Zobrazeno 1 - 6
of 6
pro vyhledávání: '"MESH: Arabs"'
Autor:
Idil I. Aigha, Hager Memmi, Lotfi Chouchane, Wijden Mahfoudh, Noureddine Bouaouina, Jingxuan Shan, Sonia Abdelhak, Sallouha Gabbouj, Elham Hassen, Rebecca Mathew, Ahlem Benhadjayed, Yassmine Remadi, Shoba P Dsouza
Publikováno v:
Breast Cancer Research and Treatment
Breast Cancer Research and Treatment, Springer Verlag, 2012, 135 (3), pp.715-24. ⟨10.1007/s10549-012-2202-6⟩
Breast Cancer Research and Treatment, Springer Verlag, 2012, 135 (3), pp.715-24. ⟨10.1007/s10549-012-2202-6⟩
Genome-wide Association Studies (GWAS) revealed novel genetic markers for breast cancer susceptibility. But little is known about the risk factors and molecular events associated with breast cancer in Arab Population. Therefore, we designed a broad s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffcde7c174fe2b743da2d13d0da814e0
https://hal-riip.archives-ouvertes.fr/pasteur-01375153
https://hal-riip.archives-ouvertes.fr/pasteur-01375153
Autor:
Frouzandeh Mahjoubi, Mohammad Esmaeil Akbari, Morteza Karimipoor, Mohammad Hamid, Sirous Zeinali
Publikováno v:
Annals of Hematology
Annals of Hematology, Springer Verlag, 2009, 88 (12), pp.1267-8. ⟨10.1007/s00277-009-0756-0⟩
Annals of Hematology, Springer Verlag, 2009, 88 (12), pp.1267-8. ⟨10.1007/s00277-009-0756-0⟩
International audience; Dear Editor, The increase of fetal hemoglobin (HbF), in adult life, is mainly due to large deletions within β-globin cluster in hereditary persistence of fetal hemoglobin (HPFH) and δβ- thalassemia or in some cases of nonde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7808a17bd463cc73f0f70f3bc50c472b
https://hal-riip.archives-ouvertes.fr/pasteur-00751227/file/fulltext2.pdf
https://hal-riip.archives-ouvertes.fr/pasteur-00751227/file/fulltext2.pdf
Autor:
Michel Michaelides, Parissa Aref, David Mansfield, Roman Carlos, Roger C. Shore, Mohsen Abbasi, Chris F. Inglehearn, Ian M. Carr, Katharine M. Blain, Hélène Dollfus, Walid El-Sayed, Ismail K. Jalili, Anthony T. Moore, Agnès Bloch-Zupan, Alan J. Mighell, Jennifer Kirkham, David A. Parry, M Shahrabi, Louise Downey, Mansour Heidari
Publikováno v:
American Journal of Human Genetics
American Journal of Human Genetics, 2009, 84 (2), pp.266-73. ⟨10.1016/j.ajhg.2009.01.009⟩
American Journal of Human Genetics, 2009, 84 (2), pp.266-73. ⟨10.1016/j.ajhg.2009.01.009⟩
International audience; The combination of recessively inherited cone-rod dystrophy (CRD) and amelogenesis imperfecta (AI) was first reported by Jalili and Smith in 1988 in a family subsequently linked to a locus on chromosome 2q11, and it has since
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1c27f7d29a94a3431a5b74061b408d8
https://www.hal.inserm.fr/inserm-00384526
https://www.hal.inserm.fr/inserm-00384526
Autor:
Latifa El Kihal, Rajae Afifi, Mohammed Hassar, Pascal Pineau, M. Benazzouz, Sayeh Ezzikouri, Abdellah Essaid El Feydi, Abdelaziz Chafik, Soumaya Benjelloun
Publikováno v:
Archives of Medical Research
Archives of Medical Research, Elsevier, 2008, 39 (2), pp.236-241. ⟨10.1016/j.arcmed.2007.09.006⟩
Archives of Medical Research, 2008, 39 (2), pp.236-241. ⟨10.1016/j.arcmed.2007.09.006⟩
Archives of Medical Research, Elsevier, 2008, 39 (2), pp.236-241. ⟨10.1016/j.arcmed.2007.09.006⟩
Archives of Medical Research, 2008, 39 (2), pp.236-241. ⟨10.1016/j.arcmed.2007.09.006⟩
International audience; Background: Hereditary hemochromatosis and SERPINA1 mutation were reported to affect liver functions. Our objective was to estimate the prevalence of HFE and SERPINA1 (formerly known as alpha1-antitrypsin, AAT) mutations and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5658b90e28110c32f640b50cd367309c
https://hal-pasteur.archives-ouvertes.fr/pasteur-02870414
https://hal-pasteur.archives-ouvertes.fr/pasteur-02870414
Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families
Autor:
Diana Zelenika, Alexander Lossos, Ali Benomar, Zohar Argov, Stephan Klebe, Alexandra Durr, Alexis Brice, Naima Bouslam, Abdelmadjid Hamri, Meriem Tazir, N. Elleuch, D. Grid, Sylvain Hanein, Giovanni Stevanin, Delphine Bacq, Vardiella Meiner, N. Birouk, Mohamed Yahyaoui, Israela Lerer
Publikováno v:
neurogenetics
neurogenetics, Springer Verlag, 2007, 8 (4), pp.307-15. ⟨10.1007/s10048-007-0097-x⟩
neurogenetics, 2007, 8 (4), pp.307-15. ⟨10.1007/s10048-007-0097-x⟩
neurogenetics, Springer Verlag, 2007, 8 (4), pp.307-15. ⟨10.1007/s10048-007-0097-x⟩
neurogenetics, 2007, 8 (4), pp.307-15. ⟨10.1007/s10048-007-0097-x⟩
Hereditary spastic paraplegia (HSP) type 15 is an autosomal recessive (AR) form of complicated HSP mainly characterized by slowly progressive spastic paraplegia, mental retardation, intellectual deterioration, maculopathy, distal amyotrophy, and mild
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baf0224f5cb7a073e32a0bab10b2fe9f
https://hal.archives-ouvertes.fr/hal-00281710
https://hal.archives-ouvertes.fr/hal-00281710
Autor:
Meriem Tazir, Pierre Pollak, Anne-Louise Leutenegger, Sabine Janin, Alexandra Durr, Ebba Lohmann, Alexis Brice, Suzanne Lesage
Publikováno v:
New England Journal of Medicine
New England Journal of Medicine, Massachusetts Medical Society, 2006, 354 (4), pp.422-3. ⟨10.1056/NEJMc055540⟩
New England Journal of Medicine, 2006, 354 (4), pp.422-3. ⟨10.1056/NEJMc055540⟩
New England Journal of Medicine, Massachusetts Medical Society, 2006, 354 (4), pp.422-3. ⟨10.1056/NEJMc055540⟩
New England Journal of Medicine, 2006, 354 (4), pp.422-3. ⟨10.1056/NEJMc055540⟩
To the Editor: Parkinson's disease is characterized by resting tremor, rigidity, and bradykinesia caused by the loss of dopaminergic neurons in the substantia nigra, a good response to levodopa, an...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afd83ada32bedb8159526e6db264795e
https://hal.archives-ouvertes.fr/hal-00221453
https://hal.archives-ouvertes.fr/hal-00221453