8 results for author:"Deymeer F." in Literature citations
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| Polymorphisms of interferon-gamma, interleukin-10, and interleukin-12 genes in myasthenia gravis. Yilmaz V., Tutuncu Y., Baris Hasbal N., Parman Y., Serdaroglu P., Deymeer F., Saruhan-Direskeneli G. Hum. Immunol. 68:544-549(2007) · Mapped (25) |
| HLA-DQ polymorphism in Turkish patients with myasthenia gravis. Saruhan-Direskeneli G., Kilic A., Parman Y., Serdaroglu P., Deymeer F. Hum. Immunol. 67:352-358(2006) · Mapped (330) |
| Slow-channel mutation in acetylcholine receptor alphaM4 domain and its efficient knockdown. Shen X.-M., Deymeer F., Sine S.M., Engel A.G. Ann. Neurol. 60:128-136(2006) · UniProtKB (1) |
| The range of chronic demyelinating neuropathy of infancy: a clinico-pathological and genetic study of 15 unrelated cases. Plante-Bordeneuve V., Parman Y., Guiochon-Mantel A., Alj Y., Deymeer F., Serdaroglu P., Eraksoy M., Said G. J. Neurol. 248:795-803(2001) · UniProtKB (1) |
| Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome. Plaster N.M., Tawil R., Tristani-Firouzi M., Canun S., Bendahhou S., Tsunoda A., Donaldson M.R., Iannaccone S.T., Brunt E., Barohn R. et al. Cell 105:511-519(2001) · UniProtKB (1) |
| Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth type 1 and HNPP patients. Bissar-Tadmouri N., Parman Y., Boutrand L., Deymeer F., Serdaroglu P., Vandenberghe A., Battaloglu E. Clin. Genet. 58:396-402(2000) · UniProtKB (2) |
| Novel muscle chloride channel mutations and their effects on heterozygous carriers. Mailaender V., Heine R., Deymeer F., Lehmann-Horn F. Am. J. Hum. Genet. 58:317-324(1996) · UniProtKB (1) |
| Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletion. Heine R., George A.L. Jr., Pika U., Deymeer F., Ruedel R., Lehmann-Horn F. Hum. Mol. Genet. 3:1123-1128(1994) · UniProtKB (1) |