Zobrazeno 1 - 10
of 227
pro vyhledávání: '"Tajir, M."'
Publikováno v:
Balkan Journal of Medical Genetics, Vol 25, Iss 1, Pp 101-104 (2023)
Turner Syndrome (TS) is a genetic disorder caused by total or partial loss of an X chromosome. The isochromosome X (i(X)) is a known variant of TS, however, double i(X) is a very rare variant, reported very few times in the literature. We report on a
Externí odkaz:
https://doaj.org/article/0bdebe62e54e49079665cdf0b2e2eceb
Autor:
Koulali H; Department of Hepato-Gastroenterology, Mohammed VI University Hospital, Oujda, Morocco.; Digestive Diseases Research Laboratory (DSRL), Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, Morocco., Azzmouri S; Department of Hepato-Gastroenterology, Mohammed VI University Hospital, Oujda, Morocco.; Digestive Diseases Research Laboratory (DSRL), Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, Morocco., Tajir M; Laboratoire de Génétique Médicale, Laboratoire Central, Centre Hospitalo-Universitaire Mohammed VI, Faculté de Médecine et de Pharmacie d'Oujda, Université Mohammed Premier, Oujda, Morocco., Zerrouki K; Laboratoire de Génétique Médicale, Laboratoire Central, Centre Hospitalo-Universitaire Mohammed VI, Faculté de Médecine et de Pharmacie d'Oujda, Université Mohammed Premier, Oujda, Morocco., Haloui A; Department of Pathology, Mohammed VI University Hospital/Faculty of Medicine, Mohammed 1st University, Oujda, Morocco., Elmqaddem O; Department of Hepato-Gastroenterology, Mohammed VI University Hospital, Oujda, Morocco.; Digestive Diseases Research Laboratory (DSRL), Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, Morocco., Zazour A; Department of Hepato-Gastroenterology, Mohammed VI University Hospital, Oujda, Morocco.; Digestive Diseases Research Laboratory (DSRL), Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, Morocco., Ismaili Z; Department of Hepato-Gastroenterology, Mohammed VI University Hospital, Oujda, Morocco.; Digestive Diseases Research Laboratory (DSRL), Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, Morocco., Kharrasse G; Department of Hepato-Gastroenterology, Mohammed VI University Hospital, Oujda, Morocco.; Digestive Diseases Research Laboratory (DSRL), Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, Morocco.
Publikováno v:
ACG case reports journal [ACG Case Rep J] 2024 Oct 31; Vol. 11 (11), pp. e01477. Date of Electronic Publication: 2024 Oct 31 (Print Publication: 2024).
Autor:
Saddouk H; Department of Dermatology, Venerology and Allergology, CHU Mohammed VI, Oujda, Morocco. Electronic address: dr.saddoukhasnae@gmail.com., Tajir M; Department of Medical Genetics, CHU Mohammed VI, Oujda, Morocco., Saadi H; Department of Obstetrics and Gynecology, CHU Mohammed VI, Oujda, Morocco., Housni B; Department of Anesthesia and Intensive Care, CHU Mohammed VI, Oujda, Morocco., Zerrouki N; Department of Dermatology, Venerology and Allergology, CHU Mohammed VI, Oujda, Morocco; Laboratory of Epidemiology, Clinical Research and Public Health. Faculty of Medicine and Pharmacy, Mohammed Premier University, Oujda, Morocco., Zizi N; Department of Dermatology, Venerology and Allergology, CHU Mohammed VI, Oujda, Morocco; Laboratory of Epidemiology, Clinical Research and Public Health. Faculty of Medicine and Pharmacy, Mohammed Premier University, Oujda, Morocco., Dikhaye S; Department of Dermatology, Venerology and Allergology, CHU Mohammed VI, Oujda, Morocco; Laboratory of Epidemiology, Clinical Research and Public Health. Faculty of Medicine and Pharmacy, Mohammed Premier University, Oujda, Morocco.
Publikováno v:
International journal of obstetric anesthesia [Int J Obstet Anesth] 2024 Oct 09, pp. 104283. Date of Electronic Publication: 2024 Oct 09.
Publikováno v:
Balkan Journal of Medical Genetics, Vol 23, Iss 1, Pp 95-98 (2020)
Ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome is a rare genetic disease with an autosomal dominant transmission, characterized by several congenital anomalies. Clinical features include ectodermal defects affecting the skin, hair
Externí odkaz:
https://doaj.org/article/399ae78977ab4dd4bbe4a81cca59457e
Autor:
Bouzid FZ; Service de Génétique, Centre de Recherche Clinique, Centre Hospitalier Universitaire Mohammed VI, Marrakech, Maroc.; Faculté de Médecine et de Pharmacie de Marrakech, Université Cadi Ayyad, Marrakech, Maroc., Hammou HA; Service de Génétique, Centre de Recherche Clinique, Centre Hospitalier Universitaire Mohammed VI, Marrakech, Maroc., Akallakh H; Service de Génétique, Centre de Recherche Clinique, Centre Hospitalier Universitaire Mohammed VI, Marrakech, Maroc., Dafir K; Service de Génétique, Centre de Recherche Clinique, Centre Hospitalier Universitaire Mohammed VI, Marrakech, Maroc.; Faculté de Médecine et de Pharmacie de Marrakech, Université Cadi Ayyad, Marrakech, Maroc., Tajir M; Service de Génétique, Centre de Recherche Clinique, Centre Hospitalier Universitaire Mohammed VI, Marrakech, Maroc.; Service de Génétique Médicale, Centre Hospitalier Universitaire Mohammed VI, Oujda, Maroc., Aboussair N; Service de Génétique, Centre de Recherche Clinique, Centre Hospitalier Universitaire Mohammed VI, Marrakech, Maroc.; Faculté de Médecine et de Pharmacie de Marrakech, Université Cadi Ayyad, Marrakech, Maroc.
Publikováno v:
The Pan African medical journal [Pan Afr Med J] 2023 Dec 01; Vol. 46, pp. 94. Date of Electronic Publication: 2023 Dec 01 (Print Publication: 2023).
Akademický článek
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Autor:
Aouni FE; Laboratoire de Génétique Médicale, Laboratoire Central, Centre Hospitalo-Universitaire Mohammed VI, BP 4806, 60049 OUJDA, Maroc, Faculté de Médecine et de Pharmacie d'Oujda, Université Mohammed Premier, Oujda, Maroc., Zerrouki K; Laboratoire de Génétique Médicale, Laboratoire Central, Centre Hospitalo-Universitaire Mohammed VI, BP 4806, 60049 OUJDA, Maroc, Faculté de Médecine et de Pharmacie d'Oujda, Université Mohammed Premier, Oujda, Maroc., Smaili F; Laboratoire de Génétique Médicale, Laboratoire Central, Centre Hospitalo-Universitaire Mohammed VI, BP 4806, 60049 OUJDA, Maroc., Ayyad A; Faculté de Médecine et de Pharmacie d'Oujda, Université Mohammed Premier, Oujda, Maroc, Service de Néonatologie et de Réanimation Néonatale, Centre Hospitalo-Universitaire Mohammed VI, Oujda, Maroc., Messaoudi S; Faculté de Médecine et de Pharmacie d'Oujda, Université Mohammed Premier, Oujda, Maroc, Service de Néonatologie et de Réanimation Néonatale, Centre Hospitalo-Universitaire Mohammed VI, Oujda, Maroc., Babakhouya A; Faculté de Médecine et de Pharmacie d'Oujda, Université Mohammed Premier, Oujda, Maroc, Service de Pédiatrie, Centre Hospitalo-Universitaire Mohammed VI, Oujda, Maroc., Amrani R; Faculté de Médecine et de Pharmacie d'Oujda, Université Mohammed Premier, Oujda, Maroc, Service de Néonatologie et de Réanimation Néonatale, Centre Hospitalo-Universitaire Mohammed VI, Oujda, Maroc., Tajir M; Laboratoire de Génétique Médicale, Laboratoire Central, Centre Hospitalo-Universitaire Mohammed VI, BP 4806, 60049 OUJDA, Maroc, Faculté de Médecine et de Pharmacie d'Oujda, Université Mohammed Premier, Oujda, Maroc.
Publikováno v:
Annales de biologie clinique [Ann Biol Clin (Paris)] 2023 Jul 21; Vol. 81 (3), pp. 304-309.
Autor:
Twigg, SRF, Ousager, LO, Miller, KA, Zhou, Y, Elalaoui, SC, Sefiani, A, Bak, GC, Hove, H, Hansen, LK, Fagerberg, CR, Tajir, M, Wilkie, AOM
Publikováno v:
Twigg, S R F, Ousager, L B, Miller, K A, Zhou, Y, Elalaoui, S C, Sefiani, A, Bak, G S, Hove, H, Kjærsgaard Hansen, L, Fagerberg, C R, Tajir, M & Wilkie, A O M 2016, ' Acromelic frontonasal dysostosis and ZSWIM6 mutation : phenotypic spectrum and mosaicism ', Clinical Genetics, vol. 90, no. 3, pp. 270-275 . https://doi.org/10.1111/cge.12721
Acromelic frontonasal dysostosis (AFND) is a distinctive and rare frontonasal malformation that presents in combination with brain and limb abnormalities. A single recurrent heterozygous missense substitution in ZSWIM6, encoding a protein of unknown
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0e115c64ceb5604ddbc07e0398227e65
https://findresearcher.sdu.dk:8443/ws/files/121727930/Twigg_et_al_2016_Clinical_Genetics.pdf
https://findresearcher.sdu.dk:8443/ws/files/121727930/Twigg_et_al_2016_Clinical_Genetics.pdf
Autor:
Elalaoui SC; Génomique et Epidémiologie Moléculaire des Maladies Génétiques (G2MG), Centre GENOPATH, Faculté de Médecine et de Pharmacie, Université Mohammed V, Rabat, Maroc.; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Maroc., Smaili W; Génomique et Epidémiologie Moléculaire des Maladies Génétiques (G2MG), Centre GENOPATH, Faculté de Médecine et de Pharmacie, Université Mohammed V, Rabat, Maroc.; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Maroc., Van-Gils J; CHU de Bordeaux, Service de Génétique Médicale, Hôpital Pellegrin, Bordeaux, France., Fergelot P; CHU de Bordeaux, Service de Génétique Médicale, Hôpital Pellegrin, Bordeaux, France.; Université Bordeaux, Laboratoire Maladies Rares: Génétique et Métabolisme (MRGM), INSERM U1211, Bordeaux, France., Ratbi I; Génomique et Epidémiologie Moléculaire des Maladies Génétiques (G2MG), Centre GENOPATH, Faculté de Médecine et de Pharmacie, Université Mohammed V, Rabat, Maroc.; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Maroc., Tajir M; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Maroc.; Faculté de Médecine et Pharmacie, Université Mohammed Premier, Oujda, Maroc., Arveiler B; CHU de Bordeaux, Service de Génétique Médicale, Hôpital Pellegrin, Bordeaux, France.; Université Bordeaux, Laboratoire Maladies Rares: Génétique et Métabolisme (MRGM), INSERM U1211, Bordeaux, France., Lacombe D; CHU de Bordeaux, Service de Génétique Médicale, Hôpital Pellegrin, Bordeaux, France.; Université Bordeaux, Laboratoire Maladies Rares: Génétique et Métabolisme (MRGM), INSERM U1211, Bordeaux, France., Sefiani A; Génomique et Epidémiologie Moléculaire des Maladies Génétiques (G2MG), Centre GENOPATH, Faculté de Médecine et de Pharmacie, Université Mohammed V, Rabat, Maroc.; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Maroc.
Publikováno v:
African health sciences [Afr Health Sci] 2021 Jun; Vol. 21 (2), pp. 960-967.
Autor:
Lhousni S; Genetics Unit, Medical Sciences Research Laboratory, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Belmokhtar KY; Genetics Unit, Medical Sciences Research Laboratory, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Belmokhtar I; Genetics Unit, Medical Sciences Research Laboratory, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Elidrissi Errahhali M; Genetics Unit, Medical Sciences Research Laboratory, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Elidrissi Errahhali M; Genetics Unit, Medical Sciences Research Laboratory, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Boulouiz R; Genetics Unit, Medical Sciences Research Laboratory, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco.; Higher Institute of Nursing Professions and Health Technologies, Oujda, Morocco., Tajir M; Medical Genetics Unit, Central Laboratory, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Charif M; Genetics, and Immuno-Cell Therapy Team, Faculty of Sciences, University Mohammed Premier, Oujda, Morocco., Zerrouki K; Medical Genetics Unit, Central Laboratory, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Benajiba N; Department of Pediatrics, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Rkain M; Department of Pediatrics, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Babakhouya A; Department of Pediatrics, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Kouismi H; Department of Pulmonology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Thouil A; Department of Pulmonology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Latrach H; Department of Endocrinology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Amrani R; Department of Neonatology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Messaoudi S; Department of Neonatology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Ayyad A; Department of Neonatology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Sidqi Z; Transfusion Regional Centre, Oujda, Morocco., Andaloussi Serraj K; Department of Internal Medicine, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Hamaz S; Department of Internal Medicine, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Alaoui H; Department of Internal Medicine, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Bachir H; Department of Internal Medicine, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Bentata Y; Nephrology and Kidney Transplantation Unit, Mohammed VI Faculty of Medicine and Pharmacy, University Hospital, University Mohammed Premier, Oujda, Morocco., Haddiya I; Nephrology and Kidney Transplantation Unit, Mohammed VI Faculty of Medicine and Pharmacy, University Hospital, University Mohammed Premier, Oujda, Morocco., Choukri M; Biochemistry Unit, Central Laboratory, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Seddik R; Genetics Unit, Medical Sciences Research Laboratory, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco.; Hematology Unit, Central Laboratory, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Bennani A; Pathology Unit, Central Laboratory, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Dikhaye S; Department of Dermatology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Oneib B; Department of Psychiatry, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Elghazouani F; Department of Psychiatry, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., El Mahi O; Department of Vascular Surgery, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Benzirar A; Department of Vascular Surgery, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Oufkir AA; Department of Plastic Surgery, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Housni B; Department of Anesthesiology and Reanimation, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Mimouni A; Department of Gynecology and Obstetrics, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Saadi H; Department of Gynecology and Obstetrics, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Belahcen M; Department of Pediatrics Surgery, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., El Harroudi T; Department of Surgical Oncology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco., Ouarzane M; Genetics Unit, Medical Sciences Research Laboratory, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco.; Faculty of Sciences, University Mohammed Premier, Oujda, Morocco., Bellaoui M; Genetics Unit, Medical Sciences Research Laboratory, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco.
Publikováno v:
BioMed research international [Biomed Res Int] 2020 Dec 08; Vol. 2020, pp. 8812609. Date of Electronic Publication: 2020 Dec 08 (Print Publication: 2020).