Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Rim, Goucha"'
Publikováno v:
Clinical Case Reports, Vol 11, Iss 2, Pp n/a-n/a (2023)
Abstract Multiple myeloma (MM) results from malignant plasma cell disorder. It represents approximately 10% of hematological malignancies and it is typically diagnosed in the elderly with a median age of 70 years and has a steep increase in incidence
Externí odkaz:
https://doaj.org/article/6cd02af503564e8d98622a489f2ade9d
Autor:
Imen Rejeb, Mouna Jerbi, Houweyda Jilani, Hanène Gaied, Yasmina Elaribi, Syrine Hizem, Raja Aoudia, Hafedh Hedri, Chiraz Zaied, Salwa Abid, Hassen Bacha, Taieb BenAbdallah, Lamia BenJemaa, Rim Goucha
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-8 (2021)
Abstract Background Karyomegalic interstitial nephritis (KIN) is a rare disease entity first described by Burry in 1974. The term KIN was introduced by Mihatsch et al. in 1979. KIN is characterized by chronic tubulointerstitial nephritis associated w
Externí odkaz:
https://doaj.org/article/d2abc6e399d04ca896b1686c49138e7d
Autor:
Mouna Jerbi, Hiba Ghabi, Hanene Gaied, Mariem Khadhar, Raja Aoudia, Rim Goucha, Taieb Ben Abdallah
Publikováno v:
Clinical Case Reports, Vol 9, Iss 2, Pp 618-622 (2021)
Abstract Unexplained deep vein thrombosis may justify screening for antineutrophil cytoplasmic antibody‐associated vasculitis as it can be an unusual presentation of this disease.
Externí odkaz:
https://doaj.org/article/7f06c7b78b154dd89cc94ba5ab2947c3
Autor:
Mouna Jerbi, Rym El Fatmi, Hanene Gaied, Dorra Belloumi, Lamia Torjemane, Raja Aoudia, Rim Goucha, Taieb Ben Abdallah, Tarek Ben Othman
Publikováno v:
Clinical Case Reports, Vol 9, Iss 1, Pp 80-85 (2021)
Abstract Proliferative glomerulonephritis with monoclonal immunoglobulin deposits is a new disorder with undefined treatment modalities. We propose cyclophosphamide‐bortezomib‐dexamethasone and autologous stem cell transplantation as a therapeuti
Externí odkaz:
https://doaj.org/article/29d95b005a96447e83c8b6c4d51cfec8
Autor:
Mouna Jerbi, Mariem Sayhi, Hanene Gaied, Hafedh Hedri, Raja Aoudia, Rim Goucha, Taieb Ben Abdallah
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 3315-3320 (2020)
Abstract Renal involvement in Niemann‐Pick disease type B is very rare. Kidney check‐up and renal biopsy should be performed in any patient presented with hypertension and kidney disease. Histology identifies the lesion, the prognosis, and guide
Externí odkaz:
https://doaj.org/article/afae3315adf94f6e8b92d56a48b1ef8d
Autor:
Hayet Kaaroud, Amel Harzallah, Mariem Hajji, Soumaya Chargui, Samia Barbouch, Sami Turki, Raja Trabelsi, Rim Goucha, Fatma Ben Moussa, Hedi Ben Maiz, Fethi Ben Hamida, Ezzeddine Abderrahim
Publikováno v:
International Journal of Nephrology, Vol 2022 (2022)
Background. Renal amyloidosis is one of the main differential diagnoses of nephrotic proteinuria in adults and the elderly. The aim of this study with the most important series in our country is to contribute to the epidemiological, clinical, and eti
Externí odkaz:
https://doaj.org/article/b5467d3fb425405186a314dbb80dedbc
Autor:
Raja Aoudia, Mohamed Mongi Bacha, Mondher Ounissi, Hanene Gaied, Mouna Jerbi, Ezzedine Abderrahim, Taieb Ben Abdallah, Rim Goucha
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 30, Iss 5, Pp 1161-1165 (2019)
Light-chain deposition disease (LCDD) reoccurs almost invariably after renal transplantation, leading to early graft loss. We report a case of LCDD with monoclonal gammopathy of renal significance diagnosed in the post-transplant period in a 28-year-
Externí odkaz:
https://doaj.org/article/0f0ba5674efd4e2698ce2b6dd6fcb7f3
Autor:
Asma Zammouri, Samia Barbouch, Mariem Najjar, Raja Aoudia, Fatima Jaziri, Hayet Kaaroud, Hafedh Hedri, Ezzeddine Abderrahim, Rim Goucha, Fethi Ben Hamida, Amel Harzallah, Taieb Ben Abdallah
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 30, Iss 6, Pp 1276-1284 (2019)
Renal involvement is rare in systemic sarcoidosis. Among renal manifestations, tubulointerstitial nephritis (TIN) is the most commonly reported finding. We conducted the current study to investigate the clinical, laboratory, and histological features
Externí odkaz:
https://doaj.org/article/0d6e15552f4c42ae9763c4d6fdd16097
Autor:
Meriam Hajji, Samia Barbouch, Amel Harzallah, Hafedh Hedri, Hayet Kaaroud, Ezzedine Abderrahim, Rim Goucha, Fathi Ben Hamida, Imen Gorsane, Taieb Ben Abdallah
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 30, Iss 1, Pp 175-184 (2019)
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disease, which usually manifests in adulthood. It is characterized by the development of multiple cysts in the kidneys and many other extrarenal manifestations.
Externí odkaz:
https://doaj.org/article/b1b3d9b24bd34a068811442141750e1e
Autor:
Ikram Mami, Amel Harzallah, Hayet Kaaroud, Raja Aoudia, Fethi Ben Hamida, Rim Goucha, Taieb Ben Abdallah
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 28, Iss 4, Pp 842-850 (2017)
Diabetic nephropathy (DN) is one of the major complications of type 2 diabetes mellitus (T2DM). The diagnosis of DN is mostly clinical. Kidney biopsy is indicated only if nondiabetic renal disease (NDRD) is suspected. This study is aimed to assess th
Externí odkaz:
https://doaj.org/article/04d338bcebec46d7a025cb2ee1224e36