Martine Cohen-Solal
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Explore the profile of Martine Cohen-Solal including associated specialties, affiliations and a list of published articles.
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140
Citations
2177
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Recent Articles
1.
Mazzaferro S, Tartaglione L, Cohen-Solal M, Hoang Tran M, Pasquali M, Rotondi S, et al.
Clin Kidney J
. 2025 Mar;
18(Suppl 1):i15-i26.
PMID: 40083954
Uremic secondary hyperparathyroidism (SHP) refers to the biochemical abnormalities that characterize CKD-MBD. However, historically parathyroid hormone (PTH) is identified as the key culprit hormone and the essential biomarker of secondary...
2.
Rabhi B, Thomasseau S, Decrouy X, Cohen-Solal M, Deckert M, Coudert A, et al.
PLoS One
. 2025 Feb;
20(2):e0318826.
PMID: 39951467
Cherubism is a rare genetic disorder caused by SH3BP2 mutations. This sterile autoinflammatory disease is characterized by jaw osteolysis, in which bone tissue is replaced by multinucleated giant cells containing...
3.
Urena Torres P, Pimentel A, Cohen-Solal M
Am J Kidney Dis
. 2025 Feb;
PMID: 39945703
No abstract available.
4.
Alvarez-Lopez A, Tabraue-Rubio R, Daza R, Colchero L, Guinea G, Cohen-Solal M, et al.
Biomimetics (Basel)
. 2025 Jan;
10(1).
PMID: 39851774
Under benign conditions, bone tissue can regenerate itself without external intervention. However, this regenerative capacity can be compromised by various factors, most importantly related with the extent of the injury....
5.
Ali D, Mirza R, Alsarraf F, Hussein S, Abu Alrob H, Appelman-Dijkstra N, et al.
J Clin Endocrinol Metab
. 2024 Dec;
PMID: 39715351
Objective: To examine the highest certainty evidence addressing the management of X-linked hypophosphatemia (XLH) in adults to inform treatment recommendations. Methods: We searched Embase, MEDLINE, Web of Science, and Cochrane...
6.
Santamaria J, Chevallier J, Dutour L, Picart A, Kergaravat C, Cieslak A, et al.
Sci Transl Med
. 2024 Dec;
16(776):eadp3171.
PMID: 39630886
Age-related thymic involution, leading to reduced T cell production, is one of the major causes of immunosenescence. This results in an increased susceptibility to cancers, infections, and autoimmunity and in...
7.
Blandin C, Collet C, Ostertag A, Funck-Brentano T, Cohen-Solal M
J Clin Endocrinol Metab
. 2024 Nov;
PMID: 39514768
Context: Osteogenesis imperfecta (OI) is a rare genetic bone disorder characterized by recurrent fractures. In adults, the value of bone mineral density (BMD) in fracture risk is unknown. Objective: We...
8.
Mancini M, Chapurlat R, Isidor B, Desjonqueres M, Couture G, Guggenbuhl P, et al.
Calcif Tissue Int
. 2024 Sep;
115(5):591-598.
PMID: 39316135
Osteoporosis is a skeletal disorder characterized by abnormal bone microarchitecture and low bone mineral density (BMD), responsible for an increased risk of fractures and skeletal fragility. It is a common...
9.
Latourte A, Jaulerry S, Combier A, Cherifi C, Jouan Y, Grange T, et al.
Ann Rheum Dis
. 2024 Aug;
83(12):1781-1790.
PMID: 39134394
Objectives: Inflammatory mediators such as interleukin 6 (IL-6) are known to activate catabolic responses in chondrocytes during osteoarthritis (OA). This study aimed to investigate the role of a downstream target...
10.
Funck-Brentano T, Cohen-Solal M, Ducray F, Mandonnet E
Bone
. 2024 Aug;
188:117221.
PMID: 39097182
Ollier Disease (OD) and Maffucci syndrome (MS) is a rare bone disorder that affects the growth and development of the bones, with an estimated prevalence of 1 in 100,000 people....