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Hassen Hadj-Kacem

Showing results (1-10 of 28) with videos related to

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Trends in Endocrinology and Metabolism: TEM|June 30, 2004
The genetics of autoimmune thyroid diseaseHammadi Ayadi, Hassen Hadj Kacem, Ahmed Rebai, et al.
Rheumatology International|April 11, 2009
DNase1 exon2 analysis in Tunisian patients with rheumatoid arthritis, systemic lupus erythematosus and Sjögren syndrome and healthy subjectsSalima Belguith-Maalej, Hassen Hadj-Kacem, Neila Kaddour, et al.
The Journal of Clinical Endocrinology and Metabolism|May 3, 2003
PDS is a new susceptibility gene to autoimmune thyroid diseases: association and linkage studyHassen Hadj Kacem, Ahmed Rebai, Noureddine Kaffel, et al.
Annales De Genetique|September 1, 2004
Androgen receptor gene CAG repeats length in fertile and infertile Tunisian menLobna Hadjkacem, Hassen Hadj-Kacem, Amel Boulila, et al.
Genetics Research|March 5, 2013
Association of intronic repetition of SLC26A4 gene with Hashimoto thyroiditis diseaseSalima Belguith-Maalej, Rihab Kallel, Mouna Mnif, et al.
Arthritis and Rheumatism|November 13, 2003
The A/T mutation in exon 2 of the DNASE1 gene is not present in Tunisian patients with systemic lupus erythematosus or in healthy subjectsPampa Chakraborty, Hassen Hadj Kacem, Kauothar Makni-Karray, et al.
Immunobiology|July 29, 2008
Thyroglobulin polymorphisms in Tunisian patients with autoimmune thyroid diseases (AITD)Salima Belguith-Maalej, Hassen Hadj Kacem, Ahmed Rebai, et al.
Genetic Testing and Molecular Biomarkers|October 11, 2017
Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing LossAbdelaziz Tlili, Abdullah Al Mutery, Walaa Kamal Eddine Ahmad Mohamed, et al.
Andrologia|July 7, 2011
Genotyping of Tunisian azoospermic men with Sertoli cell-only and maturation arrestLobna Hadjkacem-Loukil, Hassen Hadj-Kacem, Ikhlass Hadj Salem, et al.
Gene|April 9, 2017
Intronic variants of SLC26A4 gene enhance splicing efficiency in hybrid minigene assayRihab Kallel-Bouattour, Salima Belguith-Maalej, Emna Zouari-Bradai, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Trends in Endocrinology and Metabolism: TEM|June 30, 2004
The genetics of autoimmune thyroid diseaseHammadi Ayadi, Hassen Hadj Kacem, Ahmed Rebai, et al.
Rheumatology International|April 11, 2009
DNase1 exon2 analysis in Tunisian patients with rheumatoid arthritis, systemic lupus erythematosus and Sjögren syndrome and healthy subjectsSalima Belguith-Maalej, Hassen Hadj-Kacem, Neila Kaddour, et al.
The Journal of Clinical Endocrinology and Metabolism|May 3, 2003
PDS is a new susceptibility gene to autoimmune thyroid diseases: association and linkage studyHassen Hadj Kacem, Ahmed Rebai, Noureddine Kaffel, et al.
Annales De Genetique|September 1, 2004
Androgen receptor gene CAG repeats length in fertile and infertile Tunisian menLobna Hadjkacem, Hassen Hadj-Kacem, Amel Boulila, et al.
Genetics Research|March 5, 2013
Association of intronic repetition of SLC26A4 gene with Hashimoto thyroiditis diseaseSalima Belguith-Maalej, Rihab Kallel, Mouna Mnif, et al.
Arthritis and Rheumatism|November 13, 2003
The A/T mutation in exon 2 of the DNASE1 gene is not present in Tunisian patients with systemic lupus erythematosus or in healthy subjectsPampa Chakraborty, Hassen Hadj Kacem, Kauothar Makni-Karray, et al.
Immunobiology|July 29, 2008
Thyroglobulin polymorphisms in Tunisian patients with autoimmune thyroid diseases (AITD)Salima Belguith-Maalej, Hassen Hadj Kacem, Ahmed Rebai, et al.
Genetic Testing and Molecular Biomarkers|October 11, 2017
Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing LossAbdelaziz Tlili, Abdullah Al Mutery, Walaa Kamal Eddine Ahmad Mohamed, et al.
Andrologia|July 7, 2011
Genotyping of Tunisian azoospermic men with Sertoli cell-only and maturation arrestLobna Hadjkacem-Loukil, Hassen Hadj-Kacem, Ikhlass Hadj Salem, et al.
Gene|April 9, 2017
Intronic variants of SLC26A4 gene enhance splicing efficiency in hybrid minigene assayRihab Kallel-Bouattour, Salima Belguith-Maalej, Emna Zouari-Bradai, et al.
Pageof 3