Search Results - "Turki, Zinet"

Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism by Mkaouar, Rahma, Abdallah, Lamia Cherif Ben, Naouali, Chokri, Lahbib, Saida, Turki, Zinet, Elouej, Sahar, Bouyacoub, Yosra, Somai, Maali, Mcelreavey, Kenneth, Bashamboo, Anu, Abdelhak, Sonia, Messaoud, Olfa

“…The role of the prokineticin 2 pathway in human reproduction, olfactory bulb morphogenesis, and gonadotropin-releasing hormone secretion is well established…”
Get full text

A Comparative Phenotypic Study of Kallmann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes by Sarfati, Julie, Guiochon-Mantel, Anne, Rondard, Philippe, Arnulf, Isabelle, Garcia-Piñero, Alfons, Wolczynski, Slawomir, Brailly-Tabard, Sylvie, Bidet, Maud, Ramos-Arroyo, Maria, Mathieu, Michèle, Lienhardt-Roussie, Anne, Morgan, Graeme, Turki, Zinet, Bremont, Catherine, Lespinasse, James, Du Boullay, Hélène, Chabbert-Buffet, Nathalie, Jacquemont, Sébastien, Reach, Gérard, De Talence, Nicole, Tonella, Paolo, Conrad, Bernard, Despert, Francois, Delobel, Bruno, Brue, Thierry, Bouvattier, Claire, Cabrol, Sylvie, Pugeat, Michel, Murat, Arnaud, Bouchard, Philippe, Hardelin, Jean-Pierre, Dodé, Catherine, Young, Jacques

“…Context: Both biallelic and monoallelic mutations in PROK2 or PROKR2 have been found in Kallmann syndrome (KS). Objective: The objective of the study was to…”
Get full text

Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort by Jullien, Nicolas, Saveanu, Alexandru, Vergier, Julia, Marquant, Emeline, Quentien, Marie Helene, Castinetti, Frederic, Galon‐Faure, Noémie, Brauner, Raja, Marrakchi Turki, Zinet, Tauber, Maité, El Kholy, Mohamed, Linglart, Agnès, Rodien, Patrice, Fedala, Nora Soumeya, Bergada, Ignacio, Cortet‐Rudelli, Christine, Polak, Michel, Nicolino, Marc, Stuckens, Chantal, Barlier, Anne, Brue, Thierry, Reynaud, Rachel

“…Context The international GENHYPOPIT network collects phenotypical data and screens genetic causes of non‐acquired hypopituitarism. Aims To describe main…”
Get full text

Molecular basis of pituitary development defects by Turki, Zinet Marrakchi, Hamaoui, Raja Ben Belgacem, Ben Slama, Claude

“…Over the last twenty years, the progress made in molecular biology have led to the identification of many transcription factor genes, whose mutations has been…”
Get more information

Association of genetic variants in the FTO gene with metabolic syndrome: A case-control study in the Tunisian population by Elouej, Sahar, Nagara, Majdi, Attaoua, Redha, Sallem, Om Kalthoum, Rejeb, Insaf, Hsouna, Sana, Lasram, Khaled, Halim, Nizar Ben, Chargui, Mariem, Jamoussi, Henda, Turki, Zinet, Kamoun, Ines, Belfki-Benali, Hanen, Abid, Abdelmajid, Slama, Claude Ben, Bahri, Sonia, Triki, Dalenda, Romdhane, Habiba Ben, Abdelhak, Sonia, Kefi, Rym, Grigorescu, Florin

“…Abstract Aims Variants in the fat mass and obesity-associated gene ( FTO ) are associated with obesity and type 2 diabetes. However, the association of FTO…”
Get full text

Gender-specific associations of genetic variants with metabolic syndrome components in the Tunisian population by Elouej, Sahar, Rejeb, Insaf, Attaoua, Redha, Nagara, Majdi, Sallem, Om Kalthoum, Kamoun, Ines, Chargui, Mariem, Jamoussi, Henda, Turki, Zinet, Abid, Abdelmajid, Ben Slama, Claude, Bahri, Sonia, Ben Romdhane, Habiba, Abdelhak, Sonia, Kefi, Rym, Grigorescu, Florin

“…Aim of the study: Recent genome-wide association studies (GWASs) have identified many genetic variants associated with metabolic syndrome (MetS). However,…”
Get full text

Cytogenetic abnormalities in Tunisian women with premature ovarian failure by Ayed, Wiem, Amouri, Ahlem, Hammami, Wajih, Kilani, Olfa, Turki, Zinet, Harzallah, Fatma, Bouayed-Abdelmoula, Nouha, Chemkhi, Imen, Zhioua, Fethi, Slama, Claude Ben

“…To identify the distribution of chromosome abnormalities among Tunisian women with premature ovarian failure (POF) referred to the department of Cytogenetic at…”
Get more information

Association of rs9939609 Polymorphism with Metabolic Parameters and FTO Risk Haplotype Among Tunisian Metabolic Syndrome by Elouej, Sahar, Belfki-Benali, Hanen, Nagara, Majdi, Lasram, Khaled, Attaoua, Redha, Sallem, Om Kalthoum, Kamoun, Ines, Chargui, Mariem, Romdhane, Lilia, Jamoussi, Henda, Turki, Zinet, Abid, Abdelmajid, Ben Slama, Claude, Bahri, Sonia, Abdelhak, Sonia, Grigorescu, Florin, Ben Romdhane, Habiba, Kefi, Rym

“…Variants in the fat mass and obesity-associated (FTO) gene are associated with obesity and type 2 diabetes mellitus. This study aims to assess the association…”
Get more information

Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population by Kefi, Rym, Hechmi, Meriem, Dallali, Hamza, Elouej, Sahar, Jmel, Haifa, Halima, Yossra Ben, Nagara, Majdi, Chargui, Mariem, Fadhel, Sihem Ben, Romdhane, Safa, Kamoun, Ines, Turki, Zinet, Abid, Abdelmajid, Bahri, Sonia, Bahlous, Afaf, Gomis, Ramon, Baraket, Abdelhamid, Grigorescu, Florin, Normand, Christophe, Jamoussi, Henda, Abdelhak, Sonia

“…Abstract Aim of the study APOA5 has been linked to metabolic syndrome (MetS) or its traits in several populations. In North Africa, only the Moroccan…”
Get full text

A Tunisian patient with two rare syndromes: triple a syndrome and congenital hypogonadotropic hypogonadism by Cherif Ben Abdallah, Lamia, Lakhoua, Youssef, Nagara, Majdi, Khiari, Karima, Elouej, Sahar, Messaoud, Olfa, Bouyacoub, Yosra, Romdhane, Lilia, Turki, Zinet, Abdelhak, Sonia, Ben Abdallah, Nejib

“…The coexistence of triple A syndrome (AAAS) and congenital hypogonadotropic hypogonadism (CHH) has so far not been reported in the literature. This study aimed…”
Get more information

Continuous glucose monitoring in glimipiride plus metformin treated type 2 diabetic patients during the month of Ramadan by Oueslati, Ibtissem, Ben Said, Rania, Kammoun, Ines, Haouat, Emna, Ben Salem, Leila, Turki, Zinet, Ben Slama, Claude

“…Fasting during Ramadan may be a cause of poor glycaemic control in diabetic patients. To assess glucose excursions during Ramadan by using a continuous glucose…”
Get more information

A Comparative Phenotypic Study of Kalimann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes by SARFATI, Julie, GUIOCHON-MANTEL, Anne, LIENHARDT-ROUSSIE, Anne, MORGAN, Graeme, TURKI, Zinet, BREMONT, Catherine, LESPINASSE, James, DU BOULLAY, Hélène, CHABBERT-BUFFET, Nathalie, JACQUEMONT, Sébastien, REACH, Gerard, DE TALENCE, Nicole, RONDARD, Philippe, TONELLA, Paolo, CONRAD, Bernard, DESPERT, Francois, DELOBEL, Bruno, BRUE, Thierry, BOUVATTIER, Claire, CABROL, Sylvie, PUGEAT, Michel, MURAT, Arnaud, BOUCHARD, Philippe, ARNULF, Isabelle, HARDELIN, Jean-Pierre, DODE, Catherine, YOUNG, Jacques, GARCIA-PINERO, Alfons, WOLCZYNSKI, Slawomir, BRAILLY-TABARD, Sylvie, BIDET, Maud, RAMOS-ARROYO, Maria, MATHIEU, Michèle

Get full text

Hypocalcaemia due to hypoparathyroidism in β-thalassemia major. A study of a new case by Dhouib, Nawel, Turki, Zinet, Mellouli, Fethi, Ouederni, Monia, Yahiaoui, Salem, Nagi, Sonia, Kouki, Ridha, Ben Slama, Claude, Bejaoui, Mohamed

“…To report a new case of hypoparathyroidism in a child with ß-thalassemia major We report a case of a 17-year-old Tunisian girl with transfusion-dependent…”
Get more information

Renal failure in Tunisian patients with type 2 diabetes: frequency and related factors by Bouzid, Chiraz, Smida, Hajer, Kacem, Anissa, Turki, Zinet, Ben Salem, Leila, Ben Rayana, Chiheb, Slama, Ben Claude

“…Frequent screening of renal failure and good glycaemic control in diabetic patients can avoid this severe complication. To evaluate the frequency of renal…”
Get more information

Pancreatic insulinoma by Mzoughi, Zeineb, Oueslati, Imene, Attaoui, Med Amine, Marsaoui, Lobna, Askri, Anis, Khadraoui, Emna, Turki, Zinet, Ben Slama, Claude, Mestiri, Hafedh, Hendaoui, Lotfi, Gharbi, Lassaad, Khalfallah, Mohamed Taher

Get more information

Imaging diagnosis of an unilateral painful ophtalmoplegia by Nagi, Sonia, Marrakchi-Turki, Zinet, Sebaï, Rym, Kerkeni, Anis, Khouja, Nejib, Belghith, Lotfi, Touibi, Slaheddine

“…The ophtalmoplegia may be due to several lesions and the diagnosis is made by imaging modalities. We report the case of a giant aneurysm of the wright…”
Get more information