Astroglial dystrophy with Rosenthal fibers. on the adult form of Alexander disease and its clinical significance
Ule, G.; Jacob, H.
Der Nervenarzt 54(2): 69-73
1983
ISSN/ISBN: 0028-2804 PMID: 6843729 Document Number: 216697
Document emailed within 1 workday
Related Documents
Pietrini, V.; Tagliavini, F.; Tedeschi, F.; Lechi, A. 1983: Megalencephaly with formation of Rosenthal fibers in symmetric subependymal gliomatous proliferations: clinicopathologic report Clinical Neuropathology 2(1): 16-22Kim, J.J.; Kim, J.-K.; Shim, S.-C.; Choe, J.-Y.; Kim, T.-H.; Jun, J.-B.; Yoo, D.-H. 2013: MEFV gene mutations and their clinical significance in Korean patients with adult-onset Still's disease Clinical and Experimental Rheumatology 31(3 Suppl 77: 60-63
Starzynski, R.; Najwer, K. 1976: Abortive form of Melkersson-Rosenthal syndrome Wiadomosci Lekarskie 29(23): 2159-2162
Borovac, N.; Kulenović, S.; Veljkov, N.; Dzirlo, J. 1986: The adult form of Gaucher's disease Medicinski Arhiv 40(1-2): 43-45
Uhde, J. 1978: Adult form of Niemann-Pick disease Deutsche Medizinische Wochenschrift 103(20): 873
Boehme, D.H.; Leonberg, S.C.; Varagiannis, E.; Marks, N. 1980: On the neurochemistry of an adult form of ceroid lipofuscinosis (Kuf's disease) Progress in Clinical and Biological Research 39: 305-314
Spitzer, W.J. 1988: Form changes of temporomandibular joint and its clinical significance Zwr 97(10): 874-876
Selgas, R.; Temes, J.L.; Sobrino, J.A.; Viguer, J.M.; Otero, A.; Sánchez Sicilia, L. 1981: Polycystic renal disease in the adult associated with an incomplete form of Marfan's syndrome Medicina Clinica 76(7): 311-313
Zinkham, W.H. 1972: A unique form of lactate dehydrogenase in human sperm: biological and clinical significance Johns Hopkins Medical Journal 130(1): 1-10
Uchino, M.; Araki, S.; Yoshida, O.; Uekawa, K. 1983: Muscle structural proteins of the opaque fibers in Duchenne type muscular dystrophy Rinsho Shinkeigaku 23(8): 706-710
Creplet, J. 1978: Significance of TM echocardiography in adult clinical cardiology. 2 Acta Clinica Belgica 33(4): 255-271
Rampini, S.; Grauer, W.; Imhof, H.G.; Gitzelmann, R. 1986: Mucopolysaccharidosis IV-A (Maroteaux-Lamy disease, severe form): incipient compressive myelopathy, cerebrospinal fluid fistula and tracheal stenosis in an adult patient Helvetica Paediatrica Acta 41(6): 515-530
Nehrych, T.I. 2001: Diagnostic significance of isoenzymes and isoforms of alkaline phosphatase in blood serum of patients with multiple sclerosis on the clinical form of the illness Likars'ka Sprava 3: 81-85
Rosano, C.L.; Parhami, N.; Hurwitz, C. 1979: The clinical significance of protein-bound hydroxyproline fractions in sera of patients with adult rheumatoid arthritis Journal of Rheumatology 6(6): 656-663
Tallan, H.H.; Schaffner, F.; Taffet, S.L.; Schneidman, K.; Gaull, G.E. 1983: Ornithine carbamoyltransferase deficiency in an adult male patient: significance of hepatic ultrastructure in clinical diagnosis Pediatrics 71(2): 224-232
Cortes, J.E.; Kantarjian, H.; O'Brien, S.; Keating, M.; Pierce, S.; Freireich, E.J.; Estey, E. 1995: Clinical and prognostic significance of trisomy 21 in adult patients with acute myelogenous leukemia and myelodysplastic syndromes Leukemia 9(1): 115-117
Nair, R.R. 2005: Alexander's disease presenting as status epilepticus in a child Journal of Postgraduate Medicine 51(3): 244
Pierach, C.A.; Pierach, A. 1978: Alexander Pierach--early clinical chronobiologist Chronobiologia 5(2): 171-174
Hozumi, I.; Takahashi, T.; Aoki, M.; Hayashi, Y.K.; Suzuki, N.; Matsuyama, Z.; Inuzuka, T.; Nonaka, I. 2004: A patient with distal muscular dystrophy without mutations in dysferlin gene but with abnormal dysferlin localization in muscle fibers Rinsho Shinkeigaku 44(10): 699-702
Iadgarov, I.S.; Badalian, L.O.; Temin, P.A.; Arkhipov, B.A.; Bulaeva, N.V.; Amanova, Z.A. 1991: A familial form of progressive muscular dystrophy with multiple contractures of the major joints Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 91(9): 89-93