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Up‐to‐date incidence and initial characteristics of cystic fibrosis in Tunisia.
- Published in:
- Pediatric Pulmonology, 2022, v. 57, n. 10, p. 2540, doi. 10.1002/ppul.26032
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- Publication type:
- Article
High APOE epsilon 4 allele frequencies associated with Alzheimer disease in a Tunisian population.
- Published in:
- Neurological Sciences, 2012, v. 33, n. 1, p. 33, doi. 10.1007/s10072-011-0663-8
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- Publication type:
- Article
Obsessive-compulsive disorder: a new risk factor for Alzheimer disease?
- Published in:
- Neurological Sciences, 2011, v. 32, n. 5, p. 959, doi. 10.1007/s10072-011-0480-0
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- Publication type:
- Article
Autism in Phenylketonuria Patients.
- Published in:
- Journal of Child Neurology, 2016, v. 31, n. 7, p. 843, doi. 10.1177/0883073815623636
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- Publication type:
- Article
Genotypic and phenotypic characteristics of tunisian isoniazid-resistant Mycobacterium tuberculosis strains.
- Published in:
- Journal of Microbiology, 2011, v. 49, n. 3, p. 413, doi. 10.1007/s12275-011-0268-1
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- Publication type:
- Article
Missing apolipoprotein E ɛ4 allele associated with nonamnestic Alzheimer’s disease in a Tunisian population.
- Published in:
- Journal of Genetics, 2022, v. 101, n. 2, p. 1, doi. 10.1007/s12041-022-01384-9
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- Publication type:
- Article
Angiotensin-converting enzyme insertion/deletion gene polymorphism in cystic fibrosis patients.
- Published in:
- Journal of Genetics, 2016, v. 95, n. 1, p. 193, doi. 10.1007/s12041-015-0609-7
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- Publication type:
- Article
New frameshift CF mutation 3729delAinsTCT in a Tunisian cystic fibrosis patient.
- Published in:
- Journal of Genetics, 2013, v. 92, n. 1, p. 81, doi. 10.1007/s12041-013-0208-4
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- Publication type:
- Article
A gain-of-function mutation in zinc cluster transcription factor Rob1 Drives Candida albicans adaptive growth in the cystic fibrosis lung environment.
- Published in:
- PLoS Pathogens, 2024, v. 20, n. 4, p. 1, doi. 10.1371/journal.ppat.1012154
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- Publication type:
- Article
Capillarys 2 Flex Piercing: Analytical performance assessment according to CLSI protocols for HbA<sub>1c</sub> quantification.
- Published in:
- Electrophoresis, 2017, v. 38, n. 17, p. 2210, doi. 10.1002/elps.201600423
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- Publication type:
- Article
Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients.
- Published in:
- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 10, p. 1, doi. 10.1002/mgg3.2048
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- Publication type:
- Article
First study of angiotensin converting enzyme in cystic fibrosis Tunisian patients.
- Published in:
- 2014
- By:
- Publication type:
- Letter to the Editor
Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 11, p. 2115, doi. 10.1515/cclm-2013-0354
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- Publication type:
- Article
Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 8, p. 1595, doi. 10.1515/cclm-2012-0842
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- Publication type:
- Article
δ<sup>0</sup>-Thalassemia in cis of β<sup>Knossos</sup> globin gene: first homozygous description in thalassemia intermedia Libyans and first combination with codon 39 (C→T) in thalassemia intermedia Tunisian patients.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2012, v. 50, n. 10, p. 1743, doi. 10.1515/cclm-2012-0102
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- Publication type:
- Article
Preliminary national report on cystic fibrosis epidemiology in Tunisia: the actual state of affairs.
- Published in:
- African Health Sciences, 2020, v. 20, n. 1, p. 444, doi. 10.4314/ahs.v20i1.51
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- Publication type:
- Article
Cystic fibrosis in Tunisian children: a review of 32 children.
- Published in:
- African Health Sciences, 2018, v. 18, n. 3, p. 664, doi. 10.4314/ahs.v18i3.24
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- Publication type:
- Article
Congenital analbuminemia associated with compound heterozygous novel nucleotide variations in a young adult with coronary thrombosis.
- Published in:
- Annales de Biologie Clinique, 2023, v. 81, n. 2, p. 204, doi. 10.1684/abc.2023.1806
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- Publication type:
- Article
Contribution of common CFTR variants (M470V, T854, and Q1463) to cystic fibrosis in Tunisia: haplotype analysis.
- Published in:
- Annales de Biologie Clinique, 2021, v. 79, n. 1, p. 63, doi. 10.1684/abc.2021.1614
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- Publication type:
- Article
Glucose-6-phosphate dehydrogenase deficiency in Tunisian jaundiced neonates.
- Published in:
- Annales de Biologie Clinique, 2020, v. 78, n. 4, p. 411, doi. 10.1684/abc.2020.1558
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- Publication type:
- Article
Association of IVS6A GATT polymorphism of CFTR gene with cystic fibrosis: first study in CF and normal Tunisian population.
- Published in:
- Annales de Biologie Clinique, 2020, v. 78, n. 3, p. 314, doi. 10.1684/abc.2020.1555
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- Publication type:
- Article
Pseudo-Bartter syndrome as the sole manifestation of cystic fibrosis in a child with 711+G>T/IVS8-5T mutation: a new face of an old disease.
- Published in:
- Annales de Biologie Clinique, 2017, v. 75, n. 4, p. 466, doi. 10.1684/abc.2017.1268
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- Publication type:
- Article
Catalyzing precision: unraveling the diagnostic conundrum of tunisian familial hypophosphatasia case through integrative clinical and molecular approaches.
- Published in:
- Molecular Genetics & Genomics, 2024, v. 299, n. 1, p. 1, doi. 10.1007/s00438-024-02157-y
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- Publication type:
- Article
Molecular characterization of Mycobacterium tuberculosis strains resistant to isoniazid.
- Published in:
- International Journal of Mycobacteriology, 2016, v. 5, p. S151, doi. 10.1016/j.ijmyco.2016.09.070
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- Publication type:
- Article
Correction to: Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme.
- Published in:
- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01061-3
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- Publication type:
- Article
Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme.
- Published in:
- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01061-3
- By:
- Publication type:
- Article
A lower-cost protocol for sickle cell disease neonatal screening in Tunisia.
- Published in:
- Annals of Saudi Medicine, 2012, v. 32, n. 1, p. 49, doi. 10.5144/0256-4947.2012.49
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- Publication type:
- Article
Gross genomic rearrangements involving deletions in the CFTR gene: characterization of six new events from a large cohort of hitherto unidentified cystic fibrosis chromosomes and meta-analysis of the underlying mechanisms.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 5, p. 567, doi. 10.1038/sj.ejhg.5201590
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- Publication type:
- Article
Contribution of β-globin cluster polymorphisms to raise fetal hemoglobin levels in normal adults.
- Published in:
- Molecular Biology Reports, 2012, v. 39, n. 4, p. 4619, doi. 10.1007/s11033-011-1253-9
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- Publication type:
- Article
Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1b.
- Published in:
- Diabetology & Metabolic Syndrome, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13098-023-01065-2
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- Publication type:
- Article
Clopidogrel utilization in patients with coronary artery disease and diabetes mellitus: should we determine CYP2C19*2 genotype?
- Published in:
- European Journal of Clinical Pharmacology, 2018, v. 74, n. 12, p. 1567, doi. 10.1007/s00228-018-2530-5
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- Publication type:
- Article
Association of Bgl II Polymorphism in ITGA2 and (894G/T and −786T/C) Polymorphisms in eNOS Gene With Stroke Susceptibility in Tunisian Patients α2 Gene Polymorphism in α2β1 Integrin and eNOS Gene Variants and Stroke.
- Published in:
- Biological Research for Nursing, 2021, v. 23, n. 3, p. 408, doi. 10.1177/1099800420977685
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- Publication type:
- Article
Epidemiological and clinical characteristics of 66 Tunisian Sickle cell syndrome patients.
- Published in:
- African Health Sciences, 2023, v. 23, n. 3, p. 213, doi. 10.4314/ahs.v23i3.26
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- Publication type:
- Article
Association Between Alzheimer Disease and the −491T Allele of Regulatory Region Polymorphism of Apolipoprotein E in a Tunisian Population.
- Published in:
- Neurochemical Research, 2014, v. 39, n. 2, p. 244, doi. 10.1007/s11064-013-1213-y
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- Publication type:
- Article
Association between angiotensin-converting enzyme gene polymorphism and competitive anxiety in Tunisian athlete.
- Published in:
- Sport Sciences for Health, 2016, v. 12, n. 2, p. 233, doi. 10.1007/s11332-016-0280-2
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- Publication type:
- Article
Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC).
- Published in:
- 2016
- By:
- Publication type:
- journal article
The epidemiology of abnormal hemoglobins in Mediterranean high-level athletes.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Vitamin D receptor gene BsmI (rs1544410) polymorphism: role in multiple sclerosis and genotype-phenotype correlations.
- Published in:
- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09369-w
- By:
- Publication type:
- Article
Vitamin D receptor gene BsmI (rs1544410) polymorphism: role in multiple sclerosis and genotype-phenotype correlations.
- Published in:
- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09369-w
- By:
- Publication type:
- Article
Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations.
- Published in:
- Molecular Biology Reports, 2021, v. 48, n. 8, p. 5923, doi. 10.1007/s11033-021-06592-7
- By:
- Publication type:
- Article
Complete ascertainment of intragenic copy number mutations (CNMs) in the CFTR gene and its implications for CNM formation at other autosomal loci.
- Published in:
- Human Mutation, 2010, v. 31, n. 4, p. 421, doi. 10.1002/humu.21196
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- Publication type:
- Article
Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A substitution and a previously reported FGB IVS6‐10_16delTTTG deletion.
- Published in:
- Haemophilia, 2020, v. 26, n. 4, p. e194, doi. 10.1111/hae.13974
- By:
- Publication type:
- Article
Early psychiatrics symptoms in familial Alzheimer's disease with presenilin 1 mutation (I83T).
- Published in:
- Journal of Neural Transmission, 2016, v. 123, n. 4, p. 451, doi. 10.1007/s00702-015-1498-x
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- Publication type:
- Article
Association between ACE polymorphism, cognitive phenotype and APOE E4 allele in a Tunisian population with Alzheimer disease.
- Published in:
- Journal of Neural Transmission, 2016, v. 123, n. 3, p. 317, doi. 10.1007/s00702-015-1468-3
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- Publication type:
- Article
No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a Tunisian population.
- Published in:
- Journal of Neural Transmission, 2013, v. 120, n. 9, p. 1355, doi. 10.1007/s00702-013-0985-1
- By:
- Publication type:
- Article
Inherited bisalbuminemia with growth hormone deficiency.
- Published in:
- 2019
- By:
- Publication type:
- Case Study