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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
1979 2
1980 2
1983 1
1984 3
1985 2
1986 4
1987 1
1988 4
1989 1
1990 3
1991 3
1993 3
1994 2
1995 6
1996 3
1997 1
1998 2
1999 1
2000 4
2001 6
2002 5
2003 4
2004 2
2005 7
2006 9
2007 19
2008 12
2009 8
2010 20
2011 10
2012 12
2013 6
2014 6
2015 8
2016 3
2017 2
2018 5
2019 2
2020 3
2021 7
2022 3
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Article type
Publication date

Search Results

187 results
Results by year
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Page 1
Hematologically important mutations: X-linked chronic granulomatous disease (third update).
Roos D, Kuhns DB, Maddalena A, Roesler J, Lopez JA, Ariga T, Avcin T, de Boer M, Bustamante J, Condino-Neto A, Di Matteo G, He J, Hill HR, Holland SM, Kannengiesser C, Köker MY, Kondratenko I, van Leeuwen K, Malech HL, Marodi L, Nunoi H, Stasia MJ, Ventura AM, Witwer CT, Wolach B, Gallin JI. Roos D, et al. Among authors: marodi l. Blood Cells Mol Dis. 2010 Oct 15;45(3):246-65. doi: 10.1016/j.bcmd.2010.07.012. Epub 2010 Aug 21. Blood Cells Mol Dis. 2010. PMID: 20729109 Free PMC article. Review.
Pyogenic bacterial infections in humans with MyD88 deficiency.
von Bernuth H, Picard C, Jin Z, Pankla R, Xiao H, Ku CL, Chrabieh M, Mustapha IB, Ghandil P, Camcioglu Y, Vasconcelos J, Sirvent N, Guedes M, Vitor AB, Herrero-Mata MJ, Aróstegui JI, Rodrigo C, Alsina L, Ruiz-Ortiz E, Juan M, Fortuny C, Yagüe J, Antón J, Pascal M, Chang HH, Janniere L, Rose Y, Garty BZ, Chapel H, Issekutz A, Maródi L, Rodriguez-Gallego C, Banchereau J, Abel L, Li X, Chaussabel D, Puel A, Casanova JL. von Bernuth H, et al. Among authors: marodi l. Science. 2008 Aug 1;321(5889):691-6. doi: 10.1126/science.1158298. Science. 2008. PMID: 18669862 Free PMC article.
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype.
Toubiana J, Okada S, Hiller J, Oleastro M, Lagos Gomez M, Aldave Becerra JC, Ouachée-Chardin M, Fouyssac F, Girisha KM, Etzioni A, Van Montfrans J, Camcioglu Y, Kerns LA, Belohradsky B, Blanche S, Bousfiha A, Rodriguez-Gallego C, Meyts I, Kisand K, Reichenbach J, Renner ED, Rosenzweig S, Grimbacher B, van de Veerdonk FL, Traidl-Hoffmann C, Picard C, Marodi L, Morio T, Kobayashi M, Lilic D, Milner JD, Holland S, Casanova JL, Puel A; International STAT1 Gain-of-Function Study Group. Toubiana J, et al. Among authors: marodi l. Blood. 2016 Jun 23;127(25):3154-64. doi: 10.1182/blood-2015-11-679902. Epub 2016 Apr 25. Blood. 2016. PMID: 27114460 Free PMC article.
Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome.
Woellner C, Gertz EM, Schäffer AA, Lagos M, Perro M, Glocker EO, Pietrogrande MC, Cossu F, Franco JL, Matamoros N, Pietrucha B, Heropolitańska-Pliszka E, Yeganeh M, Moin M, Español T, Ehl S, Gennery AR, Abinun M, Breborowicz A, Niehues T, Kilic SS, Junker A, Turvey SE, Plebani A, Sánchez B, Garty BZ, Pignata C, Cancrini C, Litzman J, Sanal O, Baumann U, Bacchetta R, Hsu AP, Davis JN, Hammarström L, Davies EG, Eren E, Arkwright PD, Moilanen JS, Viemann D, Khan S, Maródi L, Cant AJ, Freeman AF, Puck JM, Holland SM, Grimbacher B. Woellner C, et al. Among authors: marodi l. J Allergy Clin Immunol. 2010 Feb;125(2):424-432.e8. doi: 10.1016/j.jaci.2009.10.059. J Allergy Clin Immunol. 2010. PMID: 20159255 Free PMC article.
The J Daughter Siberia Project.
Tuzankina I, Bolkov M, Nabieva U, Lázár I, Maródi L. Tuzankina I, et al. Among authors: marodi l. J Clin Immunol. 2021 Jan;41(1):262-265. doi: 10.1007/s10875-020-00894-4. Epub 2020 Oct 20. J Clin Immunol. 2021. PMID: 33078350 No abstract available.
[Wiskott-Aldrich syndrome].
Gulácsy V, Maródi L. Gulácsy V, et al. Among authors: marodi l. Orv Hetil. 2008 Jul 20;149(29):1367-71. doi: 10.1556/OH.2008.28377. Orv Hetil. 2008. PMID: 18617469 Review. Hungarian.
[Cartilage-hair hypoplasia].
Erdos M, Tóth B, Almássy Z, Tímár L, Maródi L. Erdos M, et al. Among authors: marodi l. Orv Hetil. 2008 Feb 3;149(5):209-17. doi: 10.1556/OH.2008.28256. Orv Hetil. 2008. PMID: 18218588 Review. Hungarian.
[Fabry disease--diagnostic guideline].
Constantin T, Rákóczi E, Ponyi A, Ambrus C, Kádár K, Vastagh I, Dajnoki A, Tóth B, Bokrétás G, Müller V, Katona M, Csikós M, Fiedler O, Széchey R, Varga E, Rudas G, Kertész A, Molnár S, Kárpáti S, Nagy V, Magyar P, Mahdi M, Németh K, Bereczki D, Garami M, Erdos M, Maródi L, Fekete G; Fabry Disease Work Group. Constantin T, et al. Among authors: marodi l. Orv Hetil. 2010 Feb 14;151(7):243-9. doi: 10.1556/OH.2010.28795. Orv Hetil. 2010. PMID: 20133243 Review. Hungarian.
187 results