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[Recurrent nerve palsy due to Lyme disease: report of two cases].
Martzolff L, Bouhala M, Dukic R, Saraceni O, Wilhelm JM, Bombaron P, Kieffer P. Martzolff L, et al. Rev Med Interne. 2010 Mar;31(3):229-31. doi: 10.1016/j.revmed.2009.07.012. Epub 2010 Jan 15. Rev Med Interne. 2010. PMID: 20079561 French.
[Eyes of different colours].
Hinschberger O, Martzolff L, Mostoufizadeh T, Moulana A, Klinger V, Jaeger-Bizet F, Lenoble P, Kieffer P. Hinschberger O, et al. Among authors: martzolff l. Rev Med Interne. 2012 Jun;33(6):346-7. doi: 10.1016/j.revmed.2011.07.012. Epub 2011 Aug 26. Rev Med Interne. 2012. PMID: 21872368 French. No abstract available.
Systemic lupus erythematosus and neutropaenia: a hallmark of haematological manifestations.
Meyer A, Guffroy A, Blaison G, Dieudonne Y, Amoura Z, Bonnotte B, Fiehn C, Kieffer P, Lorenz HM, Magy-Bertrand N, Maurier F, Pennaforte JL, Peter HH, Schwarting A, Sibilia J, Arnaud L, Martin T, Voll RE, Korganow AS; LBBR/Rarenet group. Meyer A, et al. Lupus Sci Med. 2020 Jul;7(1):e000399. doi: 10.1136/lupus-2020-000399. Lupus Sci Med. 2020. PMID: 32616563 Free PMC article.
Clinical characteristics and risk factors associated with severe COVID-19: prospective analysis of 1,045 hospitalised cases in North-Eastern France, March 2020.
Kaeuffer C, Le Hyaric C, Fabacher T, Mootien J, Dervieux B, Ruch Y, Hugerot A, Zhu YJ, Pointurier V, Clere-Jehl R, Greigert V, Kassegne L, Lefebvre N, Gallais F; Covid Alsace Study Group; Meyer N, Hansmann Y, Hinschberger O, Danion F; COVID Alsace Study Group. Kaeuffer C, et al. Euro Surveill. 2020 Dec;25(48):2000895. doi: 10.2807/1560-7917.ES.2020.25.48.2000895. Euro Surveill. 2020. PMID: 33272355 Free PMC article.
Adult Niemann-Pick disease type C in France: clinical phenotypes and long-term miglustat treatment effect.
Nadjar Y, Hütter-Moncada AL, Latour P, Ayrignac X, Kaphan E, Tranchant C, Cintas P, Degardin A, Goizet C, Laurencin C, Martzolff L, Tilikete C, Anheim M, Audoin B, Deramecourt V, De Gaillarbois TD, Roze E, Lamari F, Vanier MT, Héron B. Nadjar Y, et al. Among authors: martzolff l. Orphanet J Rare Dis. 2018 Oct 1;13(1):175. doi: 10.1186/s13023-018-0913-4. Orphanet J Rare Dis. 2018. PMID: 30285904 Free PMC article.
A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity.
Jeandidier E, Gervais C, Radford-Weiss I, Zink E, Gangneux C, Eischen A, Galoisy AC, Helias C, Dano L, Cammarata O, Jung G, Harzallah I, Guérin E, Martzolff L, Drénou B, Lioure B, Tancrédi C, Rimelen V, Mauvieux L. Jeandidier E, et al. Among authors: martzolff l. Cancer Genet. 2012 Jul-Aug;205(7-8):365-72. doi: 10.1016/j.cancergen.2012.04.007. Cancer Genet. 2012. PMID: 22867997
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