Prévalence de la malnutrition et de l’anémie avec carence en fer absolue et fonctionnelle dans l’insuffisance rénale chronique chez des patients non dialysés et hémodialysés de la ville d’Alger (Algérie)

Autor: Hayat Laras, Farid Haddoum, Feriel-Yasmine Baghdali, Nadia Gagi, El Hadj Ahmed Koceir, Arezki Bitam

Publikováno v: Néphrologie & Thérapeutique. 18:237-246

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4a1d8f427d2546c0d1ef10c2c0dc55f3
https://doi.org/10.1016/j.nephro.2022.03.001

[Prevalence of malnutrition and absolute and functional iron deficiency anemia in nondialysis-dependent chronic kidney disease and hemodialysis Algerian patients]

Autor: Hayat, Laras, Farid, Haddoum, Feriel-Yasmine, Baghdali, Nadia, Gagi, El Hadj Ahmed, Koceir, Arezki, Bitam

Publikováno v: Nephrologietherapeutique. 18(4)

In chronic kidney disease, anemia and malnutrition coupled with inflammation as malnutrition-inflammation complex syndrom are common and considered as morbidity-mortality factors. The link between these two factors has been described at length in the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4a596a9dbdc8f639a4a4faffe41ec04b
https://pubmed.ncbi.nlm.nih.gov/35644772

The benefits and challenges of family genetic testing in rare genetic diseases—lessons from Fabry disease

Autor: Fellype C. Barreto, Nan Chen, Huda Al Khawaja, Faisal Al Ismaili, Dau-Ming Niu, Sergey Moiseev, Gheona Altarescu, Sergey Kutsev, Sheela Nampoothiri, Mirelle Kramis, Long-Sun Ro, Juan Politei, Dominique P. Germain, Farid Haddoum, Fernando Suárez-Obando, Irina Maksimova, Dung Vu Chi, Khanh Ngoc Nguyen, Fatemeh Hadipour

Publikováno v: Molecular Genetics and Genomic Medicine
Molecular Genetics and Genomic Medicine, Wiley, 2021, 9 (5), pp.e1666. ⟨10.1002/mgg3.1666⟩
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 5, Pp n/a-n/a (2021)

Background Family genetic testing of patients newly diagnosed with a rare genetic disease can improve early diagnosis of family members, allowing patients to receive disease‐specific therapies when available. Fabry disease, an X‐linked lysosomal

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc3859260d88426bdf394d02f1263bb9
https://hal.archives-ouvertes.fr/hal-03256438/file/mgg3.1666.pdf

The benefits, challenges and regional differences of family screening in rare genetic diseases: Lessons from Fabry disease

Autor: Huda Al-Khawaja, Gheona Altarescu, Mirelle Kramis, Fellype C. Barreto, Dominique P. Germain, Long-Sun Ro, Juan Politei, Faisal Al Ismaili, Sheela Nampoothiri, Sergey Kutsev, Sergey Moiseev, Farid Haddoum, Fernando Suárez-Obando, Fatemeh Hadipour, Dung C. Vu, Dau-Ming Niu

Publikováno v: Molecular Genetics and Metabolism. 129:S61-S62

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e498d8e6504e2c3938117a8f6082e39b
https://doi.org/10.1016/j.ymgme.2019.11.142

The M694I/M694I genotype: A genetic risk factor of AA-amyloidosis in a group of Algerian patients with familial Mediterranean fever

Autor: Rowaida Z. Taha, Hatem El-Shanti, R. Sari-Hamidou, Ghalia Khellaf, Djouher Ait-Idir, Mustapha Benmansour, Farid Haddoum, Bahia Djerdjouri, Faiza Bouldjennet, Mohamed Benabadji

Publikováno v: European journal of medical genetics. 60(3)

Familial Mediterranean fever (FMF, OMIM 249100) is the most common hereditary fever, resulting from mutations in MEFV. FMF is characterized by episodic febrile attacks and polyserositis. Renal AA-amyloidosis is a major complication, which often leads

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00d939b38a63cf3a22de9554837172da
https://pubmed.ncbi.nlm.nih.gov/27956278