Zobrazeno 1 - 10
of 29
pro vyhledávání: '"H Jacobus, Gilhuis"'
Publikováno v:
Case Reports in Neurology, Vol 8, Iss 1, Pp 34-38 (2016)
Congenital hypertrophy of the hand is a rare phenomenon. The condition is characterized by hypertrophy of muscles, varies in severity and has been reported under different names. Some patients also have aberrant muscles. Electromyography is unremarka
Externí odkaz:
https://doaj.org/article/3e60729c101e438aabec70a174bbd240
Publikováno v:
Case Reports in Ophthalmology, Vol 5, Iss 3, Pp 416-422 (2014)
Purpose: To report our experience in managing a case of bilateral optic disc oedema and unilateral cystoid macular oedema with a posterior subtenon (PST) injection of triamcinolone acetonide and intravitreal bevacizumab (IVB) in a patient with polyne
Externí odkaz:
https://doaj.org/article/49cf1a90e1784e0bb0087b213d2fea35
Autor:
Peter Joseph Jongen, Keith Wesnes, Björn van Geel, Paul Pop, Hans Schrijver, Leo H. Visser, H. Jacobus Gilhuis, Ludovicus G. Sinnige, Augustina M. Brands
Publikováno v:
Multiple Sclerosis International, Vol 2015 (2015)
In persons with multiple sclerosis (MS) a lowered self-efficacy negatively affects physical activities. Against this background we studied the relationship between self-efficacy and cognitive performance in the early stages of MS. Thirty-three patien
Externí odkaz:
https://doaj.org/article/7e2e331d201a4544bec84a2f108a99c6
Autor:
Peter Joseph Jongen, Keith Wesnes, Björn van Geel, Paul Pop, Evert Sanders, Hans Schrijver, Leo H Visser, H Jacobus Gilhuis, Ludovicus G Sinnige, Augustina M Brands, COGNISEC Study Group
Publikováno v:
PLoS ONE, Vol 9, Iss 5, p e96444 (2014)
The role of cognitive domain dysfunction with respect to vocational changes in persons with Clinically Isolated Syndrome (CIS) and early Relapsing Remitting Multiple Sclerosis (eRRMS) is insufficiently known. We investigated thirty-three patients--14
Externí odkaz:
https://doaj.org/article/fa57356f940f46e8bf0f73eafed3c2cf
Publikováno v:
Journal of Pediatric Neurology. :213-218
Peripheral neuropathy in patients with merosin-negative congenital muscular dystrophy (MN-CMD) has been sporadically investigated and has been considered to be motor and demyelinating in nature on the basis of nerve conduction studies. We performed n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe29a2a30ee0fa6213cd1fc7455b823b
https://doi.org/10.1055/s-0035-1557222
https://doi.org/10.1055/s-0035-1557222
Publikováno v:
Case Reports in Ophthalmology
Case Reports in Ophthalmology, Vol 5, Iss 3, Pp 416-422 (2014)
Case Reports in Ophthalmology, Vol 5, Iss 3, Pp 416-422 (2014)
Purpose: To report our experience in managing a case of bilateral optic disc oedema and unilateral cystoid macular oedema with a posterior subtenon (PST) injection of triamcinolone acetonide and intravitreal bevacizumab (IVB) in a patient with polyne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1871f5bb9f09df6c6073204668865eb8
http://europepmc.org/articles/PMC4280463
http://europepmc.org/articles/PMC4280463
Akademický článek
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Publikováno v:
Muscle & Nerve. 48:375-380
INTRODUCTION: In this study we describe a protocol for quantitative ultrasound of facial muscles (procerus, zygomaticus major, levator labii superior, depressor anguli oris, mentalis, orbicularis oris pars labialis, orbicularis oris pars marginalis).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::239d03cd7ea380921fe8b6775d430615
https://doi.org/10.1002/mus.23769
https://doi.org/10.1002/mus.23769
Publikováno v:
Neuromuscular Disorders, 19, 714-7
Neuromuscular Disorders, 19, 10, pp. 714-7
Neuromuscular Disorders, 19, 10, pp. 714-7
Item does not contain fulltext Pathological muscular hypertrophy results from either muscular or neurogenic damage. Rarely, it is caused by a congenital malformation consisting of a unilateral muscular hyperplasia of the upper extremity. We report on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a196c6a57d2882c71ecd97a10d118f3a
https://hdl.handle.net/2066/81212
https://hdl.handle.net/2066/81212
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 159
Vogt-Koyanagi-Harada syndrome is rare in the Netherlands. However, in Asia it is one of the most common causes of panuveitis. The syndrome is characterised by a combination of panuveitis, pleocytosis in cerebral spinal fluid with or without neurologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3cd56561b9ce7824e640194a59ebff00
https://pubmed.ncbi.nlm.nih.gov/25850453
https://pubmed.ncbi.nlm.nih.gov/25850453