Found: 12
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Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations.
- Published in:
- Human Genetics, 2002, v. 111, n. 3, p. 255, doi. 10.1007/s00439-002-0755-x
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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
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
Death in Unverricht-Lundborg disease.
- Published in:
- 2009
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- Publication type:
- journal article
Death in Unverricht–Lundborg disease.
- Published in:
- Neurological Sciences, 2009, v. 30, n. 4, p. 315, doi. 10.1007/s10072-009-0102-2
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- Publication type:
- Article
Health-related Quality of Life of People with Epilepsy Compared with a General Reference Population: A Tunisian Study.
- Published in:
- Epilepsia (Series 4), 2004, v. 45, n. 7, p. 838, doi. 10.1111/j.0013-9580.2004.56903.x
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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
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- Publication type:
- Article
Association of amyotrophic lateral sclerosis and Behcet's disease: is there a relationship? A multi-national case series.
- Published in:
- Clinical Rheumatology, 2012, v. 31, n. 4, p. 733, doi. 10.1007/s10067-011-1923-y
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- Publication type:
- Article
Cheiro-Oral Syndrome and Parietal Stroke.
- Published in:
- Cerebrovascular Diseases, 1993, v. 3, n. 3, p. 183, doi. 10.1159/000108699
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- Publication type:
- Article
Systemic lupus erythematosus induced by interferon β1 therapy in a patient with multiple sclerosis.
- Published in:
- Fundamental & Clinical Pharmacology, 2012, v. 26, n. 2, p. 210, doi. 10.1111/j.1472-8206.2011.00929.x
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- Publication type:
- Article
A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous family.
- Published in:
- BMC Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2156-14-93
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- Publication type:
- Article