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Items: 30

1.

Cognition and physical functioning in patients with schizophrenia: any role for vitamin D?

Zoghbi M, Haddad C, Hallit S, Nabout R, Medlej-Hashim M, Hachem D, Azar J.

Nutr Neurosci. 2019 Feb 17:1-9. doi: 10.1080/1028415X.2019.1580830. [Epub ahead of print]

PMID:
30774039
2.

RAC1 expression and role in IL-1β production and oxidative stress generation in familial Mediterranean fever (FMF) patients.

Ibrahim JN, Jounblat R, Jalkh N, Abou Ghoch J, Al Hageh C, Chouery E, Mégarbané A, Lecron JC, Medlej-Hashim M.

Eur Cytokine Netw. 2018 Nov 1;29(4):127-135. doi: 10.1684/ecn.2018.0416.

PMID:
30698144
3.

Surfactant protein D multimerization and gene polymorphism in COPD and asthma.

Fakih D, Akiki Z, Junker K, Medlej-Hashim M, Waked M, Salameh P, Holmskov U, Bouharoun-Tayoun H, Chamat S, Sorensen GL, Jounblat R.

Respirology. 2018 Mar;23(3):298-305. doi: 10.1111/resp.13193. Epub 2017 Sep 28.

PMID:
28960651
4.

Cytokine signatures in hereditary fever syndromes (HFS).

Ibrahim JN, Jéru I, Lecron JC, Medlej-Hashim M.

Cytokine Growth Factor Rev. 2017 Feb;33:19-34. doi: 10.1016/j.cytogfr.2016.11.001. Epub 2016 Nov 22. Review.

PMID:
27916611
5.

Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation.

Masters SL, Lagou V, Jéru I, Baker PJ, Van Eyck L, Parry DA, Lawless D, De Nardo D, Garcia-Perez JE, Dagley LF, Holley CL, Dooley J, Moghaddas F, Pasciuto E, Jeandel PY, Sciot R, Lyras D, Webb AI, Nicholson SE, De Somer L, van Nieuwenhove E, Ruuth-Praz J, Copin B, Cochet E, Medlej-Hashim M, Megarbane A, Schroder K, Savic S, Goris A, Amselem S, Wouters C, Liston A.

Sci Transl Med. 2016 Mar 30;8(332):332ra45. doi: 10.1126/scitranslmed.aaf1471.

6.

Vibratory Urticaria Associated with a Missense Variant in ADGRE2.

Boyden SE, Desai A, Cruse G, Young ML, Bolan HC, Scott LM, Eisch AR, Long RD, Lee CC, Satorius CL, Pakstis AJ, Olivera A, Mullikin JC, Chouery E, Mégarbané A, Medlej-Hashim M, Kidd KK, Kastner DL, Metcalfe DD, Komarow HD.

N Engl J Med. 2016 Feb 18;374(7):656-63. doi: 10.1056/NEJMoa1500611. Epub 2016 Feb 3.

7.

Study of the association of IL-1β and IL-1RA gene polymorphisms with occurrence and severity of Familial Mediterranean fever.

Ibrahim JN, Chouery E, Lecron JC, Mégarbané A, Medlej-Hashim M.

Eur J Med Genet. 2015 Dec;58(12):668-73. doi: 10.1016/j.ejmg.2015.11.007. Epub 2015 Nov 14.

PMID:
26585190
8.

Hypovitaminosis D in a Young Lebanese Population: Effect of GC Gene Polymorphisms on Vitamin D and Vitamin D Binding Protein Levels.

Medlej-Hashim M, Jounblat R, Hamade A, Ibrahim JN, Rizk F, Azzi G, Abdallah M, Nakib L, Lahoud M, Nabout R.

Ann Hum Genet. 2015 Nov;79(6):394-401. doi: 10.1111/ahg.12133. Epub 2015 Sep 25.

9.

Ex vivo PBMC cytokine profile in familial Mediterranean fever patients: Involvement of IL-1β, IL-1α and Th17-associated cytokines and decrease of Th1 and Th2 cytokines.

Ibrahim JN, Jounblat R, Delwail A, Abou-Ghoch J, Salem N, Chouery E, Megarbane A, Medlej-Hashim M, Lecron JC.

Cytokine. 2014 Oct;69(2):248-54. doi: 10.1016/j.cyto.2014.06.012. Epub 2014 Jul 12.

PMID:
25025954
10.

Autism in children and correlates in Lebanon: a pilot case-control study.

Hamadé A, Salameh P, Medlej-Hashim M, Hajj-Moussa E, Saadallah-Zeidan N, Rizk F.

J Res Health Sci. 2013 Sep 17;13(2):119-24.

11.

Estimating the allele frequency of autosomal recessive disorders through mutational records and consanguinity: the Homozygosity Index (HI).

Gialluisi A, Pippucci T, Anikster Y, Ozbek U, Medlej-Hashim M, Mégarbané A, Romeo G.

Ann Hum Genet. 2012 Mar;76(2):159-67. doi: 10.1111/j.1469-1809.2011.00693.x. Epub 2011 Dec 21.

12.

Familial Mediterranean fever in a large Lebanese family: multiple MEFV mutations and evidence for a Founder effect of the p.[M694I] mutation.

Medlej-Hashim M, Chouery E, Salem N, Delague V, Lefranc G, Loiselet J, Mégarbané A.

Eur J Med Genet. 2011 Jan-Feb;54(1):50-4. doi: 10.1016/j.ejmg.2010.10.001. Epub 2010 Oct 15.

PMID:
20937419
13.

Population genetic data for 17 STR markers from Lebanon.

Chouery E, Coble MD, Strouss KM, Saunier JL, Jalkh N, Medlej-Hashim M, Ayoub F, Mégarbané A.

Leg Med (Tokyo). 2010 Nov;12(6):324-6. doi: 10.1016/j.legalmed.2010.08.005. Epub 2010 Sep 21.

PMID:
20863737
14.

1Novel MEFV transcripts in Familial Mediterranean fever patients and controls.

Medlej-Hashim M, Nehme N, Chouery E, Jalkh N, Megarbane A.

BMC Med Genet. 2010 Jun 9;11:87. doi: 10.1186/1471-2350-11-87.

15.

Re-assigning the DFNB33 locus to chromosome 10p11.23-q21.1.

Belguith H, Masmoudi S, Medlej-Hashim M, Chouery E, Weil D, Ayadi H, Petit C, Mégarbané A.

Eur J Hum Genet. 2009 Jan;17(1):122-4. doi: 10.1038/ejhg.2008.155. Epub 2008 Sep 10.

16.

Familial Mediterranean Fever in Lebanon: founder effects for different MEFV mutations.

Jalkh N, Génin E, Chouery E, Delague V, Medlej-Hashim M, Idrac CA, Mégarbané A, Serre JL.

Ann Hum Genet. 2008 Jan;72(Pt 1):41-7. Epub 2007 Aug 16.

17.

Country as the primary risk factor for renal amyloidosis in familial Mediterranean fever.

Touitou I, Sarkisian T, Medlej-Hashim M, Tunca M, Livneh A, Cattan D, Yalçinkaya F, Ozen S, Majeed H, Ozdogan H, Kastner D, Booth D, Ben-Chetrit E, Pugnère D, Michelon C, Séguret F, Gershoni-Baruch R; International Study Group for Phenotype-Genotype Correlation in Familial Mediterranean Fever.

Arthritis Rheum. 2007 May;56(5):1706-12.

18.

Familial Mediterranean fever in the Syrian population: gene mutation frequencies, carrier rates and phenotype-genotype correlation.

Mattit H, Joma M, Al-Cheikh S, El-Khateeb M, Medlej-Hashim M, Salem N, Delague V, Mégarbané A.

Eur J Med Genet. 2006 Nov-Dec;49(6):481-6. Epub 2006 Apr 3.

PMID:
16627024
19.

[Pre-symptomatic diagnosis of severe hereditary diseases with late onset in Lebanon: a choice or a necessity?].

Medlej-Hashim M, Mégarbané A.

Sante Publique. 2005 Dec;17(4):617-26. French. Erratum in: Sante Publique. 2006 Mar;18(1):following 162.

PMID:
16485442
20.

Familial Mediterranean fever (FMF) in Lebanon and Jordan: a population genetics study and report of three novel mutations.

Medlej-Hashim M, Serre JL, Corbani S, Saab O, Jalkh N, Delague V, Chouery E, Salem N, Loiselet J, Lefranc G, Mégarbané A.

Eur J Med Genet. 2005 Oct-Dec;48(4):412-20. Epub 2005 Jun 20.

PMID:
16378925
21.

[von Hippel-Lindau syndrome: molecular diagnosis of two Lebanese families and analysis of the genotype-phenotype correlation].

Medlej-Hashim M, Leclercq A, Salem N, Moukarzel M, Merhej S, Pigny P, Megarbane A.

J Med Liban. 2004 Jan-Mar;52(1):51-4. French.

PMID:
15881703
22.

[Familial Mediterranean Fever (FMF): from diagnosis to treatment].

Medlej-Hashim M, Loiselet J, Lefranc G, Mégarbané A.

Sante. 2004 Oct-Dec;14(4):261-6. Review. French.

23.

Amyloidosis in familial Mediterranean fever patients: correlation with MEFV genotype and SAA1 and MICA polymorphisms effects.

Medlej-Hashim M, Delague V, Chouery E, Salem N, Rawashdeh M, Lefranc G, Loiselet J, Mégarbané A.

BMC Med Genet. 2004 Feb 10;5:4.

24.

Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations.

Medlej-Hashim M, Mustapha M, Chouery E, Weil D, Parronaud J, Salem N, Delague V, Loiselet J, Lathrop M, Petit C, Mégarbané A.

Eur J Hum Genet. 2002 Jun;10(6):391-4.

25.

An unknown autoinflammatory syndrome associated with short stature and dysmorphic features in a young boy.

Mégarbané A, Sanders A, Chouery E, Delague V, Medlej-Hashim M, Torbey PH.

J Rheumatol. 2002 May;29(5):1084-7.

PMID:
12022327
26.

Familial Mediterranean fever: the potential for misdiagnosis of E148V using the E148Q usual RFLP detection method.

Medlej-Hashim M, Salem N, Chouery E, Rawashdeh M, Delague V, Haffar M, Mansour I, Naman R, Lefranc G, Loiselet J, Mégarbané A.

Clin Genet. 2002 Jan;61(1):71-3. No abstract available.

PMID:
11903360
27.

Familial Mediterranean Fever: association of elevated IgD plasma levels with specific MEFV mutations.

Medlej-Hashim M, Petit I, Adib S, Chouery E, Salem N, Delague V, Rawashdeh M, Mansour I, Lefranc G, Naman R, Loiselet J, Lecron JC, Serre JL, Mégarbané A.

Eur J Hum Genet. 2001 Nov;9(11):849-54.

28.

Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutations.

Mansour I, Delague V, Cazeneuve C, Dodé C, Chouery E, Pêcheux C, Medlej-Hashim M, Salem N, El Zein L, Levan-Petit I, Lefranc G, Goossens M, Delpech M, Amselem S, Loiselet J, Grateau G, Mégarbane A, Naman R.

Eur J Hum Genet. 2001 Jan;9(1):51-5.

29.

Genetic screening of fourteen mutations in Jordanian familial Mediterranean fever patients.

Medlej-Hashim M, Rawashdeh M, Chouery E, Mansour I, Delague V, Lefranc G, Naman R, Loiselet J, Mégarbané A.

Hum Mutat. 2000 Apr;15(4):384.

PMID:
10737992
30.

Effects of verapamil, ouabain, and ethacrynic acid on calcium retention in perfused rat kidneys.

Bikhazi AB, Medlej-Hashim M, el-Kasti M.

J Pharm Sci. 1992 Dec;81(12):1178-80.

PMID:
1491335

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