Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Al Mehdi, Krami"'
Autor:
Rachida Roky, Nadia Aadil, Al Mehdi Krami, Brahim Benaji, Ikram Errabih, Dana N. Abdelrahim, MoezAlIslam Ezzat Faris
Publikováno v:
Frontiers in Nutrition, Vol 9 (2022)
BackgroundDuring Ramadan, many patients with diabetes, renal, cardiovascular, gastrointestinal diseases, headaches, and epilepsy choose to fast even against their doctor's advice. The impact of this intermittent fasting on health and disease could be
Externí odkaz:
https://doaj.org/article/ce498084fcef4ca58f31a4018230c196
Autor:
Soukaina Essadssi, Al Mehdi Krami, Lamiae Elkhattabi, Zouhair Elkarhat, Ghita Amalou, Houria Abdelghaffar, Hassan Rouba, Abdelhamid Barakat
Publikováno v:
Journal of Immunology Research, Vol 2019 (2019)
Severe combined immunodeficiency (SCID) is the most severe form of primary immunodeficiency (PID), characterized by fatal opportunistic infections. The ADA gene encodes adenosine deaminase, an enzyme that catalyzes the irreversible deamination of ade
Externí odkaz:
https://doaj.org/article/e85042a2409444ac95a68039de425c73
Autor:
Hind Bouafi, Al Mehdi Krami, Imane Morjane, Kenza Slaoui, Houda Harmak, Hicham Charoute, Rachid Saile, Abdelhamid Barakat
Publikováno v:
Biochemical Genetics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eba730bae666f938d41a7c62b094747f
https://doi.org/10.1007/s10528-023-10342-8
https://doi.org/10.1007/s10528-023-10342-8
Autor:
Al Mehdi, Krami1,2 (AUTHOR), Fouad, Benhnini3 (AUTHOR), Zouhair, Elkarhat1 (AUTHOR), Boutaina, Belkady1,2 (AUTHOR), Yassine, Naasse1 (AUTHOR), Chaimaa, Ait El Cadi1 (AUTHOR), Najat, Sifeddine1,2 (AUTHOR), Hassan, Rouba1 (AUTHOR), Rachida, Roky2 (AUTHOR), Abdelhamid, Barakat1 (AUTHOR), Halima, Nahili1 (AUTHOR)
Publikováno v:
BioMed Research International. 12/31/2019, p1-15. 15p.
Autor:
Al Mehdi Krami, Aymane Bouzidi, Majida Charif, Ghita Amalou, Hicham Charoute, Hassan Rouba, Rachida Roky, Guy Lenaers, Abdelhamid Barakat, Halima Nahili
Publikováno v:
European Journal of Medical Genetics. 65:104515
Intellectual disability is characterized by a significant impaired intellectual and adaptive functioning, affecting approximately 1-3% of the population, which can be caused by a variety of environmental and genetic factors. In this respect, de novo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c4146b939c55f3685533e584552b368
https://doi.org/10.1016/j.ejmg.2022.104515
https://doi.org/10.1016/j.ejmg.2022.104515
Autor:
Al Mehdi Krami, Chorouk Ratib, Hicham Charoute, Hassan Rouba, Rachida Roky, Abdelhamid Barakat, Halima Nahili
Publikováno v:
Epilepsy research. 185
Epilepsy is a common serious brain condition characterized by the abnormal electrical activity of neurons. In most cases, epileptic patients respond to antiepileptic drugs. Approximately, one-third of patients prove medically intractable. The ABCB1 g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4738478fe22504f3dd80f4b986fc362e
https://pubmed.ncbi.nlm.nih.gov/35853334
https://pubmed.ncbi.nlm.nih.gov/35853334
Autor:
Chaimaa, Ait El Cadi, Al Mehdi, Krami, Hicham, Charoute, Zouhair, Elkarhat, Najat, Sifeddine, Hamid, Lakhiari, Hassan, Rouba, Abdelhamid, Barakat, Halima, Nahili
Publikováno v:
BioMed Research International
RRM2B gene encodes ribonucleoside-diphosphate reductase subunit M2 B, the p53-inducible small subunit (p53R2) of ribonucleotide reductase (RNR), an enzyme catalyzing dNTP synthesis for mitochondrial DNA. Defects in this gene may cause severe mitochon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f37322d30d720ed2fbeaf831e1ba5c34
https://pubmed.ncbi.nlm.nih.gov/32775440
https://pubmed.ncbi.nlm.nih.gov/32775440
Autor:
Hassan Rouba, Zouhair Elkarhat, Najat Sifeddine, Chaimaa Ait El Cadi, Abdelhamid Barakat, Hicham Charoute, Hamid Lakhiari, Halima Nahili, Al Mehdi Krami
Publikováno v:
BioMed Research International, Vol 2020 (2020)
RRM2B gene encodes ribonucleoside-diphosphate reductase subunit M2 B, the p53-inducible small subunit (p53R2) of ribonucleotide reductase (RNR), an enzyme catalyzing dNTP synthesis for mitochondrial DNA. Defects in this gene may cause severe mitochon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dd543204c34538d0e281841736c3bef
Publikováno v:
IBRO Reports. 6:S410
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a287cccb5a34090ecebb53444d8298a8
https://doi.org/10.1016/j.ibror.2019.07.1305
https://doi.org/10.1016/j.ibror.2019.07.1305
Autor:
Bouafi H; Laboratoire de Génomique et Génétique Humaine, Institut Pasteur du Maroc, Casablanca, Morocco.; Laboratoire Biologie et Santé, Centre de Recherche Santé et Biotechnologie, Faculté des Sciences Ben M'Sik, Hassan II University of Casablanca, Morocco., Bencheikh S; Laboratoire de Génomique et Génétique Humaine, Institut Pasteur du Maroc, Casablanca, Morocco., Mehdi Krami AL; Laboratoire de Génomique et Génétique Humaine, Institut Pasteur du Maroc, Casablanca, Morocco., Morjane I; Laboratoire de Génomique et Génétique Humaine, Institut Pasteur du Maroc, Casablanca, Morocco., Charoute H; Laboratoire de Génomique et Génétique Humaine, Institut Pasteur du Maroc, Casablanca, Morocco., Rouba H; Laboratoire de Génomique et Génétique Humaine, Institut Pasteur du Maroc, Casablanca, Morocco., Saile R; Laboratoire Biologie et Santé, Centre de Recherche Santé et Biotechnologie, Faculté des Sciences Ben M'Sik, Hassan II University of Casablanca, Morocco., Benhnini F; Laboratoire de Signalisation cellulaire, Faculté des Sciences Meknès, Université Moulay Ismail, Morocco., Barakat A; Laboratoire de Génomique et Génétique Humaine, Institut Pasteur du Maroc, Casablanca, Morocco.
Publikováno v:
BioMed research international [Biomed Res Int] 2019 Dec 04; Vol. 2019, pp. 1832084. Date of Electronic Publication: 2019 Dec 04 (Print Publication: 2019).