Published in Med Oncol on December 27, 2012
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Urinary biomarkers predict brain tumor presence and response to therapy. Clin Cancer Res (2008) 1.72
Semen parameters and sperm DNA fragmentation as causes of recurrent pregnancy loss. Urology (2011) 1.62
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Chromosomal microarray analysis in a girl with mental retardation and spina bifida. Pediatr Neurol (2011) 1.39
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Best cases from the AFIP: osmotic demyelination syndrome. Radiographics (2009) 1.04
Outcome of pediatric pineoblastoma after surgery, radiation and chemotherapy. J Neurooncol (2008) 1.00
Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations. J Hum Genet (2003) 0.97
The effects of male aging on semen quality, sperm DNA fragmentation and chromosomal abnormalities in an infertile population. J Assist Reprod Genet (2011) 0.97
Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4--KCNQ2 genes loci. Eur J Med Genet (2007) 0.96
An autosomal dominant hypophosphatemic rickets phenotype in a Tunisian family caused by a new FGF23 missense mutation. J Bone Miner Metab (2009) 0.94
Treatment of Acute Promyelocytic Leukemia with AIDA Based Regimen. Update of a Tunisian Single Center Study. Mediterr J Hematol Infect Dis (2011) 0.92
Large duplication 4q25-q34 with mild clinical effect. Ann Genet (2004) 0.92
Cathepsin S deficiency confers protection from neonatal hyperoxia-induced lung injury. Am J Respir Crit Care Med (2007) 0.91
Impact of seminal trace element and glutathione levels on semen quality of Tunisian infertile men. BMC Urol (2012) 0.90
Skewed X-chromosome inactivation pattern in SRY positive XX maleness: a case report and review of literature. Ann Genet (2003) 0.89
Altered antioxidant status and increased lipid per-oxidation in seminal plasma of tunisian infertile men. Int J Biol Sci (2011) 0.88
Cytogenetic analysis of 298 newly diagnosed cases of acute lymphoblastic leukaemia in Tunisia. Hematol Oncol (2008) 0.88
Glioma epidemiology in the central Tunisian population: 1993-2012. Asian Pac J Cancer Prev (2014) 0.87
Familial early-onset diabetes is not a typical MODY in several Tunisian patients. Tunis Med (2012) 0.87
Molecular cytogenetic characterization of variant Philadelphia translocations in chronic myeloid leukemia: genesis and deletion of derivative chromosome 9. Cancer Genet Cytogenet (2009) 0.86
Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients. Eur J Paediatr Neurol (2011) 0.85
Detection of DNA fragmentation and meiotic segregation in human with isolated teratozoospermia. J Assist Reprod Genet (2010) 0.84
BBS10 mutations are common in 'Meckel'-type cystic kidneys. J Med Genet (2010) 0.84
Treatment of acute promyelocytic leukemia with PETHEMA LPA 99 protocol: a Tunisian single center experience. Hematology (2010) 0.83
Cytogenetic and molecular aspects of absolute teratozoospermia: comparison between polymorphic and monomorphic forms. Urology (2011) 0.83
Cytogenetics and fluorescence in situ hybridization assessment of sex-chromosome mosaicism in Klinefelter's syndrome. Ann Genet (2004) 0.83
Comprehensive analysis of BCR/ABL variants in chronic myeloid leukemia patients using multiplex RT-PCR. Clin Lab (2012) 0.83
Chromosomal segregation in spermatozoa of five Robertsonian translocation carriers t(13;14). J Assist Reprod Genet (2011) 0.82
Characteristics of invasive aspergillosis in neutropenic haematology patients (Sousse, Tunisia). Mycopathologia (2014) 0.82
Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: characterization of three novel polymorphisms. Gene (2012) 0.82
Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa. Ann Neurol (2014) 0.82
Phenotype and micro-array characterization of duplication 11q22.1-q25 and review of the literature. Gene (2013) 0.81
Acute hydrocephalus secondary to obstruction of the foramen of monro and cerebral aqueduct caused by a choroid plexus cyst in the lateral ventricle. Case report. J Neurosurg (2007) 0.81
Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family. Gen Comp Endocrinol (2011) 0.81
Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III. J Hum Genet (2011) 0.81
E355G mutation appearing in a patient with e19a2 chronic myeloid leukaemia resistant to imatinib. J Clin Pathol (2010) 0.80
Chronic myeloid leukemia as a secondary malignancy after lymphoma in a child. A case report and review of the literature. Onkologie (2012) 0.80
Mutational screening of SF1 and WNT4 in Tunisian women with premature ovarian failure. Gene (2012) 0.80
Molecular prenatal diagnosis of muscular dystrophies in Tunisia and postnatal follow-up role. Genet Test (2008) 0.79
Quantitative analysis of human herpesvirus-6 and human cytomegalovirus in blood and saliva from patients with acute leukemia. J Med Virol (2014) 0.79
A masked BCR/ABL rearrangement in a case of chronic myeloid leukemia with translocation t(3;9)(p14;q34). Cancer Genet Cytogenet (2008) 0.79
Xmn I polymorphism associated with concomitant activation of Gγ and Aγ globin gene transcription on a β0-thalassemia chromosome. Blood Cells Mol Dis (2010) 0.79
High frequency of W1327X mutation in glycogen storage disease type III patients from central Tunisia. Ann Biol Clin (Paris) (2012) 0.79
Analysis of sperm aneuploidies and DNA fragmentation in patients with globozoospermia or with abnormal acrosomes. Urology (2011) 0.79
Meningeal Hemangiopericytomas and Meningomas: a Comparative Immunohistochemical and Genetic Study. Asian Pac J Cancer Prev (2015) 0.79
Array-CGH study of partial trisomy 9p without mental retardation. Am J Med Genet A (2011) 0.78
Molecular cytogenetic characterization of Philadelphia-negative rearrangements in chronic myeloid leukemia patients. J Cancer Res Clin Oncol (2011) 0.78
A cytogenetic approach to the effects of low levels of ionizing radiation (IR) on the exposed Tunisian hospital workers. Int J Occup Med Environ Health (2013) 0.78
Examination of viability and quality of ovarian tissue after cryopreservation using simple laboratory methods in ewe. Reprod Biol Endocrinol (2011) 0.78
Nasopharyngeal/nasal type NK/T lymphoma: analysis of 23 cases and current review of the literature. Kulak Burun Bogaz Ihtis Derg (2012) 0.78
Decreased eNOS protein expression in involuting and propranolol-treated hemangiomas. Arch Otolaryngol Head Neck Surg (2012) 0.77
DNA fragmentation status in patients with necrozoospermia. Syst Biol Reprod Med (2012) 0.77
Assessment of chromosomal aberrations, micronuclei and proliferation rate index in peripheral lymphocytes from Tunisian nurses handling cytotoxic drugs. Environ Toxicol Pharmacol (2010) 0.77
Progressive multifocal leukoencephalopathy in a patient with relapsed acute myelogenous leukemia. J Clin Oncol (2008) 0.76
T(1;21;8)(p34;q22;q22): a novel variant of t(8;21) in acute myeloblastic leukemia with maturation. Med Oncol (2010) 0.76
A PML/RARA chimeric gene on chromosome 12 in a patient with acute promyelocytic leukemia (M4) associated with a new variant translocation: t(12;15;17)(q24;q24;q11). Med Oncol (2013) 0.76
Pericentric inversion of chromosom 12 [Inv (12) (p12q12)] associated with idiopathic azoospermia in one infertile Tunisian man. Biochem Biophys Res Commun (2013) 0.76
[Genotoxic risk assessment of nurses handling antineoplastic drugs]. Ann Biol Clin (Paris) (2010) 0.75
A combination of micronucleus assay and fluorescence in situ hybridization analysis to evaluate the genotoxicity of formaldehyde. Arch Environ Contam Toxicol (2012) 0.75
ETV6-RUNX1 Rearrangement in Tunisian Pediatric B-Lineage Acute Lymphoblastic Leukemia. Adv Hematol (2009) 0.75
Cytogenetic profile of a large cohort of Tunisian de novo acute myeloid leukemia. Hematology (2012) 0.75
Molecular study of the perforin gene in familial hematological malignancies. Hered Cancer Clin Pract (2011) 0.75
A novel t(3;12)(q21;p13) translocation in a patient with accelerated chronic myeloid leukemia after imatinib and nilotinib therapy. Cancer Biol Med (2013) 0.75
Detection of aneuploidy rate for chromosomes X, Y and 8 by fluorescence in-situ hybridization in spermatozoa from patients with severe non-obstructive oligozoospermia. J Assist Reprod Genet (2011) 0.75
[Profiles of embryos designed by fertilization assisted and their impact on the rate of pregnancies]. Tunis Med (2010) 0.75
Multiple myeloma following essential thrombocythemia. Ann Biol Clin (Paris) (2013) 0.75
[Prognostic impact of karyotype in de novo acute myeloid leukemia: study of 139 cases]. Tunis Med (2002) 0.75
Tunisian adult's Hodgkin lymphoma Study Group. Tunis Med (2016) 0.75
Cytogenetic survey of 117 Tunisian patients with de novo myelodysplastic syndrome. Ann Genet (2002) 0.75
Nickel-Iron Nitride -Nickel Sulfide Composites for Oxygen Evolution Electrocatalysis. ACS Appl Mater Interfaces (2020) 0.75
Cytogenetic abnormalities in Tunisian de novo myelodysplastic syndrome: a comparison with other populations. Leuk Res (2008) 0.75