Maryem Ferjani
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Explore the profile of Maryem Ferjani including associated specialties, affiliations and a list of published articles.
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10
Citations
26
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Recent Articles
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Hammi Y, Charfi H, Ferjani M, Sayari T, Mrad R, Gargah T
Tunis Med
. 2024 Mar;
101(8-9):704-708.
PMID: 38445406
Introduction: Distal renal tubular acidosis (dRTA) is a rare genetic disorder due to the incapacity of the α intercalated cells to excrete protons in the collecting duct. This impaired distal...
3.
Hammi Y, Ferjani M, Meddeb R, Kacem R, Sayari T, Mrad R, et al.
Indian J Nephrol
. 2024 Jan;
33(6):426-431.
PMID: 38174310
Introduction: Nephronophthisis (NPHP) is a tubulointerstitial kidney disorder with an autosomal recessive inheritance pattern. Its genetic heterogeneity contributes to phenotype variability. The most frequent etiology of juvenile nephronophthisis is a...
4.
[Functional vesico-sphincteric disorders in children: clinical, urodynamic and evolutionary profile]
Ferjani M, Hammi Y, Sayari T, Baati R, Ouns N, Gargah T
Nephrol Ther
. 2023 Nov;
19(6):497-505.
PMID: 37915195
Background: Childhood vesico-sphincteric disorders are the cause of functional and psychological disability. They are also responsible for serious uronephrologic complications akin to neuro-bladder complications. In this study, we looked for...
5.
Ferjani M, Zaimi Y, Trad N, Hammi Y, Ayari M, Ayadi S, et al.
Int Med Case Rep J
. 2023 Oct;
16:633-639.
PMID: 37794997
Background: Nephrotic syndrome (NS) is associated with a hypercoagulable state and may be complicated by thrombotic events. Venous thrombosis is well-acknowledged, while arterial thrombosis is rather unusual. Case Presentation: We...
6.
Ferjani M, Euch M, Boumediene M, Jrad M, Ben Hamida F, Turki S, et al.
J Med Case Rep
. 2023 Jul;
17(1):306.
PMID: 37455309
Background: Takayasu arteritis is a rare and chronic granulomatous vasculitis that affects the large vessels. Takayasu arteritis targets the aorta and its branches and is still of unknown etiology. It...
7.
Hammi Y, Charfi H, Ferjani M, Sayari T, Mrad R, Gargah T
Nephrol Ther
. 2022 Oct;
18(6):541-548.
PMID: 36216732
Introduction: The distal renal tubular acidosis of children is characterized by hyperchloremic metabolic acidosis with normal anion gap, hypokalemia, hypercalciuria and nephrocalcinosis. It is secondary to the inability of alpha...
8.
Ferjani M, Euch M, Hammi Y, Sayari T, Naija O, Ben Hamida F, et al.
Clin Case Rep
. 2022 Feb;
10(2):e05423.
PMID: 35169471
Acute pancreatitis may be the first manifestation in systemic lupus erythematosus or occur during evolution. It is a rare complication, which is often associated with other visceral manifestations. Outcome is...
9.
Younsi M, Kraoua L, Meddeb R, Ferjani M, Trabelsi M, Ouertani I, et al.
Eur J Med Genet
. 2018 Oct;
62(9):103550.
PMID: 30315938
Galloway-Mowat syndrome (GAMOS [MIM 251300]) is a rare autosomal recessive disorder that manifests as a combination of nephrotic syndrome, brain abnormalities and developmental delay. It is a clinically and genetically...
10.
Mahmoud I, Jellouli M, Boukhris I, Charfi R, Ben Tekaya A, Saidane O, et al.
J Pediatr
. 2017 Jun;
187:213-219.e2.
PMID: 28602379
Objectives: To evaluate the efficacy and safety of rituximab for treating pediatric systemic lupus erythematosus (pSLE). Study Design: We performed a systematic review to evaluate the efficacy and safety of...