Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Lajmi, Y."'
Autor:
Halayem S; Department of Child and Adolescent Psychiatry, Razi Hospital La Manouba, Tunisia.; Faculty of Medicine of Tunis, University of Tunis El Manar, Tunisia., Chennoufi F; GAIA Therapeutic Farm Sidi Thabet, Tunisia., Ouali U; Faculty of Medicine of Tunis, University of Tunis El Manar, Tunisia.; Department Psychiatry A, Razi Hospital La Manouba, Tunisia., Lajmi Y; GAIA Therapeutic Farm Sidi Thabet, Tunisia., Moumni R; Department Psychiatry A, Razi Hospital La Manouba, Tunisia., Bouden A; Department of Child and Adolescent Psychiatry, Razi Hospital La Manouba, Tunisia.; Faculty of Medicine of Tunis, University of Tunis El Manar, Tunisia., Guesmi L; GAIA Therapeutic Farm Sidi Thabet, Tunisia.
Publikováno v:
La Tunisie medicale [Tunis Med] 2024 Oct 05; Vol. 102 (10), pp. 622-627. Date of Electronic Publication: 2024 Oct 05.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Grassa, A., Bornaz, E., Msolly, S., Lajmi, Y., Mezioud, A., Ghannem, Y., Abdesselem, H., Ounaissa, K., Amrouche, C.
Publikováno v:
In Annales d'Endocrinologie October 2023 84(5):681-681
Autor:
Grassa, A., Bornaz, E., Lajmi, Y., Ghannem, Y., Mezioud, A., Anane, E., Abdesselem, H., Ounaissa, K., Amrouche, C.
Publikováno v:
In Annales d'Endocrinologie October 2023 84(5):649-649
Autor:
Lajmi Y; Department of Genomic Medicine of System and Organs Diseases, Cochin Hospital, APHP Center, University Paris Cité, Paris, France., Loeuillet L; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France., Petrilli G; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France., Egloff C; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France., Nectoux J; Department of Genomic Medicine of System and Organs Diseases, Cochin Hospital, APHP Center, University Paris Cité, Paris, France., Molac C; Clinical Genetics, Maternity Port-Royal, APHP Center, University Paris Cité, Paris, France., Roux N; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France., Pannier E; Gynecology-Obstetrics Department, Port-Royal Hospital, APHP Center, University Paris Cité, Paris, France., Achaiaa A; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France., Arkoub ZA; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France., Chuon S; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France., Coussement A; Department of Genomic Medicine of System and Organs Diseases, Cochin Hospital, APHP Center, University Paris Cité, Paris, France., Dupont JM; Department of Genomic Medicine of System and Organs Diseases, Cochin Hospital, APHP Center, University Paris Cité, Paris, France., Malan V; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France., Spaggiari E; Gynecology-Obstetrics Department, Necker Hospital for Children Diseases, APHP Center, University Paris Cité, Paris, France., Razavi F; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France., Amiel J; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France., Bessières B; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France., Grotto S; Clinical Genetics, Maternity Port-Royal, APHP Center, University Paris Cité, Paris, France., Attié-Bitach T; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France.
Publikováno v:
Birth defects research [Birth Defects Res] 2023 Mar 15; Vol. 115 (5), pp. 563-571. Date of Electronic Publication: 2022 Dec 20.
Autor:
Sakka R; Human Molecular Genetics Laboratory, Faculty of Medicine of Sfax, University of Sfax, Tunisia; Center of Medical Genetics, Erasme Hospital, Université Libre de Bruxelles, Brussels, Belgium., Abdelhedi F; Human Molecular Genetics Laboratory, Faculty of Medicine of Sfax, University of Sfax, Tunisia; Medical Genetics Department, Hedi Chaker Hospital, Sfax, Tunisia. Electronic address: abdelhedi_f@yahoo.fr., Sellami H; Water Researches and Technologies Center (CERTE), University of Carthage, Tourist Road Soliman, Nabeul, Tunisia; Toxicology, Environmental Microbiology and Health Research Laboratory (LR17ES06), Faculty of Sciences of Sfax, University of Sfax, Tunisia., Pichon B; Center of Medical Genetics, Erasme Hospital, Université Libre de Bruxelles, Brussels, Belgium., Lajmi Y; Cytogenetics Department, Cochin Hospital, Assistance Publique des Hôpitaux de Paris, Sorbonne Paris Cité, Paris Descartes University, Medical School, Paris, France., Mnif M; Department of Endocrinology, Hedi Chaker Hospital, Sfax, Tunisia., Kebaili S; Department of Gynecology, HediChaker Hospital, Sfax, Tunisia., Derbel R; Human Molecular Genetics Laboratory, Faculty of Medicine of Sfax, University of Sfax, Tunisia., Kamoun H; Medical Genetics Department, Hedi Chaker Hospital, Sfax, Tunisia., Gdoura R; Toxicology, Environmental Microbiology and Health Research Laboratory (LR17ES06), Faculty of Sciences of Sfax, University of Sfax, Tunisia., Delbaere A; Fertility Clinic, Department of Gynecology and Obstetrics, Erasme Hospital, UniversitéLibre de Bruxelles, Brussels, Belgium., Desir J; Center of Medical Genetics, Erasme Hospital, Université Libre de Bruxelles, Brussels, Belgium., Abramowicz M; Center of Medical Genetics, Erasme Hospital, Université Libre de Bruxelles, Brussels, Belgium., Vialard F; Genetics Department, CHI Poissy St Germain-en-Laye, F-78300, Poissy, France; RHuMA Team, UMR-BREED, INRAE-UVSQ-ENVA, UFR-SVS, F-78180, Montigny le Bretonneux, France., Dupont JM; Cytogenetics Department, Cochin Hospital, Assistance Publique des Hôpitaux de Paris, Sorbonne Paris Cité, Paris Descartes University, Medical School, Paris, France., Ammar-Keskes L; Human Molecular Genetics Laboratory, Faculty of Medicine of Sfax, University of Sfax, Tunisia.
Publikováno v:
European journal of medical genetics [Eur J Med Genet] 2022 Nov; Vol. 65 (11), pp. 104613. Date of Electronic Publication: 2022 Sep 14.
Troubles endocriniens associés au syndrome de Prader-Willi : intérêt du diagnostic génétique précoce
Autor:
Kammoun, R., Bouassida, M., Gharbi, N., Lajmi, Y., Boujelbene, I., Ben Ayed, I., Baklouti, S., Belguith, N., Ammar Keskes, L., Masmoudi, S., Kamoun, H., Abdelhedi, F.
Publikováno v:
In Annales d'Endocrinologie October 2021 82(5):549-549
Autor:
El Arbi, K., Mnif, F., Zargni, A., Boujelben, K., Lajmi, Y., Abdelhedi, F., Ben Salah, D., Elleuch, M., Charfi, N., Rekik, N., Mnif, M., Hadj Kacem, F., Kammoun, H., Abid, M.
Publikováno v:
In Annales d'Endocrinologie October 2021 82(5):470-470
Autor:
Bouassida, M., Kammoun, R., Lajmi, Y., Guidara, S., Boujelbene, I., Mejdoub, F., Maazoun, F., Ben Ayed, I., Gharbi, N., Kamoun, H., Abdelhedi, F.
Publikováno v:
In Annales d'Endocrinologie October 2021 82(5):460-460
Autor:
Maazoun, F., Lajmi, Y., Boujelbene, I., Ben Ayed, I., Guidara, S., Kammoun, T., Kamoun, H., Abdelhedi, F.
Publikováno v:
In Annales d'Endocrinologie October 2021 82(5):328-328