:
American journal of physical medicinerehabilitation. 74
Data were collected prospectively over a 10-yr period from 53 subjects with facioscapulohumeral muscular dystrophy (FSHD) to provide a profile of impairment and disability. Manual muscle testing (MMT) indicated greater involvement of proximal muscula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cc4c203990bb042b271ef8b1705a1e16
https://pubmed.ncbi.nlm.nih.gov/7576420
https://pubmed.ncbi.nlm.nih.gov/7576420
Autor:
C M, McDonald, R T, Abresch, G T, Carter, W M, Fowler, E R, Johnson, D D, Kilmer, B J, Sigford
Publikováno v:
American journal of physical medicinerehabilitation. 74
One hundred and sixty-two patients with Duchenne muscular dystrophy (DMD) were followed over a 10-yr period to provide a profile of impairment and disability. The median height and weight of DMD boys were normally distributed before ages 9-10, but du
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bc2bd68fe5a721cfc5cc080c1e6fd826
https://pubmed.ncbi.nlm.nih.gov/7576424
https://pubmed.ncbi.nlm.nih.gov/7576424
Publikováno v:
American journal of physical medicinerehabilitation. 74
Sixty-six individuals with Limb-Girdle Syndrome (LGS) were evaluated over a 10-yr period and classified into three types: 19 severe autosomal recessive muscular dystrophy of childhood (ARMDC), alternatively referred to by some as SCARMD, 18 autosomal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::697afcd7975fb8ce67e035afd87ab451
https://pubmed.ncbi.nlm.nih.gov/7576419
https://pubmed.ncbi.nlm.nih.gov/7576419
Publikováno v:
American journal of physical medicinerehabilitation. 74
Data were collected prospectively for an impairment and disability profile for 86 hereditary motor and sensory neuropathy, types I and II (HMSN) subjects over a 10-yr period. Our data confirm that HMSN is a slowly progressive disorder that has a very
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::54df2c98b7a94b74147f99e4483381e5
https://pubmed.ncbi.nlm.nih.gov/7576421
https://pubmed.ncbi.nlm.nih.gov/7576421
Autor:
E R, Johnson, R T, Abresch, G T, Carter, D D, Kilmer, W M, Fowler, B J, Sigford, R L, Wanlass
Publikováno v:
American journal of physical medicinerehabilitation. 74
Ninety-two individuals with myotonic dystrophy (MD) were evaluated prospectively over a 10-yr period and separated into two types, 75 noncongenital (NC-MD) and 17 congenital (C-MD) MD. Muscle weakness was relatively mild and similar in both types, 4.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d1c5a4c1393bdbc26bbe6bab069b03a7
https://pubmed.ncbi.nlm.nih.gov/7576418
https://pubmed.ncbi.nlm.nih.gov/7576418