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Intrachromosomal amplification 21: A driver of acute myeloid leukemia?

EJHaem, 2023-08, Vol.4 (3), p.857-858

2023

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Visceral leishmaniasis presenting with pancytopenia and circulating blastlike lymphocytes

Blood, 2018-06, Vol.131 (25), p.2867-2867

2018

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Using the SLIPTA checklist to assess laboratory readiness for Joint Commission International accreditation

African journal of laboratory medicine, 2023, Vol.12 (1), p.1-8

2023

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P043: The status of germline variants of unknown significance in minorities: Middle Eastern patients with HBOC

Genetics in Medicine Open, 2023, Vol.1 (1), p.100062, Article 100062

2023

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Curbing the greenhouse effect by carbon dioxide adsorption with Zeolite 13X

AIChE journal, 2007-12, Vol.53 (12), p.3137-3143

2007

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Insight into the 8p23.1 duplication syndrome: Case report of a young women with infertility

Heliyon, 2023-04, Vol.9 (4), p.e15515, Article e15515

2023

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AML with inv(16)/t(16;16) and high-risk cytogenetic abnormalities: atypical features and unfavorable outcome

Hematology (Luxembourg), 2022-12, Vol.27 (1), p.636-641

2022

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KMT2A-ARHGEF12, a therapy related fusion with poor prognosis

Molecular biology reports, 2021-10, Vol.48 (10), p.7021-7027

2021

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eP314: Rare unbalanced complex chromosomal rearrangement in a case of infertility: Insight into the 8p23.1 duplication syndrome

Genetics in medicine, 2022-03, Vol.24 (3), p.S198-S198

2022

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Cryptic insertion of KMT2A, a rare t(9;11) variant

Blood, 2021-04, Vol.137 (13), p.1843-1843

2021

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Double translocation or gene insertion? A BCR/ABL1 fusion in Philadelphia-negative CML

Blood, 2020-07, Vol.136 (4), p.521-521

2020

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Molecular characterization of adult IRF4 large B-cell lymphoma with spontaneous remission

Acta oncologica, 2023-08, Vol.ahead-of-print (ahead-of-print), p.1-5

2023

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Plasma cells and lymphoid aggregates in sleeve gastrectomy specimens: Normal or gastritis?

Medicine (Baltimore), 2020-02, Vol.99 (6), p.e18926-e18926

2020

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Novel trans-2,3-enoyl-CoA reductase–like variant associated with catecholaminergic polymorphic ventricular tachycardia type 3

HeartRhythm case reports, 2023-03, Vol.9 (3), p.171-177

2023

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Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two α-Globin Gene Defects, Hb Taybe D HBA1 : C.119_121delCCA Mutation and HBA2 : C.94A > G Mutation

Hemoglobin, 2024-03, Vol.48 (2), p.1-132

2024

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Diagnosing Lymphoproliferative Disorders Using Core Needle Biopsy Versus Surgical Excisional Biopsy: Three-Year Experience of a Reference Center in Lebanon

Clinical lymphoma, myeloma and leukemia, 2020-08, Vol.20 (8), p.e455-e460

2020

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Germline pathogenic variants among high hereditary risk patients with breast and ovarian cancer and unaffected subjects in Lebanese Arab women

World journal of clinical oncology, 2024-12, Vol.15 (12), p.1481-1490

2024

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Abstract P6-02-17: A Real-World Study of BRCA1 and BRCA2 Germline Mutations among High Hereditary Risk Subjects and Patients with Breast and Ovarian Cancer in Lebanon

Cancer research (Chicago, Ill.), 2023-03, Vol.83 (5_Supplement), p.P6-P6-02-17

2023

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Comparison between the accuracy of chest computerized tomography vs. reverse transcriptase polymerase chain reaction in a tertiary care center in Lebanon; along with their correlation to mortality, morbidity and symptoms in COVID-19 patients

Human gene (Amsterdam, Netherlands), 2023-02, Vol.35, p.201150-201150, Article 201150

2023

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Molecular profiling of adult acute myeloid and lymphoid leukemia in a major referral center in Lebanon: a 10-year experience report and review of the literature

Molecular biology reports, 2019-04, Vol.46 (2), p.2003-2011

2019

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Prevalence of T790M mutation among TKI-therapy resistant Lebanese lung cancer patients based on liquid biopsy analysis: a first report from a major tertiary care center

Molecular biology reports, 2019-08, Vol.46 (4), p.3671-3676

2019

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Genetics of multifactorial disorders: proceedings of the 6th Pan Arab Human Genetics Conference

Journal of translational medicine, 2016-04, Vol.14 (96), p.96-96, Article 96

2016

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Reductive dechlorination of carbon tetrachloride by cobalamin(II) in the presence of dithiothreitol : mechanistic study, effect of redox potential and pH

Environmental science & technology, 1994-02, Vol.28 (2), p.246-252

1994

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Prevalence of thrombophilia-associated mutations and their clinical significance in a large cohort of Lebanese patients

Meta Gene, 2021-09, Vol.29, p.100936, Article 100936

2021

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Insight into the 8p23.1 duplication syndrome: Case report of a young women with infertility

Heliyon, 2023, Vol.9 (4), p.e15515-e15515

2023

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Intrachromosomal amplification 21: A driver of acute myeloid leukemia?

Visceral leishmaniasis presenting with pancytopenia and circulating blastlike lymphocytes

Using the SLIPTA checklist to assess laboratory readiness for Joint Commission International accreditation

P043: The status of germline variants of unknown significance in minorities: Middle Eastern patients with HBOC

Curbing the greenhouse effect by carbon dioxide adsorption with Zeolite 13X

Insight into the 8p23.1 duplication syndrome: Case report of a young women with infertility

AML with inv(16)/t(16;16) and high-risk cytogenetic abnormalities: atypical features and unfavorable outcome

KMT2A-ARHGEF12, a therapy related fusion with poor prognosis

eP314: Rare unbalanced complex chromosomal rearrangement in a case of infertility: Insight into the 8p23.1 duplication syndrome

Cryptic insertion of KMT2A, a rare t(9;11) variant

Double translocation or gene insertion? A BCR/ABL1 fusion in Philadelphia-negative CML

Molecular characterization of adult IRF4 large B-cell lymphoma with spontaneous remission

Plasma cells and lymphoid aggregates in sleeve gastrectomy specimens: Normal or gastritis?

Novel trans-2,3-enoyl-CoA reductase–like variant associated with catecholaminergic polymorphic ventricular tachycardia type 3

Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two α-Globin Gene Defects, Hb Taybe D HBA1 : C.119_121delCCA Mutation and HBA2 : C.94A > G Mutation

Diagnosing Lymphoproliferative Disorders Using Core Needle Biopsy Versus Surgical Excisional Biopsy: Three-Year Experience of a Reference Center in Lebanon

Germline pathogenic variants among high hereditary risk patients with breast and ovarian cancer and unaffected subjects in Lebanese Arab women

Abstract P6-02-17: A Real-World Study of BRCA1 and BRCA2 Germline Mutations among High Hereditary Risk Subjects and Patients with Breast and Ovarian Cancer in Lebanon

Comparison between the accuracy of chest computerized tomography vs. reverse transcriptase polymerase chain reaction in a tertiary care center in Lebanon; along with their correlation to mortality, morbidity and symptoms in COVID-19 patients

Molecular profiling of adult acute myeloid and lymphoid leukemia in a major referral center in Lebanon: a 10-year experience report and review of the literature

Prevalence of T790M mutation among TKI-therapy resistant Lebanese lung cancer patients based on liquid biopsy analysis: a first report from a major tertiary care center

Genetics of multifactorial disorders: proceedings of the 6th Pan Arab Human Genetics Conference

Reductive dechlorination of carbon tetrachloride by cobalamin(II) in the presence of dithiothreitol : mechanistic study, effect of redox potential and pH

Prevalence of thrombophilia-associated mutations and their clinical significance in a large cohort of Lebanese patients

Insight into the 8p23.1 duplication syndrome: Case report of a young women with infertility

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