Zobrazeno 1 - 10
of 50
pro vyhledávání: '"D W Mulder"'
Publikováno v:
Neurology. 77:1437-1437
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ef520218860aded014e0e03cfa5d0a0
https://doi.org/10.1212/01.wnl.0000407007.31963.e8
https://doi.org/10.1212/01.wnl.0000407007.31963.e8
Publikováno v:
Archives of physical medicine and rehabilitation. 72(8)
The medical records of 31 patients (19 male and 12 female) with clinical and electrophysiologic features of Wohlfart-Kugelberg-Welander syndrome were reviewed. The reported age at onset ranged from less than one year to 46 years, and the age at diagn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::29a1cef0ff3f4d4e695e2f1545178821
https://pubmed.ncbi.nlm.nih.gov/2059139
https://pubmed.ncbi.nlm.nih.gov/2059139
Akademický článek
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Autor:
D. W. Mulder
Publikováno v:
JAMA: The Journal of the American Medical Association. 280:480-480
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::656e2bfda728f9369dcc55d2f14e2f49
https://doi.org/10.1001/jama.280.5.480
https://doi.org/10.1001/jama.280.5.480
Autor:
S Ali, D W Mulder, Hill Avs., B Biryawaho, S Malamba, J Whitworth, H V Wagner, A Nunn, F Lyagoba
Publikováno v:
Human Immunology. 47:120
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06ecd26494ba97b75e966c0cece64ede
https://doi.org/10.1016/0198-8859(96)85349-3
https://doi.org/10.1016/0198-8859(96)85349-3
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 46:671-674
A sibship is reported in which two males have spastic paraparesis and Kallmann's syndrome (hypogonadotrophic hypogonadism and anosmia). One of the brothers also is color blind. The association of familial spastic paraplegia and Kallmann's syndrome ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46ce9d51e92bfc1fe454fa7810a839be
https://doi.org/10.1136/jnnp.46.7.671
https://doi.org/10.1136/jnnp.46.7.671
Publikováno v:
Neurology. 36:511-517
We analyzed the medical records of 103 patients with familial adult motor neuron disease (MND). In the 72 families, 329 members were known to be affected. Observations were compared with the sporadic and Mariana forms of MND. Clinical and laboratory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a9dc9182a129d38bba94d8e6c0996f0
https://doi.org/10.1212/wnl.36.4.511
https://doi.org/10.1212/wnl.36.4.511
Autor:
R, van den Akker, C A, Bouman-van Engelen, J C, de Jong, W M, Dolmans, A M, van Loon, D W, Mulder, J F, Shao
Publikováno v:
AIDS (London, England). 2(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9c1987e824923dad07a42a1e63119cc7
https://pubmed.ncbi.nlm.nih.gov/3129000
https://pubmed.ncbi.nlm.nih.gov/3129000
Autor:
D W, Mulder
Publikováno v:
Advances in neurology. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a943691ec7775783aeff1a823559020b
https://pubmed.ncbi.nlm.nih.gov/7180681
https://pubmed.ncbi.nlm.nih.gov/7180681
Autor:
D W, Mulder, L T, Kurland
Publikováno v:
Advances in experimental medicine and biology. 209
The etiology of motor neuron disease (MND) is unknown and treatment is limited to measures which sustain the patient. We review selected epidemiologic studies searching for a pattern in the clinical expression of MND which may reflect the operation o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3a7f85943ce380133687508b3338ff2b
https://pubmed.ncbi.nlm.nih.gov/3554910
https://pubmed.ncbi.nlm.nih.gov/3554910