Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Fawzi Bakiri"'
Autor:
Stéphane Schneebeli, Véronique Béréziat, Jacqueline Capeau, Fawzi Bakiri, Caroline Le Dour, Françoise Darcel, Corinne Vigouroux, Martine Auclair, Marie-Anne Maubert, Yves Reznik, Olivier Lascols, Marie-Line Jacquemont, Dorota Jeziorowska
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 96:E856-E862
Mutations in LMNA, encoding A-type lamins, lead to multiple laminopathies, including lipodystrophies, progeroid syndromes, and cardiomyopathies. Alterations in the prelamin-A posttranslational maturation, resulting in accumulation of farnesylated iso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c6867e8bf9e8f8dad891caa949a5083
https://doi.org/10.1210/jc.2010-2234
https://doi.org/10.1210/jc.2010-2234
Autor:
Ali El Mahdi Haddam, Lyes Yargui, Nora Soumeya Fedala, Djamila Meskine, Dalila Foudil, Fawzi Bakiri
Publikováno v:
Revue Francophone des Laboratoires. 2009:57-60
Resume L’insuffisance antehypophysaire traitee de facon conventionnelle expose a des complications metaboliques et cardiovasculaires augmentant la morbi-mortalite de facon significative. 46 patientes avec syndrome de Sheehan ont ete comparees a 51
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a2d6b3dd9d471b0b8c696e27b409d76
https://doi.org/10.1016/s1773-035x(09)70090-5
https://doi.org/10.1016/s1773-035x(09)70090-5
Autor:
Javier Herrera, Fawzi Bakiri, Joaquin Pertierra, Thierry Brue, Oscar D. Bruno, Maria Riestra, Frederic Castinetti, Olivier Perrichot
Publikováno v:
Clinical Endocrinology. 81:471-473
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::086cb931a951467e97f11def6a831db8
https://doi.org/10.1111/cen.12339
https://doi.org/10.1111/cen.12339
Autor:
Marc-Henri de Laet, Annick Rotschild, Rémi Salomon, Clothilde Penet, Stanislas Lyonnet, Ratiba Hannachi, Raja Brauner, Fawzi Bakiri, B. Chaouachi, Jean-Louis Chaussain, Arnold Munnich, Anna Pelet, Smail Hadj-Rabia
Publikováno v:
European Journal of Human Genetics. 8:613-620
Triple A syndrome (Allgrove syndrome, MIM No. 231550) is a rare autosomal recessive disorder characterised by ACTH-resistant adrenal insufficiency, achalasia of the cardia, and alacrimia. The triple A gene has been previously mapped to chromosome 12q
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edd6bb25063d645e18a8588a450f2c68
https://doi.org/10.1038/sj.ejhg.5200508
https://doi.org/10.1038/sj.ejhg.5200508
Autor:
Laurence Cattolico, Clothilde Penet, Danielle Naville, Jean-Louis Chaussain, Marc Nicolino, B. Chaouachi, Arnold Munnich, Jean Weissenbach, Smail Hadj-Rabia, Martine Begeot, Claude Mugnier, Fawzi Bakiri, Stanislas Lyonnet, Anna Tullio-Pelet, Marc-Henri de Laet, Philippe Brottier, Rémi Salomon
Publikováno v:
Nature Genetics
Nature Genetics, Nature Publishing Group, 2000, 26, pp.332-335
ResearcherID
Nature Genetics, Nature Publishing Group, 2000, 26, pp.332-335
ResearcherID
Triple-A syndrome (MIM 231550; also known as Allgrove syndrome) is an autosomal recessive disorder characterized by adrenocorticotropin hormone (ACTH)-resistant adrenal insufficiency, achalasia of the oesophageal cardia and alacrima1,2,3. Whereas sev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40572e24202fb64d427962271b0bf38b
https://hal.inrae.fr/hal-02693003
https://hal.inrae.fr/hal-02693003
Autor:
Jacqueline Capeau, Stéphane Schneebeli, Véronique Béréziat, Corinne Vigouroux, Olivier Lascols, Fawzi Bakiri, C. Le Dour
Publikováno v:
Diabetes & Metabolism. 36:A34
Introduction Les mutations du gene codant les lamines A et C, proteines nucleaires ubiquitaires, sont responsables de maladies appelees « laminopathies », parmi lesquelles des lipodystrophies et des syndromes de vieillissement accelere. Les anomali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::570a14db7a29c58d5f9a944c8782429b
https://doi.org/10.1016/s1262-3636(10)70130-0
https://doi.org/10.1016/s1262-3636(10)70130-0
Publikováno v:
Acta Endocrinologica. 112:329-335
To appreciate the aldosterone secretion status in panhypopituitarism, the steroid response to stimulation was studied in a homogeneous group of 20 female patients presenting with global hypopituitarism. Specific effects of glucocorticoid and thyroid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c0ece4c3a3eedae29d06d0554900799
https://doi.org/10.1530/acta.0.1120329
https://doi.org/10.1530/acta.0.1120329
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 56:1042-1047
To gain insight in the influence of the pituitary gland on the renin-angiotensin system plasma renin substrate (PRS) and the response of PRA to stimulation were studied in a homogeneous group of 20 female patients with the same etiology and degree of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a888c41d15613bebf6b84caf4f18719
https://doi.org/10.1210/jcem-56-5-1042
https://doi.org/10.1210/jcem-56-5-1042
Publikováno v:
The Journal of clinical endocrinology and metabolism. 58(3)
The response to an osmolar load (750 ml 2.5% NaCl solution iv preceded by 500 ml water by mouth) was studied in 20 patients with Sheehan's syndrome and 12 normal women. Sodium and osmolality were determined in plasma and urine and arginine-vasopressi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80927521c365ab28f304141adf32ee06
https://pubmed.ncbi.nlm.nih.gov/6693547
https://pubmed.ncbi.nlm.nih.gov/6693547
Autor:
Flaus-Furmaniuk, Anna1,2 (AUTHOR) anna.flaus-furmaniuk@chu-reunion.fr, Fianu, Adrian2,3 (AUTHOR), Lenclume, Victorine2 (AUTHOR), Chirpaz, Emmanuel2 (AUTHOR), Balcou-Debussche, Maryvette4 (AUTHOR), Debussche, Xavier1,2 (AUTHOR), Marimoutou, Catherine2 (AUTHOR)
Publikováno v:
BMC Endocrine Disorders. 12/13/2022, Vol. 22 Issue 1, p1-15. 15p.