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Page 1
HB Prato [alpha 31(B12)Arg----Ser] in a Calabrian family.
De Marco EV, Crescibene L, Pasqua A, Brancati C, Bria M, Qualtieri A. De Marco EV, et al. Hemoglobin. 1992;16(4):275-9. doi: 10.3109/03630269208998868. Hemoglobin. 1992. PMID: 1517104 No abstract available.
Hb D-Iran [beta 22(B4)Glu-->Gln] in southern Italy.
De Marco EV, Crescibene L, Bagalà A, Brancati C, Qualtieri A, Bria M. De Marco EV, et al. Hemoglobin. 1994 Jan;18(1):65-9. doi: 10.3109/03630269409014148. Hemoglobin. 1994. PMID: 8195010 No abstract available.
Hb J-Wenchang-Wuming or alpha 11(A9)Lys-->Gln in an Italian woman.
Qualtieri A, De Marco EV, Crescibene L, Andreoli V, Bagalà A, Scornalenchi M, Brancatl C, Greco CM. Qualtieri A, et al. Among authors: de marco ev. Hemoglobin. 1995 Sep;19(5):277-80. doi: 10.3109/03630269509005814. Hemoglobin. 1995. PMID: 8537231 No abstract available.
The dopamine D2 receptor gene is a susceptibility locus for Parkinson's disease.
Oliveri RL, Annesi G, Zappia M, Civitelli D, De Marco EV, Pasqua AA, Annesi F, Spadafora P, Gambardella A, Nicoletti G, Branca D, Caracciolo M, Aguglia U, Quattrone A. Oliveri RL, et al. Among authors: de marco ev. Mov Disord. 2000 Jan;15(1):127-31. doi: 10.1002/1531-8257(200001)15:1<120::aid-mds1019>3.0.co;2-s. Mov Disord. 2000. PMID: 10634251
Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus.
Annesi G, Gambardella A, Carrideo S, Incorpora G, Labate A, Pasqua AA, Civitelli D, Polizzi A, Annesi F, Spadafora P, Tarantino P, Cirò Candiano IC, Romeo N, De Marco EV, Ventura P, LePiane E, Zappia M, Aguglia U, Pavone L, Quattrone A. Annesi G, et al. Among authors: de marco ev. Epilepsia. 2003 Sep;44(9):1257-8. doi: 10.1046/j.1528-1157.2003.22503.x. Epilepsia. 2003. PMID: 12919402 Free article. No abstract available.
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.
Sidransky E, Nalls MA, Aasly JO, Aharon-Peretz J, Annesi G, Barbosa ER, Bar-Shira A, Berg D, Bras J, Brice A, Chen CM, Clark LN, Condroyer C, De Marco EV, Dürr A, Eblan MJ, Fahn S, Farrer MJ, Fung HC, Gan-Or Z, Gasser T, Gershoni-Baruch R, Giladi N, Griffith A, Gurevich T, Januario C, Kropp P, Lang AE, Lee-Chen GJ, Lesage S, Marder K, Mata IF, Mirelman A, Mitsui J, Mizuta I, Nicoletti G, Oliveira C, Ottman R, Orr-Urtreger A, Pereira LV, Quattrone A, Rogaeva E, Rolfs A, Rosenbaum H, Rozenberg R, Samii A, Samaddar T, Schulte C, Sharma M, Singleton A, Spitz M, Tan EK, Tayebi N, Toda T, Troiano AR, Tsuji S, Wittstock M, Wolfsberg TG, Wu YR, Zabetian CP, Zhao Y, Ziegler SG. Sidransky E, et al. Among authors: de marco ev. N Engl J Med. 2009 Oct 22;361(17):1651-61. doi: 10.1056/NEJMoa0901281. N Engl J Med. 2009. PMID: 19846850 Free PMC article.
Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson's disease - a multicenter study.
von Otter M, Bergström P, Quattrone A, De Marco EV, Annesi G, Söderkvist P, Wettinger SB, Drozdzik M, Bialecka M, Nissbrandt H, Klein C, Nilsson M, Hammarsten O, Nilsson S, Zetterberg H. von Otter M, et al. Among authors: de marco ev. BMC Med Genet. 2014 Dec 12;15:131. doi: 10.1186/s12881-014-0131-4. BMC Med Genet. 2014. PMID: 25496089 Free PMC article.
45 results