Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rita Medlej"'
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:
Neuroradiology. 62:891-894
Monocarboxylate transporter 1 (MCT1) deficiency was first described in 2014 by Hasselt et al. as a novel genetic cause of recurrent ketoacidosis. Patients present in the first year of life with acute episodes of ketoacidosis triggered by fasting or i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d2eacf34170bb7cf352a7400c4bd674
https://doi.org/10.1007/s00234-020-02435-7
https://doi.org/10.1007/s00234-020-02435-7
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:
Endocrine Research. 27:99-108
Genetic factors are involved in the development of diabetic nephropathy in type-1 diabetes. We are examining the association of the angiotensin-converting enzyme (ACE), insertion/deletion (I/D) polymorphism with the presence of diabetic nephropathy i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48319be1dad100d07c7652e17d203305
https://doi.org/10.1081/erc-100107173
https://doi.org/10.1081/erc-100107173
Autor:
David R. Repaske, James W. Findling, Ebrû K. Gültekin, John A. Phillips, George Halaby, M.R.S. Krishnamani, Rita Medlej
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 82:51-56
Autosomal dominant neurohypophyseal diabetes insipidus (ADNDI) is a familial form of diabetes insipidus due to progressive vasopressin deficiency with onset typically at 1-6 yr of age. Affected individuals demonstrate specific degeneration of the vas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39d0d0200ace4ce3c481001bf9cd244c
https://doi.org/10.1210/jcem.82.1.3660
https://doi.org/10.1210/jcem.82.1.3660
Autor:
Catherine Chevalier, Jean-Marc A. Lobaccaro, Charles Sultan, Rita Medlej, Charles Belon, Jean-Paul Guthmann, René-Benoit Galifer, Paul Czernichow, Philippe Berta, Robert Dumas
Publikováno v:
Clinical Endocrinology. 38:197-201
Summary OBJECTIVE We explored the possibility of a genetic anomaly in the sex determining region of the Y chromosome, SRY gene, known to be equated to the testis determining region. PATIENTS Four patients with bilateral congenital anorchia, absence o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab8b8dcf8db9bb1a8be2978df0a91ec8
https://doi.org/10.1111/j.1365-2265.1993.tb00993.x
https://doi.org/10.1111/j.1365-2265.1993.tb00993.x
Autor:
Georges, El Hajj, Ali Fadlallah, Yahya, Rita, Medlej, Ghada, Sebaaly, Mirna, Souaid, Georges, Halaby
Publikováno v:
Le Journal medical libanais. The Lebanese medical journal. 57(4)
In this article, we analyze the clinical and biological data concerning the autoimmune thyroid diseases in patients recruited in an endocrinology clinic at the university hospital center of Hôtel-Dieu de France between March 2005 and November 2005.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5bbcca36d47a9bfdb5447b103aac3837
https://pubmed.ncbi.nlm.nih.gov/20027797
https://pubmed.ncbi.nlm.nih.gov/20027797