Fatma Majdoub
Overview
Explore the profile of Fatma Majdoub including associated specialties, affiliations and a list of published articles.
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11
Citations
13
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Recent Articles
1.
Layo-Carris D, Lubin E, Sangree A, Clark K, Durham E, Gonzalez E, et al.
Eur J Hum Genet
. 2024 Jul;
32(8):1032.
PMID: 39060653
No abstract available.
2.
Smal N, Majdoub F, Janssens K, Reyniers E, Meuwissen M, Ceulemans B, et al.
Eur J Hum Genet
. 2024 Jul;
32(11):1378-1386.
PMID: 38965372
This study aimed to uncover novel genes associated with neurodevelopmental disorders (NDD) by leveraging recent large-scale de novo burden analysis studies to enhance a virtual gene panel used in a...
3.
Layo-Carris D, Lubin E, Sangree A, Clark K, Durham E, Gonzalez E, et al.
Eur J Hum Genet
. 2024 Apr;
32(8):928-937.
PMID: 38678163
Bryant-Li-Bhoj syndrome (BLBS), which became OMIM-classified in 2022 (OMIM: 619720, 619721), is caused by germline variants in the two genes that encode histone H3.3 (H3-3A/H3F3A and H3-3B/H3F3B) [1-4]. This syndrome...
4.
Nessib D, Majdoub F, Ferjani H, Kaffel D, Maatallah K, Hamdi W
Rev Prat
. 2024 Feb;
73(8):890-894.
PMID: 38354015
CLINICAL EXAMINATION OF THE CHILD'S FOOT. The clinical examination of the child's foot is part of the musculoskeletal examination and requires a good knowledge of morphological and physiological features of...
5.
Ferjani H, Majdoub F, Nessib D, Kaffel D, Triki W, Maatallah K, et al.
Tunis Med
. 2023 Sep;
101(1):15-18.
PMID: 37682255
Introduction: The decrease in muscle function and mass is defined as sarcopenia. Known for a long time as an age-related disorder, sarcopenia is nowadays well recognized in childhood. Juvenile idiopathic...
6.
Nessib D, Ferjani H, Majdoub F, Ben Aissa R, Gzam Y, Kaffel D, et al.
Curr Rheumatol Rev
. 2023 Sep;
20(1):88-96.
PMID: 37670695
Objective: The purpose of this study was to describe the distribution of Anterior Chest Wall (ACW) arthropathies in a tertiary care center and identify clinical, biological and imaging findings to...
7.
Majdoub F, Ferjani H, Nessib D, Kaffel D, Maatallah K, Hamdi W
Ann Pediatr Endocrinol Metab
. 2023 Jul;
28(2):98-106.
PMID: 37401056
Osteogenesis imperfecta (OI) is an inherited skeletal disorder that leads to bone fragility and multiple fractures. Given advances in the genetic understanding of existing phenotypes and newly discovered mutations, therapeutic...
8.
Nessib D, Majdoub F, Ferjani Lassoued H, Kaffel D, Matallah K, Hamdi W
Joint Bone Spine
. 2023 Feb;
90(3):105539.
PMID: 36758894
No abstract available.
9.
Majdoub F, Nessib D, Ferjani H, Kaffel D, Triki W, Maatallah K, et al.
Musculoskeletal Care
. 2023 Feb;
PMID: 36757930
Introduction: Fibromyalgia (FM) is a chronic musculoskeletal condition characterised by reduced quality of life and severe limitations in daily living activities. Considering the wide spectrum of symptoms and the ineffectiveness...
10.
Rabhi E, Ferjani H, Majdoub F, Nessib D, Kaffel D, Maatallah K, et al.
Int J Rheum Dis
. 2023 Feb;
26(6):1149-1151.
PMID: 36737415
Primary pachydermoperiostosis is a rare genetic disease affecting the skin and musculoskeletal system. In contrast to secondary hypertrophic osteoarthropathy, primary pachydermoperiostosis is considered a benign condition. While a variety of...