Search Results - "Medlej, R."

The effect of vildagliptin relative to sulphonylureas in Muslim patients with type 2 diabetes fasting during Ramadan: the VIRTUE study by Al-Arouj, M, Hassoun, A A K, Medlej, R, Pathan, M F, Shaltout, I, Chawla, M S, Hristoskova, S, Ditommaso, S, Kadwa, M Y

“…To assess, in a real-world setting, the effect of vildagliptin compared with sulphonylurea (SU) treatment on hypoglycaemia in Muslim patients with type 2…”
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Diabetes Mellitus and Optic Atrophy: A Study of Wolfram Syndrome in the Lebanese Population by Medlej, R., Wasson, J., Baz, P., Azar, S., Salti, I., Loiselet, J., Permutt, A., Halaby, G.

“…Wolfram syndrome (WFS) is a rare hereditary neurodegenerative disorder also known as DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, and…”
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Survey bedsores and nosocomial infections in two rehabilitation centers in Lebanon and profile of inpatient by Ghoussoub, K, Sakkal, J, Ibrahim, S, Sleilati, G, Choueiri-Medlej, R, Hage, A

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Genetics of autoimmune thyroid disease in the Lebanese population by Farra, C., Awwad, J., Fadlallah, A., Sebaly, G., Hage, G., Souaid, M., Ashkar, H., Medlej, R., Gannageh, M. H., Halaby, G.

“…This study aims to investigate the association of human leukocyte antigen (HLA) class II genes and cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) with…”
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Predictors of intra-operative parathyroid hormone decline in subjects operated for primary hyperparathyroidism by minimally invasive parathyroidectomy by Gannagé-Yared, M. H., Abboud, B., Amm-Azar, M., Saab, A., Khalife, S., Halaby, G., Atallah, C., Medlej, R., Jambart, S.

“…Background : The predictors of intra-oprerative PTH (IOPTH) decline during minimally invasive parathyroidectomy (MIP) for primary hyperparathyroidism have been…”
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Malignant struma ovarii: an unusual presentation by Checrallah, A, Medlej, R, Saadé, C, Khayat, G, Halaby, G

“…Malignant struma ovarii is a rare disease; only a few cases are well documented in the literature. Thus, the overall prognosis and modalities of treatment are…”
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Enquête sur les escarres et les infections nosocomiales dans deux centres de réhabilitation au Liban et profil des patients hospitalisés by Ghoussoub, K, Sakkal, J, Ibrahim, S, Sleilati, G, Choueiri-Medlej, R, Hage, A

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IDF21-0616 Observational study on covid 19 and type 1 diabetes in the Chronic Care Center Lebanon by Maalouf Nawfal, P., Medlej, R., Abou Nasr, T., Abi Saad, M., Bitar, C., Sadek, C., Chaaya, I., Najjar, J., Ajouz, J., Mourad, M.

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Screening for Y-derived sex determining gene SRY in 40 patients with Turner syndrome by Medlej, R, Lobaccaro, J M, Berta, P, Belon, C, Leheup, B, Toublanc, J E, Weill, J, Chevalier, C, Dumas, R, Sultan, C

“…In Turner patients, the presence of a Y chromosome or derivative Y is correlated with the risk of gonadoblastoma induction. "Marker" chromosomes originating…”
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THE DD GENOTYPE OF THE ACE GENE POLYMORPHISM IS ASSOCIATED WITH DIABETIC NEPHROPATHY IN TYPE-1 DIABETICS by Azar, Sami T., Zalloua, Pierre A., Medlej, Rita, Halabi, George

“…Genetic factors are involved in the development of diabetic nephropathy in type-1 diabetes. We are examining the association of the angiotensin-converting…”
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Symptoms, hormones, and glucose fluxes during a gradual hypoglycaemia induced by intraperitoneal vs venous insulin infusion in Type I diabetes by Selam, J L, Medlej, R, M'bemba, J, Chevalier, A, Guyon, F, Ashworth, L, Slama, G

“…Intraperitoneal (IP) insulin infusion with programmable implantable pumps is associated with a reduction in hypoglycaemic events when compared to intensive…”
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PCR analysis and sequencing of the SRY sex determining gene in four patients with bilateral congenital anorchia by Lobaccaro, J M, Medlej, R, Berta, P, Belon, C, Galifer, R B, Guthmann, J P, Chevalier, C, Czernichow, P, Dumas, R, Sultan, C

“…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…”
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SRY and male sex determination by Sultan, C, Lobaccaro, J M, Medlej, R, Poulat, F, Berta, P

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Management of hyperandrogenism in adolescent girls by Sultan, C, Medlej, R, Chevalier, C, Lobaccaro, J M

“…Hyperandrogenism in adolescent girls can be a troubling problem because of the difficulty in establishing a diagnosis and in prescribing appropriate therapy…”
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Effects of vildagliptin relative to sulfonylureas in Muslim patients with type 2 diabetes fasting during Ramadan: influence of age and treatment with/without metformin in the VIRTUE study by Hassoun AAK, Pathan MF, Medlej RC, Alarouj M, Shaltout I, Chawla MS, Knap D, Vaz JA

“…Ahmed AK Hassoun,1 Md Faruque Pathan,2 Rita C Medlej,3,4 Monira Alarouj,5 Inass Shaltout,6 Manoj S Chawla,7 Ditte Knap,8 Julius A Vaz9 1Dubai Diabetes Centre,…”
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Role of early fundoscopy for diagnosis of wolfram syndrome in type 1 diabetic patients by BAZ, P, AZAR, S. T, MEDLEJ, R, BEJJANI, R, HALABI, G, SALTI, I

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Extrapontine myelinolysis: treatment with TRH by Chemaly, R, Halaby, G, Mohasseb, G, Medlej, R, Tamraz, J, el-Koussa, S

“…Central pontine and extra-pontine myelinolysis are a well known complication of hyponatremia. Other causes may be present. We report a case of head injury in a…”
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Endocrinologic recovery after treatment of an intrasellar aneurysm by Slaba, S, Medlej, R, Smayra, T, Zafatayeff, S, Nohra, G, Okais, N, Halaby, G

“…Cavernous intrasellar aneurysms are rare, but may be clinically mistaken for an hypophyseal tumor, thus the need for a preoperative diagnosis. We report on a…”
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A rare manifestation of hypothyroidism: intestinal obstruction. Report of 2 cases and review of the literature by Abboud, B, Sayegh, R, Medlej, R, Halaby, G, Saade, C, Farah, P

“…Gastrointestinal manifestations of hypothyroidism are unfrequent. They consist particularly in hypomotility, intestinal atony, and pseudoobstruction. A high…”
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Heterogeneity in clinical manifestation of autosomal dominant neurohypophyseal diabetes insipidus caused by a mutation encoding Ala-1→Val in the signal peptide of the arginine vasopressin/neurophysin II/copeptin precursor by REPASKE, D. R, MEDLEJ, R, GÜLTEKIN, E. K, KRISHNAMANI, M. R. S, HALABY, G, FINDLING, J. W, PHILLIPS, J. A

“…Autosomal dominant neurohypophyseal diabetes insipidus (ADNDI) is a familial form of diabetes insipidus due to progressive vasopressin deficiency with onset…”
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