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MeSH Review

Cranial Nerve Diseases

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Disease relevance of Cranial Nerve Diseases


High impact information on Cranial Nerve Diseases


Chemical compound and disease context of Cranial Nerve Diseases


Biological context of Cranial Nerve Diseases


Gene context of Cranial Nerve Diseases


  1. CARD15 mutations in familial granulomatosis syndromes: a study of the original Blau syndrome kindred and other families with large-vessel arteritis and cranial neuropathy. Wang, X., Kuivaniemi, H., Bonavita, G., Mutkus, L., Mau, U., Blau, E., Inohara, N., Nunez, G., Tromp, G., Williams, C.J. Arthritis Rheum. (2002) [Pubmed]
  2. Clinical and histopathologic studies of two families with lattice corneal dystrophy and familial systemic amyloidosis (Meretoja syndrome). Starck, T., Kenyon, K.R., Hanninen, L.A., Beyer-Machule, C., Fabian, R., Gorn, R.A., McMullan, F.D., Baum, J., McAdam, K.P. Ophthalmology (1991) [Pubmed]
  3. Controlled clinical trial of IV cyclophosphamide versus IV methylprednisolone in severe neurological manifestations in systemic lupus erythematosus. Barile-Fabris, L., Ariza-Andraca, R., Olguín-Ortega, L., Jara, L.J., Fraga-Mouret, A., Miranda-Limón, J.M., Fuentes de la Mata, J., Clark, P., Vargas, F., Alocer-Varela, J. Ann. Rheum. Dis. (2005) [Pubmed]
  4. Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein. Haltia, M., Prelli, F., Ghiso, J., Kiuru, S., Somer, H., Palo, J., Frangione, B. Biochem. Biophys. Res. Commun. (1990) [Pubmed]
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  10. Role of Blink Reflex in diagnosis of subclinical cranial neuropathy in Diabetic Mellitus type II. Kazem, S.S., Behzad, D. Electromyography and clinical neurophysiology. (2005) [Pubmed]
  11. Cranial neuropathy heralding otherwise occult AIDS-related large cell lymphoma. Berger, J.R., Flaster, M., Schatz, N., Droller, D., Benedetto, P., Poblete, R., Post, M.J. Journal of clinical neuro-ophthalmology. (1993) [Pubmed]
  12. Neurologic complications associated with gold therapy for rheumatoid arthritis. Fam, A.G., Gordon, D.A., Sarkozi, J., Blair, G.R., Cooper, P.W., Harth, M., Lewis, A.J. J. Rheumatol. (1984) [Pubmed]
  13. Danish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type). Maury, C.P., Liljeström, M., Boysen, G., Törnroth, T., de la Chapelle, A., Nurmiaho-Lassila, E.L. J. Clin. Pathol. (2000) [Pubmed]
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  15. Spontaneous intracranial hypotension with unique strabismus due to third and fourth cranial neuropathies. Brady-McCreery, K.M., Speidel, S., Hussein, M.A., Coats, D.K. Binocular vision & strabismus quarterly. (2002) [Pubmed]
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