Clair A Francomano
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Explore the profile of Clair A Francomano including associated specialties, affiliations and a list of published articles.
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62
Citations
1115
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Recent Articles
1.
Schubart J, Schaefer E, Mills S, Knight D, Shen C, Francomano C
Mayo Clin Proc Innov Qual Outcomes
. 2025 Jan;
9(1):100586.
PMID: 39790860
Objective: To determine the financial impact of Ehlers-Danlos syndromes (EDS) on patients in the United States by examining the medical expenses incurred by patients. Patients And Methods: We used a...
2.
Halverson C, Cao S, Perkins S, Francomano C
Genet Med Open
. 2024 Dec;
1(1):100812.
PMID: 39669244
Purpose: The extent of comorbidity and misdiagnosis had been unclear for patients with hypermobile Ehlers-Danlos Syndrome (hEDS), a hereditary connective tissue disorder. The objectives of the study were to (1)...
3.
Schubart J, Mills S, Rodeo S, Francomano C
BMC Musculoskelet Disord
. 2024 Oct;
25(1):846.
PMID: 39448975
Background: Patients with Ehlers-Danlos syndromes (EDS) often experience high rates of joint subluxations and dislocations, and associated pain that may require surgical interventions. Orthopaedic surgical management is challenging in this...
4.
Zhou Y, Shoala T, Kline A, Francomano C, Collins M, Ferguson M, et al.
Ophthalmic Genet
. 2024 Sep;
45(6):596-601.
PMID: 39264219
Importance: Alström syndrome is a rare genetic disorder characterized by retinopathy and has life-threatening complications. Alström syndrome is frequently misdiagnosed or confused with other early childhood disorders with retinopathy. Understanding...
5.
Francomano C, Maitland A, Krakow D, Maier C
Front Med (Lausanne)
. 2024 Aug;
11:1364308.
PMID: 39104859
No abstract available.
6.
Schubart J, Schaefer E, Knight D, Mills S, Francomano C
Front Public Health
. 2024 Jul;
12:1365712.
PMID: 39022417
Introduction: Patients with Ehlers-Danlos syndromes (EDS) and hypermobility spectrum disorders (HSD) have significant health challenges that are well-documented, however their impact in terms of cost is not known. Our research...
7.
Gensemer C, Beck T, Guo L, Petrucci T, Morningstar J, Kornblau I, et al.
Res Sq
. 2024 Jul;
PMID: 38947032
Hypermobile Ehlers-Danlos syndrome (hEDS) is a common heritable connective tissue disorder that lacks a known genetic etiology. To identify genetic contributions to hEDS, whole exome sequencing was performed on families...
8.
Wagner W, Doyle T, Francomano C, Knight D, Halverson C
Orphanet J Rare Dis
. 2024 Mar;
19(1):122.
PMID: 38486236
Background: The Ehlers-Danlos Syndromes (EDS) are a group of connective tissue disorders that are hereditary in nature and characterized by joint hypermobility and tissue fragility. The complex nature of this...
9.
Schubart J, Mills S, Francomano C, Stuckey-Peyrot H
Front Med (Lausanne)
. 2024 Jan;
10:1291189.
PMID: 38235272
Introduction: Individuals with Ehlers-Danlos syndromes (EDS) often have complex and multi-faceted symptoms across the lifespan. Pain and the related symptoms of fatigue and sleep disorders are common. The objective of...
10.
Henderson Sr F, Schubart J, Narayanan M, Tuchman K, Mills S, Poppe D, et al.
Neurosurg Rev
. 2024 Jan;
47(1):27.
PMID: 38163828
Craniocervical instability (CCI) is increasingly recognized in hereditary disorders of connective tissue and in some patients following suboccipital decompression for Chiari malformation (CMI) or low-lying cerebellar tonsils (LLCT). CCI is...