Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Kamal Hirbli"'
Publikováno v:
Journal of Clinical and Translational Endocrinology Case Reports, Vol 30, Iss , Pp 100134- (2023)
Background: Thyroid hemiagenesis (TH) is a rare disorder that is usually clinically silent unless associated with other thyroidal pathologies. We present a case of a TH patient with Graves’ disease (GD). To our knowledge, this is the first ever cas
Externí odkaz:
https://doaj.org/article/1e8b0c82d7494f16bbd60ef03ecd7fbb
Publikováno v:
Journal of Clinical and Translational Endocrinology Case Reports, Vol 30, Iss , Pp 100133- (2023)
Externí odkaz:
https://doaj.org/article/a699b32855db4e77a3732a9de8df3fa7
Publikováno v:
Journal of Clinical and Translational Endocrinology Case Reports, Vol 26, Iss , Pp 100128- (2022)
Background: Thyroid hemiagenesis (TH) is a rare disorder that is usually clinically silent unless associated with other thyroidal pathologies. We present a case of a TH patient with Graves' disease (GD). To our knowledge, this is the first ever case
Externí odkaz:
https://doaj.org/article/9df34948290f40e696cb487a134d8172
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-4 (2021)
Abstract Background Androgen insensitivity syndrome is a rare X-linked disorder of sex development, caused by mutations in the androgen receptor. In this case, a 13-year-old child, reared as female, presenting for primary amenorrhea, was diagnosed wi
Externí odkaz:
https://doaj.org/article/a0f9f949421645418560ab02887068dc
Publikováno v:
Journal of Diabetes Mellitus. 13:77-92
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::208cff4f4ec8e42f985c7ca844d16e82
https://doi.org/10.4236/jdm.2023.132008
https://doi.org/10.4236/jdm.2023.132008
Publikováno v:
Cureus
We report a case of fixed drug eruption in a 58-year-old lady treated for diabetes with four pharmacologically different anti-diabetic agents that were used at separate times of therapy. Skin manifestations, including erythema, blisters, and ulcers,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03150ac388a43b5d5ef4c692c470b40e
https://doi.org/10.7759/cureus.18599
https://doi.org/10.7759/cureus.18599
Autor:
Rita Medlej, Mohamed M. El-Zaheri, Paola Atallah, Charles Saab, Kamal Hirbli, Omar M. Abu-Hijleh, Nadim Jarrah, Fares Haddad, Emile Andari, Hiba Hajar
Publikováno v:
Journal of Diabetes Mellitus. 10:73-87
Introduction: Type 2 Diabetes Mellitus (T2DM) has witnessed a rise in its prevalence worldwide and in the Middle East region. The overall burden associated with the disease is well characterized, but little is known about patient satisfaction in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3a42819dacfc274ae440c95a4af5a1d
https://doi.org/10.4236/jdm.2020.102007
https://doi.org/10.4236/jdm.2020.102007
Publikováno v:
Journal of Clinical and Translational Endocrinology: Case Reports. :100133
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97ede4e54c70cbfbb05f297dd7902c52
https://doi.org/10.1016/j.jecr.2022.100133
https://doi.org/10.1016/j.jecr.2022.100133
Publikováno v:
Journal of Medical Case Reports
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-4 (2021)
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-4 (2021)
Background Androgen insensitivity syndrome is a rare X-linked disorder of sex development, caused by mutations in the androgen receptor. In this case, a 13-year-old child, reared as female, presenting for primary amenorrhea, was diagnosed with comple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4389cfd3dcf34e34712703e6aa97f0e
https://doi.org/10.1186/s13256-021-02738-0
https://doi.org/10.1186/s13256-021-02738-0
Autor:
Pierre Zalloua, Michella Ghassibe-Sabbagh, Hatem El-Shanti, Jihane Romanos, Angelique K. Salloum, Dominique Gauguier, Yasmine Akle, Francis Mouzaya, Yasser Al-Sarraj, Kamal Hirbli, Daniel E. Platt, Marc Haber
Publikováno v:
Scientific Reports
Genome-wide association studies (GWAS) of multiple populations with distinctive genetic and lifestyle backgrounds are crucial to the understanding of Type 2 Diabetes Mellitus (T2DM) pathophysiology. We report a GWAS on the genetic basis of T2DM in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::add9fe6c4658ba7fffaee22b678fe29b