Florence Marchelli
Overview
Explore the profile of Florence Marchelli including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
7
Citations
319
Followers
0
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Recent Articles
1.
Aloui C, Neumann L, Bergametti F, Sartori E, Herbreteau M, Maillard A, et al.
JAMA Netw Open
. 2024 Apr;
7(4):e247034.
PMID: 38630472
Importance: Cerebral small vessel diseases (CSVDs) account for one-fifth of stroke cases. Numerous familial cases remain unresolved after routine screening of known CSVD genes. Objective: To identify novel genes and...
2.
Bellicha A, Bel Lassen P, Poitou C, Genser L, Marchelli F, Aron-Wisnewsky J, et al.
Obes Surg
. 2022 Apr;
32(7):1-9.
PMID: 35486289
Purpose: Little is known about the consequences of COVID-19 lockdowns on physical activity (PA), eating behavior, and mental health in post-bariatric surgery (BS) patients. We aimed to analyze the relations...
3.
Bel Lassen P, Poitou C, Genser L, Marchelli F, Aron-Wisnewsky J, Ciangura C, et al.
Obesity (Silver Spring)
. 2020 Sep;
29(1):24-28.
PMID: 32875723
Objective: Obesity is a major risk factor for severe forms of coronavirus disease (COVID-19), but little is known about the post-bariatric surgery (BS) setting. The prevalence of likely COVID-19 and...
4.
Collet T, Dubern B, Mokrosinski J, Connors H, Keogh J, Mendes de Oliveira E, et al.
Mol Metab
. 2017 Oct;
6(10):1321-1329.
PMID: 29031731
Objective: Pro-opiomelanocortin (POMC)-derived peptides act on neurons expressing the Melanocortin 4 receptor (MC4R) to reduce body weight. Setmelanotide is a highly potent MC4R agonist that leads to weight loss in...
5.
Denier C, Labauge P, Bergametti F, Marchelli F, Riant F, Arnoult M, et al.
Ann Neurol
. 2006 Oct;
60(5):550-556.
PMID: 17041941
Objective: To compare clinical features of CCM1, CCM2, and CCM3 mutation carriers. Methods: A detailed clinical and molecular analysis of 163 consecutive cerebral cavernous malformation (CCM) families was performed. Results:...
6.
Riant F, De Fusco M, Aridon P, Ducros A, Ploton C, Marchelli F, et al.
Hum Mutat
. 2005 Aug;
26(3):281.
PMID: 16088919
Familial hemiplegic migraine (FHM) is an autosomal dominant form of migraine with aura. The disease is caused by mutations of at least three genes among which two have been identified,...
7.
Denier C, Labauge P, Brunereau L, Cave-Riant F, Marchelli F, Arnoult M, et al.
Ann Neurol
. 2004 Feb;
55(2):213-20.
PMID: 14755725
Cerebral Cavernous Malformations (CCM/OMIM 604214) are vascular malformations causing seizures and cerebral hemorrhages. They occur as a sporadic and autosomal dominant condition, the latter being characterized by the presence of...