C A Francomano
Overview
Explore the profile of C A Francomano including associated specialties, affiliations and a list of published articles.
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101
Citations
2760
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Recent Articles
1.
Henderson Sr F, Francomano C, Koby M, Tuchman K, Adcock J, Patel S
Neurosurg Rev
. 2019 Jan;
42(4):915-936.
PMID: 30627832
A great deal of literature has drawn attention to the "complex Chiari," wherein the presence of instability or ventral brainstem compression prompts consideration for addressing both concerns at the time...
2.
Zhang Z, Fan J, Becker K, Graff R, Lee G, Francomano C
Osteoarthritis Cartilage
. 2006 Jan;
14(5):449-59.
PMID: 16414292
Objective: The chondron is a basic unit of articular cartilage that includes the chondrocyte and its pericellular matrix (PCM). This current study was designed to investigate the effects of the...
3.
Platte P, Papanicolaou G, Johnston J, Klein C, Doheny K, Pugh E, et al.
Am J Med Genet C Semin Med Genet
. 2003 Jul;
121C(1):71-80.
PMID: 12888987
Obesity is thought to have a genetic component with the estimates of heritability ranging from 0.25-0.40. As part of an ongoing study of obesity in the Old Order Amish, seven...
4.
Jia L, Ho N, Park S, Powell J, Francomano C
Am J Med Genet
. 2002 Mar;
106(4):275-81.
PMID: 11891679
The Skeletal Gene Database (SGD) is an integrated resource that provides comprehensive information about bone-related genes, mRNA, and proteins expressed in human and mouse, with rich links to numerous other...
5.
Peters K, Horne R, Kong F, Francomano C, Biesecker B
Clin Genet
. 2001 Oct;
60(4):283-92.
PMID: 11683774
We investigated the perceptions of and adherence to medication and physical activity guidelines in 174 adults with Marfan syndrome. Over 80% of those prescribed beta- and Ca2+-channel blockade reportedly adhere...
6.
Peters K, Kong F, Horne R, Francomano C, Biesecker B
Clin Genet
. 2001 Oct;
60(4):273-82.
PMID: 11683773
We present data from an exploratory study of 174 adults with Marfan syndrome regarding their cognitive perceptions of the condition as postulated by the self-regulatory model (Leventhal H, Benyamini Y,...
7.
Mastroianni M, Shotland L, Davis J, Ondrey F, Balog J, Rudy S, et al.
Arch Otolaryngol Head Neck Surg
. 2001 Sep;
127(9):1061-8.
PMID: 11556853
Objectives: To characterize the natural history and possible mechanisms of hearing loss in Stickler syndrome (OMIM 108300; or hereditary progressive arthro-ophthalmopathy) and to determine if the auditory phenotype is a...
8.
Rose P, Ahn N, Levy H, Magid D, Davis J, Liberfarb R, et al.
J Pediatr Orthop
. 2001 Aug;
21(5):657-63.
PMID: 11521037
Stickler syndrome is an autosomal dominant connective tissue disorder with a prevalence similar to that of Marfan syndrome. No previous study has examined hip pain or abnormalities in a large...
9.
Iwata T, Li C, Deng C, Francomano C
Hum Mol Genet
. 2001 Jun;
10(12):1255-64.
PMID: 11406607
Several gain-of-function mutations in a receptor tyrosine kinase, fibroblast growth factor receptor 3 (FGFR3), cause dwarfism in humans. Two particularly severe dwarfisms, thanatophoric dysplasia type II (TDII) and severe achondroplasia...
10.
Rose P, Levy H, Ahn N, Sponseller P, Magyari T, Davis J, et al.
Genet Med
. 2001 Jun;
2(5):278-82.
PMID: 11399208
Purpose: To compare the Berlin and Ghent diagnostic criteria for Marfan syndrome and evaluate the utility of screening for dural ectasia in the diagnosis of Marfan syndrome. Methods: Review of...