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Results: 13

1.

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.

PMID:
25125949
[PubMed]
Free PMC Article
2.

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.

PMID:
22762240
[PubMed - in process]
Free PMC Article
3.

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
[PubMed - indexed for MEDLINE]
4.

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
[PubMed - indexed for MEDLINE]
5.

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
[PubMed - indexed for MEDLINE]
6.

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.

PMID:
18319074
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

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
[PubMed - indexed for MEDLINE]
8.

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
[PubMed - indexed for MEDLINE]
9.

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
[PubMed - indexed for MEDLINE]
10.

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
[PubMed - indexed for MEDLINE]
11.

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.

PMID:
14713176
[PubMed - indexed for MEDLINE]
12.

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.

PMID:
14652796
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

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
[PubMed - as supplied by publisher]

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