List of works - Myrna Medlej-Hashim

1Novel MEFV transcripts in Familial Mediterranean fever patients and controls

scientific article

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

scientific article

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

scientific article published on May 2007

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

scientific article published on December 1, 1992

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

scientific article published on 21 December 2011

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

scientific article

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

scientific article published on November 2001

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

scientific article

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.

scientific article published on January 2001

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

scientific article published on 15 October 2010

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

scientific article

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

scientific article published in January 2002

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

scientific article published in June 2002

Population genetic data for 17 STR markers from Lebanon.

scientific article

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

scientific article published on 10 September 2008

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

scientific article published on 01 December 2005

List of works by Myrna Medlej-Hashim

1Novel MEFV transcripts in Familial Mediterranean fever patients and controls

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

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

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

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

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

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

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

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.

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

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

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

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

Population genetic data for 17 STR markers from Lebanon.

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

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