Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Chiraz Bouchlaka"'
Publikováno v:
Climacteric : the journal of the International Menopause Society. 18(4)
Osteopenia is characterized by intermediate values of bone mineral density (BMD) as compared to normal and osteoporotic subjects. BMD, a surrogate phenotype for osteoporosis, is influenced in part by genetic factors. Among the genes associated with B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e326a6038171389d4fe8c79685f6533
https://pubmed.ncbi.nlm.nih.gov/25603555
https://pubmed.ncbi.nlm.nih.gov/25603555
Autor:
R. Ben Mousli, A. Ben Osman, S. Ghedamsi, Mourad Mokni, Koussay Dellagi, Samir Boubaker, R. Elkares, Cherine Charfeddine, Chiraz Bouchlaka, D. Baccouche, Sonia Abdelhak
Publikováno v:
British Journal of Dermatology. 149:1108-1115
Summary Background Mal de Meleda (MDM) is a rare autosomal recessive skin disorder which belongs to the clinically and genetically heterogeneous group of palmoplantar keratodermas (PPK). Clinically, MDM is characterized by erythema and hyperkeratosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a1adf51ad21bedb2f7002be69788d9c
https://doi.org/10.1111/j.1365-2133.2003.05606.x
https://doi.org/10.1111/j.1365-2133.2003.05606.x
Autor:
Bechir Zouari, Hejer El Mahmoudi, H. Sahli, Serge Ferrari, Rim Sassi, Amel Benammar Elgaaied, Slaheddine Sellami, Chiraz Bouchlaka Souissi
Publikováno v:
BMC Musculoskeletal Disorders
BMC Musculoskeletal Disorders, Vol. 15, No 144 (2014)
BMC Musculoskeletal Disorders, Vol. 15, No 144 (2014)
Background Osteoporosis is a highly heritable trait. Among the genes associated with bone mineral density (BMD), the low-density lipoprotein receptor-related protein 5 gene (LRP5) has been consistently identified in Caucasians. However LRP5 contribut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5fb0e1a53a6264dd2152d9cedd69638
https://doi.org/10.1186/1471-2474-15-144
https://doi.org/10.1186/1471-2474-15-144
Autor:
Myriam, Ammar, Chiraz, Bouchlaka-Souissi, Ines, Zaraa, Cindy, Helms, Nejib, Doss, Fatma, Bouazizi, Raouf, Dhaoui, Amel Ben, Ossman, Amel Ben, Ammar-el Gaied, Mourad, Mokni
Publikováno v:
International journal of dermatology. 51(11)
The pathogenesis of all forms of psoriasis remains obscure. Segregation analysis and twin studies together with ethnic differences in disease frequency all point to an underlying genetic susceptibility to psoriasis, which is both complex and likely t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2ad2b3a9957b15adb4b8cb724d553c19
https://pubmed.ncbi.nlm.nih.gov/23067081
https://pubmed.ncbi.nlm.nih.gov/23067081
Autor:
Myriam, Ammar, Ines, Zaraa, Chiraz, Bouchlaka-Souissi, Nejib, Doss, Raouf, Dhaoui, Amel, Ben Osman, Mourad, Mokni, Amel, Ben Ammar El Gaaied
Publikováno v:
La Tunisie medicale. 90(7)
Psoriasis is a chronic inflammatory skin disease often benign, affecting 2-3% of the total world population. Psoriasis is a multifactorial disease.To present recent advances in the immunologic mechanisms and susceptibility genes involved in the patho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9dab8bf188cb8bbfefa55ebeb4862ed5
https://pubmed.ncbi.nlm.nih.gov/22811223
https://pubmed.ncbi.nlm.nih.gov/22811223
Autor:
Abdelkarim Ayadi, Koussay Dellagi, Sonia Abdelhak, M. Tahar Sfar, B. Mahjoub, Mahbouba Sioud, Neji Gueddich, Zouheir Belhadjali, Chokri Maktouf, Ahmed Rebai, Chiraz Bouchlaka
Publikováno v:
Journal of Human Genetics
Journal of Human Genetics, Nature Publishing Group, 2007, 52 (3), pp.262-270. ⟨10.1007/s10038-007-0110-0⟩
Journal of Human Genetics, Nature Publishing Group, 2007, 52 (3), pp.262-270. ⟨10.1007/s10038-007-0110-0⟩
International audience; Megaloblastic anaemia 1 (MGA1) is a rare autosomal recessive condition characterized by selective intestinal vitamin B12 malabsorption and proteinuria. More than 200 MGA1 patients have been identified worldwide, but the diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1aba697bf297dcb582b77be76c3fc70d
https://pubmed.ncbi.nlm.nih.gov/17285242
https://pubmed.ncbi.nlm.nih.gov/17285242
Autor:
Mourad Mokni, Samir Boubaker, Cherine Charfeddine, Amel Ben Osman, Ahmed Rebai, Selma Kassar, Chiraz Bouchlaka, Sonia Abdelhak, Hela Zribi
Publikováno v:
Journal of Human Genetics
Journal of Human Genetics, Nature Publishing Group, 2006, 51 (10), pp.841-845. ⟨10.1007/s10038-006-0002-8⟩
Journal of Human Genetics, Nature Publishing Group, 2006, 51 (10), pp.841-845. ⟨10.1007/s10038-006-0002-8⟩
International audience; Transgressive palmoplantar keratoderma (PPK) is the phenotypic hallmark of Mal de Meleda (MDM, MIM 24300). It is characterized by erythema and hyperkeratosis that extend to the dorsal face of the hands and feet. The disease is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5517c0db7013f25f2da5ee7edf8d6e1d
https://hal-riip.archives-ouvertes.fr/pasteur-01375261
https://hal-riip.archives-ouvertes.fr/pasteur-01375261
Autor:
Hela Ben Abid, Chiraz Bouchlaka, Lamia Aissaoui, Koussay Dellagi, Sonia Abdelhak, Hmida Slama, Moez Elloumi, Ahlem Amouri, Sondes Hadiji, Ali Saad, Tarek Ben Othman, Houda Elloumi, Hafedh Makni
Publikováno v:
Genetic testing. 8(3)
We report on the effectiveness of molecular studies regarding Fanconi anemia (FA) for a better selection of bone marrow graft donors and for post-transplant follow up. Ten unrelated FA patients and their families were analyzed by microsatellite marke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5205bcd3ef956a821f80c8f4a95c3a3
https://pubmed.ncbi.nlm.nih.gov/15727250
https://pubmed.ncbi.nlm.nih.gov/15727250
Publikováno v:
La Tunisie medicale. 82(5)
Fanconi anemia (FA) is an autosomal recessive rare disease characterized by progressive pancytopenia, congenital malformations and predisposition to acute myeloid leukemia. Fanconi anemia is genetically heterogeneous, with at least eight complementat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cc405c2c86097ea0c318191867709ae9
https://pubmed.ncbi.nlm.nih.gov/15453041
https://pubmed.ncbi.nlm.nih.gov/15453041
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