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Items: 16

1.

Persistent Hg contamination and occurrence of Hg-methylating transcript (hgcA) downstream of a chlor-alkali plant in the Olt River (Romania).

Bravo AG, Loizeau JL, Dranguet P, Makri S, Björn E, Ungureanu VG, Slaveykova VI, Cosio C.

Environ Sci Pollut Res Int. 2016 Jun;23(11):10529-41. doi: 10.1007/s11356-015-5906-4. Epub 2015 Dec 11.

PMID:
26662302
2.

The potential of organic substrates based on mushroom substrate and straw to dissipate fungicides contained in effluents from the fruit-packaging industry - Is there a role for Pleurotus ostreatus?

Karas PA, Makri S, Papadopoulou ES, Ehaliotis C, Menkissoglu-Spiroudi U, Karpouzas DG.

Ecotoxicol Environ Saf. 2016 Feb;124:447-54. doi: 10.1016/j.ecoenv.2015.11.022. Epub 2015 Nov 28.

PMID:
26624931
3.

Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.

Hamza W, Ali Pacha L, Hamadouche T, Muller J, Drouot N, Ferrat F, Makri S, Chaouch M, Tazir M, Koenig M, Benhassine T.

BMC Med Genet. 2015 Jun 12;16:36. doi: 10.1186/s12881-015-0180-3.

4.

Ultrastructural aspects of the effects of L-carnitine administration on epithelial cells in the aging rat tongue.

Barlagiannis D, Dietrich E, Papaliagkas V, Makri S, Toskas A, Papamitsou T.

Hippokratia. 2014 Jan;18(1):32-6.

5.

Enhanced interleukin-1β production of PBMCs from patients with gout after stimulation with Toll-like receptor-2 ligands and urate crystals.

Mylona EE, Mouktaroudi M, Crisan TO, Makri S, Pistiki A, Georgitsi M, Savva A, Netea MG, van der Meer JW, Giamarellos-Bourboulis EJ, Joosten LA.

Arthritis Res Ther. 2012 Jul 4;14(4):R158. doi: 10.1186/ar3898.

6.

Pantothenate kinase-associated neurodegeneration: clinical description of 10 patients and identification of new mutations.

Assami S, Azzedine H, Nouioua S, Mundwiller E, Mahoui S, Makri S, Djemai M, Grid D, Brice A, Hamadouche T, Stevanin G, Tazir M.

Mov Disord. 2011 Aug 1;26(9):1777-9. doi: 10.1002/mds.23648. Epub 2011 Mar 25. No abstract available.

PMID:
21442655
7.

Early onset collagen VI myopathies: Genetic and clinical correlations.

Briñas L, Richard P, Quijano-Roy S, Gartioux C, Ledeuil C, Lacène E, Makri S, Ferreiro A, Maugenre S, Topaloglu H, Haliloglu G, Pénisson-Besnier I, Jeannet PY, Merlini L, Navarro C, Toutain A, Chaigne D, Desguerre I, de Die-Smulders C, Dunand M, Echenne B, Eymard B, Kuntzer T, Maincent K, Mayer M, Plessis G, Rivier F, Roelens F, Stojkovic T, Taratuto AL, Lubieniecki F, Monges S, Tranchant C, Viollet L, Romero NB, Estournet B, Guicheney P, Allamand V.

Ann Neurol. 2010 Oct;68(4):511-20. doi: 10.1002/ana.22087.

PMID:
20976770
8.

Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophy.

Makri S, Clarke NF, Richard P, Maugenre S, Demay L, Bonne G, Guicheney P.

Neuromuscul Disord. 2009 Jan;19(1):26-8. doi: 10.1016/j.nmd.2008.09.016. Epub 2008 Dec 11.

PMID:
19084400
9.

ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency.

Lagier-Tourenne C, Tazir M, López LC, Quinzii CM, Assoum M, Drouot N, Busso C, Makri S, Ali-Pacha L, Benhassine T, Anheim M, Lynch DR, Thibault C, Plewniak F, Bianchetti L, Tranchant C, Poch O, DiMauro S, Mandel JL, Barros MH, Hirano M, Koenig M.

Am J Hum Genet. 2008 Mar;82(3):661-72. doi: 10.1016/j.ajhg.2007.12.024.

10.

Pertussis outbreak detected by active surveillance in Cyprus in 2003.

Theodoridou M, Hadjipanagis A, Persianis N, Makri S, Hadjichristodoulou C.

Euro Surveill. 2007 May 1;12(5):E11-2.

PMID:
17991391
11.

Pathogenicity of environmental isolates of V. cholerae in mice.

Makri S, Purdy AE, Bartlett D, Fierer J.

Microbes Infect. 2007 Sep;9(11):1351-8. Epub 2007 Jul 5.

PMID:
17890125
12.

Brain MRI abnormalities in muscular dystrophy due to FKRP mutations.

Quijano-Roy S, Martí-Carrera I, Makri S, Mayer M, Maugenre S, Richard P, Berard C, Viollet L, Leheup B, Guicheney P, Pinard JM, Estournet B, Carlier RY.

Brain Dev. 2006 May;28(4):232-42. Epub 2005 Dec 20.

PMID:
16368217
13.

Collagen VI status and clinical severity in Ullrich congenital muscular dystrophy: phenotype analysis of 11 families linked to the COL6 loci.

Demir E, Ferreiro A, Sabatelli P, Allamand V, Makri S, Echenne B, Maraldi M, Merlini L, Topaloglu H, Guicheney P.

Neuropediatrics. 2004 Apr;35(2):103-12.

PMID:
15127309
14.

Lowering of furosemide dosage after clinical stabilization in patients with congestive heart failure.

Alexopoulos GP, Anastasiou-Nana MI, Rapti ACh, Margari ZJ, Terrovitis JV, Mitsibounas D, Makri S, Nanas JN.

Acta Cardiol. 2003 Dec;58(6):513-7.

15.

New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families.

Louhichi N, Triki C, Quijano-Roy S, Richard P, Makri S, Méziou M, Estournet B, Mrad S, Romero NB, Ayadi H, Guicheney P, Fakhfakh F.

Neurogenetics. 2004 Feb;5(1):27-34. Epub 2003 Dec 2.

16.

Helicobacter pylori infection in upper gastrointestinal bleeding in patients with hereditary hemorrhagic disorders.

Eleftheriadis N, Makri S, Aggouridaki C, Pithara E, Makris P.

Eur J Intern Med. 2002 Dec;13(8):480-484.

PMID:
12446191
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